Bi quantum dots implanted 2D C-doped BiOCl nanosheets: Enhanced visible light photocatalysis efficiency and reaction pathway

光催化 材料科学 杂原子 兴奋剂 可见光谱 光化学 表面等离子共振 半导体 量子点 密度泛函理论 载流子 纳米技术 催化作用 光电子学 纳米颗粒 化学 有机化学 计算化学 戒指(化学)
作者
Ye He,Jieyuan Li,Kanglu Li,Minglu Sun,Chaowei Yuan,Ruimin Chen,Jianping Sheng,Geng Leng,Fan Dong
出处
期刊:Chinese Journal of Catalysis [China Science Publishing & Media Ltd.]
卷期号:41 (9): 1430-1438 被引量:89
标识
DOI:10.1016/s1872-2067(20)63612-9
摘要

The simultaneous integration of heteroatom doping and surface plasmon resonance (SPR) modulation on semiconductor photocatalysts could be capable of improving visible light utilization and charge separation, achieving better solar light conversion and photocatalysis efficiency. For this purpose, we have designed a novel Bi quantum dots (QDs) implanted C-doped BiOCl photocatalyst (C/BOC/B) for NOx removal. The feasibility was firstly evaluated through density functional theory (DFT) calculations methods, which indicates that the enhanced photocatalytic performance could be expected owing to the synergistic effects of doped C heteroatoms and loaded Bi QDs. Then, the C/BOC/B was synthesized via a facile hydrothermal method and exhibited efficient and stable visible light photocatalytic NO removal. The results found that the doped C atoms can serve as electron guides to induce oriented charge transfer from Bi QDs to BiOCl, while the Bi QDs can act as light-capture and electron-donating sites. The reaction pathway and mechanism for NO conversion was unveiled by in situ Fourier-transform infrared spectroscopy combined with DFT calculation. The enhanced adsorption of reactants and intermediates could promote the overall reaction efficiency and selectivity in photocatalytic NO conversion. This work could provide a new perspective on the mechanistic understanding of the synergistic effects toward non-metal doping and SPR effects in semiconductor photocatalysts, and this presented technique could be extended for other semiconductor materials.
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