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用于可控光催化还原二氧化碳产物的Z型α-FeO/CdS负载PdAg双金属合金纳米颗粒的修饰

Decoration of PdAg Dual-Metallic Alloy Nanoparticles on Z-Scheme α-FeO/CdS for Manipulable Products Photocatalytic Reduction of Carbon Dioxide.

作者信息

Yang Shuhui, Ke Xi, Zhang Menglong, Luo Dongxiang

机构信息

Institute of Semiconductors, South China Normal University, Guangzhou, China.

School of Chemistry and Chemical Engineering/Institute of Clean Energy and Materials/Guangzhou, Key Laboratory for Clean Energy and Materials/Huangpu Hydrogen Innovation Center, Guangzhou University, Guangzhou, China.

出版信息

Front Chem. 2022 Jul 22;10:937543. doi: 10.3389/fchem.2022.937543. eCollection 2022.

DOI:10.3389/fchem.2022.937543
PMID:35936090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9353514/
Abstract

Metal nanoparticles have been extensively used as co-catalysts in photocatalytic systems in order to pursue improvements in both reaction kinetics and selectivity. In this work, PdAg dual-metallic nanoparticles synthesized by the co-reduction method were decorated on a well-established α-FeO/CdS Z-scheme photoactive material as a co-catalyst to study their performance for promoting the photoreduction of CO. Herein, α-FeO and CdS were synthesized on fluorine-doped tin oxide (FTO) glass by hydrothermal and SILAR (successive ionic layer adsorption and reaction) methods, respectively. The direct Z-scheme charge transfer path between FeO and CdS and the effective electron migration toward the PdAg mainly contributed to the excellent photocatalytic CO reduction performance. The controllable work function based on Pd (5.12) and Ag (4.26) constructed an appropriate band alignment with α-FeO/CdS and displayed favorable production for CH rather than CO. The optimum ratio of PdAg 1:2 performed a 48% enhancement than pure Pd for photoreduction of CO. Meanwhile, the enhanced charge separation improved the photoelectrochemical performance and photocurrent generation, and reduced the electrical resistance between components. This work provided insights into the dual-metallic co-catalyst for boosting the activity and selectivity of photocatalytic CO reduction.

摘要

金属纳米颗粒已被广泛用作光催化体系中的助催化剂,以提高反应动力学和选择性。在这项工作中,通过共还原法合成的PdAg双金属纳米颗粒被修饰在一种成熟的α-FeO/CdS Z型光活性材料上作为助催化剂,以研究其促进CO光还原的性能。在此,α-FeO和CdS分别通过水热法和连续离子层吸附反应(SILAR)法在氟掺杂氧化锡(FTO)玻璃上合成。FeO和CdS之间直接的Z型电荷转移路径以及向PdAg的有效电子迁移主要促成了优异的光催化CO还原性能。基于Pd(5.12)和Ag(4.26)的可控功函数与α-FeO/CdS构建了合适的能带排列,并显示出对CH而非CO的良好生成效果。PdAg 1:2的最佳比例在CO光还原方面比纯Pd表现出48%的增强。同时,增强的电荷分离改善了光电化学性能和光电流产生,并降低了组件之间的电阻。这项工作为双金属助催化剂提高光催化CO还原的活性和选择性提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/4ec315c44de3/fchem-10-937543-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/490a1cc21057/fchem-10-937543-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/20c08eb93343/fchem-10-937543-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/3da783848b6e/fchem-10-937543-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/7de18aa043f1/fchem-10-937543-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/4ec315c44de3/fchem-10-937543-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/490a1cc21057/fchem-10-937543-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/20c08eb93343/fchem-10-937543-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/3da783848b6e/fchem-10-937543-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/7de18aa043f1/fchem-10-937543-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828a/9353514/4ec315c44de3/fchem-10-937543-g005.jpg

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本文引用的文献

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Influence of NO on the activity of Pd/θ-AlO catalyst for methane oxidation: Alleviation of transient deactivation.一氧化氮对钯/θ-氧化铝催化剂甲烷氧化活性的影响:缓解瞬态失活
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