Richeng Lin 1†Yanming Zhu 1†Liang Chen 2†Wei Zheng 1,*[ ... ]Xiaoping Ouyang 2,5,***
Author Affiliations
Abstract
1 State Key Laboratory of Optoelectronic Materials and Technologies, School of Materials, Sun Yat-Sen University, Guangzhou 510275, China
2 State Key Laboratory of Intense Pulsed Radiation Simulation and Effect and Radiation Detection Research Center, Northwest Institute of Nuclear Technology, Xi’an 710024, China
3 School of Nuclear Science and Technology, Xi’an Jiaotong University, Xi’an 710049, China
4 CAS Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Key Laboratory of Nanomaterials, Fujian Institute of Research On the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China
5 School of Materials Science and Engineering, Xiangtan University, Xiangtan 411105, China
Large-size scintillators with high efficiency and ultrafast radiation fluorescence have shown more potential in the applications to ionizing radiation detection of medical diagnosis, nuclear control and high-energy physics. Currently, although traditional scintillators have made tremendous progress in scintillation efficiency, there are still challenges left in fluorescence lifetime. Faced with that problem, we adopted 2-inch ZnO as the substrate and doped gallium as activator to realize an ultrafast fluorescence excited by α-ray, of which the decay time is only 600 ps that is the shortest scintillation decay time reported so far. The results show that the shallow donor related with gallium not only effectively suppresses band-edge self-absorption, but makes ultrafast radiation possible, which gets gallium-doped ZnO as a potential scintillator for high-quality ultrafast dynamic imaging proved.
PhotoniX
2022, 3(1): 9
Author Affiliations
Abstract
State Key Laboratory of Optoelectronic Materials and Technologies, School of Materials, Sun Yat-sen University, Guangzhou, 510275 Guangdong, China
Black phosphorus has a strong Raman anisotropy on the basal and cross planes due to its orthorhombic crystal structure. However, almost all the studies on black phosphorus’ anisotropy focus on basal plane with the cross plane neglected. Here, we performed a systematic angle-resolved polarized Raman scattering on both the basal and cross planes of black phosphorus and obtained its integral Raman tensors. It is discovered that when the polarization direction of excitation light is along different crystal axes, the Raman intensity ratio (Ixx : Iyy: Izz) of $$ {A}_g^1 $$ mode is 256:1:5. Besides, via calculation, it is confirmed that the strong Raman anisotropy mainly comes from different differential polarizability alone different directions. This phenomenon is also observed when it comes to the $$ {A}_g^2 $$ mode.
PhotoniX
2020, 1(1): 17
Author Affiliations
Abstract
1 State Key Laboratory of Optoelectronic Materials and Technologies, School of Materials, Sun Yat-sen University, Guangzhou 510275, China
2 Key Laboratory of Materials Physics, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031, China
3 e-mail: zhengw37@mail.sysu.edu.cn
This publisher’s note corrects the order of the fourth author’s name in Photon. Res.6, 991 (2018)2327-912510.1364/PRJ.6.000991.
Photonics Research
2018, 6(12): 12001101
Author Affiliations
Abstract
1 State Key Laboratory of Optoelectronic Materials and Technologies, School of Materials, Sun Yat-sen University, Guangzhou 510275, China
2 Key Laboratory of Materials Physics, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031, China
3 e-mail: zhengw37@mail.sysu.edu.cn
Raman spectroscopy is a versatile tool widely used for comprehensive probing of crystal information. However, generally when applied in narrow-band-gap van der Waals crystals, it is liable to form a “bug,” especially in transition-metal-dichalcogenides (TMDs). That is, several resonant Raman-scattering (RS) modes will inevitably appear in the Raman spectra with strong intensity, interfering with the desired signal of optical-phonon modes. Here, we propose cross-sectional polarized Raman scattering capable of regulating the intensity of RS modes in accordance with quasi-sinusoidal rules. Typically, for MoS2 and WS2, when the polarization vector of excited light is along the c axis of the crystal, all RS modes are nearly completely “expunged” from the Raman spectra. The mechanism is that the absorption of most TMDs with a space group of R3m for the light polarized along the c axis is infinitesimal, thus forming a small coupling intensity of electronic states excited optically and acoustic-phonon modes at point M, which in turn restrain the appearance of RS modes. The regulating strategy proposed can be applied to other van der Waals crystals so as to obtain a high signal-to-noise ratio Raman spectrum.
Photonics Research
2018, 6(11): 11000991

关于本站 Cookie 的使用提示

中国光学期刊网使用基于 cookie 的技术来更好地为您提供各项服务,点击此处了解我们的隐私策略。 如您需继续使用本网站,请您授权我们使用本地 cookie 来保存部分信息。
全站搜索
您最值得信赖的光电行业旗舰网络服务平台!