NiFe Layered Double Hydroxide Electrocatalyst Prepared via an Electrochemical Deposition Method for the Oxygen Evolution Reaction

被引:19
作者
Kumar, Murugesan Praveen [1 ]
Sasikumar, Moorthy [2 ]
Arulraj, Arunachalam [1 ,3 ]
Rajasudha, Venugopalan [4 ]
Murugadoss, Govindhasamy [5 ]
Kumar, Manavalan Rajesh [6 ]
Peera, Shaik Gouse [7 ]
Mangalaraja, Ramalinga Viswanathan [1 ]
机构
[1] Adolfo Ibanez Univ, Fac Engn & Sci, Diagonal Torres 2640, Santiago 7941169, Chile
[2] Bishop Heber Coll, Dept Phys, Thiruchirapalli 620023, Tamil Nadu, India
[3] Univ Atacama, Fac Ciencias Nat, Dept Fis, Av Copayapu 485, Copiapo 1531772, Chile
[4] Annai Vailankanni Arts & Sci Coll, Dept Chem, Thanjavur 613007, Tamil Nadu, India
[5] Sathyabama Inst Sci & Technol, Ctr Nanosci & Nanotechnol, Chennai 600119, Tamil Nadu, India
[6] Ural Fed Univ, Inst Nat Sci & Math, Ekaterinburg 620002, Russia
[7] Keimyung Univ, Dept Environm Sci, 1095 Dalgubeol Daero, Daegu 42601, South Korea
基金
新加坡国家研究基金会;
关键词
OER; NiFe-LDH electrocatalyst; electrochemical deposition; (Oxy)hydroxides phases; long-time stability; HYDROGEN EVOLUTION; IRON; NANOPARTICLES; CATALYSTS; COMPOSITE; ALLOY;
D O I
10.3390/catal12111470
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
Herein, we aimed to obtain NiFe layered double hydroxide (LDH) with a controlled phase and surface morphology as a highly active and stable oxygen evolution catalyst via the electrochemical deposition method, which was thermodynamically stable for the oxygen evolution reaction (OER) in an alkaline medium. The NiFe-LDH sample was analyzed by sophisticated instruments and tested as an electrocatalyst on Toray carbon (TC). The NiFe-LDH electrocatalyst showed an excellent performance with lower overpotential of 0.27 V at 35 mA cm(-2) and higher density of 125 mA cm(-2) for OER in the 1 M KOH electrolyte solution. Moreover, the prepared catalyst exhibited unpredictable long-time stability for 700 h. From our knowledge, NiFe-LDH is a robust highly stable electrocatalyst compared to the recent reports.
引用
收藏
页数:12
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