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

IF 13.1 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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低配位铋-氧空位缺陷团簇制备具有优异CO2还原性能的黑色In2O3光催化剂
氧化铟(In2O3)是一种广泛应用于CO2还原的催化剂,但其固有的特性,如宽带隙和低活性表面,需要对其进行改性以实现宽波长吸收和增强表面活性。然而,通过单一材料调制方法同时实现这些目标仍然具有挑战性。在这里,我们提出了一种简单而创新的策略来开发一种黑色催化剂BixIn2-xO3-y,它在氧缺陷负载的In2O3上含有明显的低配位铋。这种方法诱导了局部结构和载流子的变化,导致了非常高的可见光吸收和卓越的表面活性。原位漫反射红外傅立叶变换光谱(DRIFTS)证实,即使在黑暗中,BixIn 2-xO3-y表面上的CO2也会自发解离成CO,强调了催化剂的活性增强。与原始的In2O3相比,BixIn2-xO3-y显示出大约24倍的CO产量。表征技术,包括扩展x射线吸收精细结构(EXAFS)和x射线吸收近边结构(XANES)分析,以及密度泛函理论(DFT)计算,表明还原样品中的氧空位降低了铋的平均配位数和有效氧化态。我们的研究结果表明,异常低配位的铋掺杂剂更好地促进了靠近铋(Bi-Vö)而不是靠近铟的氧空位的形成,这导致了局部结构和载流子的变化。这些Bi-Vö团簇增强了光收集、电荷分离和CO2吸附/活化/还原。重要的是,我们的方法展示了广泛应用的前景,解决了催化剂改性以减少二氧化碳的关键挑战,并为该领域的进一步发展提供了机会。
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来源期刊
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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