催化作用
甲醇
甲醇燃料
阳极
材料科学
直接甲醇燃料电池
阴极
化学工程
氧还原反应
铂金
氧化还原
对偶(语法数字)
无机化学
纳米技术
化学
电化学
有机化学
电极
工程类
物理化学
艺术
文学类
作者
Yuanhui Zuo,Wenchao Sheng,Wen‐Quan Tao,Zhuo Li
标识
DOI:10.1016/j.jmst.2021.10.031
摘要
One fundamental challenge in exploiting direct methanol fuel cells (DMFCs) is the preparation of inexpensive, high active electrocatalysts, which are highly active and durable for the two half-reactions, i.e., the methanol oxidation reaction (MOR) at the anode and the oxygen reduction reaction (ORR) at the cathode. Platinum group metals-based catalysts have been known the governing dual-functional electrocatalysts based on the literature reports. But these catalysts are expensive and commercialize the DMFC less attractive. In addition to the high-cost, there are also methanol crossover, CO poisoning, long-term instability, and other problems as for Pt-based spurs. For the dual-role MOR & ORR catalysts, methanol crossover is inevitable to a certain extent on the current development of DMFC with losses in terms of cell voltage. In this regard, one strategy is to exploit high selective anodic/cathodic electrocatalysts to capitalize the energy density at a high concentration of methanol. According to the summary results, there are mainly two types of dual-role electrocatalysts: one is Pt-support/co-catalyst (designated as P-S/C) for MOR/ORR, the other is catalyst/co-catalyst (designated as C/C) for MOR/ORR. This paper aims to review the design and construction of the various dual-role catalysts and give some discussion briefly.
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