卤化物
钙钛矿(结构)
异质结
钝化
光伏
热稳定性
材料科学
能量转换效率
铯
甲脒
钙钛矿太阳能电池
图层(电子)
化学
相(物质)
化学工程
光电子学
三卤化物
纳米技术
无机化学
光伏系统
结晶学
有机化学
工程类
生物
生态学
作者
Ziren Zhou,Shuang Yang,Kaixuan Xu,Hong Qiao,Jin Xie,Zeqing Lin,Bing Ge,Jingjing He,Mengjiong Chen,Jun Zhang,Yu Hou,Hua Yang
标识
DOI:10.1021/acs.jpclett.9b03414
摘要
The insertion of organic spacers into halide perovskite slabs has offered a trade-off between the efficiency and stability of perovskite solar cells (PSCs). The layered structure of diammonium-intercalated cesium lead halide perovskites is virtually unexplored, in contrast to several works on the monoammonium system. In this report, we find that perovskite with 1,4-butanediammonium (BDA) and cesium cations can only form n = 1 and n = 2 layered isologues defined by the chemical formula of (BDA)Csn–1Pbn(I0.7Br0.3)3n+1, while the n = 3–4 ones will self-construct into unique heterostructures comprising separated quantum wells (QWs; n = 1–2) and 3D (n = ∞) perovskites. We highlight that the 2D/3D heterostructures show a structural resemblance to that of bulk heterojunction in organics, thus improving the charge separation and transport more than surface passivation. Solar cells based on the (BDA)Cs3Pb4I9.1Br3.9 (n = 4) absorbing layer delivered a power conversion efficiency (PCE) reaching 9.49% with ideal light and thermal stability.
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