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通过自组装二维介电层实现具有隧道结的高效宽带隙钙钛矿太阳能电池

Highly Efficient Wide Bandgap Perovskite Solar Cells With Tunneling Junction by Self-Assembled 2D Dielectric Layer.

作者信息

Lee Minwoo, Lim Jihoo, Choi Eunyoung, Soufiani Arman Mahboubi, Lee Seungmin, Ma Fa-Jun, Lim Sean, Seidel Jan, Seo Dong Han, Park Ji-Sang, Lee Wonjong, Lim Jongchul, Webster Richard Francis, Kim Jincheol, Wang Danyang, Green Martin A, Kim Dohyung, Noh Jun Hong, Hao Xiaojing, Yun Jae Sung

机构信息

School of Materials Science and Engineering, University of New South Wales, Sydney, NSW, 2052, Australia.

Australian Centre for Advanced Photovoltaics (ACAP), School of Photovoltaic and Renewable Energy Engineering, University of New South Wales, Sydney, NSW, 2052, Australia.

出版信息

Adv Mater. 2024 Oct;36(41):e2402053. doi: 10.1002/adma.202402053. Epub 2024 Aug 15.

Abstract

Reducing non-radiative recombination and addressing band alignment mismatches at interfaces remain major challenges in achieving high-performance wide-bandgap perovskite solar cells. This study proposes the self-organization of a thin two-dimensional (2D) perovskite BAPbBr layer beneath a wide-bandgap three-dimensional (3D) perovskite CsFAPb(IBr), forming a 2D/3D bilayer structure on a tin oxide (SnO) layer. This process is driven by interactions between the oxygen vacancies on the SnO surface and hydrogen atoms of the n-butylammonium cation, aiding the self-assembly of the BAPbBr 2D layer. The 2D perovskite acts as a tunneling layer between SnO and the 3D perovskite, neutralizing the energy level mismatch and reducing non-radiative recombination. This results in high power conversion efficiencies of 21.54% and 19.16% for wide-bandgap perovskite solar cells with bandgaps of 1.7 and 1.8 eV, with open-circuit voltages over 1.3 V under 1-Sun illumination. Furthermore, an impressive efficiency of over 43% is achieved under indoor conditions, specifically under 200 lux white light-emitting diode light, yielding an output voltage exceeding 1 V. The device also demonstrates enhanced stability, lasting up to 1,200 hours.

摘要

减少非辐射复合以及解决界面处的能带对准失配问题,仍然是实现高性能宽带隙钙钛矿太阳能电池的主要挑战。本研究提出在宽带隙三维(3D)钙钛矿CsFAPb(IBr)下方自组装一层薄的二维(2D)钙钛矿BAPbBr层,在氧化锡(SnO)层上形成2D/3D双层结构。这一过程由SnO表面的氧空位与正丁基铵阳离子的氢原子之间的相互作用驱动,有助于BAPbBr二维层的自组装。二维钙钛矿充当SnO与三维钙钛矿之间的隧穿层,消除能级失配并减少非辐射复合。这使得带隙为1.7和1.8 eV的宽带隙钙钛矿太阳能电池的功率转换效率分别高达21.54%和19.16%,在1个太阳光照下开路电压超过1.3 V。此外,在室内条件下,特别是在200勒克斯的白色发光二极管光下,实现了超过43%的令人印象深刻的效率,输出电压超过1 V。该器件还表现出增强的稳定性,可持续长达1200小时。

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