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用于水氧化的晶面工程BiVO光催化剂:寿命增益与能量损失

Facet-Engineered BiVO Photocatalysts for Water Oxidation: Lifetime Gain Versus Energetic Loss.

作者信息

He Tianhao, Zhao Yue, Benetti Daniele, Moss Benjamin, Tian Lei, Selim Shababa, Li Rengui, Fan Fengtao, Li Qian, Wang Xiuli, Li Can, Durrant James R

机构信息

Department of Chemistry, Centre for Processable Electronics, Imperial College London, London W12 0BZ, U.K.

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory for Clean Energy, Dalian 116023, China.

出版信息

J Am Chem Soc. 2024 Oct 2;146(39):27080-27089. doi: 10.1021/jacs.4c09219. Epub 2024 Sep 21.

Abstract

A limiting factor to the efficiency of water Oxygen Evolution Reaction (OER) in metal oxide nanoparticle photocatalysts is the rapid recombination of holes and electrons. Facet-engineering can effectively improve charge separation and, consequently, OER efficiency. However, the kinetics behind this improvement remain poorly understood. This study utilizes photoinduced absorption spectroscopy to investigate the charge yield and kinetics in facet-engineered BiVO (F-BiVO) compared to a non-faceted sample (NF-BiVO) under operando conditions. A significant influence of preillumination on hole accumulation is observed, linked to the saturation and, thus, passivation of deep and inactive hole traps on the BiVO surface. In DI-water, F-BiVO shows a 10-fold increase in charge accumulation (∼5 mΔOD) compared to NF-BiVO (∼0.5 mΔOD), indicating improved charge separation and stabilization. With the addition of Fe(NO), an efficient electron acceptor, F-BiVO demonstrates a 30-fold increase in the accumulation of long-lived holes (∼45 mΔOD), compared to NF-BiVO (∼1.5 mΔOD) and an increased half-time, from 2 to 10 s. Based on a simple kinetic model, this increase in hole accumulation suggests that facet-engineering causes at least a 50-100 meV increase in band bending in BiVO particles, thereby stabilizing surface holes. This energetic stabilization/loss results in a retardation of OER relative to NF-BiVO. This slower catalysis is, however, offset by the observed increase in density and lifetime of photoaccumulated holes. Overall, this work quantifies how surface faceting can impact the kinetics of long-lived charge accumulation on metal oxide photocatalysts, highlighting the trade-off between lifetime gain and energetic loss critical to optimizing photocatalytic efficiency.

摘要

金属氧化物纳米颗粒光催化剂中析氧反应(OER)效率的一个限制因素是空穴和电子的快速复合。晶面工程可以有效地改善电荷分离,从而提高OER效率。然而,这种改善背后的动力学仍知之甚少。本研究利用光致吸收光谱来研究在操作条件下,与无晶面样品(NF-BiVO)相比,晶面工程化的BiVO(F-BiVO)中的电荷产率和动力学。观察到预照明对空穴积累有显著影响,这与BiVO表面深层和非活性空穴陷阱的饱和以及钝化有关。在去离子水中,与NF-BiVO(约0.5 mΔOD)相比,F-BiVO的电荷积累增加了10倍(约5 mΔOD),表明电荷分离和稳定性得到改善。加入有效的电子受体Fe(NO)后,与NF-BiVO(约1.5 mΔOD)相比,F-BiVO的长寿命空穴积累增加了30倍(约45 mΔOD),半衰期从2秒增加到10秒。基于一个简单的动力学模型,空穴积累的这种增加表明晶面工程使BiVO颗粒中的能带弯曲至少增加了50-100 meV,从而稳定了表面空穴。这种能量稳定/损失导致相对于NF-BiVO的OER延迟。然而,这种较慢的催化作用被光积累空穴密度和寿命的增加所抵消。总体而言,这项工作量化了表面晶面如何影响金属氧化物光催化剂上长寿命电荷积累的动力学,突出了寿命增加和能量损失之间的权衡对于优化光催化效率至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80d8/11450740/7cba487592cd/ja4c09219_0001.jpg

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