Constructing Stable and Potentially High-Performance Hybrid Organic-Inorganic Perovskites with “Unstable” Cations
A new family of functional hybrid organic-inorganic perovskites (HOIPs) is theoretically designed based on the following chemical insights: when a proton is adhered to molecules like water or ethanol, the newly formed larger-sized cations (e.g., H5O2+, C2H5OH2+, and CH3SH+) entail low electron affin...
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doaj-1256dad131414835ad1a856777d9ea972020-11-25T03:13:29ZengAmerican Association for the Advancement of ScienceResearch2639-52742020-01-01202010.34133/2020/1986576Constructing Stable and Potentially High-Performance Hybrid Organic-Inorganic Perovskites with “Unstable” CationsQing Yang0Menghao Wu1Xiao Cheng Zeng2School of Physics,Huazhong University of Science and Technology,Wuhan,Hubei 430074,ChinaSchool of Physics,Huazhong University of Science and Technology,Wuhan,Hubei 430074,ChinaDepartment of Chemistry,University of Nebraska,Lincoln,NE 68588,USAA new family of functional hybrid organic-inorganic perovskites (HOIPs) is theoretically designed based on the following chemical insights: when a proton is adhered to molecules like water or ethanol, the newly formed larger-sized cations (e.g., H5O2+, C2H5OH2+, and CH3SH+) entail low electron affinities mimicking superalkalis; they are conjugated acids of weak bases that cannot survive in solution, while their chemistry behavior in the HOIP frameworks, however, may be markedly different due to greatly enhanced cohesive energies of the proton, which facilitate the formation of new HOIPs. First-principles computations show that the putative formation reactions for these newly designed HOIPs typically release much more energy compared with the prevailing HOIP MAPbI3, suggesting the likelihood of facile solution-based fabrications, while the suppression of reverse formation suggests that the humidity stability may be markedly enhanced. During their formations, halide acids are unlikely to react with ethanol or methanethiol without the presence of metal halides, a condition further favoring their stability. The proposed structure of (H5O2)PbI3 may also clarify the origin of the long-speculated existence of HPbI3. Importantly, density functional theory computations suggest that many of these HOIPs possess not only direct bandgaps with values within the optimal range for solar light absorbing but also more desirable optical absorption spectra than that of MAPbI3, where their ferroelectric polarizations also benefit photovoltaics. The stability and photovoltaic efficiency may be even further improved for the newly designed two-dimensional (2D) HOIPs and 2D/3D hybrid HOIP structures.http://dx.doi.org/10.34133/2020/1986576 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Qing Yang Menghao Wu Xiao Cheng Zeng |
spellingShingle |
Qing Yang Menghao Wu Xiao Cheng Zeng Constructing Stable and Potentially High-Performance Hybrid Organic-Inorganic Perovskites with “Unstable” Cations Research |
author_facet |
Qing Yang Menghao Wu Xiao Cheng Zeng |
author_sort |
Qing Yang |
title |
Constructing Stable and Potentially High-Performance Hybrid Organic-Inorganic Perovskites with “Unstable” Cations |
title_short |
Constructing Stable and Potentially High-Performance Hybrid Organic-Inorganic Perovskites with “Unstable” Cations |
title_full |
Constructing Stable and Potentially High-Performance Hybrid Organic-Inorganic Perovskites with “Unstable” Cations |
title_fullStr |
Constructing Stable and Potentially High-Performance Hybrid Organic-Inorganic Perovskites with “Unstable” Cations |
title_full_unstemmed |
Constructing Stable and Potentially High-Performance Hybrid Organic-Inorganic Perovskites with “Unstable” Cations |
title_sort |
constructing stable and potentially high-performance hybrid organic-inorganic perovskites with “unstable” cations |
publisher |
American Association for the Advancement of Science |
series |
Research |
issn |
2639-5274 |
publishDate |
2020-01-01 |
description |
A new family of functional hybrid organic-inorganic perovskites (HOIPs) is theoretically designed based on the following chemical insights: when a proton is adhered to molecules like water or ethanol, the newly formed larger-sized cations (e.g., H5O2+, C2H5OH2+, and CH3SH+) entail low electron affinities mimicking superalkalis; they are conjugated acids of weak bases that cannot survive in solution, while their chemistry behavior in the HOIP frameworks, however, may be markedly different due to greatly enhanced cohesive energies of the proton, which facilitate the formation of new HOIPs. First-principles computations show that the putative formation reactions for these newly designed HOIPs typically release much more energy compared with the prevailing HOIP MAPbI3, suggesting the likelihood of facile solution-based fabrications, while the suppression of reverse formation suggests that the humidity stability may be markedly enhanced. During their formations, halide acids are unlikely to react with ethanol or methanethiol without the presence of metal halides, a condition further favoring their stability. The proposed structure of (H5O2)PbI3 may also clarify the origin of the long-speculated existence of HPbI3. Importantly, density functional theory computations suggest that many of these HOIPs possess not only direct bandgaps with values within the optimal range for solar light absorbing but also more desirable optical absorption spectra than that of MAPbI3, where their ferroelectric polarizations also benefit photovoltaics. The stability and photovoltaic efficiency may be even further improved for the newly designed two-dimensional (2D) HOIPs and 2D/3D hybrid HOIP structures. |
url |
http://dx.doi.org/10.34133/2020/1986576 |
work_keys_str_mv |
AT qingyang constructingstableandpotentiallyhighperformancehybridorganicinorganicperovskiteswithunstablecations AT menghaowu constructingstableandpotentiallyhighperformancehybridorganicinorganicperovskiteswithunstablecations AT xiaochengzeng constructingstableandpotentiallyhighperformancehybridorganicinorganicperovskiteswithunstablecations |
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