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Sn类钙钛矿太阳电池薄膜的掺杂改性研究
引用本文:檀满林,杨帅,马清,符冬菊,李冬霜,王晓伟,张维丽,陈建军,张化宇.Sn类钙钛矿太阳电池薄膜的掺杂改性研究[J].无机化学学报,2016,32(9):1565-1571.
作者姓名:檀满林  杨帅  马清  符冬菊  李冬霜  王晓伟  张维丽  陈建军  张化宇
作者单位:深圳清华大学研究院, 深圳 518057,深圳清华大学研究院, 深圳 518057;哈尔滨工业大学深圳研究生院, 深圳 518055,深圳清华大学研究院, 深圳 518057,深圳清华大学研究院, 深圳 518057,深圳清华大学研究院, 深圳 518057,深圳清华大学研究院, 深圳 518057,深圳清华大学研究院, 深圳 518057,深圳清华大学研究院, 深圳 518057,哈尔滨工业大学深圳研究生院, 深圳 518055
基金项目:深圳市科技计划项目(No.CXZZ20150323160924557,JCYJ20160301100700645)和广东省科技计划(No.2014A010106004,2016B020244001)资助。
摘    要:采用一步法分别制备了Sn类CH3NH3Sn I3和Pb类CH3NH3Pb I3钙钛矿太阳电池薄膜材料,并对其表面形貌、微观结构、吸收光谱和电池器件性能进行了表征和测试。研究结果表明:Sn类钙钛矿材料的吸收光谱相对于Pb类钙钛矿材料发生了明显的红移,吸收截止波长从800 nm上升到950 nm左右,光学带隙由1.45 e V降低至1.21 e V左右;Sn类钙钛矿材料的光谱吸收范围明显扩大,但吸收强度有所降低,相应太阳电池器件的光电转换效率也明显低于Pb类钙钛矿太阳电池,分别为2.05%和6.71%。而Br的掺杂可使Sn类钙钛矿材料带隙变宽,吸收光子能量增大,电池器件的开路电压也相应提高。当Br含量由0增加至完全替代I时,Sn类钙钛矿材料逐渐由黑褐色转变为黄色,光学带隙增大至1.95 e V,但吸收截止波长由950 nm降低至650nm。值得提及的是当Br含量为0.5时,电池器件的光电转换效率可由最初的2.05%提升至2.94%。

关 键 词:钙钛矿太阳电池  甲铵锡碘  掺杂改性
收稿时间:2016/4/19 0:00:00
修稿时间:2016/7/28 0:00:00

Doping Modification of Stannic Perovskite Based Thin Films for Solar Cell Applications
TAN Man-Lin,YANG Shuai,MA Qing,FU Dong-Ju,LI Dong-Shuang,WANG Xiao-Wei,ZHANG Wei-Li,CHEN Jian-Jun and ZHANG Hua-Yu.Doping Modification of Stannic Perovskite Based Thin Films for Solar Cell Applications[J].Chinese Journal of Inorganic Chemistry,2016,32(9):1565-1571.
Authors:TAN Man-Lin  YANG Shuai  MA Qing  FU Dong-Ju  LI Dong-Shuang  WANG Xiao-Wei  ZHANG Wei-Li  CHEN Jian-Jun and ZHANG Hua-Yu
Institution:Research Institute of Tsinghua University in Shenzhen, Shenzhen, Guangdong 518057, China,Research Institute of Tsinghua University in Shenzhen, Shenzhen, Guangdong 518057, China;Harbin Institute of Technology Shenzhen Graduate School, Shenzhen, Guangdong 518055, China,Research Institute of Tsinghua University in Shenzhen, Shenzhen, Guangdong 518057, China,Research Institute of Tsinghua University in Shenzhen, Shenzhen, Guangdong 518057, China,Research Institute of Tsinghua University in Shenzhen, Shenzhen, Guangdong 518057, China,Research Institute of Tsinghua University in Shenzhen, Shenzhen, Guangdong 518057, China,Research Institute of Tsinghua University in Shenzhen, Shenzhen, Guangdong 518057, China,Research Institute of Tsinghua University in Shenzhen, Shenzhen, Guangdong 518057, China and Harbin Institute of Technology Shenzhen Graduate School, Shenzhen, Guangdong 518055, China
Abstract:The plumbic and stannic perovskite solar cell materials such as CH3NH3SnI3 and CH3NH3PbI3 were obtained by one step preparation with the surface morphology, microstructure, spectral absorption and device performance were investigated respectively. The spectral absorption of stannic perovskite material were found to expand wider and have an obvious red-shift compared to plumbic perovskite, with the absorption edge increased from 800 to 950 nm and the optical band gap reduced from 1.45 to 1.21 eV. But the conversion efficiency of stannic perovskite solar cell demonstrated significantly lower than that of plumbic perovskite, 2.05% and 6.71% respectively, due to a downshift of absorption intensity. However, bromine (Br) doping could broaden the band gap and thus give rise to the open circuit voltage of solar cell device accordingly. As the doping content increased from 0 to be totally replacement of iodine, the color of stannic perovskite turned gradually from dark brown to yellow, and the optical band gap increased up to 1.95 eV. At the same time, a blue shift of spectra absorption was observed, reducing from 950 to 650 nm. Noteworthy is that the solar cell conversion efficiency increased from initial 2.05% to 2.94% at the doping content of 0.5.
Keywords:perovskite solar cell  stannic perovskite  doping modification
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