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理解交联甲基碘化铅晶体中的氢键相互作用:迈向减少水分和光降解途径

Understanding Hydrogen Bonding Interactions in Crosslinked Methylammonium Lead Iodide Crystals: Towards Reducing Moisture and Light Degradation Pathways.

作者信息

Nimens Wendy J, Lefave Sarah J, Flannery Laura, Ogle Jonathan, Smilgies Detlef-M, Kieber-Emmons Matthew T, Whittaker-Brooks Luisa

机构信息

Department of Chemistry, University of Utah, 315 S 1400 E, Salt Lake City, UT, 84112, USA.

Cornell High Energy Synchrotron Source (CHESS), Cornell University, Ithaca, NY, 14853, USA.

出版信息

Angew Chem Int Ed Engl. 2019 Sep 23;58(39):13912-13921. doi: 10.1002/anie.201906017. Epub 2019 Aug 19.

Abstract

Methylammonium lead halide perovskite-based solar cells have demonstrated efficiencies as high as 24.2 %, highlighting their potential as inexpensive and solution-processable alternatives to silicon solar cell technologies. Poor stability towards moisture, ultraviolet irradiation, heat, and a bias voltage of the perovskite layer and its various device interfaces limits the commercial feasibility of this material for outdoor applications. Herein, we investigate the role of hydrogen bonding interactions induced when metal halide perovskite crystals are crosslinked with alkyl or π-conjugated boronic acid small molecules (-B(OH) ). The crosslinked perovskite crystals are investigated under continuous light irradiation and moisture exposure. These studies demonstrate that the origin of the interaction between the alkyl or π-conjugated crosslinking molecules is due to hydrogen bonding between the -B(OH) terminal group of the crosslinker and the I of the [PbI ] octahedra of the perovskite layer. Also, this interaction influences the stability of the perovskite layer towards moisture and ultraviolet light irradiation. Morphology and structural analyses, as well as IR studies as a function of aging under both dark and light conditions show that π-conjugated boronic acid molecules are more effective crosslinkers of the perovskite crystals than their alkyl counterparts thus imparting better stability towards light and moisture degradation.

摘要

基于甲铵铅卤化物钙钛矿的太阳能电池已展现出高达24.2%的效率,凸显了其作为硅太阳能电池技术廉价且可溶液加工替代品的潜力。钙钛矿层及其各种器件界面在湿度、紫外线照射、热和偏置电压方面稳定性较差,限制了这种材料在户外应用中的商业可行性。在此,我们研究了金属卤化物钙钛矿晶体与烷基或π共轭硼酸小分子(-B(OH)₂)交联时诱导的氢键相互作用的作用。对交联的钙钛矿晶体在连续光照和湿气暴露下进行了研究。这些研究表明,烷基或π共轭交联分子之间相互作用的起源是由于交联剂的-B(OH)₂端基与钙钛矿层[PbI₆]八面体的I之间形成了氢键。此外,这种相互作用影响了钙钛矿层对湿气和紫外线照射的稳定性。形态学和结构分析以及在黑暗和光照条件下作为老化函数的红外研究表明,π共轭硼酸分子比其烷基对应物更有效地交联钙钛矿晶体,从而赋予更好的抗光和抗湿气降解稳定性。

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