纳米晶
可见光谱
催化作用
材料科学
光催化
漫反射红外傅里叶变换
带隙
太阳能燃料
光化学
氧气
吸附
红外线的
光谱学
量子产额
纳米技术
光电子学
化学
光学
物理化学
荧光
物理
量子力学
有机化学
生物化学
作者
Lianjun Liu,Yuqiu Jiang,Huilei Zhao,Jiatang Chen,Jianli Cheng,Kesong Yang,Ying Li
标识
DOI:10.1021/acscatal.5b02098
摘要
This work for the first time reports engineered oxygen-deficient, blue TiO2 nanocrystals with coexposed {101}-{001} facets (TiO2–x{001}-{101}) to enhance CO2 photoreduction under visible light. The TiO2–x{001}-{101} material demonstrated a relatively high quantum yield (0.31% under UV–vis light and 0.134% under visible light) for CO2 reduction to CO by water vapor and more than 4 times higher visible light activity in comparison with TiO2 with a single {001} plane or {101} plane and TiO2(P25). Possible reasons are the exposure of more active sites (e.g., undercoordinated Ti atoms and oxygen vacancies), the facilitated electron transfer between {001} and {101} planes, and the formation of a new energy state (Ti3+) within the TiO2 band gap to extend the visible light response. An in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) study was applied to understand the roles of coexposed {001}-{101} facets and Ti3+ sites in activating surface intermediates. The in situ DRIFTS analysis suggested that the coexposed {001}-{101} facets increased the capacity of reversible CO2 adsorption and that the combination of {001}-{101} and Ti3+ enhanced the activation and conversion kinetics of adsorbed species. The visible light responsive TiO2–x{001}-{101} material is not oxidized after long-term exposure to an air environment. This work is a significant contribution to the design of efficient and stable solar fuel catalysts.
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