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有机-无机杂化钙钛矿的氢键作用与稳定性

Hydrogen Bonding and Stability of Hybrid Organic-Inorganic Perovskites.

作者信息

El-Mellouhi Fedwa, Marzouk Asma, Bentria El Tayeb, Rashkeev Sergey N, Kais Sabre, Alharbi Fahhad H

机构信息

Qatar Environment and Energy Research Institute (QEERI), Hamad Bin Khalifa University, P.O. Box 5825, Doha, Qatar.

College of Science and Engineering, Hamad Bin Khalifa University, Doha, Qatar.

出版信息

ChemSusChem. 2016 Sep 22;9(18):2648-2655. doi: 10.1002/cssc.201600864. Epub 2016 Sep 8.

Abstract

In the past few years, the efficiency of solar cells based on hybrid organic-inorganic perovskites has exceeded the level needed for commercialization. However, existing perovskites solar cells (PSCs) suffer from several intrinsic instabilities, which prevent them from reaching industrial maturity, and stabilizing PSCs has become a critically important problem. Here we propose to stabilize PSCs chemically by strengthening the interactions between the organic cation and inorganic anion of the perovskite framework. In particular, we show that replacing the methylammonium cation with alternative protonated cations allows an increase in the stability of the perovskite by forming strong hydrogen bonds with the halide anions. This interaction also provides opportunities for tuning the electronic states near the bandgap. These mechanisms should have a universal character in different hybrid organic-inorganic framework materials that are widely used.

摘要

在过去几年中,基于有机-无机杂化钙钛矿的太阳能电池效率已超过商业化所需水平。然而,现有的钙钛矿太阳能电池(PSC)存在一些内在不稳定性,这阻碍它们达到工业成熟度,因此稳定PSC已成为一个至关重要的问题。在此,我们提议通过加强钙钛矿框架中有机阳离子与无机阴离子之间的相互作用来化学稳定PSC。特别地,我们表明用替代的质子化阳离子取代甲铵阳离子可通过与卤化物阴离子形成强氢键来提高钙钛矿的稳定性。这种相互作用还为调节带隙附近的电子态提供了机会。这些机制在广泛使用的不同有机-无机杂化框架材料中应具有普遍性。

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