期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 125, 期 21, 页码 11756-11764出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.1c02870
关键词
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资金
- Department of Energy, Office of Science, Basic Energy Sciences [SC0012541]
- Department of Science & Technology (DST) of Govt. of India [JNC/AO/A. 0610-1(3)/2018-03]
- Science & Engineering Research Board (SERB) of the Govt. of India [RJF/2020/000106]
- Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Bangalore
- Ras al Khaimah Centre for Advanced Materials
This study explores the feasibility of forming double perovskite halides using the Goldschmidt tolerance factor and the radius ratio of trivalent metals. The rarity of double perovskite iodides is rationalized based on these descriptors. Using this model, it is predicted that there may be over 300 unknown double perovskite iodides with various organic and inorganic cations in the A site.
Following on the heels of the remarkable lead halide perovskite optoelectronic materials, interest in lead-free halide perovskites has grown rapidly in the past decade. Double perovskite halides with the general formula A(2)M(I)M(III)X(6) (where A is a large monovalent cation in the perovskite A site, M-I is a univalent metal, M-III is a trivalent metal, and X is a halide) represent one of the promising classes of such materials, and of these, the iodides are particularly interesting since their band gaps are expected to be similar to those found in the iconic lead-containing phases, APbI(3). However, the successful synthesis of A(2)M(I)M(III)I(6) iodides appears to have been elusive. In this work, we examine the likelihood that double perovskite halides will form using a combination of the Goldschmidt tolerance factor and the radius ratio of the trivalent metals, M-III, and rationalize the rarity of double perovskite iodides in terms of these descriptors. Using this model as the formability criterion, we predict the possible existence of more than 300 hitherto unknown double perovskite iodides with organic and inorganic cations in the A site.
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