光催化
异质结
氮气
固氮
电子转移
化学
辐照
电子
化学工程
材料科学
氨
光化学
纳米技术
催化作用
光电子学
有机化学
物理
核物理学
量子力学
工程类
作者
Xin Huang,Rui Du,Yuanyuan Zhang,Jingyu Ren,Qisheng Yang,Kangning Wang,Ni Yang,Yuqi Yao,Razium Ali Soomro,Li Guo,Chunming Yang,Danjun Wang,Bin Xu,Feng Fu
标识
DOI:10.1016/j.jcis.2024.03.018
摘要
Photocatalytic nitrogen fixation presents an eco-friendly approach to converting atmospheric nitrogen into ammonia (NH3), but the process faces challenges due to rapid interface charge recombination. Here, we report an innovative charge transfer and oriented accumulation strategy using an In-O-Mo bond-modulated S-scheme heterostructure composed of In2O3/Bi2MoO6 (In/BMO) synthesized using a simple electrostatic assembly. The unique interfacial arrangement with optimal photocatalyst configuration (3 % In/BMO) enabled enhanced photogenerated electron separation and transfer, leading to a remarkable nitrogen fixation rate of approximately 150.9 μmol·gcat−1·h−1 under visible light irradiation. The performance of the photocatalyst was 9-fold and 27-fold higher than that of its pristine components, Bi2MoO6 and In2O3, respectively. The experimental and theoretical evaluation deemed interfacial In-O-Mo bonds crucial for rapid transfer and charge-oriented accumulation. Whereas the generated internal electric field drove the spatial separation and transfer of photo-generated electrons and holes, significantly enhancing the photocatalytic N2-to-NH3 conversion efficiency. The proposed work lays the foundation for designing S-scheme heterostructures with highly efficient interfacial bonds, offering a promising avenue for substantial improvements in photocatalytic nitrogen fixation.
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