首页> 外文期刊>Advanced functional materials >Defective MWCNT Enabled Dual Interface Coupling for Carbon-Based Perovskite Solar Cells with Efficiency Exceeding 22
【24h】

Defective MWCNT Enabled Dual Interface Coupling for Carbon-Based Perovskite Solar Cells with Efficiency Exceeding 22

机译:碳基钙钛矿太阳能电池的MWCNT双界面耦合缺陷,效率超过22

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Suffering from sluggish charge transfer kinetics, carbon-based perovskitesolar cells (C-PSCs) lag far behind the Ag/Au-based normal PSCs in powerconversion efficiency (PCE). Herein, the use of defective multi-walled CNT(D-MWCNT) is demonstrated to tune the charge transfer kinetics regardinghole transport layer (HTL) and the interface between HTL and carbon electrode.Benefiting from the electrostatic dipole moment interaction between theterminal oxygen-containing groups of D-MWCNT and 2,2′,7,7′-tetrakis(N,Ndi-p-methoxyphenylamine)-9,9′-spirobifluorene, an interface coupling atmolecular level is established and in turn, allows rapid charge transfer byedge effect induced electron redistribution and 1D hyper-channels. Meanwhile,a seamless connection between HTL and carbon electrode is achievedin a novel modular C-PSCs due to D-MWCNT induced interface coupling withgraphene at nanometer scale. Based on this strategy, high PCEs up to 22.07(with a certified record PCE of 21.9 to date for C-PSCs) and excellent operationalstability have been achieved.
机译:碳基钙钛矿太阳能电池(C-PSCs)受电荷转移动力学迟缓的影响,在功率转换效率(PCE)方面远远落后于Ag/Au基普通PSC。本文展示了使用缺陷多壁CNT(D-MWCNT)来调节空穴传输层(HTL)以及HTL与碳电极之间界面的电荷转移动力学。利用D-MWCNT末端含氧基团与2,2′,7,7′-四(N,Ndi-对甲氧基苯胺)-9,9′-螺二芴之间的静电偶极矩相互作用,在分子水平上建立了界面耦合,进而通过边缘效应诱导的电子再分布和一维超通道实现快速电荷转移。同时,由于D-MWCNT诱导与石墨烯在纳米尺度上的界面耦合,在新型模块化C-PSCs中实现了HTL和碳电极之间的无缝连接。基于这一策略,已经实现了高达22.07%的高PCE(迄今为止C-PSC的认证记录PCE为21.9%)和出色的运行稳定性。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号