PDF Principles and Applications of Up Converting Phosphor Technology Ruifu Yang Ebook Full Chapter
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Ruifu Yang Editor
Principles and
Applications of
Up-converting
Phosphor
Technology
Principles and Applications of Up-converting
Phosphor Technology
Ruifu Yang
Editor
123
Editor
Ruifu Yang
State Key Laboratory of Pathogen
and Biosecurity
Beijing Institute of Microbiology
and Epidemiology
Beijing, China
This Springer imprint is published by the registered company Springer Nature Singapore Pte Ltd.
The registered company address is: 152 Beach Road, #21-01/04 Gateway East, Singapore 189721,
Singapore
Contents
v
vi Contents
Abstract The upconversion (UC) luminescent materials typically refer to the mate-
rials doped with rare earth (RE) ions or transition metal ions as the luminescence
centers, among which the lanthanides ions possess superior UC efficiency. UC lumi-
nescence (UCL) is a kind of anti-Stokes process, which absorbs two or more photons
with a low energy while emits one photon with a high energy. The energy difference
between the absorbed and emitted photons are typically much larger than kT (k is the
Boltzmann constant and T is the Kelvin temperature). At present, the UCL covers
the whole visible spectrum range, which can be applied in many fields including the
solid laser, the multicolor display technology, the optical data storage, the biological
probe, and the bio-imaging. Especially in the biological field, the UC materials can
penetrate a much depth in the body benefiting from its infrared light excitation, and
meanwhile, the florescence emission from the organic molecules can be avoided.
Therefore, the UC materials yield many unique features in the detection and the
identification of the biomolecules. Here, in this chapter, a fundamental description
of the UC processes and the properties of the UC materials is provided. Section 1.1
provides a brief introduction to the UCL materials and the main UCL processes.
Section 1.2 describes the necessary mechanisms and the processes involved in the
UCL. Section 1.3 introduces the methods for improving the luminescent performance
of the UCL materials.
With the materials upon the excitation of certain energy, such as light, heat, electrical
stress, and without chemically changed, it will give the excess energy and back
to its equilibrium state. If the energy is given as the electromagnetic wave in the
visible or near visible range, the phenomenon is called as luminescence (Xu et al.
2004). Luminescent materials include the semiconductor luminescent materials, the
materials with discrete luminescent centers, some special structured materials (like
quantum well), and so on.
Generally, the material will emit photons with a smaller energy than the absorbed
photons, and the difference between the emission spectrum and the absorption spec-
trum is called as the Stokes shift (as can be seen in Fig. 1.1a). If the material emits
photons with higher energy than the absorbed photons, the difference is called as the
anti-Stokes shift. The materials with anti-Stokes shift contain UC materials, mul-
tiphoton absorption materials, hot band absorption, and triplet-triplet annihilation
(Zhu et al. 2017), which possess many unique properties in the application. The
different emission processes can be seen from Fig. 1.1b–f. In a Stokes shift process,
1 hv1
heat
1 hv1
Fig. 1.1 Stokes shift and anti-Stokes shift luminescence processes. a Absorption and emission
spectra of the Stokes shift materials; b Stokes shift luminescence process; c two-photon absorption
process; d hot band absorption process; e triplet-triplet annihilation process; f UC process (O’Brien
1946)
1 Upconversion Luminescent Materials … 3
according to the general luminescent materials, the electron at the ground state cap-
tures the energy of the incident photon and jumps to the excited state, and then it back
to the ground state by emitting a photon with lower energy and losing the excessive
energy. In the two-photon absorption process, the electron absorbs two photons with
low energy and jumps to the excited state, followed by emitting one photon with
high energy. In the hot band absorption process, the electron absorbs the hot energy
and the photon simultaneously, and then emits a photon with high energy. In the
triplet-triplet annihilation process which mainly occurs in the organic materials, two
triplet excitons with low energy generate one singlet exciton with high energy.
In the UC process, the electrons capture two or more photons by absorption or
energy transfer, and then gives photons with high energy when electrons transit to
a lower state or the ground states (the energy difference is much larger than kT).
The UC process is an important example of the anti-stokes shift, which effectively
increases the photon energy by a factor of 2 or more. Hence, the UC process can
translate the infrared light to the visible light. Different from other multiple photon
absorption process, the UC process can occur at low excitation density.
The discovery and the research of the UCL phenomenon starts from the middle of
last century. Before 1940s, it was found that a type of phosphor could emit visible light
upon excitation with infrared light (O’Brien 1946), and this phenomenon was defined
as the UCL. However, this actually is a kind of infrared stimulated luminescence.
In 1959, Bloebergen et al. proposed a design of the infrared quantum counter by
translating the infrared photons into visible photons through a sequential absorption
process of the ions (Bloembergen 1959), i.e., the sequential absorption by the excited
states of the ions, which is the earliest description of achieving UCL via excited
state absorption. In the middle of 1960s, Auzel et al. investigated the UCL from
the materials co-doped with RE ions (Auzel 1966). They discovered the UCL in
the materials with Yb3+ ions co-doped with other RE ions such as Er3+ , Tm3+ , and
Pr3+ . They attributed the UCL to the addition de Photons par Transferts d’Energie
(APTE) i.e., the energy transfer upconversion (ETU) (Cresswell et al. 1978; Zhou
et al. 2012; Auzel 1973) by exciting Yb3+ . The concept of ETU by other ions to
boost UCL increases the UCL efficiency by a large content, and also it makes the
realizing of lasers with single frequency pumping to be possible. In 1979, Chivian
et al. discovered the photon avalanche (PA) UC process in the infrared quantum
counter based on Pr3+ ions.
Besides the RE ions, some transition metal ions as the luminescent centers are
also found to be able to exhibit UCL. In 1978, Cresswell et al. utilized Re4+ ion to
replace Yb3+ ion in Yb–Tm system in Cs2 NaYCl6 matrix, which enabled the UC
from the infrared light to green light (Cresswell et al. 1978). Auzel et al. observed
UC emission from MgF2 :Ni2+ (Moncorgé et al. 2006). In addition, Ti2+ (3 d2 ) ion,
Cr3+ (3 d3 ) ion, Mo3+ (4 d3 ) ion and Os4+ (5 d4 ) ion are also proved to be able to exhibit
UCL (Auzel 2004). However, due to the strong Stokes shift of d ions in the medium
crystal field, the UCL from the transition metal ions is not as efficient as that from
the RE ions.
The UC materials were mainly utilized in the field of lasers in the initial stage
since they were discovered, which could convert the infrared light to the visible laser.
4 D. Song et al.
In 1971, Johnson et al. firstly realized the green laser from UCL using flash gun as the
pump at 77K utilizing BaY2 F8 : Yb/Ho and BaY2 F8 : Yb/Er UC materials (Xu et al.
2004). In 1987, Antipenko et al. realized the laser by UCL of BaY2 F8 : Er material
at room temperature. At present, the lasers in violet, blue, green, and red spectrum
are all be realized by using UCL at room temperature, and the highest power reaches
1238 mW and the slope efficiency reaches 46.6% (Fujimoto et al. 2013). The UCL
can also be utilized in solar cells, which can convert the infrared part of the solar
spectrum to the visible region where the solar cell is able to absorb. Hence, the
absorption of the solar spectrum by the solar cells can be improved (Huang et al.
2013). However, due to the relatively low UC efficiency of the UC materials, the
improvement in the final efficiency of the solar cells is few. The UCL also possess
advantages in other applications, such as 3D displays and anti-forgery technologies.
An extreme important application of the UC materials is in the biological fields.
With the developments of the biological technologies, labeling, imaging, and detect-
ing of the biomolecules by means of the luminescence become more and more impor-
tant. A variety of materials, including fluorescent protein, organic dyes, organometal-
lic compounds, semiconductor quantum dots and so on, can be used as the fluores-
cence probe. However, the excitation of these materials requires the photons with
high energy, which may damage the DNA and cells (Zhou et al. 2012). Moreover,
the biomolecules may also be excited simultaneously, which also emit light and
disturbs the detection. Therefore, the anti-Stokes shift materials with the ability of
converting near-infrared to visible light are of great advantages in this field. The UC
nanoparticles with lanthanide metal ions as the luminescent centers are capable of
emitting visible light at a low excitation influence, which are successfully applied in
biological labeling, imaging, and thereby.
Typically, the luminescence only involves one ground state and one excited state.
In UCL, there are many metastable excite states involved. The superposition of
the energy from these intermediate states enables the conversion from low energy
photons to high energy photons. Ions with f and d levels contain the metastable states,
and hence in theoretically, the RE ions with f level (4f, 5f) and the transition metal
ions with d level (3d, 4d, 5d) are able to create UCL.
As each type of ions has their certain energy levels, so the UC processes are
also different among different ions. There are basically three kinds of UC processes,
including the excited state absorption (ESA), the photon-avalanche (PA) and the
energy transfer upconversion (ETU, or addition de photon par transferts d’energie,
APTE). A schematic illustration of the different UC processes is shown in Fig. 1.2.
The UCL based on ESA process is realized through the sequential absorption at
the excited state, as shown in Fig. 1.2a, the electron jumps to the metastable excited
state E1 by absorbing a pump photon and then jumps the excited state E2 by absorbing
another pump photon. The transition from E2 to the ground state G creates a photon
1 Upconversion Luminescent Materials … 5
Fig. 1.2 Schematic illustration of the UC processes. a Excited state absorption (ESA); b energy
transfer upconversion (ETU); c photon-avalanche (PA). The red, dashed grey and green arrows
represent the absorption process, the energy transfer process and the emission process, respectively
with higher energy that equals to the sum of two pump photons. The UCL based
on ETU process also involves the metastable excited state absorption, whereas the
metastable excited state absorption is assisted by the energy transfer from another RE
ion instead of direct absorption of the pump photon in ESA process. As can be seen
in Fig. 1.2b, the electron of one RE ion absorbs the pump photon and jumps to the
metastable excited state E1, followed by obtaining additional energy from adjacent
ion through energy transfer and then jumping to a higher excited state E2, realizing
the energy upconversion. The PA process is shown in Fig. 1.2c, the electrons are
populated at the metastable excited state by nonresonant absorption and then jump
to a higher excited state by the resonant absorption of the pump light.
In these three processes, the UC efficiency of the ESA process is relatively low,
and the UC efficiency of the ETU process is the highest. Therefore, the efficient
UC materials are based on the ETU process. The performance of some typical UC
materials based on different processes are listed in Table 1.1 (Auzel 1973, 1975,
1990; Nakazawa and Shionoya 1970; Auzel and Pecile 1973, 1976; Page et al. 1998;
Chamarro and Cases 1988; Wu et al. 1994; Hubert et al. 1986; Salley et al. 2001;
Hehlen et al. 2001).
Table 1.1 Performance of the UC materials based on different processes (Auzel 1973, 1975, 1990;
Nakazawa and Shionoya 1970; Auzel and Pecile 1973, 1976; Page et al. 1998; Chamarro and Cases
1988; Wu et al. 1994; Hubert et al. 1986; Salley et al. 2001; Hehlen et al. 2001)
Matrix RE ions Process Temp (K) Effiiency References
(cm2 /W)n−1
YF3 Yb3+ –Er3+ APTE (ETU) 300 ∼
= 10−3 Auzel (1973)
SrF2 Er3+ ESA 300 ∼
= 10−5 Auzel (1973)
YF3 Yb3+ –Tb3+ Cooperative 300 ∼ 10−6
= Auzel (1973)
sensitization
YbPO4 Yb3+ Cooperative 300 ∼
= 10−8 Auzel (1990),
luminescence Nakazawa and
Shionoya
(1970)
CaF2 Eu3+ Two-photon 300 ∼
= 10−13 Auzel (1973)
absorption
YF3 Yb3+ –Er3+ APTE (ETU) 300 2.8 × 10−1 Auzel and
Pecile (1973)
vitroceramics Yb3+ –Er3+ APTE (ETU) 300 2.8 × 10−1 Auzel (1975)
NaYF4 Yb3+ –Tm3+ APTE (ETU) 300 3.4 × 10−2 Auzel and
Pecile (1976)
YF3 Yb3+ –Tm3+ APTE (ETU) 300 4.25 × 10−2 Auzel and
Pecile (1976)
vitroceramics Yb3+ –Tm3+ APTE (ETU) 300 8.5 × 10−2 Auzel and
Pecile (1976)
NaYF4 , Yb3+ –Er3+ APTE (ETU) 300 10−2 to Page et al.
Na2 Y3 F11 2 × 10−4 (1998)
NaYF4 Yb3+ –Er3+ APTE (ETU) 300 2.5 × 10−4 Hehlen et al.
(2001)
NaYF4 Yb3+ –Tm3+ APTE (ETU) 300 5.5 × 10−2 Page et al.
(1998)
NaYF4 Yb3+ –Tm3+ APTE (ETU) 300 3 × 10−7 Hehlen et al.
(2001)
fluorohanfnate Yb3+ –Tm3+ APTE (ETU) 300 6.4 × 10−3 Chamarro and
glass Cases (1988)
fluorohanfnate Yb3+ –Ho3+ APTE (ETU) 300 8.4 × 10−4 Chamarro and
glass Cases (1988)
vitroceramics Yb3+ –Tm3+ APTE (ETU) 300 3.5 × 10−1 Wu et al.
(1994)
vitroceramics Yb3+ –Tm3+ APTE (ETU) 300 3.6 × 10−3 Wu et al.
(1994)
ThBr4 U4+ ESA 300 2 × 10−6 Hubert et al.
(1986)
SrCl2 Yb3+ –Yb3+ Cooperative 100 1.7 × 10−10 Salley et al.
luminescence (2001)
SrCl2 Yb3+ –Tb3+ Cooperative 300 8 × 10−8 Salley et al.
sensitization (2001)
1 Upconversion Luminescent Materials … 7
Fig. 1.3 Elements with the ability of emitting UCL in periodic table of elements
(4f6 ), Gd3+ (4f7 ), Tb3+ (4f8 ), Dy3+ (4f9 ), Ho3+ (4f10 ), Er3+ (4f11 ), Tm3+ (4f12 ),
Tm2+ (4f13 )), actinides ions (U4+ (5f2), U3+ (5f5 )), and transition metal ions
(Ti2+ (3d2 ), Cr3+ (3d3 ), Mn2+ (3d5 ), Ni2+ (3d8 ), Cu2+ (3d9 ), Mo3+ (4d3 ), Re4+
(5d3 ), Os4+ (5d4 )).
high, leading to the low UC efficiency. Hence, this chapter mainly focuses on the
UC materials consisted of RE ions, especially the lanthanide ions.
(2) The parameters for evaluating the UC materials
In general, the parameters for evaluating the UCL performance of the UC mate-
rials are the quantum yield (ηQY ) and the conversion efficiency (ηCE ).
The quantum yield ηQY of the UC materials can be expressed by the following
equation
where nem and nabs represent for the numbers of the emitted photons and the absorbed
photons, respectively. In the UCL, the maximum ηQY for a two-photon absorption
scheme is 50% while for a three-photon absorption scheme is 33%. The measurement
of the absolute quantum yield of the UC materials can be found in the published
literatures including “Measurement of photoluminescence quantum yields. Review”
(The Journal of Physical Chemistry, 1971, 75, 991–1024) (Lee et al. 2004) and
“Measuring the absolute quantum efficiency of luminescent materials” (Journal of
luminescence, 2005, 115, 77–90) (Rohwer and Martin 2005).
The conversion efficiency ηCE of the UC materials can be expressed by the fol-
lowing equation
where Pem and Pabs represent for the power of the emitted photons and the absorbed
photons, respectively. As the power of the photons is determined by their wave-
lengths, so the conversion efficiency is not equal to the quantum yield.
Many factors may influence the UC efficiency of the materials, the following are
some important ones.
(a) The energy level structure and the doping concentration of the ions.
The energy difference between the higher energy level and the next lower level
effects the radiation rate of the higher energy level. The bigger the energy difference
is, the lower the non-radiation rate is, which will result a higher radiation rate and
then the higher efficient upconversion luminescence, and vice versa. Generally, a
higher content of doped ions can cause the concentration quench of the upconversion
luminescence due to the cross-relaxation between different ions. In order to avoid
this phenomenon, a low content of doped ions and a high excitation can be combined
to achieve efficient upconversion luminescence (Kaminskii 2013).
The effect of the host matrix includes the following aspects. (I) The phonon energy
of the host matrix will affect the multiphonon relaxation and the phonon-assisted
energy transfer of excited RE ions, which is one of the key factors related with the
1 Upconversion Luminescent Materials … 9
upconversion efficiency. (II) The crystal symmetry of the host matrix will influence
the electric dipole transition probability of lanthanide ions. Therefore, lanthanide
ions with different radius are doped to induce the lattice expansion or shrinkage to
adjust the crystal symmetry of the host matrix (Han et al. 2014; Zhao et al. 2013).
Or co-doping the transition metal ions increases the electron–phonon interaction of
lanthanide ions by the d orbit effect of transition metal ions (Han et al. 2014; Tang
et al. 2015).
By increasing the temperature, the multiphonon relaxation rate of the higher energy
level also increases, whereas the efficiency of upconversion luminescence will
decrease. In addition, the energy transfer probability assisted by absorbed phonons
will increase and thereby emitted phonons will decrease when the temperature
increases.
The energy level structure and the electron transition between energy levels of RE
ions are determined by the system Hamiltonian. For a free trivalent RE ion, the
Hamiltonian is as follows
H E is the Hamiltonian of the electron system, and H S.O. refers to the most important
magnetic interaction (spin-orbit interaction) of f electrons. H O , as a main part of H E ,
describes the interaction between each valence electron with the atomic kernel, which
provides the electronic orbits of the 4f valence electrons forming the (4f)N electron
configuration. V is the perturbation term, describing the Coulomb interactions among
the 4f electrons. V makes the (4f)N electron configuration splitting to a series of states
with different energy, each of which can be marked with L and S (the LS terms).
10 D. Song et al.
Generally, the mixed configuration induced by V is not obvious and can be ignored.
For a large number of 4f electrons, L and S may represent more than one state, and
an additional quantum number α is introduced.
The Hamiltonian H S.O describing the spin-orbit interaction, which can be under-
stood as magnetic dipole–dipole interactions between the spin and angular moment
of the electrons, can be expressed as follows,
HS.O. = ξ(ri )li · Si (1.4)
i
H electron-static field describes the interaction between electrons and static field. Ionic
energy levels split under the influence of the static field produced by the crystalline
environment, as shown in Fig. 1.4 which is the 4f energy levels of trivalent RE ions.
Meanwhile, the interaction between ions with the static field will influence the free
ion Hamiltonian, which results in the change of the whole energy levels.
H electron-lattice describes the influence of lattice waves on electrons. It will influence
the light transition form and intensity and relates with the non-radiative relaxation.
H lattice is the lattice vibration energy expressed by phonon mode.
1 Upconversion Luminescent Materials … 11
35000
6P
30000 7/2 1D
2
5G
25000 6
5D
2
Energy (cm -1)
1G
5D 4
3P 4
20000 0 5D
1 4F 5S
1D 9/2 2
2
4G 5F 4F
5/2 5D 4 9/2
15000 0 6F
3/2 5I 4I
3F
2,3
4 9/2 3H
1G 5I 4
4 6F 5 4I
5I 11/2 11/2 2F
3H 5/2
10000 3F
4F
3/2
1 5I
6 5
4 4I 5I 7F 4I
15/2 5 0 13/2 3F
7F 5I 4
5I 6 7
4I 7
5000 2F
7/2 13/2
3H
5 4I
11/2 6H
13/2
0
Ground= 2F5/2 4I
9/2
5I
4 6H 7F 7F 6H 5I 4I 2F
3H 3H
state 4 5/2 0 6 15/2 8 15/2 6 7/2
La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu
n= 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14
(1) The basic principles on the transition (Huang 2002; Yen and Selzer 1981)
D represents the electric dipole moment operator μ or the magnetic dipole moment
operator M, the summation extends over all states of |i and | f .
When the total spin of |i state and | f state is different, the matrix element is
equal to zero. The spin selection rule for the electron transition is S = 0. However,
the spin is not an effective quantum number due to the spin-orbit coupling, so the
spin selection rule is not strictly followed. Generally, the spin allowed transition (S
= 0) is stronger than the spin forbidden transition (S = 0).
In spectroscopy, another dimensionless parameter called the oscillator strength is
defined as
1 8π 2
2
f = | f |D|i| (1.8)
gi 3he2
12 D. Song et al.
In this
equation,
m is the mass of an electron, v is the frequency of the transition,
hv = E f − E i , gi is the degeneracy of the state |i, for RE ions, it usually equals
to 2J + 1.
The light absorption intensity Iv (l) is determined by measure the light absorption
coefficient α(v):
Iv (l) is the transmission intensity of light v through the thickness l. The absorption
cross section is defined as σ (v) = α(v)/N , where N is the number of the lumines-
cence center per volume. If the absorption is due to the electric dipole transition,
there is the relationship between σ (ν), f ED and S ED :
2
−1 1 π e2 n2 + 2 1
σ (v)dv = N σ (v)dv = · fE D
4π ε0 mc 3 n
2
1 8π 3 v n2 + 2 1 1
= · SE D (1.10)
4π ε0 3hc 3 n ga
If the radiation transition is the electric dipole transition, the Einstein spontaneous
emission rate A between the state |i and | f is:
2
1 8π 2 v 2 e2 n2 + 2
A E D (v) = · n fE D
4π ε0 mc3 3
2
1 64π 4 v 2 n2 + 2 1
= ·n SE D (1.11)
4π ε0 3hc 3 3 ga
The above equation also fits to the magnetic dipole transition when substitute f ED
and S ED by f MD and S MD ,((n2 + 2)/3)2 by n2 , respectively.
The relationship between the Einstein stimulated radiation rate B with the Einstein
spontaneous emission rate A is:
The energy level of all free RE ions is constituted by the same (4f)N configurations
and has the same parity. Electric dipole transitions within (4f)N configurations are
forbidden and magnetic dipole transition is allowed. When RE ions were doped in
crystals, their luminescence were detected thanks to the contributions from config-
urations of opposite parity of (4f)N−1 5d to the wave functions of the (4f)N configu-
rations by the odd parity terms of the crystalline potential expansion. Therefore, the
matrix elements of electric dipole operator between the mixed-parity eigenfunctions
are nonzero. Then the equation of transition rates within (4f)N configurations was
deduced by B. R. Judd and G. S. Ofelt starting from the point of mixed-parity con-
figurations due to the static crystal field effect, which is called as J–O theory and is
the only one theory to calculate the luminescence intensity of RE ions. Also it can
be used in amorphous materials.
Adopting the static model, the system Hamiltonian should be H = H f + V, H f is
the Hamiltonian of free ions, V is the crystalline potential and comes from the inter-
action between electrons and crystal field. Judd and Ofelt thought that the expression
of the crystalline potential can be separated into even parity and odd parity parts. The
odd parity parts caused the mixing of the opposite parity of (4f)N−1 (n’l’) configura-
tions into (4f)N configuration, then electric-dipole transitions happened. Therefore,
it required that the coefficient Atp (t is odd values) is not equal completely to zero
(Non central coordination field):
V = Veven + Vodd = At p D (t)
p
t, p
N
4π
D (t)
p = r tj [ ]1/2 · Yt, p (θ j , φ j ) (1.13)
j
(2t + 1)
β| is the wavefunction of different parity excited configurations, E(A) and E(β)
is the eigenvalues of A| and β|, respectively.
The electric dipole moment operator P can be decomposed as (P(1)q ) in the direction
of x, y, and z, so there are transitions corresponding to various polarization. When
q = 0, it is π polarization, q = ±1 corresponds to the σ polarization. The matrix
elements of P(1)q is not equal to zero due to the mixing of odd parity.
(1) A|Vodd |β β Pq(1) A A Pq(1) β β|Vodd |A
B Pq B = − − (1.16)
β
E(A) − E(β) β
E(A ) − E(β)
Here the summation is for all |β configurations with opposite parity. It is diffi-
cult to calculate above equation because that all E(β), |β and the odd components
of crystal field contribute to the mixing of opposite parity configurations. At the
same time in 1962, Judd and Ofelt independently made an important hypothesis to
simply this calculation. They used a constant E irrelevant with ϕ, J, M and β to
substitute E(A)–E(β) and E(A’)–E(β). It means that the energy splitting in the same
configuration is far smaller than the energy difference of different configurations.
Therefore, to calculate above equation 1.16 we can get all J–O parameters. How-
ever, it is difficult to distinguish exactly the absorption lines corresponding to the
transition between the components of two levels of the RE ions doped in crystal or
amorphous materials. In experiment, it needs to sum the transition probabilities of
all components of two levels, which is the line strength:
2
j j =
S ed |b| D|a|2 = e2 Ωλ f N ϕ J U (λ) f N ϕ J (1.17)
a,b λ=2,4.6
U (λ) is the reduced matrix element, which can be referred from the reference
(Zhao et al. 2013) or other references. Ω λ is not related to J, but only related to the
crystal field parameters, so it can be used as the adjusted parameter.
process, the electron at the ground state (G) of the luminescence center absorbs a
photon with the frequency of ω1 and is excited to the metastable excited state E2 .
Subsequently, the electron at E2 absorbs another photon with the frequency of ω2
and is excited to the higher excited state E3 . The electron transition from E3 to G
gives a photon with the frequency of ω. It is clear that ω > ω1 , ω2 . Hence, the UCL
is achieved.
The electron transition in the ESA process can be either direct transition or
phonon-assisted transition. Generally, the ESA process requires two pump lasers,
one of which resonates with the ground state absorption (GSA) and the other one
resonates with the excited state absorption. In some conditions, one laser pump may
also be possible, including (i) the absorption energy of the ground state and the
excited state are uniform or the absorption energy difference can be compensated by
the phonons, and (ii) the transitions are in homogeneously broadened in some irreg-
ular materials. The ESA process occurs inner one ion, and hence, it is not affected
by the concentration of the RE ions which avoids the losses induced by the energy
transfer between RE ions.
(2) Examples of the UCL based on ESA process (Xu and Su 2004)
With the pump by Kr+ ion laser at 647.1 nm, the luminescence from the excited states
3
H4 , 1 G4 , 1 D2 , and 1 I6 of LaF3 :Tm3+ can be observed, as shown in Fig. 1.6. The UCL
from the higher excited states (1 G4 , 1 D2 or 1 I6 ) is caused by the ESA process. The
excitation steps are as follows. The electron absorbs the first photon and jumps from
the ground state 3 H6 to the excited state 3 F2 . As the states 3 F2 , 3 F3, and 3 H4 are very
close, the electron quickly relaxes to the state 3 H4 . The electron may absorb another
photon and jumps from the state 3 H4 to 1 D2 , or backs to the ground state by giving
an infrared photon. The electron at the state 1 D2 may back to the ground state or the
state 3 F4 by giving a visible photon. The electron at the state 3 F4 may absorb other
one or two photons and jumps to much higher states (1 G4 or 3 P1 ). As the states 3 P1
and 1 I6 are very close, so the electron at 3 P1 will quickly relax to 1 I6 . Therefore, the
UCL can be observed from the excited states 1 G4 , 1 D2 , and 1 I6 .
16 D. Song et al.
The photon avalanche (PA, or absorption avalanche) process was firstly discovered in
LaCI3 :Pr3+ material system (Chivian et al. 1979). In this system, the pump frequency
is resonant to the excited state absorption from 3 H5 to 3 P1 state of Pr3+ ion. Beyond a
critical pump intensity, the luminescence from 3 P1 or 3 P0 state of Pr3+ ion is enhanced
sharply, and accordingly the absorption of the pump is also increased sharply. This
is the PA phenomenon. The PA process was also revealed in other material systems
like LaBr3: Sm3+ (Krasutsky 1983) and CeCl3 :Nd3+ (Pelletier-Allard and Pelletier
1991). As PA produces population in an excited state with energy exceeding that of
the pump photon, it is possible to realize UCL.
The photon avalanche process combines the excited state absorption and the
energy transfer processes. As shown in Fig. 1.7, it shows the condition in a four-
level system, where G, m1 , and m2 are the ground state and two metastable states,
respectively, E is the excited state emitting photons. The pump laser with the fre-
quency of ω enables the resonant absorption from m1 to E, which is a characteristic
of PA process. Though the ground state absorption may be not resonant to the pump,
a small amount of electrons may absorb the pump photons and jumps to the excited
states between E and m2 , then relax to m2 . The electron at m2 jumps to m1 and simul-
taneously transfers the energy to an electron at the ground state G to m1 . Meanwhile,
the electron transition from E to m1 may excite two electrons from G to m1 . Hence,
the resonant pumping of electrons from m1 to E makes the electron population at E
1 Upconversion Luminescent Materials … 17
m2
'
ω
m1
increasing like avalanche. The electron transition from E to G gives a photon with a
higher frequency of ω (ω > ω ), leading to the UCL.
Another characteristic of PA process is an excitation power threshold (Kueny et al.
1989; Guy et al. 1994), which divides the excitation into two different stages. In the
condition of a weaker excitation than the threshold, the UCL is quite weak and the
crystal is transparent for the pump. In the condition of a stronger excitation than the
threshold, the intensity of the UCL is enhanced by several orders and the absorption
of the pump light is strong. Moreover, the concentration of the RE ions shall be high
enough to enable the population of the metastable states by energy transfer.
The UC laser based on PA process avoids the photo-induced degradation of host
materials observed in the laser based on the down-conversion emission by violet
light excitation. Compared with the laser based on ESA process, the laser based on
PA process only requires one resonant transition, it means only pump light needed.
Hence, PA process is also an ideal pump scheme for the UC laser with high dopant
concentration. More information on the mechanisms and the application in lasers of
the PA process can be found in the review of《Photon avalanche upconversion in
rare earth laser materials》(Joubert 1999).
In CdF2 :Tm3+ system, the PA-induced UC emission, which converts the red excita-
tion light to the blue light, can be observed at 77K. The pump light with a wavelength
of 647.7 nm is resonant to the 3 H4 –1 D2 transition from Tm3+ ions, which produces
the blue emission peaking around 450 nm (Ofelt 1962). In LiYF4 :Tm3+ system, the
PA-induced UC emission is also proved, which converts the NIR excitation light to
the UV light (Kueny et al. 1993). In this system, the pump photons with a wavelength
of 1.04 μm enables the avalanche excitation of 3 F4 –3 F2 transition, which populates
the energy level with a wavenumber of 15,000 cm−1 ; subsequently, the population
of the high energy state with a wavenumber of 35,000 cm−1 is realized by multiple
energy transfer processes, leading to the UV emission.
18 D. Song et al.
The energy transfer can occur between either same kind or different kinds of RE
ions. Thus, the UCL based on the energy transfer includes two different types (Xu
et al. 2004), (i) the energy transfer between the same kind of ions at the excited states,
and (ii) the sequential energy transfer between different kinds of ions (the generally
defined energy transfer upconversion (ETU) process). Similar to the definitions in
the phosphor field, the ions which absorb light and give the energy are called as the
sensitizer (or donor), while the ions accepting the energy and giving the photons are
called as the activator (or acceptor).
There are four types of energy transfer process that include the resonant radiative
energy transfer, the resonant non-radiative energy transfer, phonon-assisted non-
radiative energy transfer, and the cross-relaxation between the same kind of ions. In
the resonant radiative energy transfer, the sensitizer emits a photon, followed by the
photon absorption by the activator. This type of energy transfer depends on the shape
of the sample, and also the overlap between the emission spectrum of the sensitizer
and the absorption spectrum of the activator. The resonant radiative energy transfer
is rarely employed in the UCL.
The resonant non-radiative energy transfer, i.e., the Föster energy transfer, is the
most important type in UCL. In this scheme, the sensitizer ion at its excited state
transfers its energy to the acceptor ion through the Coulomb interactions before it is
able to emit a photon, and the overlap of the wave functions between the two ions are
not essential. Föster firstly considered this type of energy transfer as dipole–dipole
interactions (Föster 1948). He assumed that the interaction is strongest in the con-
dition that the electric dipole transitions are all permitted in these two ions (Auzel
1973). The transfer probability is given by:
2π e 0 2
PS A = S A |HS A | S 0 Ae ρ E (1.18)
S, A the sensitizer center and the activator center, respectively
HAS interaction Hamiltonian
e, o the excited state and the ground state, respectively
ρE density of states provided by the vibrational motion contributing to the line
broadening of the transition.
E1 E1 E1
hv1 hv hv
hv hv1
energy from sensitizer ions (Auzel 1966), as shown in Fig. 1.9b. This kind of energy
transfer is also defined as the sequential energy transfer. The transfer probability can
then be rewritten as:
2π e 0 2
PS A = S A |HS A | S 0 Aee ρ E (1.21)
where S 0 Aee the wave function for the system where the sensitizer is in its ground
state and the activator in a doubly excited state.
The energy transfer from the sensitizer to the activator decreases the electrons and
lifetime of the excited state of the sensitizer, resulting in the weak emission or the
absence of the luminesce from the sensitizer ions. As the excited state of the sensitizer
is excited by a photon with low energy, the energy transfer enables the activator ion
to jump to its high excited states of which the energy may be higher double, triple
or even quadruple than that of the excitation photons. When the activator ion jumps
from the high excited state to its lower state, it will emit a photon with high energy.
As the activator contains several excited states and only one ground state, the electron
population of higher excited states will be achieved by the energy transfer through
the energy superposition of several pump photons. This implies the probability of
the multiphoton upconversion. Thereby, people understood that the energy difference
between different levels, instead of the absolute energy of the energy level, is more
important to the energy transfer between ions. The energy transfer between the same
kind of ions is also called the cross-relaxation upconversion, as shown in Fig. 1.9c
Besides the successive energy transfer described above, the cooperative effect
of ions by their mutual interaction also be used to explain anti-Stokes lumines-
1 Upconversion Luminescent Materials … 21
cence, such as the cooperative sensitization (Fig. 1.9d) and cooperative luminescence
(Fig. 1.9e). In a cooperative sensitization process as can be seen from Fig. 1.9e, the
united two excited sensitizer ions transfer their energy to an activator ion meanwhile,
which enable the acceptor ion to jumps to its high excited energy level. The coopera-
tive luminescence is the emission in a single process of one photon from two excited
interacting ions.
All of the above energy transfer processes are due to the interactions between
the RE ions, so they depend on the concentrations of the RE ions. If the energy
between the sensitizer and the activator is mismatched in the energy transfer process,
the energy difference can be compensated by the phonon. In practice, the energy
difference of the different energy transfer process can be used to estimate which
energy transfer process is the most probable. The outstanding advantage of utilizing
energy transfer process to realize the upconversion laser is that it only requires single
pump with a certain frequency.
The UCL of Pr3+ ion based on ETU process. Upon the pump of two lasers with
the wavelength of 1017 nm and 835 nm, respectively, Pr3+ ions doped in fluoride
host can emit visible lights at different wavelengths. As shown in Fig. 1.10 of the
upconversion processes of Pr3+ in fluoride glass LaF3 , the excitation processes are
as follows. The electron at ground state 3 H4 absorbs a photon with the wavelength of
1017 nm and jumps to the excited state 1 G4 , followed by jumping to upper excited
states 3 P0 , 3 P1, and 1 I6 upon excitation at 835 nm. The transitions from 3 P0 , 3 P1, and
1
I6 states to different lower excited states exhibit the UCL at different wavelengths,
as can be seen in Fig. 1.10.
The UCL from Yb3+ –Tm3+ system based on ETU process. Figure 1.11
schematically illustrates the UC process based on the energy transfer from Yb3+
ions to Tm3+ ions. Yb3+ ions are excited by an infrared light with a wavelength of
980 nm, accompanied by the electron transition from the ground state 2 F7/2 to the
excited state 2 F5/2 , which transfer the energy to the neighboring Tm3+ ions and back to
the ground states. The Tm3+ ions are excited from the ground state 3 H6 to the excited
state 3 H5 . Afterward, the Tm3+ ions at the excited state 3 H5 are further excited to
the upper excited states by absorbing the energy transferred from neighboring Yb3+
ions. The Tm3+ ions at the upper excited states back to the ground state and emit the
UCL.
In the UCL process, one or more UC process may be involved. For example, in Yb–Er
co-doped system, ETU and ESA probably simultaneously exist in the UCL process.
The sequential absorption in the ESA process is due to the combination absorption
by many excited states of the activator ions, whereas in the ETU process is due to
the absorption by the ground state of the sensitizer ions (the excited state absorption
relies on the energy transfer). Hence, in ETU process, the excitation spectra derive
from the sensitizer ions, and this feature can be utilized to distinguish whether ETU
1 Upconversion Luminescent Materials … 23
or ESA is the main processes creating UCL (Nadort et al. 2016). For instance, in
NaYF4 :2%Er, 18%Yb system (Suyver et al. 2005), only the transition 2 F7/2 → 2 F5/2
of Yb3+ ions is observed in the excitation spectrum, which means that the UCL of
this system is mainly due to ETU from the sensitizer Yb3+ ions to the activator Er3+
ions. In NaYF4 :2%Er system (Suyver et al. 2005), the excitation spectrum contains
many transitions such as 4 I15/2 → 4 I1/2 and 4 I11/2 → 4 F7/2 , which implies that ESA
is the main process for the sequential absorption of photons by Er3+ ions.
The light absorption rate in different upconversion processes is also different. In
ESA UC process, the absorption by the ground state and metastable excited states
occurs in nanosecond time scale (Zhao et al. 2016), and thus, the time to UCL
is also fast. The corresponding transient photoluminescence (PL) decays mono-
exponentially with the elapsing time, as shown in Fig. 1.12a. In ETU process, it
requires a long time as the luminescence of the activator can be produced under at
least twice energy transfer procedure. In the related transient PL, the PL intensity
firstly increases with the elapsing time (generally in the time scale of microseconds)
and then decreases. Hence, in the decay profile of the UCL governed by ETU process,
the decay rate of the sensitizer, the rate of the energy transfer and the PL decay rate
of the activator are all included. In the material system in which simultaneously exist
two kinds of UC processes, the PL intensity of the activator decays bi-exponentially
(Fig. 1.12b).
The PA process features an excitation threshold, so its existence can be evaluated
by the relation between the luminescence intensity and the excitation power. The
UCL intensity I generally changes exponentially with the excitation power P, as
shown in Fig. 1.13a (Sangeetha and van Veggel 2009), and no threshold power can
be observed. In contrast, in PA process, the intense UCL can only be observed upon
a certain excitation power. As can be seen from Fig. 1.13b (Singh et al. 2011),
which shows the UCL based on the PA process from LaF3 :Er3+ /Yb3+ system. It is
clear that in condition of a lower excitation power than the threshold, few UCL can
be observed, while the non-radiative and the downconversion processes govern the
transitions. Upon the threshold, the UCL intensity is increased sharply, indicating
(a) (b)
Intensity (a.u.)
Intensity (a.u.)
GSA/ESA GSA/ETU
Time (a.u.)
Time (a.u.)
Fig. 1.12 The evolution of upconversion luminescence over time after the excitation from
a GSA/ESA and b GSA/ETU processes
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It had engaged itself, before I commenced my observations, upon a
roast gigot of mutton, which happened to lie near it. This it soon
nearly finished. It then cast a look of fearful omen at a piece of cold
beef, which lay immediately beyond, and which, being placed within
reach by some kind neighbour, it immediately commenced to, with
as much fierceness as it had just exemplified in the case of the
mutton. The beef also was soon laid waste, and another look of
extermination was forthwith cast at a broken pigeon-pie, which lay
still farther off. Hereupon the eye had scarcely alighted, when the
man nearest it, with laudable promptitude, handed it upwards.
Scarcely was it laid on the altar of destruction, when it disappeared
too, and a fourth, and a fifth, and a sixth look, were successively cast
at other dishes, which the different members of the party as
promptly sent away, and which the Mouth as promptly dispatched.
By this time all the rest of the party were lying upon their oars,
observing with leisurely astonishment the progress of the surviving,
and, as it appeared to them, endless feeder. He went on, rejoicing in
his strength, unheeding their idleness and wonder, his very soul
apparently engrossed in the grand business of devouring. They
seemed to enter into a sort of tacit compact, or agreement, to indulge
and facilitate him in his progress, by making themselves, as it were,
his servitors. Whatever dish he looked at, therefore, over the wide
expanse of the table, immediately disappeared from its place. One
after another, they trooped off towards the head of the table, like the
successive brigades which Wellington dispatched, at Waterloo,
against a particular field of French artillery; and still, dish after dish,
like said brigades, came successively away, broken, diminished,
annihilated. Fish, flesh, and fowl disappeared at the glance of that
awful eye, as the Roman fleet withered and vanished before the
grand burning-glass of Archimedes. The end of all things seemed at
hand. The Mouth was arrived at a perfect transport of voracity! It
seemed no more capable of restraining itself than some great engine,
full of tremendous machinery, which cannot stop of itself. It had no
self-will. It was an unaccountable being. It was a separate creature,
independent of the soul. It was not a human thing at all. It was
everything that was superhuman—everything that was immense—
inconceivably enormous! All objects seemed reeling and toppling on
towards it, like the foam-bells upon a mighty current, floating
silently on towards the orifice of some prodigious sea-cave. It was
like the whirlpool of Maëlstrom, everything that comes within the
vortex of which, for miles around, is sure of being caught,
inextricably involved, whirled round and round and round, and then
down that monstrous gulph—that mouth of the mighty ocean, the
lips of which are overwhelming waves, whose teeth are prodigious
rocks, and whose belly is the great abyss!
Here I grew dizzy, fainted, and—I never saw the Mouth again.
RICHARD SINCLAIR;
OR, THE POOR PRODIGAL IN THE AISLE.
By Thomas Aird.
Chapter I.
With the calmness almost of despair, when the closing eve took
away his chance of seeing any more stray passengers that day, the
poor youth groped his way to his marble slab, and again sat down
with a strange vacuity of heart, as if it would refuse further thought
of his dismal situation. A new fear came over him, however, when
daylight thickened at the grated window of his low room, and the
white marbles grew dark around him. And not without creeping
horror did he remember that from this very aisle it was that old
Johnny Hogg, a former sexton, was said to have seen a strange vile
animal issue forth one moonlight night, run to a neighbouring
stream, and after lapping a little, hurry back, trotting over the blue
graves, and slinking through beneath the table stones, as if afraid of
being shut out from its dull, fat haunt. Hurriedly, yet with keen
inspection, was young Sinclair fascinated to look around him over
the dim floor; and while the horrid apprehension came over him,
that he was just on the point of seeing the two eyes of the gloating
beast, white and muddy from its unhallowed surfeits, he drew up his
feet on the slab on which he sat, lest it should crawl over them. A
thousand tales—true to boyish impressions—crowded on his mind;
and by this rapid movement of sympathetic associations, enough of
itself, while it lasts, to make the stoutest heart nervous, and from the
irritation of his body from other causes, so much was his mind
startled from its propriety that he thought he heard the devil ranging
through the empty pews of the church; and there seemed to flash
before his eyes a thousand hurrying shapes, condemned and fretted
ghosts of malignant aspect, that cannot rest in their wormy graves,
and milky-curdled babes of untimely birth, that are buried in
twilights, never to see the sun.
Soon, however, these silly fears went off, and the tangible evil of
his situation again stood forth, and drove him to renew his cries for
assistance, and his attacks upon the door, ere he should be quite
enfeebled by hunger and disease. Again he had to sit down, after
spending his strength in vain.
By degrees, he fell into a stupor of sleep, peopled with strange
dreams, in all of which, from natural accordance with his waking
conviction that he had that day seen his mother’s burial, her image
was the central figure. In danger she was with him—in weariness—in
captivity; and when he seemed to be struggling for life, under
delirious fever, then, too, she was with him, with her soft assuaging
kiss, which was pressed upon his throbbing brow, till his frenzy was
cooled away, and he lay becalmed in body and in spirit beneath her
love. Under the last modification of his dream, he stood by confused
waters, and saw his mother drowning in the floods. He heard her
faintly call upon his name; her arms were outstretched to him for
help, as she was borne fast away into the dim and wasteful ocean;
and, unable to resist this appeal, he stripped off his clothes and
plunged in to attempt her rescue. So vivid was this last part of his
vision, that in actual correspondence with the impulse of his dream,
the poor prodigal in the aisle threw off his clothes to the shirt to
prepare himself for swimming to her deliverance. One or two cold
ropy drops, which at this moment fell from the vaulted roof upon his
neck, woke him distinctly, and recalled him to a recollection of his
situation as a captive. But being unable to account for his being
naked, he thought that he had lost, or was about to lose, his reason;
and, weeping aloud like a little child, he threw himself upon his
knees, and cried to God to keep fast his heart and mind from that
dismal alienation. He was yet prostrate when he heard feet walking
on the echoing pavement of the church; and at the same time a light
shone round about him, filling the whole aisle, and showing
distinctly the black letters on the white tombstones.
His first almost insane thought was that a miraculous answer was
given to his prayer, and that, like the two apostles of old, he had won
an angel from heaven to release him from his midnight prison. But
the footsteps went away again by the door, and ceased entirely;
whilst at the same time the light was withdrawn, leaving him to curse
his folly, which, under an absurd hope, had lost an opportunity of
immediate disenthralment. He was about to call aloud, to provoke a
return of the visitation, when, through the grated window of the
aisle, he observed a light among the graves, which he set himself to
reconnoitre. It was one of those raw, unwholesome nights, choked up
with mists to the very throat, which thicken the breath of old men
with asthma, and fill graveyards with gross and rotten beings; and,
though probably not more than twenty yards distant, Sinclair could
not guess what the light was, so tangled and bedimmed was it with
the spongy vapours.
At length he heard human voices, and was glad to perceive the
light approaching his window. When the men, whom he now saw
were two in number, had got within a few yards of him, he called out,
—
“I pray you, good people, be not alarmed; I have been locked up in
this aisle to-day, and must die of hunger in it if you do not get me
out. You can get into the church, and I doubt not you will find the key
of this aisle-door in the sexton’s closet. Now, I hope you have enough
of manhood not to let me remain in this horrid place from any silly
fears on your part.”
Instead of answering to this demand, the fellows took instantly to
their heels, followed by the vehement reproaches of our hero, whose
heart at the same time was smitten by the bitter reflection, that every
chance of attracting attention to his captivity was likely to be
neutralized by the superstitious fears of such as might hear him from
his vault. In a few minutes the light again approached, and after
much whispering betwixt themselves, one of the men demanded who
and what the prisoner was.
“I can only tell you farther,” replied Sinclair, “that I fell asleep in
this place during the sermon,—no very creditable confession, you will
observe,—and that, when I awoke, I found myself fairly entrapped.”
The men retired round the church, and with joy Richard heard
next minute the rattling of the keys as they were taken from the
sexton’s closet. In another minute he heard the door of his dungeon
tried; it opened readily; and with a start, as if they thought it best at
once to rush upon their danger, his two deliverers, whom he
recognised to be of his native village, advanced a little into the aisle,
the foremost bearing the light, which he held forward and aloft,
looking below it into the interior, to be aware for what sort of captive
they had opened. No sooner did Sinclair stand disclosed to them,
naked as he was to the shirt—for he had not yet got on his clothes—
than the sternmost man, with something between a yell and a groan,
bended on his knees, whilst his hair bristled in the extremity of his
terror, and catching hold of his companion’s limbs, he looked
through betwixt them upon the naked spirit of the aisle. The
foremost man lowered the light by inches, and cried aloud,—
“Fear-fa’ me! take haud o’ me, Geordie Heart! It’s the yellow dead
rising from their graves. Eh! there’s the lightning! and is yon no an
auld crooked man i’ the corner?”
“Will Balmer! Will Balmer! whaur are ye?” cried the other, from
between Will’s very knees, which, knocking upon the prostrate man’s
cheeks, made him chatter and quiver in his wild outcry.
“Oh! there’s the lightning again! Gin we could but meet wife and
bairns ance mair!” ejaculated the foremost man.
“Lord have mercy on my widow and sma’ family!” echoed the
sternmost.
“Tout! it’s but the laird’s drucken mulatto after a’!” said the
former, gathering a little confidence.
“Oh, if it were! or but a man wi’ the jaundice, our days might be
lengthened,” cried the latter.
Richard advanced to explain; but at that moment the dull
firmament in the east, which had been lightning from time to time
(as often happens previously to very rainy weather), opened with
another sheeted blaze of white fire, the reflection of which on
Richard’s yellow face, as he came forward, seemed to the terrified
rustics a peculiar attribute of his nature. With a groan, he in the van
tried a backward retreat; but being straitened in the legs, he tumbled
over his squatted companion. Leaving his neighbour, however, to sit
still upon his knees, he that was the foremost man gathered himself
up so well, that he crept away on his hands and feet, till, getting right
below the bell-rope at the end of the church, he ventured to rise and
begin to jow it, making the bell toll at an unusual rate. The inmates
of the manse were immediately alarmed; and first came the
minister’s man, who demanded the meaning of such ill-timed,
ringing.
“Oh! Tam Jaffray! Tam Jaffray! sic a night’s in this kirkyard! If sae
be it’s ordeened that I may ring an’ live, I’ll haud to the tow. Oh! Tam
Jaffray! Tam Jaffray! what’s become o’ puir Geordie Heart? If the
Wandering Jew o’ Jerusalem, or the Yellow Fever frae Jamaica, is no
dancing mother-naked in the aisle, then it behoves to be the dead
rising frae their graves. I trust we’ll a’ be found prepared! Rin for a
lantern, Tam.—Eh! look to that lightning!”
A light was soon brought from the manse; and a number of people
from the village having joined the original alarmists, a considerable
muster advanced to the aisle door just as Sinclair was stepping from
it. Taking the light from one of the countrymen, he returned to the
relief of the poor villager, who was still upon his knees, and who,
with great difficulty, was brought to comprehend an explanation of
the whole affair. The crowd made way as Sinclair proceeded to leave
the graveyard; but whether it was that they were indignant because
the neighbourhood had been so much disturbed, or whether they
considered that proper game was afoot for sportive insolence, they
began to follow and shout after him—
“Come back, ye yellow neegur! we’ll no send ye!—stop him! Come
back, ye squiff, and we’ll gie ye a dead subject!—Stop the
resurrectionist!—After him, gie him a paik, and see if he’s but a batch
o’ badger skins dyed yellow—hurrah!”
Sinclair wishing, for several reasons, to be clear at once of the mob,
was in the act of springing over the dyke into the plantation already
mentioned, when he was struck by a stick on the head, which
brought him back senseless to the ground. The crowd was instantly
around the prostrate youth, and in the caprice or better pity of
human nature, began to be sorry for his pale condition.
“It was a pity to strike the puir lad that gate,” said one. “Some folk
shouldna been sae rash the day, I think,” remarked another. “Stand
back,” cried Tam Jaffray, pushing from right to left; “stand back, and
gie the puir fallow air. Back, Jamieson, wi’ your shauchled shins; it
was you that cried first that he was a resurrectionist.”
The clergyman now advanced and asked what was the matter.
“It’s only a yellow yorlin we’ve catched in the aisle,” cried an
insolent clown, who aspired to be the prime wit of the village; “he
was a bare gorblin a few minutes syne, and now he’s full feathered.”
This provoked a laugh from groundlings of the same stamp, and the
fellow, grinning himself, was tempted to try another bolt,—“And he’s
gayan weel tamed by this time.”
“Peace, fellow,” said the minister, who had now seen what was
wrong; “peace, sir, and do not insult the unfortunate. I am ashamed
of all this.”
By the directions of the clergyman, the poor prodigal was carried
into the manse, where he soon recovered from the immediate
stunning effects of the blow he had received.
“How is all this?” was his first question of surprise, addressed to
his host. “May I request to know, sir, why I am here?”
“In virtue of a rash blow, which we all regret,” answered the
minister.
“I crave your pardon, sir,” returned the youth. “I can now guess
that I am much indebted to your kindness.”
“May we ask you, young man,” said the clergyman, “how it has
happened that you have so alarmed our peaceful neighbourhood?”
The poor prodigal succinctly stated the way of his imprisonment in
the aisle; and with this explanation the charitable old clergyman
seemed perfectly satisfied. Not so, however, was his ruling elder,
who, deeming his presence and authority indispensable in any
matter for which the parish bell could be rung, had early rushed to
the scene of alarm, and was now in the manse, at the head of a
number of the villagers. He, on the contrary, saw it necessary to
remark (glancing at his superior for approbation),—
“Sae, mind, young man, in times future, what comes of sleeping in
the time of two peeous and yedifying discoorses.”
“A good caution, John,” said the mild old minister; “but we must
make allowances.”
“Was it you that struck me down?” said Richard eagerly to an old
man, who, with evident sorrow working in his hard muscular face,
stood watching this scene with intense interest, and who, indeed, was
his own father.
Smitten to the heart by this sudden question of the youth,
ashamed of his own violent spirit on such a night, and grieved, after
the explanation given, for the condition of the poor lad before him,
old Sinclair groaned, turned quickly half round, shifted his feet in the
agony of avowal,—then seizing his unknown prodigal boy by the
hand, he wrung it eagerly, and said,—
“There’s my hand, young man, in the first place; and now, it was
me indeed that struck you down, but I thought——”
“Oh! my prophetic conscience!” interrupted the poor prodigal,
whilst he looked his father ruefully in the face, and returned fervently
the squeeze of his hand. “Make no apologies to me, thou good old
man; thy blow was given under a most just dispensation.”
“I sent two neighbours,” said the old man, still anxious to explain,
“to see that all was right about the grave. I heard the alarm, and
came off wi’ my stick in my hand. I heard them crying to stop ye, for
ye were a resurrectionist. I saw ye jumping suspiciously into the
planting. Ye maun forgie me the rest, young man, for I thought ye
had been violating the grave of a beloved wife.”
“My own poor mother!” sobbed forth the prodigal.
Old Sinclair started—his strong chest heaved—the recollection of
his rash blow, together with the circumstance that it had been
dispensed on such a solemn night, and near the new grave of one
whose gentle spirit had been but too much troubled by the harshness
and waywardness of both husband and son, came over his heart with
the sudden conviction that his boy and himself were justly punished
by the same blow, for their mutual disrespect in former years.
Yearning pity over that son’s unhappy appearance, and the natural
flow of a father’s heart, long subdued on behalf of his poor lost
prodigal, were mingled in the old man’s deep emotion; and he sought
relief by throwing himself in his boy’s arms, and weeping on his
neck.
His sturdy nature soon recovered itself a little; yet the bitter spray
was winked from his compressed eyes as he shook his head; and the
lower part of his face quivered with unusual affliction, as he said in a
hoarse whisper—
“My own Richard!—my man, has your father lived to strike you to
the ground like a brute beast, and you sae ill?—on the very day, too,
o’ your mother’s burial, that loved ye aye sae weel! But come away wi’
me to your father’s house, for ye are sick as death, and the auld man
that used ye ower ill is sair humbled the night, Richard!”
The prodigal’s heart could not stand this confession of a father. His
young bosom heaved as if about to be rent to pieces; the mother, and
hysterica passio of old Lear, rose in his straitened throat,
overmastering the struggling respiration, and he fell back in a violent
fit. His agonized parent ran to the door, as if seeking assistance, he
knew not what or where; then checking himself in a moment, and
hastening back, yet without looking on his son, he grasped the
clergyman strongly by the hand, crying out, “Is he gone?—is my
callant dead?”
Ordering the people to withdraw from around the prostrate youth,
whose head was now supported by the clergyman’s beautiful and
compassionate daughter, the kind old pastor led forward the
agonised father, and pointing to his reviving son, told him that all
would soon be well again. With head depressed upon his bosom, his
hard hands slowly wringing each other, while they were wetted with
the tears which rained from his glazed eyes, old Sinclair stood
looking down upon the ghastly boy, whose eye was severely swollen,
whilst his cheek was stained with the clotted blood which had flowed
from the wound above the temples, inflicted by his own father.
After standing a while in this position, the old man drew a white
napkin from his pocket, and, as if himself unable for the task, he gave
it to one of his neighbours, and pointed to the blood on the face of his
prodigal boy, signifying that he wished it wiped away. This was done
accordingly; and, in a few moments more, Richard rose, recovered
from his fit, and modestly thanking the clergyman and his beautiful
daughter for their attentions to him, he signified his resolve to go
home immediately with his father. The kind old minister would fain
have kept him all night, alleging the danger of exposing himself in
such a state to the night air; but the youth was determined in his
purpose; and old Sinclair cut short the matter by shaking the hand of
his pastor, whilst, without saying a word, he looked him kindly in the
face to express his thanks, and then by leading his son away by the
arm.
The villagers, who had crowded into the manse, judging this one of
those levelling occasions when they might intrude into the best
parlour, allowed the father and son to depart without attempting
immediately to follow—nature teaching them that they had no right
to intermeddle with the sacred communings of the son and father’s
repentance and forgiveness, or with the sorrow of their common
bereavement. Yet the rude throng glanced at the minister, as if
surprised and disappointed that the thing had ended so simply; then
slunk out of the room, apprehensive, probably, of some rebuke from
him. The ruling elder, however, remained behind, and wherefore
not?
THE BARLEY FEVER—AND REBUKE.
By D. M. Moir (“Delta”).
Sages their solemn een may steek,
And raise a philosophic reek,
And, physically, causes seek
In clime and season;
But tell me Whisky’s name in Greek,
I’ll tell the reason.—Burns.