方解石
沸石
催化作用
铜
甲醇
过电位
无机化学
化学工程
电化学
硫化铜
热液循环
材料科学
离子交换
化学
电极
离子
物理化学
冶金
有机化学
工程类
作者
Pengyan Wei,Fang Fang,E Yifeng,Yuying Jiang,Peng Chen,Hongzhu Xing,Kun Qian
标识
DOI:10.1016/j.ijhydene.2023.01.090
摘要
CuxS derivatives perform high activity in MOR (methanol oxidation reaction) through the co-operation of Cu and S. In order to further improve their performance, the composition and structure are regulated through the co-growth process of copper sulfide heterojunction and SOD (sodalite code) zeolite framework. Under the hydrothermal condition, the introduced Cu0 and Cu+ ions are clustered on the zeolitic surface and inner cages. The S2- anions are selectively located at the zeolite cage to balance the framework charge arisen from the incorporation of Cu+. In the electrochemical process, the optimized Cu2S/SOD zeolite electrode reveals an extra high efficiency of 8847 A g−1 at an extra low overpotential of 0.374 V with an excellent resistance to catalyst poisoning in high concentration of methanol. This work opens up a new method for the design and industrial application of non-precious metal electrocatalysts with high energy density based on porous zeolite materials.
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