化学
锐钛矿
X射线光电子能谱
二氧化钛
镍
水解
无机化学
钛
化学计量学
核化学
打赌理论
亲核细胞
化学工程
催化作用
光催化
有机化学
工程类
作者
Xiaoming Zhu,Yongchao Zheng,Likun Chen,Jina Wu,Sheng-Song Li,Xin Yi,Mingjun Su,Yan Cui
标识
DOI:10.1016/j.arabjc.2021.103678
摘要
Here, Nickel doped anatase TiO2 samples were prepared and characterized by X-ray diffraction, transmission electron microscope, X-ray photoelectron spectroscopy, specific surface area (BET), porosity determination (BJH) and CO2-TPD experiments. DFT calculation was conducted to investigate the oxygen vacancy formation energies and hydroxyl groups activity. The as-prepared Ni2+ doped TiO2 samples were used for heterogeneous degradation of chemical warfare agents (CWAs) and a high degradation rate, 92.2% and > 99.5% for sulfur mustard (HD) within 1 h and 12 h, > 99.5% for soman (GD) in less than 30 min, and > 99.5% for VX in less than 5 min was achieved, which were significantly enhanced compared with commercial P25 and anatase TiO2 nanoparticles under identical conditions. The formation of non-toxic hydrolysis products confirmed the nucleophilic hydrolysis pathway via surface reaction. Integration of experimental and computational methods could well illustrate that surface structure changes of TiO2 after Ni2+ doping was the main reason for the superior stoichiometric activity towards CWAs.
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