Na-Dependent Ultrafast Carrier Dynamics of CdS/Cu(In,Ga)Se2 Measured by Optical Pump-Terahertz Probe Spectroscopy

被引:19
作者
Lee, Woo-Jung [1 ]
Cho, Dae-Hyung [1 ]
Wi, Jae-Hyung [1 ]
Han, Won Seok [1 ]
Chung, Yong-Duck [1 ,2 ]
Park, Jaehun [3 ]
Bae, Jung Min [4 ]
Cho, Mann-Ho [4 ]
机构
[1] Elect & Telecommun Res Inst, Components & Mat Res Lab, Taejon 305700, South Korea
[2] Korea Univ Sci & Technol, Dept Adv Device Engn, Taejon 305350, South Korea
[3] POSTECH, Pohang Accelerator Lab, Fs THz Lab, Pohang 790784, South Korea
[4] Yonsei Univ, Inst Phys & Appl Phys, Seoul 120749, South Korea
关键词
CU(IN; GA)SE-2; SOLAR-CELLS; THIN-FILMS; CUINSE2; PHOTOLUMINESCENCE; SEMICONDUCTORS; EFFICIENCY; LIFETIME; NANOWIRES; LAYERS;
D O I
10.1021/acs.jpcc.5b02282
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
To investigate the origin of the Na effect on photovoltaic (PV) devices, Cu(In,Ga)Se-2 (CIGS) and CdS/CIGS layers were grown on borosilicate (BS) and soda-lime glass (SLG), respectively. The defect states and nonequilibrium carrier dynamics of the samples were measured using photoluminescence (PL) and optical pump-THz probe (OPTP) spectroscopy. From the PL results, we discovered that different shallow donor-acceptor levels were formed in the CIGS layer grown on BS and SLG, respectively. In the OPTP results, relaxation times of photocarriers excited from the CdS/CIGS layer were clearly distinguishable, and are explained by the formation of different defect states depending on substrates. In BS, deep defect level 'DX states' were formed in the E-g near the p-n junction, which induce trapping photocarriers, resulting in shortening relaxation time. In SLG, there was no "DX state", which clearly demonstrates the positive effect of Na atoms at the p-n junction on performance of PV devices.
引用
收藏
页码:20231 / 20236
页数:6
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