节点文献

介孔钙钛矿太阳能电池中二氧化锡基电子传输层的合理设计:比传统双层结构更具动力学优势(英文)

Rational design of SnO2-based electron transport layer in mesoscopic perovskite solar cells:more kinetically favorable than traditional double-layer architecture

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 董庆顺薛源王适王立铎陈凡张森迟日涵赵亮史彦涛

【Author】 Qingshun Dong;Yuan Xue;Shi Wang;Liduo Wang;Fan Chen;Sen Zhang;Rihan Chi;Liang Zhao;Yantao Shi;Key Laboratory of Organic Optoelectronics & Molecular Engineering of Ministry of Education,Department of Chemistry,Tsinghua University;State Key laboratory of Fine Chemicals,School of Chemistry,Dalian University of Technology;

【机构】 Key Laboratory of Organic Optoelectronics & Molecular Engineering of Ministry of Education,Department of Chemistry,Tsinghua UniversityState Key laboratory of Fine Chemicals,School of Chemistry,Dalian University of Technology

【摘要】 本文采用点分布SnO2和TiO2介孔层中的纳米粒子组成的"协同层"作为高效介孔钙钛矿太阳能电池的电子传输层衬层.基于该新策略,电荷复合和能量损失路径被有效阻隔,使得之前报道的SnO2基电子传输层介孔钙钛矿太阳能电池中的强烈电荷复合被有效抑制.同时,整个介孔钙钛矿太阳能电池的串联电阻显著降低.新型的电子传输层动力学上更有利的电子传输有效提升了介孔钙钛矿太阳能电池的光伏性能,并明显抑制了电池的回滞.

【Abstract】 Here,the interfacial synergism of discontinuous spot shaped SnO2 and TiO2 mesoporous nanocomposite as electron transfer layer(ETL) underlayer is presented in highly efficient mesoscopic perovskite solar cells(M-PSCs). Based on this new strategy,strong charge recombination observed in previous SnO2-based ETLs is suppressed to a great extent as the pathways of charge recombination and energy loss are blocked effectively. Meanwhile,the internal series resistance of entire M-PSC is decreased remarkably. The new ETL is more kinetically favorable to electron transfer and thus results in significant photovoltaic improvement and alleviated hysteresis effect of M-PSCs.

【基金】 supported by the National Natural Science Foundation of China (51402036,51273104 and 91433205);the International Science & Technology Cooperation Program of China (2013DFA51000)
  • 【文献出处】 Science China Materials ,中国科学:材料科学(英文版) , 编辑部邮箱 ,2017年10期
  • 【分类号】TM914.4
  • 【被引频次】5
  • 【下载频次】261
节点文献中: 

本文链接的文献网络图示:

本文的引文网络