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Synthesis of a Visible‐Light‐Responsive Perovskite SmTiO 2 N Bifunctional Photocatalyst via an Evaporation‐Assisted Layered‐Precursor Strategy
Author(s) -
Bao Yunfeng,
Du Shiwen,
Qi Yu,
Li Gao,
Zhang Peng,
Shao Guosheng,
Zhang Fuxiang
Publication year - 2021
Publication title -
advanced materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.707
H-Index - 527
eISSN - 1521-4095
pISSN - 0935-9648
DOI - 10.1002/adma.202101883
Subject(s) - materials science , visible spectrum , photocatalysis , water splitting , bifunctional , nitride , perovskite (structure) , chemical engineering , band gap , mesoporous material , photochemistry , inorganic chemistry , nanotechnology , catalysis , optoelectronics , organic chemistry , chemistry , layer (electronics) , engineering
Development of visible‐light‐responsive oxynitride photocatalysts has been highly inspired for promising solar‐to‐chemical conversion, but the number of Ti‐based oxynitrides is scarce because of the relatively low thermal stability of Ti 4+ ions under ammonia flow. Here, the feasible synthesis of a novel perovskite SmTiO 2 N from the layered NaSmTiO 4 precursor is demonstrated to exhibit wide visible‐light response with a bandgap of ≈2.1 eV and to show effective water reduction and oxidation functionalities under visible‐light irradiation. The successful preparation mainly results from the synergistic effect of the layered structure of NaSmTiO 4 and the evaporation spillover of Na + ions, both of which are favorable for ammonia diffusion to accelerate the substitution of nitrogen to oxygen atoms and to shorten the nitridation time. The thermodynamic and kinetic feasibility of SmTiO 2 N for water splitting are investigated in detail, and its optimal apparent quantum efficiency (AQE) of water oxidation reaches 16.7% at 420 ± 10 nm, higher by far than that of most previous visible‐light‐responsive photocatalysts. Interestingly, a series of oxynitrides RTiO 2 N (R = La, Pr, Nd) are similarly synthesized by the alkali‐metal evaporation‐assisted layered‐precursor strategy, demonstrating its generality to prepare visible‐light‐responsive (oxy)nitride photocatalysts containing reducible metals for solar energy conversion.