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In Situ Formation of Bismuth‐Based Perovskite Heterostructures for High‐Performance Cocatalyst‐Free Photocatalytic Hydrogen Evolution
Author(s) -
Tang Yunqi,
Mak Chun Hong,
Liu Rugeng,
Wang Zuankai,
Ji Li,
Song Haisheng,
Tan Chunyan,
Barrière Frédéric,
Hsu HsienYi
Publication year - 2020
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202006919
Subject(s) - materials science , perovskite (structure) , heterojunction , bismuth , photocatalysis , iodide , halide , chemical engineering , aqueous solution , catalysis , nanotechnology , inorganic chemistry , optoelectronics , chemistry , organic chemistry , metallurgy , engineering
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.