Post-synthetic halide conversion and selective halogen capture in hybrid perovskites

被引:112
|
作者
Solis-Ibarra, D. [1 ]
Smith, I. C. [1 ]
Karunadasa, H. I. [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
NUCLEOPHILIC CONTRIBUTION; OLEFIN BROMINATION; HALONIUM CATIONS; SOLAR-CELLS; EFFICIENCY; SOLVATION; SOLVENT;
D O I
10.1039/c5sc01135c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reaction with halogen vapor allows us to post-synthetically exchange halides in both three- (3D) and two-dimensional (2D) organic-inorganic metal-halide perovskites. Films of 3D Pb-I perovskites cleanly convert to films of Pb-Br or Pb-Cl perovskites upon exposure to Br-2 or Cl-2 gas, respectively. This gas-solid reaction provides a simple method to produce the high-quality Pb-Br or Pb-Cl perovskite films required for optoelectronic applications. Reactivity with halogens can be extended to the organic layers in 2D metal-halide perovskites. Here, terminal alkene groups placed between the inorganic layers can capture Br-2 gas through chemisorption to form dibromoalkanes. This reaction's selectivity for Br-2 over I-2 allows us to scrub Br-2 to obtain high-purity I-2 gas streams. We also observe unusual halogen transfer between the inorganic and organic layers within a single perovskite structure. Remarkably, the perovskite's crystallinity is retained during these massive structural rearrangements.
引用
收藏
页码:4054 / 4059
页数:6
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