Role of Noncovalent Interactions on the Electrocatalytic Oxidation of Ethanol in Alkali Metal Hydroxide Solutions

被引:9
|
作者
Han, Chenjie [1 ]
Lyu, Yeqing [1 ]
Wang, Shaona [1 ]
Liu, Biao [1 ]
Zhang, Yi [1 ]
Du, Hao [1 ,2 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Green Proc & Engn, Natl Engn Res Ctr Green Recycling Strateg Met Res, Inst Proc Engn, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
ethanol; electro-oxidation; faraday efficiency; noncovalent interactions; ELECTROCHEMICAL DETERMINATION; ELECTROOXIDATION; ELECTRODE; CATALYSTS; MEDIA; ACID; CO2; NANOPARTICLES; EFFICIENCY; DIFFUSION;
D O I
10.1021/acsami.1c20964
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ethanol is considered to be one of the most promising fuels for fuel cells. However, ethanol fuel cells have a sluggish Faraday efficiency due to complex interactions between the electrolyte, electrode, and ethanol. Recent studies have further suggested that noncovalent interactions originated from the hydrated alkali metal cations and the adsorbed OHad at the Pt electrode surface also played an important role in the electron transfer. In this regard, the noncovalent interactions in different alkali metal hydroxide (AMH) solutions have been systematically investigated in this study, and it was observed that the noncovalent interactions could result in the occupation of the Pt electrode surface active sites and sluggish migration of ethanol molecules in the electrical double layer, significantly affecting the electrooxidation efficiency. Further, it was concluded that the electro-oxidation efficiency in different AMH solutions followed the order of K+ > Na+ > Rb+ > Cs+ > Li+ due to the noncovalent interactions.
引用
收藏
页码:5318 / 5327
页数:10
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