材料科学
X射线光电子能谱
分解水
光催化
锐钛矿
镧系元素
制氢
二氧化钛
带隙
光化学
离子
化学工程
催化作用
化学
光电子学
生物化学
有机化学
工程类
冶金
作者
Hyekyung Cho,Hyunku Joo,Hansung Kim,Jieun Kim,Kyoung-Soo Kang,Hyeonmin Jung,Jaekyung Yoon
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2022-08-05
卷期号:12 (8): 866-866
被引量:12
标识
DOI:10.3390/catal12080866
摘要
Highly ordered TiO2 nanotubes (TNTs) decorated with a series of lanthanide ions (Ln3+ = Ho3+, Tb3+, Eu3+, Yb3+, and Er3+) were prepared through an electrochemical process and anodization. The composition, structure, and chemical bond of the as-prepared photocatalysts were characterized through scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, ultraviolet photoelectron spectroscopy, and ultraviolet diffuse reflectance spectroscopy. Furthermore, the electrochemical characteristics of the catalysts were analyzed and photoelectrochemical properties were investigated through water splitting. All samples were prepared in the anatase phase without changing the crystal structure. The holmium-doped TNT photocatalyst exhibited the best performance with a hydrogen evolution rate of 90.13 μmol cm−2h−1 and photoconversion efficiency of 2.68% (0 V vs. RHE). Photocatalytic efficiency increased because of the expansion of the absorption wavelength range attributed to the appropriate positioning of the band structure and reduced electron/hole pair recombination resulting from the unhindered electron movement. This study demonstrated the preparation of high-potential solar-active photocatalysts through the synergetic effects of the work function, band edge, and bandgap changes caused by the series of lanthanide combinations with TNTs.
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