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金属卤化物钙钛矿的可逆甲醇化

Reversible Methanolation of Metal Halide Perovskites.

作者信息

Rosales Bryan A, Mundt Laura E, Schelhas Laura T, Wheeler Lance M

机构信息

National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States.

SLAC National Accelerator Laboratory, 2575 Sand Hill Road, Menlo Park, California 94025, United States.

出版信息

J Am Chem Soc. 2022 Jan 19;144(2):667-672. doi: 10.1021/jacs.1c10942. Epub 2022 Jan 5.

Abstract

The low formation energies inherent in metal halide perovskites enable the structure to be easily broken and remade with little energy input. In this work, we leverage low formation energy to demonstrate 0D/3D structural transformations induced by reversible intercalation of methanol to yield dramatic control of visible light absorption. We identify a methanolated structure that features sheets of 0D isolated [PbI] octahedra separated by MAI and methanol. Methanol and water reversibly displace each other in the 0D complex by controlling the chemical potential of the system via Le Chatelier's principle. The weaker H-bonding of methanol compared to water effectively reduces the complex dissociation temperature from 70 to 50 °C, rendering the methanol complex more desirable for an array of next-generation applications spanning low-power-consumption memory to switchable photovoltaics.

摘要

金属卤化物钙钛矿固有的低形成能使得该结构能够在很少的能量输入下轻松地被破坏和重塑。在这项工作中,我们利用低形成能来证明由甲醇可逆嵌入诱导的0D/3D结构转变,从而实现对可见光吸收的显著控制。我们确定了一种甲醇化结构,其特征是由MAI和甲醇分隔的0D孤立[PbI]八面体片层。通过勒夏特列原理控制体系的化学势,甲醇和水在0D络合物中可逆地相互取代。与水相比,甲醇较弱的氢键有效地将络合物的解离温度从70℃降低到50℃,使得甲醇络合物对于从低功耗存储器到可切换光伏的一系列下一代应用更具吸引力。

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