光催化
材料科学
X射线光电子能谱
锐钛矿
异质结
带隙
可见光谱
兴奋剂
纳米技术
化学工程
催化作用
光电子学
化学
生物化学
工程类
作者
Tao Liu,Aori Qileng,Nuermaimaitijiang Wubulikasimu,Zhixiong Liu,Weipeng Liu,Yingju Liu
出处
期刊:ChemNanoMat
[Wiley]
日期:2023-08-26
卷期号:9 (10)
被引量:4
标识
DOI:10.1002/cnma.202300343
摘要
Abstract As a green photocatalyst, TiO 2 has been widely used in adsorption, desorption and redox reactions, but the wide energy band and moderate visible light absorption have greatly inhibited its applications in photocatalysis. The effective method of enhancing the performance of catalysts is the development of heterojunction and metal‐nonmetal co‐doping. Herein, Fe−N co‐doped TiO 2 heterojunction photocatalysts (Fe x Ti@C) were successfully synthesized by calcining a self‐sacrificial template (NH 2 −MIL‐125(Ti)) injected with Fe 3+ solution. X‐ray diffraction (XRD), transmission electron microscopy (TEM), X‐ray photoelectron spectroscopy (XPS), N 2 adsorption/desorption analysis, and photoelectrochemical tests were used to characterize Fe x Ti@C, showing multiple rutile/anatase TiO 2 heterojunction structure, low bandgap, and significant absorption in visible light. In addition, the Ti−O−Fe tetrahedra and more oxygen vacancies were provided since the doped N is from the pristine MOF and the radii of Fe 3+ and Ti 4+ are similar, which improved the photocatalytic efficiency of CO 2 reduction to CH 4 , especially the Fe 0.8 Ti@C reached 7.8‐fold and 10.2‐fold CH 4 yield increase compared with the original TiMOF template and the undoped Ti@C, respectively. This work presents a simple method for the fabrication of low bandgap semiconductors, and also makes a new attempt at the synergistic effect between the in‐situ elements and valence bonds of MOF‐derived catalysts.
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