阴极
电化学
双功能
降级(电信)
过渡金属
材料科学
兴奋剂
傅里叶变换红外光谱
催化作用
无机化学
金属
化学
化学工程
电极
冶金
有机化学
物理化学
光电子学
计算机科学
电信
工程类
作者
Pei Su,Wenyang Fu,Zhongzheng Hu,Jiana Jing,Minghua Zhou
标识
DOI:10.1016/j.apcatb.2022.121457
摘要
In electrochemical advanced oxidation processes (EAOPs), a series of transition metal encapsulated nitrogen-doped carbon nanotubes ([email protected], M=Fe, Co, Ni, Cu) as bifunctional cathodes were synthesized to compare and uncover their activity trends, fulfilling the self-sufficient electrocatalytic degradation. The sulfamethazine (SMT) degradation activity trends were follows: [email protected]>[email protected]>[email protected]>[email protected] cathode at pH≤ 7, while the [email protected] cathode exhibited the highest activity at pH 9 due to the more 1O2 and atomic H*. In-situ Fourier transformed infrared (FTIR) spectroscopy and density functional theory (DFT) calculation suggested that the atomic H* was easier to generate under the action of pyridinic N on [email protected] cathode. Overall, various pollutants degradation on [email protected] cathode performed with good stability with low leaching iron (0.12 mg L−1) and low energy consumption (<0.3 kWh∙log−1∙m−3). This study sheds light on different mechanisms of reactive species production on [email protected] cathode, thus providing guidance for the selectivity between [email protected] via active species and pollutants.
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