原子精确的金属纳米簇三明治异质结稳健和高效的光催化CO2还原为甲醇

IF 6.1 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Rui Lu, Aimin Yao, Yali Dai, Haijiao Yin, Chengqi Li, Yuanxin Du, Manzhou Zhu
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引用次数: 0

摘要

开发结构明确、反应性和稳定性优异的多相纳米催化剂对了解催化机理和实际工业应用具有重要意义。本文报道了原子精密金属纳米团簇夹层异质结(MIL-125-NH2-Au25(L-Cys)18/g-C3N4,简称M-A/C)的构建。与二元化合物相比,M-A/C在可见光照射下可以高效、选择性地光催化CO2还原为甲醇,且由于保护壳的存在,活性和稳定性显著增强。此外,三元M-A/C异质结不仅拓宽了光吸收区域,增强了CO2吸附,而且扩大了界面电荷转移通道,有利于光催化性能的提高。此外,精确结构和原位光谱的结合揭示了从CO2到CH3OH的演变。这项工作为设计高效、稳定的原子精密金属团簇异质结催化剂开辟了一条有希望的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Atomically precise metal nanocluster sandwich heterojunction for robust and efficient photocatalytic CO2 reduction to methanol
Developing heterogeneous nanocatalyst with well-defined structure and excellent reactivity and stability is vital for understanding catalytic mechanism and practical industrial application. Herein, we report the construction of atomically precise metal nanocluster sandwich heterojunction (MIL-125-NH2-Au25(L-Cys)18/g-C3N4, M-A/C for short). Compared with the binary counterparts, the M-A/C efficiently and selectively photocatalyzes CO2 reduction to methanol under visible light irradiation with remarkably enhanced activity and stability, due to the protective shell. Moreover, the ternary M-A/C heterojunction not only broadens light absorption region, strengthens CO2 adsorption, but also expands interface charge transfer channel, benefiting for photocatalytic performance. Additionally, the integrating of precise structure and in situ spectrometry unveils the evolution from CO2 to CH3OH. This work opens a promising avenue to design highly-efficient and robust atomically precise metal cluster-based heterojunction catalyst.
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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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