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用于增强光阳极活性的二氧化钛纳米管的水热钴掺杂

Hydrothermal Cobalt Doping of Titanium Dioxide Nanotubes towards Photoanode Activity Enhancement.

作者信息

Wtulich Mariusz, Szkoda Mariusz, Gajowiec Grzegorz, Gazda Maria, Jurak Kacper, Sawczak Mirosław, Lisowska-Oleksiak Anna

机构信息

Department of Chemistry and Technology of Functional Materials, Chemical Faculty, Gdańsk University of Technology, 80-233 Gdańsk, Poland.

Faculty of Mechanical Engineering and Ship Technology, Institute of Machine Technology and Materials, Gdansk University of Technology, 80-233 Gdansk, Poland.

出版信息

Materials (Basel). 2021 Mar 19;14(6):1507. doi: 10.3390/ma14061507.

Abstract

Doping and modification of TiO nanotubes were carried out using the hydrothermal method. The introduction of small amounts of cobalt (0.1 at %) into the structure of anatase caused an increase in the absorption of light in the visible spectrum, changes in the position of the flat band potential, a decrease in the threshold potential of water oxidation in the dark, and a significant increase in the anode photocurrent. The material was characterized by the SEM, EDX, and XRD methods, Raman spectroscopy, XPS, and UV-Vis reflectance measurements. Electrochemical measurement was used along with a number of electrochemical methods: chronoamperometry, electrochemical impedance spectroscopy, cyclic voltammetry, and linear sweep voltammetry in dark conditions and under solar light illumination. Improved photoelectrocatalytic activity of cobalt-doped TiO nanotubes is achieved mainly due to its regular nanostructure and real surface area increase, as well as improved visible light absorption for an appropriate dopant concentration.

摘要

采用水热法对TiO纳米管进行掺杂和改性。向锐钛矿结构中引入少量钴(0.1原子%)会导致可见光谱中光吸收增加、平带电位位置改变、黑暗中析氧阈值电位降低以及阳极光电流显著增加。通过扫描电子显微镜(SEM)、能谱仪(EDX)、X射线衍射(XRD)方法、拉曼光谱、X射线光电子能谱(XPS)和紫外可见反射率测量对该材料进行了表征。电化学测量与多种电化学方法一起使用:计时电流法、电化学阻抗谱、循环伏安法以及在黑暗条件和太阳光照射下的线性扫描伏安法。钴掺杂TiO纳米管光催化活性的提高主要归因于其规则的纳米结构和真实表面积的增加,以及在适当掺杂浓度下可见光吸收的改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f217/8003354/002257607707/materials-14-01507-g001.jpg

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