Oxygen Evolution Reaction on Single-Walled Carbon Nanotubes Noncovalently Functionalized with Metal Phthalocyanines

被引:34
作者
Alzate-Carvajal, Natalia [1 ]
Bolivar-Pineda, Lina M. [2 ]
Meza-Laguna, Victor [2 ]
Basiuk, Vladimir A. [2 ]
Basiuk, Elena, V [3 ]
Baranova, Elena A. [1 ]
机构
[1] Univ Ottawa, Dept Chem & Biol Engn, CCRI, 161 Louis Pasteur, Ottawa, ON K1N 6N5, Canada
[2] Univ Nacl Autonoma Mexico, Inst Ciencias Nucl, Ciudad De Mexico 04510, Mexico
[3] Univ Nacl Autonoma Mexico, Inst Ciencias Aplicadas & Tecnol, Ciudad De Mexico 04510, Mexico
基金
加拿大自然科学与工程研究理事会;
关键词
water electrolysis; oxygen evolution reaction; metal phthalocyanines; carbon nanotubes; alkaline media; EFFICIENT BIFUNCTIONAL ELECTROCATALYST; THIN-FILM; REDUCTION; OXIDATION; IRON; NI; CATALYSTS; FE; MEMBRANE; GRAPHENE;
D O I
10.1002/celc.201901708
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
This work reports the facile preparation of single-walled carbon nanotubes (SWCNTs) noncovalently functionalized with 3d transition metal (II) phthalocyanines MPcs (M=Mn, Fe, Co and Ni) and their electrochemical evaluation towards the oxygen evolution reaction (OER) in alkaline media. The modification of SWCNTs with MPcs improved the potential required for the oxygen evolution reaction in 0.1 M and 1 M KOH by lowering the potential by approximately 120 mV in comparison with unmodified SWCNTs, at a current density of 10 mA cm(-1). The onset potential of the hybrids is close to the bulk Ni electrode in 1 M KOH and significantly outperforms Ni and Ir black electrodes in 0.1 M KOH solution. Nickel, cobalt and iron phthalocyanines showed auto-activation during extended cyclic voltammetry and long-term chronoamperometric measurements in both KOH concentrations. The excellent electrocatalytic activity of hybrids obtained and the straightforward method of their synthesis opens the possibility of exploring the proposed materials for applications in anion exchange membrane water electrolysis (AEMWE).
引用
收藏
页码:428 / 436
页数:9
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