Exceptionally Low-Coordinated Bismuth–Oxygen Vacancy Defect Clusters for Generating Black In2O3 Photocatalysts with Superb CO2 Reduction Performance

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2025-01-09 DOI:10.1021/acscatal.4c03491
Farzin Nekouei, Christopher J. Pollock, Tianyi Wang, Zhong Zheng, Yanzhao Zhang, Zelio Fusco, Huanyu Jin, Thrinath Reddy Ramireddy, Ary Anggara Wibowo, Teng Lu, Shahram Nekouei, Farzaneh Keshtpour, Julien Langley, Elwy H. Abdelkader, Nicholas Cox, Zongyou Yin, Hieu Nguyen, Alexey Glushenkov, Siva Karuturi, Zongwen Liu, Li Wei, Hao Li, Yun Liu
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Abstract

Indium oxide (In2O3) is a widely used catalyst for CO2 reduction, yet its inherent properties, such as a wide band gap and low-active surface, necessitate a modification to achieve broad-wavelength absorption and enhanced surface activity. However, simultaneously achieving these goals through a single material modulation approach remains challenging. Here, we present a simple yet innovative strategy to develop a black catalyst, BixIn2–xO3–y, comprising notably low-coordinated bismuth on oxygen-defect-laden In2O3. This approach induces local structural and charge carrier changes, resulting in remarkably high visible light absorption and preeminent surface activity. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) confirms the spontaneous dissociation of CO2 species into CO even in the dark on the BixIn 2–xO3–y surface, underscoring the catalyst’s enhanced activity. Compared to pristine In2O3, BixIn2–xO3–y exhibits approximately 24 times greater CO production. Characterization techniques, including extended X-ray absorption fine structure (EXAFS) and X-ray absorption near-edge structure (XANES) analyses, along with density functional theory (DFT) calculations, reveal that oxygen vacancies in the reduced sample decrease both the average coordination number of bismuth and its effective oxidation state. Our findings indicate that the unusually low-coordinated bismuth dopant preferably promotes the formation of oxygen vacancies close to bismuth (Bi-Vö) rather than near indium, which induces local structural and charge carrier changes. These Bi-Vö clusters enhance light harvesting, charge separation, and CO2 adsorption/activation/reduction. Importantly, our approach demonstrates promise for a wide range of applications, addressing key challenges in catalyst modification for CO2 reduction and offering opportunities for further advancement in this field.

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ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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