材料科学
光催化
碘化物
异质结
铋
钙钛矿(结构)
卤化物
水溶液
化学工程
催化作用
纳米技术
光化学
无机化学
光电子学
物理化学
有机化学
化学
冶金
工程类
作者
Yunqi Tang,Chun Hong Mak,Rugeng Liu,Zuankai Wang,Ji Li,Haisheng Song,Chunyan Tan,Frédéric Barrière,Hsien‐Yi Hsu
标识
DOI:10.1002/adfm.202006919
摘要
Abstract Solar‐to‐fuel conversion with organic–inorganic hybrid halide perovskites has attracted growing attention as a result of their excellent optoelectronic properties as well as the low temperature of the solution based fabrication process. However, the most comprehensively developed hybrid perovskite materials are comprised of the toxic metal lead, raising concerns about environmental health threats. Herein, a lead‐free bismuth (Bi)‐based hybrid perovskite showing in situ growth of heterojunctions is successfully developed at the interface of methylammonium bismuth iodide (MA 3 Bi 2 I 9 ) and tri(dimethylammonium) hexa‐iodobismuthate (DMA 3 BiI 6 ) by a facile solvent engineering technique. The air‐stable MA 3 Bi 2 I 9 /DMA 3 BiI 6 perovskite heterostructure with enhanced photoinduced charge separation exhibit outstanding visible‐light‐induced photocatalytic activity for H 2 evolution in aqueous hydrogen iodide solution. The powdered MA 3 Bi 2 I 9 /DMA 3 BiI 6 heterostructured composite (BBP‐5) shows a H 2 evolution rate of 198.2 µmol h −1 g −1 without the addition of Pt co‐catalysts under 100 mW cm −2 of visible‐light (λ ≥ 420 nm) illumination.
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