Space-confined growth of halide perovskite nanocrystals for enhanced photocatalytic hydrogen evolution

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2025-03-06 DOI:10.1016/j.mcat.2025.114981
Xue Li, Miaomiao Gao, Yaqiang Wu, Hui Fu, Qianqian Zhang, Jinghang Chen, Zeyan Wang, Zhaoke Zheng, Hefeng Cheng, Yuanyuan Liu, Baibiao Huang, Peng Wang
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Abstract

Halide perovskites, as emerging semiconductor materials, exhibit great potential in photocatalytic hydrogen evolution. However, perovskite powders prepared through the conventional co-precipitation method typically form large-sized particles with diameters of several tens of micrometers, resulting in low specific surface area and limited active sites, which seriously compromise their catalytic efficiency. Herein, a spatially confined growth method is developed to grow small-sized mixed halide perovskite FAPbBr3-xIx (FA = CH(NH2)2+) nanocrystals within MCM-41 molecular sieve for photocatalytic hydroiodic acid splitting. This developed method significantly increases the specific surface area, provides more reaction sites, and promotes the separation of carriers for the perovskite nanocrystal. When loading with Pt as the cocatalyst, 40 % MCM-41@FAPbBr3-xIx composite demonstrates excellent photocatalytic H2 evolution activity of 2260 μmol h−1. This work presents an inspiring advancement in confined growth tactics for perovskite nanocrystals to achieve efficient photocatalytic hydrogen evolution.

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增强光催化析氢的卤化物钙钛矿纳米晶体的空间受限生长
卤化物钙钛矿作为一种新兴的半导体材料,在光催化析氢方面具有很大的潜力。然而,通过常规共沉淀法制备的钙钛矿粉末通常形成直径几十微米的大颗粒,导致比表面积低,活性位点有限,严重影响其催化效率。本文采用空间受限生长方法,在MCM-41分子筛内生长小尺寸混合卤化物钙钛矿FAPbBr3-xIx (FA = CH(NH2)2+)纳米晶体,用于光催化氢碘酸裂解。该方法显著提高了钙钛矿纳米晶体的比表面积,提供了更多的反应位点,促进了载体的分离。当负载Pt作为助催化剂时,40% MCM-41@FAPbBr3-xIx复合材料的光催化析氢活性为2260 μmol h−1。这项工作在钙钛矿纳米晶体的受限生长策略方面取得了令人鼓舞的进展,以实现有效的光催化析氢。
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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