制作
双层
钙钛矿(结构)
异质结
材料科学
电介质
卤化物
带隙
溶解
基质(水族馆)
光伏系统
纳米技术
极性(国际关系)
图层(电子)
相(物质)
光电子学
化学工程
化学
结晶学
无机化学
膜
医学
生物化学
有机化学
生物
病理
海洋学
地质学
替代医学
细胞
生态学
工程类
作者
Siraj Sidhik,Yafei Wang,Michael C. De Siena,Reza Asadpour,Andrew Torma,Tanguy Terlier,Kevin Ho,Wenbin Li,Anand B. Puthirath,Xinting Shuai,Ayush Agrawal,Boubacar Traoré,Matthew R. Jones,Rajiv Giridharagopal,Pulickel M. Ajayan,Joseph Strzalka,David S. Ginger,Claudine Katan,Muhammad A. Alam,Jacky Even,Mercouri G. Kanatzidis,Aditya D. Mohite
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2022-09-22
卷期号:377 (6613): 1425-1430
被引量:261
标识
DOI:10.1126/science.abq7652
摘要
Realizing solution-processed heterostructures is a long-enduring challenge in halide perovskites because of solvent incompatibilities that disrupt the underlying layer. By leveraging the solvent dielectric constant and Gutmann donor number, we could grow phase-pure two-dimensional (2D) halide perovskite stacks of the desired composition, thickness, and bandgap onto 3D perovskites without dissolving the underlying substrate. Characterization reveals a 3D–2D transition region of 20 nanometers mainly determined by the roughness of the bottom 3D layer. Thickness dependence of the 2D perovskite layer reveals the anticipated trends for n-i-p and p-i-n architectures, which is consistent with band alignment and carrier transport limits for 2D perovskites. We measured a photovoltaic efficiency of 24.5%, with exceptional stability of T 99 (time required to preserve 99% of initial photovoltaic efficiency) of >2000 hours, implying that the 3D/2D bilayer inherits the intrinsic durability of 2D perovskite without compromising efficiency.
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