Crystalline and porous CoSe dendrimeric architectures for efficient oxygen evolution reaction

被引:16
|
作者
Bilal, Muhammad [1 ]
Rashid [1 ]
Altaf, Amna [1 ]
Baig, Nadeem [2 ]
Chotana, Ghayoor Abbas [3 ]
Ashraf, Raja Shahid [4 ]
Rasul, Shahid [5 ,6 ]
Nafady, Ayman [7 ]
Ul-Hamid, Anwar [8 ]
Sohail, Manzar [1 ]
机构
[1] Natl Univ Sci & Technol, Sch Nat Sci, Dept Chem, H-12, Islamabad 44000, Pakistan
[2] King Fahd Univ Petr & Minerals, Interdisciplinary Res Ctr Membranes & Water Secur, Dhahran 31261, Saudi Arabia
[3] Lahore Univ Management Sci, Syed Babar Ali Sch Sci & Engn, Dept Chem & Chem Engn, Lahore 54792, Pakistan
[4] Univ Lahore, Dept Chem, Govt Coll, Lahore 54000, Pakistan
[5] Newcastle Univ, Sch Engn, Newcastle Upon Tyne NE1 7RU, Northd, England
[6] Northumbria Univ, Fac Engn & Environm, Newcastle Upon Tyne NE1 8ST, Northd, England
[7] King Saud Univ, Coll Sci, Dept Chem, Riyadh 11451, Saudi Arabia
[8] King Fahd Univ Petr & Minerals, Core Res Facil, Dhahran 31261, Saudi Arabia
关键词
CoSe; Electrocatalyst; Oxygen evolution reaction; Water splitting; Renewable energy; COBALT SELENIDE NANOSTRUCTURES; RATIONAL DESIGN; IRON SELENIDE; WATER; ELECTROCATALYST; CATALYSTS; NANOPARTICLES; NANOSHEETS; OXIDATION; CO0.85SE;
D O I
10.1016/j.fuel.2022.124324
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Developing an efficient and economical electrocatalyst for oxygen evolution reaction is the key challenge to renewable energy technologies. Metal selenides are attractive candidates for electrocatalytic water oxidation because they provide suitable surface-active sites for the reaction. Herein, we report less explored hexagonal cobalt selenide (CoSe) preparation for oxygen evolution reaction through the facile and environmentally benign one-step hydrothermal method. Reaction conditions were precisely tailored to develop highly crystalline and porous dendrimeric architectures of CoSe. Owing to its exclusive porous and dendrimeric crystalline network and large electrochemical surface area, the superior CoSe electrocatalyst (that is 16H) showed excellent electrochemical activity with remarkably low overpotential (250 mV at 10 mA cm(-2)) and very high current density (570 mA cm(-2)) in a small potential window. The Tafel slope of 16H sample was 56 mV dec(-1), indicating the faster kinetics at the catalyst surfaces. Moreover, it also showed excellent stability under harsh oxidative conditions in a 24-hour long stability test experiment.
引用
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页数:8
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