Pulse electrodeposition of CoFe thin films covered with layered double hydroxides as a fast route to prepare enhanced catalysts for oxygen evolution reaction

被引:54
作者
Sakita, Alan M. P. [1 ,2 ]
Della Noce, Rodrigo [3 ]
Valles, Elisa [2 ,4 ]
Benedetti, Assis V. [1 ]
机构
[1] UNESP Univ Estadual Paulista, Inst Quim, BR-14800900 Araraquara, Brazil
[2] Ge CPN Thin Films & Nanostruct Electrodeposit Grp, Dpt Ciencia Mat & Quim Fis, Marti & Franques 1, Barcelona 08028, Spain
[3] Univ Lisbon, Inst Super Tecn, Dept Chem Engn, CQE, P-1049001 Lisbon, Portugal
[4] Univ Barcelona, Inst Nanocience & Nanotechnol IN2UB, Barcelona, Spain
关键词
Ultra-fast electrodeposition; CoFe alloy; CoFe-layered double hydroxide; Oxygen evolution reaction; Water splitting; ALLOY NANOPARTICLES; WATER OXIDATION; COBALT; IRON; CARBON; NUCLEATION; GROWTH; FE; REDUCTION; CORROSION;
D O I
10.1016/j.apsusc.2017.11.042
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
A novel, ultra-fast, and one-step method for obtaining an effective catalyst for oxygen evolution reaction is proposed. The procedure consists in direct electrodeposition, in a free-nitrate bath, of CoFe alloy films covered with layered double hydroxides (LDH), by potentiostatic mode, in continuous or pulsed regime. The catalyst is directly formed on glassy carbon substrates. The best-prepared catalyst material reveals a mixed morphology with granular and dendritic CoFe alloy covered with a sponge of CoFe-LDH containing a Cl interlayer. An overpotential of eta 10 mA = 286 mV, with a Tafel slope of 48 mV dec(-1), is obtained for the OER which displays the enhanced properties of the catalyst. These improved results demonstrate the competitiveness and efficacy of our proposal for the production of OER catalysts. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1153 / 1160
页数:8
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