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具有NiO/TiO₂纳米复合结构的表面光催化活性的制备与表征

Preparation and Characterization of Surface Photocatalytic Activity with NiO/TiO₂ Nanocomposite Structure.

作者信息

Chen Jian-Zhi, Chen Tai-Hong, Lai Li-Wen, Li Pei-Yu, Liu Hua-Wen, Hong Yi-You, Liu Day-Shan

机构信息

Institute of Electro-Optical and Materials Science, National Formosa University, Huwei, Yunlin 63201, Taiwan.

Industrial Technology Research Institute South, Liujia Shiang, Tainan 734, Taiwan.

出版信息

Materials (Basel). 2015 Jul 13;8(7):4273-4286. doi: 10.3390/ma8074273.

DOI:10.3390/ma8074273
PMID:28793439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5455623/
Abstract

This study achieved a nanocomposite structure of nickel oxide (NiO)/titanium dioxide (TiO₂) heterojunction on a TiO₂ film surface. The photocatalytic activity of this structure evaluated by decomposing methylene blue (MB) solution was strongly correlated to the conductive behavior of the NiO film. A -type NiO film of high concentration in contact with the native -type TiO₂ film, which resulted in a strong inner electrical field to effectively separate the photogenerated electron-hole pairs, exhibited a much better photocatalytic activity than the controlled TiO₂ film. In addition, the photocatalytic activity of the NiO/TiO₂ nanocomposite structure was enhanced as the thickness of the -NiO film decreased, which was beneficial for the migration of the photogenerated carriers to the structural surface.

摘要

本研究在二氧化钛(TiO₂)薄膜表面实现了氧化镍(NiO)/二氧化钛(TiO₂)异质结的纳米复合结构。通过分解亚甲基蓝(MB)溶液评估该结构的光催化活性,其与NiO薄膜的导电行为密切相关。与本征型TiO₂薄膜接触的高浓度A型NiO薄膜形成了强大的内电场,有效地分离了光生电子 - 空穴对,其光催化活性比对照TiO₂薄膜要好得多。此外,随着NiO薄膜厚度的减小,NiO/TiO₂纳米复合结构的光催化活性增强,这有利于光生载流子向结构表面迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/886bc585464a/materials-08-04273-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/fab7f906677b/materials-08-04273-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/c5b891863ae1/materials-08-04273-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/37664e6cccfc/materials-08-04273-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/177038f7af22/materials-08-04273-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/c26ddfc4c1d2/materials-08-04273-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/9f71b627888d/materials-08-04273-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/886bc585464a/materials-08-04273-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/fab7f906677b/materials-08-04273-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/d1a9a005dd34/materials-08-04273-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/63ace5c60b32/materials-08-04273-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/c5b891863ae1/materials-08-04273-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/37664e6cccfc/materials-08-04273-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/177038f7af22/materials-08-04273-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/c26ddfc4c1d2/materials-08-04273-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/9f71b627888d/materials-08-04273-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebe/5455623/886bc585464a/materials-08-04273-g009.jpg

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