光催化
联轴节(管道)
材料科学
领域(数学)
催化作用
纳米技术
化学
复合材料
数学
生物化学
纯数学
作者
Mengpei Jiang,Keke Huang,Jinghai Liu,Dan Wang,Ying Wang,Xia Wang,Zhida Li,Xiyang Wang,Zhibin Geng,Xiangyan Hou,Shouhua Feng
出处
期刊:Chem
[Elsevier BV]
日期:2020-07-21
卷期号:6 (9): 2335-2346
被引量:101
标识
DOI:10.1016/j.chempr.2020.06.033
摘要
Summary
Solar-driven CO2 conversion is an attractive option for producing usable fuels and chemicals. However, traditionally synthesized TiO2 materials suffer from the low activity of CO2 conversion into multi-carbon products. In this study, for the first time, strong magnetic fields were introduced into the synthesis of TiO2. By regulating the splitting ratio of high-angle and low-angle quantum orbitals, we developed a new type of TiO2{100} facets containing more active low-coordinate Ti atoms. In-situ Fourier transform infrared spectroscopy (FTIR) and DFT calculations both revealed that the interfacial charge redistribution and lattice structure of such TiO2{100} are beneficial to the coupling of adsorbed CO∗. This enables highly efficient conversion of CO2 into C2H5OH with a yield rate of 6.16 μmol g−1 h−1, which is 22-fold higher than that of pristine TiO2. This strategy provides a new platform for desirable photocatalyst synthesis and furthers our understanding of the relationship between atomic orbital control and CO2 conversion.
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