Single crystal growth, optical absorption and luminescence properties under VUV-UV synchrotron excitation of type III Ce3+:KGd(PO3)4, a promising scintillator material.

Scintillator materials have gained great interest for many applications, among which the medical applications stand out. Nowadays, the research is focused on finding new scintillator materials with properties that suit the needs of each application. In particular, for medical diagnosis a fast and intense response under high-energy radiation excitation is of great importance. Here, type III Ce3+-doped KGd(PO3)4 single crystals with high crystalline quality are grown and optically characterized as a new promising scintillator material. The 4f → 5d electronic transitions of Ce3+ are identified by optical absorption. The optical absorption cross section of Ce3+ for the electronic transition from the 2F5/2 to the 5d1 level is 370 × 10-20 cm2. The luminescence of KGd0.996Ce0.004(PO3)4 crystal by exciting the 5d levels of Ce3+ with VUV-UV synchrotron radiation shows down-shifting properties with strong emissions at 322 and 342 nm from the 5d1 to 2F5/2 and 2F7/2 levels of Ce3+ with a short decay time of ~16 ns, which is very suitable for scintillator applications. Moreover, these intense emissions are also observed when Gd3+ is excited since an energy transfer from Gd3+ to Ce3+ exists.

Introduction

Scintillator materials have gained great interest for a large number of applications, such as in medical imaging techniques (X-ray computed tomography, positron emission tomography), high energy and nuclear physics, non-destructive testing, amongst others[1-4]. An ideal scintillator material should satisfy different properties, mainly high density, fast emission and a high light yield[5]. Many efforts are dedicated to find novel scintillator materials with the best properties for different applications, especially in the case of medical applications with the aim to reduce the ionizing radiation exposure to the patient in diagnostic techniques[6].

In scintillator materials which contain lanthanide ions, the emissions in the ultraviolet and visible regions suitable for scintillation applications are produced mainly by the 5d → 4f electronic transitions of these ions, which act as scintillator centres. Typical scintillator materials are Ce3+-doped crystals, such as Ce3+:Lu2SiO5 and Ce3+:LaBr3. Both crystals present some drawbacks, such as difficulty for crystal growth and hygroscopicity, respectively[7,8]. Multicomponent garnet crystals doped with Ce3+ are also used in medical imaging and gamma spectroscopy due to high light yield and high density, but with poorer timing performance compared with lutetium-yttrium oxyorthosilicate crystals[9]. Ce3+ emission bands are based on the 5d to 4f electronic level transitions, usually as a doublet since the arrival states, 2F5/2 and 2F7/2, are separated by around 2000 cm−1 [10]. These electronic transitions are allowed and have a very short decay time in the order of nanoseconds[11], which could be suitable for scintillator applications.

Crystalline alkali and rare earth polyphosphates, MRE(PO3)4 (where M is an alkali cation, M = Li, Na and K; RE is a rare earth cation), have been recently studied as candidates for scintillator applications[2] due to their broad transparency range in the ultraviolet region, its relatively high density and the possibility to incorporate Ce3+ and Pr3+ ions which are characterized by fast emissions in many hosts. They have been also intensively studied for other optical applications due to the low concentration quenching of the luminescence at high concentration of the active Ln3+ ions[12]. Ce3+ luminescence in phosphate compounds have been deeply studied, by Blasse and Dirken[13] in LiLaP4O12, by Shalapska et al.[12] in LiYP4O12, Zhong et al.[14] in 2007 in AGdP4O12 (being A = Cs, K, Na and Li) and Novais et al.[15] in 2014 in the non-centrosymmetric monoclinic phase NaYP2O7.

Among them, KGd(PO3)4 is a suitable crystal to incorporate different Ln3+ ions substituting the Gd3+ ions of the structure, is not hygroscopic, presents a good chemical stability[16] and its density is 3.538 mg·m−3 [17]. Besides, it is a deep-ultraviolet crystal closing at 160 nm[18] indicating a large band gap, which potentially could allow that the 5d energy levels of some Ln3+ ions be located between the conduction band and the valence band.

The existence of the radioisotope 40K (0.0117% natural abundance) may limit its usefulness for some applications by increasing the background radiation. However, as mentioned in the review of Nikl[19], other radioactive isotopes are also present in several used scintillator crystals such as 176Lu, 87Rb, and 138La contributing in a background signal. Besides, other promising scintillator materials identified in the literature also contain K as ion, such as: K2LaI5:Ce3+, being attractive by its fast decay time of 24 ns, together with a relative high density[20]; and KSr2I5:Eu2+ with a very high yield[21].

Finally, we have already reported the feasibility of growing these crystals within the non-centrosymmetric monoclinic crystalline phase with high crystalline quality[18,22]. This compound presents a polymorphism related to the degree of condensation of the phosphoric anions: the PO4 forms chains in the type III phase (space group: P21) and type IV phase (space group: P21/n), belonging to the group of polyphosphates, and the PO4 forms rings in the type B phase (space group: C2/c) belonging to the group of cyclophosphates[22]. High quality bulk single crystals of Ln3+-doped non-centrosymmetric KGd(PO3)4 (space group: P21) have been already grown by us by the Top Seeded Solution Growth technique. The unit cell parameters for undoped KGd(PO3)4 are a = 7.255(4) Å, b = 8.356(5) Å, c = 7.934(5) Å, β = 91.68(5)° and Z = 2 refined by single crystal X-ray diffraction[17].

Potassium and Ce3+ stoichiometric phosphate, KCe(PO3)4, also presents polymorphism; in this compound, the phosphoric anions can form chains in the type III phase (space group: P21)[23]. Since KCe(PO3)4 also presents the type III crystalline phase, it is expected that the non-centrosymmetric phase (type III) KGd(PO3)4 can be doped with high concentration of Ce3+.

Thus, KGd(PO3)4 as a host and Ce3+ as doping element (hereafter Ce3+:KGdP) is a promising combination to obtain a new scintillator material. The aim of our research is to growth non-centrosymmetric Ce:KGdP single crystals from high temperature solutions with different Ce3+ doping concentrations in order to carry out a study of the luminescence properties of these crystals under synchrotron VUV excitation and discuss the potential of this crystalline phase of KGdP for scintillator applications.

Results and Discussion

Bulk single crystal growth

Table 1 summarizes the growth conditions of the different single crystal growth experiments carried out in this work and some features of the crystals obtained.

Table 1

Crystal growth conditions and crystals obtained from about 100 g of solution.

Exp. number	[Ce2O3]/([Gd2O3] + [Ce2O3]) in the solution [at.%]	Growth interval [K]	Crystal weight [g]	Crystal dimensions along a*×b × c* directions [mm]	Growth rate [ × 10−3 g·h−1]
1	0.25	27.4	0.62	3.1 × 9.9 × 9.9	1.55
2	0.50	30	1.62	6.1 × 15.1 × 10.9	3.61
3	0.50	29	1.65	5.4 × 14.9 × 11.4	3.84
4	1.00	31	1.31	3.9 × 13.2 × 12.2	2.78
5	1.00	32	1.76	6.0 × 15.7 × 11.5	3.58
6	2.00	34.3	1.68	4.9 × 15.5 × 13.3	3.25

The saturation temperature of the solutions was determined to be at around 950 K. As expected this saturation temperature is similar to the one reported for the crystal growth of Yb-doped KGdP crystals, grown in similar experimental conditions[24] and lower than reported for undoped KGdP[16]. Lower crystallization temperature would mean higher viscosity in the solution, which can affect negatively to the crystal quality and the growth rate of the crystals.

These crystals were colourless, transparent, and generally free from inclusions and cracks. The size of the crystals obtained along a* × b × c* directions were 3.1–6.1 × 9.9–15.7 × 9.9–13.3 mm and the weight of the crystals ranged from 0.62 to 1.76 g. In all cases, the crystal dimension along the b crystallographic axis was higher than the dimensions in a* and c* directions. Comparing the a* dimension with previous reported grown crystals, in this case the dimensions are smaller. One of the reasons of these smaller crystal dimensions is the lower amount of growth solution in the crucible due to the smaller crucible diameter. In addition, changes in the thermal vertical gradient, especially in the first centimetre of the solution, and different position of the stirrer in relation to the crystal growing can also contribute to produce changes in the crystal dimensions.

The crystal growth rates were generally higher than 3 × 10−3 g·h−1. In previous reports, the crystal growth rate was around 8-9 × 10−3 g·h−1 for undoped KGdP[25] and around 7 × 10−3 g·h−1 for Nd-doped KGdP[18]. Several reasons can induce this slower crystal growth, which are the different composition of the solution with a reduced amount of solute in it, the total mass of the solution which in the present work is lower, and finally, the presence of cerium in the solution. However, it is significant to point out the difficulty of the growing high quality crystals due to the high viscosity of the solution, around 19 Pa·s at 950 K, and how by choosing and designing accurate crystal growth conditions, such as appropriate stirring of the solution by the use of stirrer and cooling ramps, high crystalline quality crystals have been obtained. Crystal growth is very difficult in highly viscous solutions, since due to the low molecular mobility inside them, the growth units find difficulties to reach the crystal surface.

As an example, Fig. 1 shows an as-grown Ce3+:KGdP single crystal with the platinum stirrer and a morphological scheme with the crystalline faces observed in this crystal. The crystal scheme corresponds to the crystalline habit of type III phase of KGdP.

Figure 1

(a) As-grown single crystal of Ce3+:KGdP and platinum stirrer, (b) As-grown single crystal of Ce3+:KGdP and (c) Crystal scheme with the faces observed.

The distribution coefficient of Ce3+ in KGdP was calculated using the EPMA results according to the formula: KCe = ([Ce]/([Ce] + [Gd]))crystal/([Ce]/([Ce] + [Gd]))solution. The stoichiometry of the crystals and the Ce3+ distribution coefficients are shown in Table 2. The cerium distribution coefficient is larger than one; this means that the Ce3+ distribution inside the crystal may be not homogeneous. Besides, the distribution coefficient of Ce3+ is larger than the observed one for Yb and similar to the one reported for Nd[18,24]. This last fact can be related to the different ionic radii of the lanthanide doping ions.

Table 2

EPMA results for Ce:KGdP. KCe denotes the distribution coefficient of the Ce3+ in the crystal.

Ce3+ at.% in solution	K Ce	Ce3+ concentration [cm−3]	Chemical formula
0.25	1.77	1.667 × 1019	KGd0.996Ce0.004(PO3)4
0.5	1.30	2.501 × 1019	KGd0.994Ce0.006(PO3)4
1	1.88	7.919 × 1019	KGd0.981Ce0.019(PO3)4
2	1.28	1.084 × 1020	KGd0.974Ce0.026(PO3)4

In addition, X-ray powder diffraction analysis was made to study the effect on the unit cell parameters of KGdP when it is doped with Ce3+ ions. For undoped KGdP, with non-centrosymmetric crystalline structure, the unit cell parameters are a = 7.2510(4) Å, b = 8.3498(2) Å, c = 7.9240(2) Å, β = 91.823(3)°, with Z = 2 and the unit cell volume is 479.51(3) Å3. In the case of KCe0.026Gd0.974(PO3)4 crystals, the unit cell parameters are a = 7.2520(4) Å, b = 8.3524(2) Å, c = 7.9265(2) Å, β = 91.826(3)°, with Z = 2 and the unit cell volume is 479.88(3) Å3. As can be seen, the unit cell parameters and the unit cell volume slightly increase when KGdP is doped with Ce3+ ions. This is expected since the ionic radius of Ce3+ with coordination VIII is higher than the ionic radius of Gd3+ with the same coordination (1.143 Å and 1.053 Å, respectively)[26]. Moreover, by acquiring the X-ray diffraction pattern for obtaining the unit cell parameters of the Ce3+-doped crystals, it is proved that the crystalline phase of the crystals is the type III one (space group: P21).

Ce3+ spectroscopy in KGd(PO3)4 single crystals

Optical absorption

As it is known, the 5d electrons present a strong interaction with the crystal field, which determines the position of the 5d energy levels and its high dependence with the crystal host[27-29]. These bands are also wide due to the 5d electron interaction with the lattice phonons. In the non-centrosymmetric KGdP crystalline phase, Ce3+ substitutes the Gd3+ ions in a C1 position inside a GdO8 distorted dodecahedra. The 5d level splits in five non-degenerated crystal-field levels.

Figure 2 shows the unpolarised optical absorption coefficient of KGd0.996Ce0.004(PO3)4 at room temperature and the inset displays the unpolarised optical absorption cross section of 2F5/2→5d1 transition of Ce3+ in the same crystal at room temperature. As can be seen in this Figure, the strongest bands are assigned to the 4f→5d vibronic transitions. The wavelengths assigned to each 4f→5d1, 5d2, 5d3, 5d4 and 5d5 absorptions are resumed in Table 3. The wavelength values for the 4f→5d electronic transitions in other hosts are also summarised in Table 3.

Figure 2

Unpolarised optical absorption coefficient of KGd0.996Ce0.004(PO3)4 at room temperature. Propagation direction is along b axis. Labels in purple indicate the absorption transitions of Gd3+ and labels in pink those of Ce3+. Inset: Unpolarised optical absorption cross section of 2F5/2→5d1 transition of Ce3+ in KGd0.996Ce0.004(PO3)4 at room temperature.

Table 3

Spectroscopic properties and crystallographic space groups of Ce3+ doped phosphates.

Compound	Space group	Rav (Gd-O) [Å]	CF	λ5, λ4, λ3, λ2, λ1 [nm]	D(A)[cm−1]	εcfs [cm−1]	εc[cm−1]	Reff [Å]	αsp [10−30 m3]	Ref.
KGd0.996Ce0.004(PO3)4	P21	2.4065	ddh	194, 215, 226, 243.5, 302.5	16282	18489	7944	2.447	1.479	This work
KGd0.99Ce0.01P4O12	C2/c	2.408	ddh	193, 209, 221, 245, 307	16767	19240	7570	2.453	1.431	[14]
NaGd0.99Ce0.01(PO3)4	P21/n	—2.401	—ddh	—, —, 223, 256, 297196, 207, 218, 254, 297	—15670	—17350	—7582	—2.443	—1.398	[2, 14]
NaPr0.9Ce0.1P4O12	P21/n	—	ddh	195, 230, 252, 268, 295	15442	17300	7332	—	—	[12]
LiLa0.95Ce0.05P4O12	C2/c	—	ddh	—, —, —, —, 278	13369	—	—	—	—	[13]

Note: Rav = average distance, CF = coordination figure, ddh = dodecahedron, λ5, λ4, λ3, λ2, λ1 = absorption bands of the 5d levels, D(A) = spectroscopic redshift, εc = centroid shift, εcfs = crystal field splitting, Reff = effective distance of Gd-O, and αsp = spectroscopic polarizability.

The broad band centred at 302.5 nm (33058 cm−1, 4.10 eV) (see Fig. 2) corresponds to the first spin-allowed 4f→5d transition from ground state to the first 5d level (5d1) of Ce3+ in the KGdP host. This value is very close to the reported values in other crystalline phosphates, such as 310 nm for K3La(PO4)2[30], and 307 nm for the centrosymmetric KGdP (space group: C2/c)[14]. It is worth to point out that the photons at 194, 244 and 302.5 nm excite both Ce3+ and Gd3+ ions; whereas the other identified wavelengths, 214 and 226 nm, excite predominantly only Ce3+ ions.

The centroid position of the 5d energy levels of Ce3+ in a free ion is 51230 cm−1 [28]. Due to the large interaction of the 5d electron with the crystal field of the host A, the first dipole allowed 4f→5d transition is shifted in relation with the free ion value; this shift is defined as the spectroscopic redshift, D(A)[28]. The spectroscopic redshift of Ce3+ due to the type III KGdP host is D(KGdP) = 16282 cm−1. As mentioned by Dorenbos et al., this depression is expected to be the same for each Ln3+ ion used as scintillator centre in the same KGdP host[31].

As described by Dorenbos et al.[32], the polyphosphate compounds have a large fraction of strongly bonding phosphate atoms, which cause that the D(A) is amongst the smallest, and the crystal field splitting, εcfs, and the bandgap amongst the largest of all oxide compounds. By comparing the values of the D(A) of Table 3, it can be observed how this value decreases as smaller is the alkaline ion (K > Na > Li); this tendency in the phosphates was already observed by Dorenbos[31].

Table 3 shows the spectroscopic redshift, D(A), as well as the centroid shift, εc, crystal field splitting, εcfs, effective distance of Gd-O bond, Reff, and spectroscopic polarizability, αsp, for the type III KGdP host and others. D(A), εc and εcfs were calculated by using the optical absorption spectrum in Fig. 2; Reff and αsp were calculated considering the εc, as in the reference[14], and the crystallographic data of the undoped non-centrosymmetric KGdP[22].

The crystal field splitting, εcfs (the energy difference between the 5d1 and the 5d5) for the non-centrosymmetric KGdP is smaller than in the centrosymmetric one. This fact does not follow the expected behaviour since εcfs is determined by the strength of the crystal field, related to the shape and the size of the coordination polyhedron, and considering the same polyhedral shape, the smaller the bond length and larger distortion, the higher the crystal field splitting[28]. Comparing the two hosts, the non-centrosymmetric KGdP crystal presents shorter bond length than the centrosymmetric one, and they have similar distortion in the cation site. This different crystal field suffered by the Ce3+ ions may be related to effects in the second coordination sphere.

The centroid shift, εc (energy difference between the centroid value of the 5d of the free electron and the one inside the crystal) may be related to the ligand polarization and has no dependence on the crystal field splitting value. As it can be seen in the same table, the εc for the non-centrosymmetric KGdP in comparison with the centrosymmetric one is higher. Taking into account the ligand polarization model[29], the fact that the non-centrosymmetric KGdP has a εc value larger than the centrosymmetric one, should be attributed to the major contribution of the effective distances, Reff, in the value of centroid shift (εc ∝ Reff−6).

All discussed parameters until now are dependent of the crystalline host, so they are also related to the Ce3+ concentration in the crystal and temperature. The spectroscopic values for non-centrosymmetric KGdP have been calculated for KGd0.996Ce0.004(PO3)4 and at room temperature.

Moreover, as 4f→5d transitions are parity allowed transitions, it was also expected a high value of optical absorption cross section. The observed value is 370 × 10−20 cm2 at 302.5 nm for Ce3+ in the type III KGdP crystal. The 4f→4f transitions in lanthanide ions are very weakly influenced by the crystal field and for this reason the position of such absorption transitions of Gd3+ are the expected ones and have been labelled by using the Dieke’s diagram[10].

Optical emission

Figure 3 shows the emission spectra of KCe0.004Gd0.996(PO3)4 under λexc = 244 nm (5.09 eV), 226 nm (5.49 eV), 214 nm (5.80 eV) and 194 nm (6.40 eV), which correspond to the excitation to the 5d2, 5d3, 5d4 and 5d5 energy levels, respectively, of Ce3+ in the KGdP host. The intensities have been corrected by the excitation photon flux values. From this Figure, it can be seen an intense doublet peak centred at 322 and 342 nm corresponding to the 5d1→2F5/2 and 5d1→2F7/2 transitions, respectively, of Ce3+ in KGdP. The energy difference between these two emission peaks is consistent with the energy difference between the 4f levels of Ce3+, 2F5/2 and 2F7/2 levels, as can be seen in the Dieke’s diagram[10]. This emission appears by exciting the sample under all these four different excitation wavelengths, in which the emission intensities are in accordance with the values of absorption coefficient for each excitation wavelength. The intensity of emission when the sample is excited at 194 nm is lower than when it is excited at 214 nm, despite their similar absorption coefficient values. This behaviour might be attributed to a depopulation of the 5d5 level of Ce3+ due to energy transfer to the 4f levels of Gd3+.

Figure 3

Optical emission spectra of KGd0.996Ce0.004(PO3)4 under 244, 226, 214 and 194 nm excitation. Labels in purple (inset) indicate the transitions of Gd3+ and labels in pink those of Ce3+.

It is worth saying that the 6P7/2→8S7/2 transition of Gd3+ which should appear as a sharp emission around 311 nm, being common in many hosts[33-36], is not present in the non-centrosymmetric KGd1−xCex(PO3)4 crystals, as observed in Fig. 3. The same behaviour is observed in the KGd0.981Ce0.019(PO3)4 and KGd0.974Ce0.026(PO3)4 crystals, referring to the emissions of Ce3+ and Gd3+ under the wavelength excitation 244, 226, 214 and 194 nm. By comparing the emission spectrum obtained under VUV excitation and that obtained under X-ray excitation of four highly similar hosts[2,14,37] to our compound, it has been observed that the 6P7/2→8S7/2 transition of Gd3+ is not present under VUV excitation, and it does not appear by exciting the compound with X-rays, either. Thus, in type III Ce:KGdP, since the above mentioned 4f→4f transition of Gd3+ is not observed (Fig. 3), it is expected that it will not appear under X-ray excitation. This is a favourable feature for scintillator use because the emissions which are of interest in this application are based on 5d→4f transitions, instead of the 4f→4f transitions, since the 5d levels have very short decay times, in the order of nanoseconds. However, it should be noted that similar spectra are not always obtained when the compound is excited with VUV radiation and with X-rays.

From the work done by Zhong et al.[14] similar results were observed in KGdP4O12 host with type B phase (space group: C2/c). The 5d1→2F5/2 and 5d1→2F7/2 transitions appear at 323 and 343 nm, respectively. When Ce:KGdP4O12 is excited at 193 nm (2F5/2→5d5), the emission of Gd3+ at 311 nm looks very weak as a hump in the band corresponding to the 5d1→2F5/2 emission. Therefore, this emission of Gd3+ is extraordinarily rare in comparison with the emissions of Ce3+ in the type III KGdP. In a similar phosphates, this Gd3+ emission appears more intense than the emission peaks corresponding to 5d1→2F5/2, 2F7/2 transitions of Ce3+ in Ce:LiGdP4O12 (space group: C2/c) under 292 nm (2F5/2→5d1), 273 nm (8S7/2→6IJ Gd3+) and 188 nm (2F5/2→5d5) excitation, and in Ce:NaGdP4O12 (space group: P21/n) under 298 nm (2F5/2→5d1) and 273 nm (8S7/2→6IJ Gd3+) excitation[14].

In the inset of Fig. 3, it can be seen how several weak peaks appeared in the spectral range from 560 to 640 nm when the KCe0.004Gd0.996(PO3)4 sample is excited at 194 nm. These four weak peaks centred at 578, 592, 613 and 633 nm correspond to 4f→4f transitions of Gd3+, being the 6G11/2,9/2,5/2→6P7/2, 6G7/2→6P7/2, 6G11/2,9/2,5/2→6P3/2 and 6G7/2→6P3/2 transitions, respectively. This may occur since the 8S7/2→6G13/2 absorption transition of Gd3+ about 194 nm is overlapped with the 2F5/2→5d5 of Ce3+, as can be seen in Fig. 2. The energy levels of Gd3+ and Ce3+ in KGdP and the possible energy transfer mechanism are shown in Fig. 4. Returning to Figs 2 and 3, since the absorption from 2F5/2 ground state of Ce3+ to its 5d1 level appears at 302.5 nm and the emission corresponding to the 5d1→2F5/2 transition appears at 322 nm, the Stokes shift in the type III KGdP host is ΔS = 2002 cm−1. By observing the work done by Shalapska et al.[12], the absorption peak corresponding to 2F5/2→5d1 transition of Ce3+ in Ce:NaPrP4O12 (space group: P21/n) appear at 295 nm, and the 5d1→2F5/2 and 5d1→2F7/2 transitions appear as emissions at 310 and 328 nm. The characteristics of Ce3+-luminescence in LiYP4O12 host have also been studied by Shalapska et al.[38]. In this host, the absorption peaks corresponding to 2F5/2→5d1 transition of Ce3+ appear at 295 and the 5d1→2F5/2 and 5d1→2F7/2 transitions appear at 312 and 333 nm. From the experimental data mentioned, the Stokes shifts are ΔS(KGdP4O12) = 1614 cm−1, ΔS(NaPrP4O12) = 1640 cm−1 and ΔS(LiYP4O12) = 1847 cm−1. Thus, the Stokes shift of type III KGd(PO3)4 host is higher [ΔS = 2002 cm−1] than the calculated in the three hosts mentioned above, but still slightly below the most frequent Stokes shift measured in 240 different compounds, being 2200 cm−1 [27]. The Stokes shift is induced by lattice relaxation at the excited states. Hence, the higher the value of Stokes shift is, the larger the relaxation of the electron at the excited state is before emitting electromagnetic radiation, resulting in higher non-radiative losses[39,40]. The Stokes shift is not dependent of the lanthanide ion, but only depends on the host. So, it can be extrapolated for future doping ions in the KGdP crystal[31].

Figure 4

Energy levels diagram of Ce3+ and Gd3+ in KGd0.996Ce0.004(PO3)4 and the emission mechanism. ET = Energy Transfer.

Moreover, it is also interesting to observe the intensity ratios of the peaks corresponding to 5d1→2F5/2 and 5d1→2F7/2 transitions of Ce3+, since it varies with the doping level. As the Ce3+ doping is higher, the peak corresponding to the transition from 5d1 to 2F5/2 becomes less intense compared to the transition to 2F7/2. The evolution of this ratio of intensities versus Ce3+ concentration can be seen in Fig. 5. This behaviour may be due to the presence of reabsorption of the emission corresponding to the 5d1→2F5/2 transition by the neighbouring Ce3+ atoms.

Figure 5

Intensity ratio of the emission peaks belonging to the 5d1 →2F5/2 transition (I1) versus the emission peaks belonging to 5d1→2F7/2 transition (I2) of Ce3+ under 226 nm excitation (2F5/2→5d3).

Figure 6 shows the excitation spectrum of KGd0.981Ce0.019(PO3)4 at room temperature for the emission wavelengths λemi = 342 nm (5d1→2F7/2 of Ce3+) and λemi = 592 nm (6G7/2→6P7/2 of Gd3+) with the electronic transitions labelled. In the case of the excitation spectrum for the emission of Ce3+, it can be observed that these emissions take place when Ce3+ is excited and also when Gd3+ is excited. Therefore, this reaffirms that an energy transfer from Gd3+ to Ce3+ occurs. In addition, from the same spectrum (Fig. 6a), the complete band of the 5d5 level of Ce3+ has been observed complementing the assignment of 5d levels energy values in the absorption measurements.

Figure 6

Excitation spectra of KCe0.019Gd0.981(PO3)4 for the emission wavelengths of (a) 342 nm (5d1→2F7/2 of Ce3+) and (b) 592 nm (6G7/2→6P7/2 of Gd3+). Labels in purple indicate the transitions of Gd3+ and labels in pink those of Ce3+.

From Fig. 6b, it can be seen how the emission at 592 nm is produced mainly when Gd3+ cations are directly excited. Similar behaviours have been observed for the emissions centred at 578, 613 and 633 nm, all corresponding to 4f→4f electronic Gd3+ transitions.

The energy of the exciton creation (Eex), that is, bound electron and hole pairs, in type III KGdP has been predicted that appears at 164 nm (7.57 eV) by the calculations explained below. First, the energy of the onset of the fundamental absorption (Efa) of type III KGdP has been established at 172 nm (7.22 eV) by overlapping a straight line along the ultraviolet absorption edge observed in the transmission spectrum of Nd:KGd(PO3)4 crystal[18]. This same procedure was used in the work done by Ueda et al.[41]. Then, the estimated value of Eex has been obtained by adding 0.35 eV to Efa since these measurements have been performed at room temperature[42]. Hence, the band corresponding to Eex could appear centred at 164 nm in the excitation spectra (Fig. 6), although it would not be appreciated due to an overlapping with the 8S7/2→4F9/2 transition of Gd3+.

From the value of Eex, it can be calculated the approximate energy difference from the bottom of the conduction band to the top of the valence band (EVC); being approximately 1.08 times the energy of the exciton creation[42]. Therefore, the estimated value for type III KGdP is EVC = 8.17 eV (152 nm).

Decay time measurements

Ce3+-doped crystals were excited at 302.5 nm (2F5/2→5d1 of Ce3+), 194 nm (8S7/2→6G13/2 of Gd3+ and 2F5/2→5d5 of Ce3+) and 174 nm (8S7/2→6H15/2 of Gd3+). It should be noted that in order to gain in photon flux reaching to the sample, the excitation beam had a bandwidth of around 7%, being not purely monochromatic. Figure 7a shows the luminescence decay curves for the emission at λemi = 322 nm of Ce3+-doped KGdP crystals with different doping concentrations and at different excitation wavelengths. As can be seen in the Figure, the decay curves can be fitted by a single exponential decay. The lifetime obtained for 5d1 level of Ce3+ in this host is around 16 ns. No significant changes in the lifetime value were obtained either due to the change of the wavelength of excitation or the different Ce3+ concentration in the crystals.

Figure 7

(a) Fast component of the luminescence decay curves of Ce3+-doped KGdP crystals with different doping concentrations and at different excitation wavelengths for λemi = 322 nm. (b) Slow component of the decay curve of KGd0.974Ce0.026(PO3)4 under excitation at 302.5 nm for λemi = 342 nm.

This measured lifetime of the 5d1 level of Ce3+ in the KGdP crystal is similar or even shorter than the measured ones in other scintillator materials[3,12,14,43]. By comparing this value with the obtained in the centrosymmetric KGdP (space group: C2/c, 21.1 ns), the lifetime of the 5d1 level of Ce3+ in type III KGdP (space group: P21) is significantly lower[14].

It has been also observed that in type III Ce3+:KGdP crystals, the 5d1→2F5/2,2F7/2 decay is not only composed by a fast component, but also by a slow component. This fact was observed when the intensity of the emission does not reach zero value because of the short interpulse time in the synchrotron measurements. To measure in the appropriate magnitude this slow component, the lifetime was measured in a conventional fluorimeter. Figure 7b shows the slow component of this decay curve in the KGd0.974Ce0.026(PO3)4 crystal under excitation at λexc = 302.5 nm for the emission at λemi = 342 nm. In this Figure, it can be seen the exponential fit of the slow component resulting in a decay time around 8 ms. This slow component has been already observed in other Ce3+-doped phosphates, as in Ce:NaPrP4O12[12], and Ce:CsGd(PO3)4[14]. In the first case, it was only observed at high energy excitations and it was attributed to trapping effect which makes the host-cerium energy transfer process more difficult, but in the case of Ce:CsGd(PO3)4, the slow component was observed when solely the Gd3+ ion was excited and not the Ce3+ ions. The long component in the Ce3+-doped non-centrosymmetric KGdP crystal has been observed when exciting at short wavelength values (Fig. 7a) and also when exciting directly to the 5d1 level (Fig. 7b). Therefore, the origin of this slow component could be attributed to some contribution of the trapping effect, but the contribution of the Gd3+ emission corresponding to the electronic transition 6P7/2→8S7/2 cannot be disregarded since the lifetime of this emitting 6P7/2 level of Gd3+ is of the same order (4.9 ms in NaY0.80Gd0.20PO4[34] and 6.36 ms in NaGd(PO3)4[44].

Conclusions

Type III Ce3+-doped bulk single crystals have been grown by Top Seeded Solution Growth-Slow cooling technique from self-fluxes in high crystalline quality. Till a Ce3+ doping level of 2 at% substituting Gd3+ in solution, no effect of the cerium doping has been observed in the crystalline quality of the single crystals. The maximum optical absorption cross section has been measured for the electronic transition from the ground state of Ce3+ until the 5d1 level, being the value at 302.5 nm around 370 × 10−20 cm2. The spectroscopic redshift of the 5d energy levels of Ce3+ in the type III KGdP host is 16282 cm−1. Under ultraviolet excitation, a doublet emission peak centred at 322 and 342 nm has been observed in all grown crystals, corresponding to the 5d1→2F7/2 and 5d1→2F5/2 transitions of Ce3+, respectively. No important Gd3+ 4f→4f emissions have been clearly observed by exciting at this range. By last, the lifetime of the 5d1 level of Ce3+ in type III KGdP has been measured by setting the doublet emission peak and a lifetime around 16 ns has been obtained, which is similar or even shorter than the lifetime of the same level of Ce3+ in other hosts. In addition, the presence of a slow component has been observed by setting the same emission peak. The reported results confirm the potentiality of the Ce3+-doped type III KGd(PO3)4 crystals for scintillation applications.

Experimental

Single crystal growth

Ce3+:KGdP single crystals with non-centrosymmetric monoclinic structure (space group: P21) have been grown from high temperature solutions. The solvent used was an excess of K2O and P2O5 (self-flux), so that it does not contain foreign ions that could be introduced as impurities in the crystalline structure. The compositions of the growth solutions, chosen on the basis of the primary crystallization region of KGdP in the K2O-Gd2O3-P2O5 ternary system, previously determined[22,45], were K2O:((1−x)Gd2O3 + x Ce2O3):P2O5 = 36:4:60 (mol%) with x in the range 0–0.02. The solutions, with a weight of about 100 g, were prepared in a platinum cylindrical crucible of 40 mm in diameter. The reagents used were K2CO3 anhydrous (Alfa Aesar A. Johnson Matthey Company, 99%), NH4H2PO4 (Fluka Analytical, ≥99.0%) and both Gd2O3 and Ce2(CO3)3 from Aldrich with a purity of 99.9%.

Due to the relatively high level of dynamic viscosity of the solutions[25], the mixing of the solution was produced by using high axial thermal gradient (3.0 K·mm−1 in depth), with the coolest point at the center of the solution surface (the solution density decreases with increasing the temperature), accompanied by the use of a platinum stirrer (20 mm in diameter) located at about 12 mm below the surface of the solution, rotating at 55 rpm. The growth was carried out on an undoped KGdP seed with a orientation with the b crystallographic direction tangential to the rotation direction, because in previous works it has been proved that this crystalline orientation gives excellent results in terms of crystal quality[16]. The seed, located in contact with the solution surface at about 10 mm from the rotation axis, was joined with the stirrer and rotated together[25].

The saturation temperature of the solution was accurately determined by measuring the growth and dissolution rates of the KGdP seed as a function of the temperature. Beginning at the determined saturation temperature, cooling rates of 0.1 K·h−1 for the firsts 15 K and 0.05 K·h−1 for the next 10–15 K were applied to achieve the required supersaturation of the solution for crystal growth. After finishing the cooling ramps or when the crystal was big enough, it was slowly removed from the solution. To avoid thermal shocks in the crystal, it was cooled to room temperature inside the furnace at a rate of 20–25 K·h−1.

The composition of the crystals was determined by Electron Probe Microanalysis with Wavelength Dispersive Spectroscopy (EPMA-WDS) using a JEOL JXA-8230. The standard used to measure K, Gd, P and O was a KGdP single crystal, while the Ce content in the crystals was measured using CeO2 as standard. The measures were made with an accelerating voltage of 20 kV and a current of 20 nA. The measuring time for K, Gd, P and O was 10 s for peak and 5 s for background, while in the case of Ce the measuring time was 120 s for peak and 60 s for background, because of its low concentration in the crystals. Kα X-ray lines of K, P and O and Lα X-ray lines of Gd and Ce were used for the composition measurements. The dispersive crystals were PETJ for K, LIFH for Gd, PETL for P and Ce and LDE1 for O measurements. Under these conditions, the detection limit of Ce was 195 ppm.

X-ray powder diffraction

The unit cell parameters of KGdP with Ce3+ doping up to 2 at.% in solution were determined by X-ray powder diffraction. The equipment used was a D5000 Siemens X-ray powder diffractometer in a θ-θ configuration with the Bragg-Brentano geometry. The measurements were carried out with step size of 0.03° and a step time of 7 s and recorded in the range 2θ = 10–70°. The unit cell parameters were refined using the TOPAS program[46].

Optical characterization

The grown crystals were cut in plates perpendicular to the crystallographic a*, b and c* directions with a diamond saw, lapped with Al2O3 suspension with particle size of 9 and 3 μm, successively, and polished with colloidal suspension of amorphous silicon dioxide with a mean particle size of 0.2 μm. These plates were used for optical absorption and emission studies. The optical absorption of Ce3+ in KGdP has been studied at room temperature using a 0.25 at.% Ce:KGdP plate parallel to the (001) crystallographic plane with a thickness of 0.11 mm and the equipment used was a CARY 5000 UV-Vis-NIR Spectrophotometer.

The emission spectroscopy of Ce3+-doped KGdP single crystals under vacuum ultraviolet excitation was carried out in the wavelength range from 120 to 248 nm (10–5 eV). Experiments were performed in the DESIRS beamline at SOLEIL Synchrotron (France, proposal num. 20151215, Standard). The samples were placed in a vacuum chamber which can be evacuated to around 10−5 bar. A Lithium Fluoride window at the entrance of the vacuum chamber separates it from the synchrotron line. The monochromatic synchrotron light reached perpendicularly to the KGdP plate. The emitted light from the sample was collected at 45° by a silica lens, focused at the entrance of an optical fibre connected to a Jaz spectrometer, Ocean Optics with a minimum spectral resolution of 0.3 nm. The emission spectra were recorded from 192 to 886 nm.

Lifetime measurements were also made in the DESIRS beamline at SOLEIL Synchrotron in a single bunch mode of operation to obtain pulsed radiation with full width at half-maximum pulse duration of 50 ps and interpulse time duration of 1.12 ms (proposal number 20161324, Standard). The crystals were placed at the same vacuum chamber, with the same configuration that in the emission measurements. The output emission of the crystal, focused with the same silica lens, was guided with an optical fibre to an ANDOR Shamrock 193i spectrograph (grating 150 lines/mm) coupled to an iStar Intensified Charge Coupled Device camera with fast response (DH734–18F-03 model). To increase the photon flux reaching the sample, once the vacuum in the chamber was enough high (at least 2 × 10−5 bars), the optical window between the vacuum chamber and the synchrotron line was removed. Long components of the time decays have been checked and measured by a conventional fluorimeter Cary Eclipse Fluorescence Spectrophotometer.