Advances in Condensed Matter Physics
Volume 2017 (2017), Article ID 5304791, 6 pages
https://doi.org/10.1155/2017/5304791

Research Article

Surface Plasmon Resonance Enhanced Spontaneous Upconversion and Stimulated Emissions in Glass Ceramics Containing Ba₂LaF₇ Nanocrystals

Sai Li,¹ Wei Lu,² Qihua Yang,¹ Dacheng Zhou,1,3 Jianbei Qiu,1,3 Xuhui Xu,1,3 and Xue Yu1,3

¹College of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093, China
²University Research Facility in Materials Characterization and Device Fabrication, The Hong Kong Polytechnic University, Hung Hom, Hong Kong
³Key Laboratory of Advanced Materials of Yunnan Province, Kunming 650093, China

Correspondence should be addressed to Xue Yu; yuyu6593@126.com

Received 19 June 2017; Accepted 10 August 2017; Published 13 September 2017

Academic Editor: Zaiquan Xu

Copyright © 2017 Sai Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Glass ceramics containing Yb³⁺, Er³⁺ codoped Ba₂LaF₇ nanocrystals were fabricated via melt quenching method and the subsequent heating treatment. The formation of Ba₂LaF₇ nanocrystals in the glass ceramics was confirmed by X-ray diffraction (XRD) and transmission electron microscope (TEM). The spontaneous upconversion (UC) emission and the stimulated counterpart as a random lasing action of Er³⁺, which were related to the characteristic transitions of Er³⁺ ions, were achieved in the Yb³⁺, Er³⁺-doped Ba₂LaF₇ nanocrystals embedded glass ceramic hybrid. Furthermore, the absorption spectra verified the surface plasmon resonance (SPR) band of Ag, which precipitated from the matrix glasses as Ag nanoparticles (NPs). By incorporating Ag NPs in the glass ceramic hybrid, spontaneous UC emission intensity of Er³⁺ in visible region was significantly enhanced, while the threshold of the random lasing was decreased from 480 to 350 nJ/cm².

1. Introduction

The integration of novel luminescent nanometer materials into glassy matrix can bring about new and promising optical hybrid materials and photonic devices in recent years [1]. Great enhancement of optical emission efficiency was realized in fluorosilicate glasses by the growth of the lanthanide doped fluoride nanocrystals embedded in the glass matrix [2]. Lanthanide-containing UC nanocrystals have become distinct candidates for biomedical imaging, anticounterfeiting, biological sensing, solar energy management, data storage, and 3D volumetric displays, which enable higher-energy emissions in the ultraviolet to visible spectral range by upconverting two or more near-infrared excitation photons [3, 4]. Once lanthanide ions are located inside the fluoride nanocrystals, they will be in the low phonon energy environment. So the multiphonon relaxation rates can be significantly reduced from some excited states [5, 6]. Oxyfluoride glass ceramics combine the favorable properties of fluoride crystal (low refractive index and phonon energy) and the oxide glasses (high chemical stability and large solubility of rare-earth (RE) ions). Thus, oxyfluoride glass ceramics have potential applications in the fields of luminescence applications and laser [7].

Er³⁺-doped UC materials are popular due to their high luminescence quenching concentration compared to other rare-earth ions. In addition, Er³⁺ ions have a large spectral overlap with Yb³⁺, and Yb³⁺ ions can absorb the photons of 980 nm effectively. Therefore, Yb³⁺ and Er³⁺ codoping materials can enhance the UC efficiency through the energy transfer, which demonstrated that the Yb³⁺ and Er³⁺ codoping materials exhibit excellent luminescent properties. SPR arises by the collective oscillation of electrons on the metal nanoparticles, which can have either beneficial or deleterious effect depending on the position of the SPR peak and the distance of the luminophore from the metal surface [8, 9]. Recently, SPR has been energetically used to improve the emission efficiency of luminescent materials and devices. For example, the photoluminescence (PL) intensity in the dye-doped polymers [10], CdSe quantum dots [11], Si quantum dots [12], ZnO films [13, 14], and InGaN quantum wells [15] was improved significantly due to the SPR excitation. In contrast to the continuous efforts to spontaneous emissions, little knowledge has been known in the stimulated counterparts. However, the incorporation of metallic nanostructures into optical gain media may lead to a breakthrough of laser devices, that is, to beat the diffraction limit with regard to both of the physical dimension and optical mode size [16]. Besides, the enhanced local field occurring in hot spots is particularly important to trigger low threshold lasing resonance because it can locally enhance the pump rate of gain media [7, 17].

Thus, in this work, Yb³⁺, Er³⁺-doped Ba₂LaF₇ glass ceramic as an effective UC material was synthesized via conventional melt quenching technique and the subsequently heat treatment. Besides, a nanosecond laser pumped random lasing action has been achieved in the silicate oxyfluoride glass ceramics containing Ba₂LaF₇ nanocrystals. By incorporating Ag NPs, spontaneous UC emission intensity of Er³⁺ in visible region was drastically enhanced, while the threshold of the random lasing decreased significantly from 450 to 350 nJ/cm².

2. Experimental

The glass ceramic samples were prepared according to the following composition (mol%): 45SiO₂-15Al₂O₃-12Na₂CO₃-20BaF₂-6.5LaF₃-1YbF₃-0.5ErF₃ doped with wt% of Ag₂O by the conventional melt quenching technique (, 0.1, 0.3, 0.5, 0.7), denoted as 0 Ag, 0.1 Ag, 0.3 Ag, 0.5 Ag, and 0.7 Ag. About 10 g of original material was fully mixed and then melted in an air atmosphere at 1500°C for 45 min. The crucible was covered with an alumina cap to avoid volatilization loss. The molten glass was cast into a carbon plate maintained at about 300°C. The glass samples were annealed at 500°C for 8 h to avoid internal stress. The obtained glass was thermally treated at 670°C for 2 h to induce crystallization.

XRD was performed using a D8 Focus diffractometer (Bruker) with Cu-Kα radiation ( nm) in the 2θ range from 20° to 70°. The UC photoluminescence spectra in the wavelength range of 450 to 700 nm were recorded by using a HITACHIF-7000. Fluorescence spectrophotometer was under the excitation of 980 nm laser diode with the power of 2 W. The absorption spectra were recorded in the wavelength range from 350 to 600 nm using a Model U-4100 Spectrophotometer. To detect the nucleation and growth of Ag NPs, a TEM (JEM-2100) operating at an accelerating voltage of 200 kV was used. For the laser measurement, a Continuum Panther EX optical parametric oscillator and a 355 nm frequency-tripled Continuum Powerlite DLS 9010 Q-switched Nd: YAG laser were used to generate 980 nm pump pulses of width and repetition rate of ≈6 ns and 10 Hz, respectively. The laser beam of diameter equal to 8 mm was focused on the surface of the glass ceramics by a cylindrical lens with focal length of 100 mm. Light emitted from the side of the glass was recorded by an optical fiber connected to a spectrum analyzer (Oriel MS257 monochromator with spectral resolution ≈ 0.1 nm). The sample was placed in a temperature regulating chamber with N₂ (Linkam DSC 600 stage system). For the sample under pulse excitation, the temperature rise was negligible due to the influence of the optical pumping. However, for continuous wave excitation samples, the average temperature of the sample must be offset 18 K.

3. Results and Discussion

Figure 1(a) shows the differential scanning calorimetry (DSC) spectrum of the 0.5 Ag sample. As can be seen in this figure, there are three temperature parameters: the glass transition temperature () located in the vicinity of 574°C and temperature of two crystallization peaks (, ) located at the vicinity of 630°C and  745°C. According to the differential thermal analysis (DTA) results analysis, in this study, all the prepared glasses were heat-treated at 670°C for 2 h to precipitate nanocrystals. Figure 1(b) displays the XRD patterns of the samples by modulating the Ag concentration, respectively. All the diffraction peaks of the samples are in good agreement with hexagonal Ba₂LaF₇ (the standard JCPDS 48-0099). No second phase is detected in the XRD pattern, revealing that the high purity cubic phase of Ba₂LaF₇ has been fabricated.

(a)

(b)

Figure 1: (a) DSC of 0.5 Ag sample. (b) XRD patterns of glass ceramic samples with different Ag concentration.

The TEM micrograph of the 0 Ag sample in Figure 2(a) demonstrates that Ba₂LaF₇ nanocrystals with the diameter of 7–12 nm distribute homogeneously among the glass matrix. HR-TEM image of Figure 2(b) shows the presence of clear and resolved lattice fringes of 0 Ag sample. The inset in Figure 2(b) is the enlargement of HR-TEM image of the corresponding sample. As shown in the inset of Figure 2(b), the interplanar distance between the adjacent fringes is determined to be 0.427 nm, which matches well, respectively, with those of the (111) plane of the cubic Ba₂LaF₇. The TEM image of the 0.5 Ag sample is shown in Figure 2(c), indicating the presence of near-spherical NPs distributed homogeneously in the glass matrix with the particle size of about 2 to 4 nm. Figure 2(d) is the HR-TEM image of 0.5 Ag sample and the enlargement of HR-TEM image of the corresponding (the inset of Figure 2(d)). It shows that the interplanar distance between the adjacent fringes is determined to be 0.261 nm ascribed to the (200) planes of Ag. Thus, it is unambiguous evidence that Ag NPs are randomly distributed in the glass matrix.

(a)

(b)

(c)

(d)

Figure 2: (a) TEM micrograph of 0 Ag sample: the inset is the SAED pattern of the 0 Ag sample. (b) HR-TEM image of 0 Ag sample: the inset is the enlargement of HR-TEM image of the corresponding sample. (c) TEM micrograph of 0.5 Ag sample. (d) HR-TEM image of 0.5 Ag sample: the inset is the enlargement of HR-TEM image of the corresponding sample.

Figure 3(a) shows the UC photoluminescence spectra of 0 Ag, 0.1 Ag, 0.3 Ag, 0.5 Ag, and 0.7 Ag samples pumped by 980 nm with 60 W/cm² excitation density. The characteristic green (540 nm) and red (658 nm) emissions, corresponding to ⁴S3/2⁴I15/2 and ⁴F9/2⁴I15/2 transitions of Er³⁺, respectively, are simultaneously observed. The UC emission intensity is greatly improved with increasing concentration of Ag₂O, and the maximum enhancement is realized when the concentration of Ag₂O is up to 0.5 wt%. Then, the UC emission intensity decreases with further increase of Ag₂O concentrations. The inset exhibits the absorption spectra of the 0 Ag, 0.1 Ag, 0.3 Ag, 0.5 Ag, and 0.7 Ag samples. Absorption bands attributed to 4f-4f transitions of Er³⁺ ions corresponding to transitions starting from the ground state to the excited states are observed. As shown in the inset, the absorption spectra of the sample with Ag₂O show a distinctive band centered at 420 nm that is attributed to the SPR associated with the Ag NPs [18]. The primary reason for such fluorescence intensification of RE ions which is attributed to a local field enhancement induced by SPR of metal NPs has been accepted [19–23].

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(b)

Figure 3: (a) UC luminescence spectra of samples with different Ag concentration under the excitation of 980 nm laser diode: the inset is absorption spectra of samples by modulating the Ag concentration. (b) Room temperature luminescence decay curves of ⁴S3/2⁴I15/2 (Er³⁺) transition of the 0 Ag, 0.1 Ag, 0.3 Ag, 0.5 Ag, and 0.7 Ag samples.

In order to investigate the dependence of the UC emission intensities on the Ag₂O concentrations in detail, the emission decay curves of the ⁴S3/2⁴I15/2 transitions of Er³⁺ in the series of Ag doped samples were measured under the 980 nm excitation, as displayed in Figure 3(b). The effective experimental lifetime can be evaluated as follows:

where represents the luminescence intensity at time after the cut-off of the excitation light. The lifetime of the transitions of ⁴S3/2⁴I15/2 is determined to be 0.400, 1.122, 1.459, 0.982, and 0.732 ms in the 0 Ag, 0.1 Ag, 0.3 Ag, 0.5 Ag, and 0.7 Ag samples, respectively. The lifetime decreases after the first increase, and the variation tendency agrees well with the change of UC luminescence intensities of green emission. The lifetime result is an evidence of an accelerating energy transfer from Yb³⁺ to Er³⁺ with increasing Ag NPs content [24, 25], which indicates that some energy transfer from fluorescent Ag NPs to Er³⁺ cannot be totally ignored.

Interestingly, microcavities can be realized by randomly embedding Ba₂LaF₇:Yb³⁺, Er³⁺ nanocrystals inside the glass and random lasing action can be achieved in the glass ceramic. The optically pumped spectra of 0.5 Ag sample were collected under the 980 nm nanosecond laser beam; it was found that the Ag NPs decorated glass ceramics containing Ba₂LaF₇ nanocrystals exhibit a similar optically pumped random lasing characteristic as the corresponding glass ceramics without Ag. Figure 4(a) shows the lasing characteristics of the glass ceramics with the decoration of Ag NPs under different 980 nm pulsed excitation power at room temperature. As the pump energy exceeds an excitation threshold, , of 385 nJ/cm² (i.e., kink of the light-light curve as shown in Figure 4(b)), one sharp peak emerges from the emission spectrum. In addition, further increase of the excitation intensity increases the number of sharp peaks. In this case, the sharp peaks represent the formation of closed-loop paths for light (i.e., the realization of microcavities due to the coherent optical feedback from the Ag NPs). Figure 4(b) provides a direct proof of the central role of local field enhancement in the emergence of low threshold lasing resonance, and the threshold of the lasing decreased from 480 to 350 nJ/cm² with decorating of Ag NPs. It can be safe to say that the enhanced local field occurring in hot spots is particularly important to trigger low threshold lasing resonance since it can locally enhance the pump rate of gain media [26, 27]. The corresponding plot of Fourier transform spectrum, as shown in Figure 4(c), exhibits periodic features, indicating the formation of closed-loop paths, and the round-trip cavity length of the random modes inside the glass hybrid is ca. 9.81 μm. The inset of Figure 4(a) is the photograph of the 0.5 Ag under the excitation of 980 nm nanosecond laser. It is clearly seen that a collimated output beam is emitted from one of the edge facets from the glass. The green spot projected behind a lens represents an output beam of lasing. This indicates that the output beam is highly directional and spatially coherent at a particular direction.

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(b)

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Figure 4: (a) Emission spectra of 0.5 Ag sample under different pump intensity of 980 nm nanosecond lasers: the inset is the photograph of 0.5 Ag sample under excitation of 980 nm nanosecond. (b) Integrated emission intensity of 0 Ag and 0.5 Ag samples versus pumping energy density. (c) Plot of Fourier transform (FT) patterns of the lasing spectra of the 0.5 Ag sample.

4. Conclusions

The spontaneous UC emissions intensity of Er³⁺ is drastically improved with the Ag NPs emerged in Ba₂LaF₇ glass ceramic for the contribution of the SPR and some of the energy transfer from Ag NPs to Er³⁺. Meanwhile, the stimulated emission as a random lasing action is achieved in this hybrid material. It is found that the incorporation of Ag NPs is advantageous in reducing the threshold of the lasing action. Therefore, the new class of hybrid glasses allows for fiber-based devices to be developed for photonic applications or as a useful tool for tailoring light-nanoparticles interactions study.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

This work was financially supported by the National Nature Science Foundation of China (61565009, 61308091), the Foundation of Natural Science of Yunnan Province (2016FB088), the Young Talents Support Program of Faculty of Materials Science and Engineering, Kunming University of Science and Technology (14078342), and the Postdoctoral Science Foundation of China (2013M540720).

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