非阻塞I/O
X射线光电子能谱
材料科学
催化作用
碳纤维
拉曼光谱
镍
阳极
氧化物
金属
氢
无机化学
分析化学(期刊)
化学工程
物理化学
化学
电极
冶金
复合材料
生物化学
物理
光学
有机化学
色谱法
复合数
工程类
作者
Xiaofeng Li,Xiaohui Liu,Jiamao Hao,Lijun Li,Yanfang Gao,Yousong Gu,Zhenzhu Cao,Jinrong Liu
出处
期刊:ACS omega
[American Chemical Society]
日期:2022-07-07
卷期号:7 (28): 24646-24655
被引量:23
标识
DOI:10.1021/acsomega.2c02479
摘要
A strong metal-support interaction (SMSI) type catalyst has been synthesized and applied to a molten hydroxide direct carbon fuel cell (MHDCFC) to enhance the reaction activity of the anode carbon fuel through the interaction between the metal Ni and the support CeO2. Two catalysts have been prepared by a direct precipitation method (denoted NiO@CeO2) and a hydrothermal method (denoted NiO-CeO2), which are reduced by H2 to obtain Ni@CeO2 and Ni-CeO2, respectively. X-ray photoelectron spectroscopy (XPS), Raman, and temperature-programmed hydrogen reduction (H2-TPR) analysis results show that there are obvious oxygen vacancies and a Ni-O-Ce interface structure in NiO-CeO2 and Ni-CeO2, which is induced by the interaction between Ni and CeO2. The calculation results of current density and power density show that the performance of the MHDCFC is significantly improved in the presence of Ni-CeO2. The function fitting curves of the logarithm of the reaction rate constant (ln k) and the reciprocal of the temperature (1/T) show that the slope of the curve is decreased significantly after the addition of Ni-CeO2. In combination with density functional theory (DFT), the anode carbon reaction path is simulated in the MHDCFC, and the calculation results show that the reaction energy for the anodic carbon to generate carbon dioxide is decreased by 1.03 eV in the presence of Ni-CeO2.
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