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非晶态C@TiO中氧空位和介孔结构在光催化CO还原中的协同效应。

Synergistic effects of oxygen vacancies and mesoporous structures in amorphous C@TiO for photocatalytic CO reduction.

作者信息

Yuan Binxia, Liu Yuhao, Qian Hong, Zhu Rui, Zhang Chengxi, Luan Weiling

机构信息

College of Energy and Mechanical Engineering, Shanghai University of Electric Power, Shanghai 201306, P.R. China.

Department of Optoelectronic Information Science and Engineering, Jiangsu University of Science and Technology, Zhenjiang 212100, China.

出版信息

iScience. 2024 Jun 25;27(7):110377. doi: 10.1016/j.isci.2024.110377. eCollection 2024 Jul 19.

DOI:10.1016/j.isci.2024.110377
PMID:39055922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11269941/
Abstract

In this study, the theoretical calculations proves that the combination of oxygen vacancy and amorphous carbon films in TiO (V-CT) can effectively reduce the energy bandgap and work function. The minimum Gibbs free energies required for the CORR reaction of V-CT are 0.20 eV, which is lower than pure TiO. The amorphous c@TiO nanomaterials with oxygen vacancy and mesoporous structures (V-MCT) are prepared with the P123 surfactant as the template and oxalic acid as an inducer. The electron paramagnetic resonance indicates the presence of abundant oxygen vacancy defects in the samples. UV-vis spectra indicate that the mesoporous structure enhances light absorption capacity. The photocatalytic CO reduction tests show that the highest conversion rates for CH and CO of V-MCT are 14 μmol g h and 10.66 μmol g h, respectively. The electron consumption rate of V-MCT is 12.43 times higher than that of commercial TiO (P200).

摘要

在本研究中,理论计算证明,TiO(V-CT)中氧空位与非晶碳膜的结合可有效降低能带隙和功函数。V-CT的CORR反应所需的最小吉布斯自由能为0.20 eV,低于纯TiO。以P123表面活性剂为模板、草酸为诱导剂制备了具有氧空位和介孔结构的非晶c@TiO纳米材料(V-MCT)。电子顺磁共振表明样品中存在大量氧空位缺陷。紫外可见光谱表明介孔结构增强了光吸收能力。光催化CO还原试验表明,V-MCT对CH和CO的最高转化率分别为14 μmol g h和10.66 μmol g h。V-MCT的电子消耗率比商用TiO(P200)高12.43倍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dbe/11269941/49a27a814869/gr8.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dbe/11269941/437dcfd53250/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dbe/11269941/22b543f7513c/gr1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dbe/11269941/4854890dffab/gr3.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dbe/11269941/bf939e9ac6ef/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dbe/11269941/b3c2a12265fb/gr6.jpg
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本文引用的文献

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In-situ incorporation of Copper(II) porphyrin functionalized zirconium MOF and TiO for efficient photocatalytic CO reduction.原位掺入铜(II)卟啉功能化锆金属有机框架和二氧化钛以实现高效光催化二氧化碳还原
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Electrochemical Reduction of Carbon Dioxide at TiO/Au Nanocomposites.
TiO/Au纳米复合材料上二氧化碳的电化学还原
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