机构地区:[1]Renewable Energy Conversion and Storage Center,Solar Energy Conversion Center,Institute of Photoelectronic Thin Film Devices and Technology,Nankai University,Tianjin 300350,People’s Republic of China [2]Key Laboratory of Photoelectronic Thin Film Devices and Technology of Tianjin,Tianjin 300350,People’s Republic of China [3]Haihe Laboratory of Sustainable Chemical Transformations,Tianjin 300192,People’s Republic of China [4]Engineering Research Center of Thin Film Photoelectronic Technology of Ministry of Education,Tianjin 300350,People’s Republic of China [5]Collaborative Innovation Center of Chemical Science and Engineering(Tianjin),Tianjin 300072,People’s Republic of China [6]Center of Single‑Molecule Sciences,Institute of Modern Optics,Tianjin Key Laboratory of Micro‑Scale Optical Information Science and Technology,College of Electronic Information and Optical Engineering,Nankai University,38 Tongyan Road,Jinnan District,Tianjin 300350,People’s Republic of China [7]Shenzhen Research Institute of Nankai University,16Th Floor,Yantian Science and Technology Building,Haishan Street,Yantian District,Shenzhen 518083,People’s Republic of China
出 处:《Nano-Micro Letters》2024年第9期557-570,共14页纳微快报(英文版)
基 金:the financial support of National Key Research and Development Program of China(Grant No.2023YFB4202503);the Joint Funds of the National Natural Science Foundation of China(Grant No.U21A2072);Natural Science Foundation of China(Grant No.62274099);Natural Science Foundation of Tianjin(No.20JCQNJC02070);China Postdoctoral Science Foundation(No.2020T130317);the Overseas Expertise Introduction Project for Discipline Innovation of Higher Education of China(Grant No.B16027);Tianjin Science and Technology Project(Grant No.18ZXJMTG00220);Key R&D Program of Hebei Province(No.19214301D);provided by the Haihe Laboratory of Sustainable Chemical Transformations;the Fundamental Research Funds for the Central Universities,Nankai University.
摘 要:Monolithic textured perovskite/silicon tandem solar cells(TSCs)are expected to achieve maximum light capture at the lowest cost,potentially exhibiting the best power conversion efficiency.However,it is challenging to fabricate high-quality perovskite films and preferred crystal orientation on commercially textured silicon substrates with micrometersize pyramids.Here,we introduced a bulky organic molecule(4-fluorobenzylamine hydroiodide(F-PMAI))as a perovskite additive.It is found that F-PMAI can retard the crystallization process of perovskite film through hydrogen bond interaction between F^(−)and FA^(+)and reduce(111)facet surface energy due to enhanced adsorption energy of F-PMAI on the(111)facet.Besides,the bulky molecular is extruded to the bottom and top of perovskite film after crystal growth,which can passivate interface defects through strong interaction between F-PMA+and undercoordinated Pb^(2+)/I^(−).As a result,the additive facilitates the formation of large perovskite grains and(111)preferred orientation with a reduced trap-state density,thereby promoting charge carrier transportation,and enhancing device performance and stability.The perovskite/silicon TSCs achieved a champion efficiency of 30.05%based on a silicon thin film tunneling junction.In addition,the devices exhibit excellent longterm thermal and light stability without encapsulation.This work provides an effective strategy for achieving efficient and stable TSCs.
关 键 词:Perovskite crystallization (111)preferred orientation Defect passivation Perovskite/silicon tandem solar cells
分 类 号:TM914.4[电气工程—电力电子与电力传动]
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