Deposition of CeO2 on TiO2 nanorods electrode by dielectric barrier discharge plasma to enhance the photoelectrochemical performance in high chloride salt system

Deposition of CeO2 on TiO2 nanorods electrode by dielectric barrier discharge plasma to enhance the photoelectrochemical performance in high chloride salt system
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介质阻挡放电等离子体在TiO2纳米棒电极上沉积CeO2以增强高氯盐体系中的光电化学性能

DOI:
10.1016/j.seppur.2021.119252
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发表时间:
2021-12
影响因子:
8.6
通讯作者:
Zhang Yi
Zhang Yi
中科院分区:
工程技术1区
文献类型:
--
作者:
Ma Hao;Yuan Chenchen;Wang Xiaomin;Wang Hongjun;Long Yupei;Chen Yuqi;Wang Qi;Cong Yanqing;Zhang Yi

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In this study, cerium oxide (CeO2) was deposited on TiO2nanorods (TiO2-NRs) through the one-step deposition by using dielectric barrier discharge (DBD) plasma treatment, where this was a simple and efficient means of synthesizing a CeO2/TiO2-NR electrode. The results of X-ray diffraction indicated that CeO2(1 1 1) was successfully loaded on the TiO2-NRs, and the peak shifted in the positive direction after DBD discharge-induced modification, indicating that a bond between CeO2and TiO2had been formed in the CeO2/TiO2-NR electrode. Based on X-ray photoelectron spectroscopy, the ratio of Ce3+/Ce4+increased due to plasma modification to enhance the oxygen vacancy of the CeO2/TiO2-NRs in the lattice structure. The CeO2/TiO2-NR composite electrode delivered the best photoelectrochemical (PEC) performance at a modified input voltage of 45 V and a deposition time of 10 min due to DBD discharge. The efficiency of removal of phenol from simulated seawater with a high salt system yielded the highest value of 97.1% for the CeO2/TiO2-NR electrodes through the PEC process at 3 V and UV–visible irradiation. A mechanism of the PEC performance of the CeO2/TiO2-NRs electrode was proposed, whereby a heterojunction was formed between TiO2and CeO2to increase the effect of oxygen storage, and active chlorine ions were produced in the high chloride salt system to enhance the degradation of pollutants.
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