In situ alloying silver/copper nanostructure as efficient electrocatalysts toward electrochemical water splitting

被引:0
|
作者
Abbood, Manal A. [1 ]
Althomali, Raed H. [2 ]
Al-dolaimy, F. [3 ]
Portilla, Roxana Madueno [4 ]
Abdullaev, Sherzod Shukhratovich [5 ]
Laime, Maria Del Carmen Delgado [6 ]
Hassan, Zahraa F. [7 ]
Abbas, Ahmed hussien R. [8 ]
Alsaalamy, Ali Hashiem [9 ]
机构
[1] Univ Technol Baghdad, Dept Appl Sci, Div Med & Ind Mat Sci, Baghdad, Iraq
[2] Prince Sattam Bin Abdulaziz Univ, Coll Arts & Sci, Dept Chem, Wadi Al Dawasir 11991, Saudi Arabia
[3] Al Zahraa Univ Women, Karbala 56001, Iraq
[4] Natl Amazonian Univ Madre Dios, Fac Engn, Acad Dept Med Vet Zootech, Puerto Maldonado, Peru
[5] New Uzbekistan Univ, Fac Chem Engn, Tashkent, Uzbekistan
[6] Univ Nacl Jose Maria Arguedas, Agroind Engn Dept, Andahuaylas 03701, Peru
[7] Al Ayen Univ, Coll Dent, Thi Qar, Iraq
[8] Islamic Univ, Coll Tech Engn, Najaf, Iraq
[9] Imam Jaafar Al Sadiq Univ, Coll Tech Engn, 66002, Al Muthanna, Iraq
关键词
Hydrogen electroreduction; Ag/Cu catalyst; Water splitting; Electrochemistry; OXYGEN EVOLUTION; HYDROGEN; PERFORMANCE;
D O I
10.1007/s11581-023-05264-9
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrochemical water splitting for hydrogen production has gained significant attention in the renewable energy field. In this study, we have developed a simple and reproducible method to synthesize silver-copper nanocomposites as efficient catalysts for water splitting. Despite silver's lower activity toward both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), our Ag/Cu catalyst exhibits improved catalytic activity compared to similar composition electrocatalysts. Notably, the Ag/Cu catalyst demonstrates a remarkably lower overpotential of 203 mV at 100 mA cm-2 for HER and only 205 mV at 100 mA cm-2 for OER. Moreover, the catalyst exhibits enhanced charge transfer ability with lower charge resistance for both OER and HER, indicating its critical role in electrocatalytic activity.
引用
收藏
页码:433 / 444
页数:12
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