制作
双层
钙钛矿(结构)
材料科学
纳米技术
光电子学
工程物理
化学工程
化学
物理
膜
替代医学
病理
工程类
生物化学
医学
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
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2022-09-22
卷期号:377 (6613): 1425-1430
被引量:328
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 T99 (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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