Enhanced up-conversion luminescence in transparent glass-ceramic containing KEr3F10:Er3+ nanocrystals and its application in temperature detection.

Transparent Er3+ doped glass-ceramics containing KEr3F10:Er3+ nanocrystals were prepared via the traditional melt-quenching technique. The micro-structures, optical properties and up-conversion luminescence behaviors of the Er3+ doped glass-ceramics were systemically studied using X-ray diffraction, absorption and up-conversion luminescence spectra. Under the excitation of a laser at 980 nm, the intensity of red emission of the glass-ceramics increases more than 70 times after heat treatment compared with that of the precursor glass ceramic. Moreover, the fluorescence intensity ratio of the thermally coupled energy levels (2H11/2 and 4S3/2) shows a good linear relationship with temperature and maintains relatively high sensitivities of 0.398% per K at 303-573 K, which indicates that the glass ceramics have promising applications in temperature detection. This journal is © The Royal Society of Chemistry.

Introduction

In recent years, rare earth (RE) ion doped up-conversion materials, including nanoparticles, glasses and glass-ceramics, have attracted wide attention because of their excellent characteristics and potential application prospects in solid-state lasers, multi-color displays, optical processing sensors, solar cells, bio-imaging etc.[1-8]

Compared with traditional oxyfluoride glass, RE doped transparent fluoride glass-ceramics have excellent optical properties and mechanical properties. They have a higher refractive index, lower local phonon energy and lower non-radiative relaxation probability, so high luminescence efficiency of REs has been observed.[9,10] In view of this, a large number of oxyfluoride glass-ceramics have been studied and considered as excellent hosts for rare earth ions to realize efficient up-conversion luminescence.[11-19] In these systems, the doping ions usually enter the crystalline lattice mainly through the diffusion of rare earth ions from the glass matrix to the precipitated crystals, which is greatly affected by the diffusion activation energy and diffusion coefficient of the RE ions in the glass.[20] Usually, at lower crystallization temperatures, the low diffusion coefficient of rare earth ions in the glass hinders their bonding in the crystal, while at high crystallization temperatures, the rapid growth of the grains significantly reduces the transparency of the glass-ceramics, thus resulting in unfavorable optical performance. Therefore, it is meaningful to prepare oxyfluoride glass-ceramics with good stability and transparency.

Among many rare earth ions, Er3+ ions is considered as the most ideal rare earth ions for near-infrared up-conversion due to its rich 4f–4f transition level. Moreover, Er3+ ions have a couple of thermally coupled energy levels (TCEL), 2H11/2 and 4S3/2 levels. Therefore, application of Er3+ doped glass-ceramics as optical temperature sensors has attracted increasing attention in recent years.[21-24] What's more, there is no report on optical temperature measurement of Er3+ doped KEr3F10 glass-ceramics. Therefore, it is of great significance to study the up-conversion luminescence and temperature sensing properties of Er3+ doped KEr3F10 glass-ceramics.

In this paper, highly transparent glass-ceramics containing KEr3F10 nanoparticles were successfully fabricated by properly designing the oxyfluoride glass composition. Unlike previously reported cases, glass-ceramics are formed directly by self-crystallization during melt quenching, and Er3+ is directly incorporated into the crystalline lattice rather than entering the already formed lattice during heat treatment. After heat treatment, the luminescence is enhanced more than 70 times. In addition, based on the fluorescence intensity ratio (FIR) technology, the temperature sensing characteristics of the glass-ceramic are also investigated.

Experiment

Precursor samples were prepared by melt-quenching method. The precursor glass (PG) compositions (mol%) is 22.5 KF-22.5 ZnF2-65 SiO2, ErF3 (0.1, 0.3, 0.5, 1, 1.5, 3 mol%). SiO2 (99.9%), ZnF (99.9%), KF (99.5%) and ErF3 (99.99%) were used as raw materials. About 20 g of a mixture of raw materials was placed into a covered platinum crucible and melted at 1450 °C for 30 minutes. Then, the glass melt was poured onto a 300 °C preheated stainless-steel plate and pressed by another plate to obtain the PG samples. After releasing the internal stress by heating at 450 °C for 3 h, the PG samples were crystallized by heat-treatment at 625 °C for 10 h to fabricate transparent glass ceramic (GC). All of the samples were polished carefully prior to optical measurements.

X-ray diffraction (XRD) patterns were acquired using a Philips X′ Pert PRO SUPER X-ray diffractometer (40 kV, 40 mA) equipped with a Cu Kα radiation source. The absorption spectra of the glass-ceramic samples were measured by a UV-Vis-NIR spectrophotometer Lambda 900 (PerkinElmer, USA). The morphology and crystal size of the nanocrystals in GC were obtained by high-resolution transmission electron microscope (HRTEM, 2100F, JEOL, Japan) The emission spectra of the samples were obtained using a computer Triax 320 type spectrometer (Jobin-Yvon Corp.) with a 980 nm continuous-wave laser. The pump power was adjusted through neutral density filters. The temperature-dependent spectra of the samples in the range of 298 to 573 K were also measured by the above spectrometers equipped with a temperature controller (FOTEK MT48-V-E, Taiwan). Except for the temperature dependent up-conversion luminescence spectra, all of the above tests were performed at room temperature.

Results and discussion

Fig. 1(a) shows the XRD patterns of different concentration Er3+ doped samples. PG shows weak diffraction peaks when the Er3+ doping concentration reaches 0.5%. The diffusion peak is caused by the amorphous glass phase, while the weak diffraction peaks means that a small amount of nanocrystals have formed after melt-quenching. XRD patterns of PG and GC are shown in Fig. 1(b). After heat treatment at 625 °C for 10 h, the diffraction peaks of GC sample corresponding to KEr3F10 nanocrystals (PDF no. 26-1311) become intense, which indicates that more nanocrystals are formed after the heat treatment. TEM images of GC sample are shown in Fig. 1(c). TEM micrograph reveals that KEr3F10 nanocrystals are homogeneously dispersed in amorphous glassy phase. The corresponding selected area electron diffraction (SAED) patterns indicate that glass-ceramics are composite materials that contain amorphous glasses and nanocrystals. The HRTEM image shows the resolved lattice fringes and the value of the associated interplanar spacing d is about 0.463 nm, which corresponds to (−2 0 7) crystal plane of KEr3F10 (d = 0.462 nm).

Fig. 1

(a) XRD patterns of different concentration Er3+ doped glass samples; (b) XRD pattern of PG, GC samples and standard XRD data of PDF card no. 26-1311 for KEr3F10; (c) TEM micrograph of GC and corresponding SAED pattern. (d) HRTEM image of GC.

Fig. 2(a) shows the upconversion spectra of PG and GC samples doped with 1% (mol) Er3+ excited by 980 nm laser. The emission bands located at 523 nm, 543 nm and 665 nm are assigned to 2H11/2 → 4I15/2, 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2 transition emissions of Er3+, severally.[25,26] It is clear that the up-conversion spectra of the sample show obvious Stark splitting at 543 and 665 nm. After heat treatment, the upconversion intensity of GC is greatly enhanced; although a few Er3+ ions have already participated into KEr3F10 nanocrystals before heat treatment. Specifically, the upconversion intensity of red emission of the GC enhances by more than 70 times compared to that of the PG. The enhance of upconversion luminescence may be due to the incorporation of Er3+ ions into KEr3F10 nanocrystals with lower phonon energy and the enrichment of Er3+ resulting in the change of the energy transfer mode between Er3+. From the transmission spectra of PG and GC samples shown in Fig. 2(b), it can be observed that PG and GC maintain good transparency and the transparency of GC is up to 76% in visible region. It can be seen that KEr3F10 glass-ceramics are transparent with excellent uniformity, indicative of homogeneous crystallization of these samples.

Fig. 2

(a) Upconversion spectra of PG and GC samples excited by 980 nm laser; (b) transmission spectra of PG and GC samples and the inset is the photograph of PG and GC.

For the upconversion process, upconversion emission intensity I is proportional to the nth power of the pump power P, that is[27]where n is the number of pump photons absorbed per upconversion photon emitted. A plot of log I versus log P yields a straight line with slope n. Fig. 3(a) and (b) show the power dependences of upconversion of PG and GC samples, respectively. For PG, the slopes n values are 1.81 ± 0.03 and 1.69 ± 0.03 for green and red emission, respectively. As to GC, n values are 1.79 ± 0.03 and 1.73 ± 0.03. The results reveal that both red and green upconversion emissions are caused by two-photon process.

Fig. 3

(a) Dependence of upconversion intensity on pump power for PG sample; (b) dependence of upconversion intensity on pump power for GC sample.

Fig. 4(a) shows the fluorescent lifetime curves of Er3+ 4F9/2 → 4I15/2 (666 nm) emission in PG and GC samples upon 980 nm LD. The prolongation of upconversion emission lifetime shows that the non-radiative relaxation rate of Er3+ in the GC sample decreases, which proves that Er3+ ions are preferentially enriched in KEr3F10 nanocrystals with lower phonon energy. The fluorescent lifetime curve of GC can be well fitted with a double exponential unction, which indicates that GC samples have multi-luminescent centers.

Fig. 4

(a) The fluorescence decay curves of Er3+ 4F9/2 → 4I15/2 (666 nm) emission in PG and GC samples (λex = 980 nm). (b) Energy level diagram of Er3+ and possible up-conversion mechanisms.

To understand the upconversion mechanism, the energy level diagram of Er3+ and possible upconversion mechanisms are shown in Fig. 4(b). Firstly, Er3+ ions in the ground state of 4I15/2 absorb a 980 nm phonon and be pumped to the intermediate excited state of 4I11/2 through ground state absorption (GSA). Then, these ions at 4I11/2 level can be excited to higher emitting levels through two famous upconversion processes: (1) excited state absorption (ESA), (2) energy transfer (ET). ESA process is a single ion process. The ET process involves two ions and therefore the rate depends largely on the distance between the active ions.

Because only a bit of KEr3F10:Er3+nanocrystals form in PG, a small amount of Er3+ ions merge into KEr3F10:Er3+ nanocrystals with low phonon energy and most of Er3+ are persisted in the glass phase, which can be confirmed by the weak stark splitting in PG (see Fig. 2(a)). ET and ESA process are responsible for the 2H11/2, 4S3/2 and 4F9/2 emission levels. ESA maybe the dominant process due to the uniform dispersion of Er3+ ions in the glass and the relatively long distance between Er3+ ions.

By absorbing one 980 nm photon, Er3+ ions at 4I11/2 level are stimulated to the level of 4F7/2 by ESA process, and then non-radiatively relax to the level of 2H11/2 and 4S3/2 levels. Finally, Er3+ ions at 2H11/2 and 4S3/2 emitting further relax to 4I15/2 level and produce upconversion emissions at 525 and 543 nm, respectively. For the red emission, there are two possible ways, including multi-phonon non-radiative relaxation from the upper level of 4S3/2 and a ESA processes: Er3+ ions absorb another photon from 4I13/2 level.[22,27] Intermediate excited states in 4I13/2 can be filled by multi-phonon non-radiation processes at 4I11/2 level and high radiation processes at 4S3/2 level.[18] Finally, the Er3+ ions radiation at 4F9/2 level relaxes to 4I15/2 ground state and produce red emission at 666 nm.

For GC sample, since the distance of Er3+–Er3+ is further shortened, the up-conversion mechanism belongs to ET process, which is a more efficient way for Er3+ ions at 4I11/2 level to be excited to higher emitting levels and produce stronger up-conversion luminescence. An excited Er3+ ion at 4I11/2 level relaxes non-radiatively to 4I15/2 level and transfers its excitation energy to a neighboring Er3+ ion at the same level, promoting the latter to 4F7/2 level: 4I11/2 + 4I11/2 → 4I15/2 + 4F7/2.[25] The red luminescent 4F9/2 level can be excited by the ET process: 4I13/2 + 4I11/2 → 4F9/2 + 4I15/2.[27] The emission intensity enhancement of red is more than green after further heat treatment, which can be considered as another energy transfer process, 4F7/2 + 4I15/2 → 4I11/2 + 4I11/2. Since the 4F7/2 level plays an important role in the green light emission process, the red emission in Fig. 2(a) is stronger than the green emission.

Fig. 5(a) is normalized upconversion spectra of the GC sample in the temperature range of 303–573 K under a 980 nm LD excitation. It is obvious that the intensity of 2H11/2 → 4I15/2 transition (525 nm) and 4S3/2 → 4I15/2 transition (543 nm) increases obviously as the temperature raises. Fig. 5(b) shows the temperature dependence of FIR between 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2 transitions of Er3+. Interestingly, the intensity of Er3+ exhibits a significantly different temperature dependent luminescence behavior compare to previous studies.[18,21-24]. The FIR of the TCEL (2H11/2 and 4S3/2) shows good linear temperature dependence. From 303 to 573 K the following linear dependence of FIR on temperature is found for KEr3F10:Er3+:

Fig. 5

(a) The normalized green up-conversion spectra of GC sample in the temperature range of 303–573 K under 980 nm LD excitation; (b) temperature dependence of FIR between 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2 transitions of Er3+.

It is different from the general temperature sensors that the sensitivity is enhanced first and then weakened. The sensitivity of GC sample maintains a relative high value of 0.398% per K at 303–573 K. This value is larger than most of other Er3+ ions doped glass and glass ceramics as listed in Table 1. The fluorescent lifetime curve of the glass ceramic sample can be well fitted with a double exponential function, which indicates that the sample has multi-luminescent centers. For the system with multiple luminescent centers, the number of particles in each excited state varies due to the energy transfer between ions, which may not obey Boltzmann distribution strictly.[28] This result indicates that KEr3F10:Er3+ glass-ceramics is a promising optical temperature sensing.

Sensitivity of several optical temperature sensors based on up-conversion emission from 2H11/2 and 4S3/2 levels of Er3+ ion

Sensing materials	Temperature range (K)	S max (10−3/K)	Temperature (K)	Ref.
KEr3F10:Er3+GC	303–573	3.98	303–573	This work
Sr2YbF7:Er3+GC	300–500	6.21	560	21
CaF2:Er3+glass	303–573	2.38	483	23
CaF2:Er3+GC	303–573	1.63	453	23
Na5Gd9F32:Er3+GC	300–510	1.79	499	22
K3YF6:Er3+GC	300–510	1.27	300	18
NaYF4:Er3+/Yb3+GC	298–693	0.35	560	24

Conclusion

Er3+-doped transparent KEr3F10 glass-ceramics were prepared via the melt-quenching method and subsequent heat treatment process. Significant Stark splitting, enhanced up-conversion emission in glass ceramics and extended fluorescent lifetime indicate that Er3+ preferentially enters KEr3F10 nanocrystals with low phonon energy and shorter Er3+–Er3+ distance after heat treatment. The FIR of the 525 nm and 543 nm shows good linear dependence and high sensitivity, which suggests that the explored KEr3F10 GC doped with Er3+ shows great potential for optical temperature sensing.

Conflicts of interest

There are no conflicts to declare.