Non-Precious Metal/Metal Oxides and Nitrogen-Doped Reduced Graphene Oxide based Alkaline Water-Electrolysis Cell

被引:41
|
作者
Vineesh, Thazhe Veettil [1 ]
Sekar, Archana [1 ]
Rajappa, Sivamathini [2 ]
Pal, Shubhadeep [1 ]
Alwarappan, Subbiah [2 ]
Narayanan, Tharangattu N. [1 ]
机构
[1] Tata Inst Fundamental Res, TCIS, Hyderabad 500075, Andhra Prades, India
[2] CSIR, Cent Electrochem Res Inst, CECRI, Karaikkudi 630003, Tamil Nadu, India
关键词
doping; electrochemistry; graphene; membranes; water splitting; OXYGEN EVOLUTION; HIGH-PERFORMANCE; CO3O4; ELECTROCATALYST; NANOPARTICLES; CATALYST; HYDROGEN;
D O I
10.1002/cctc.201701018
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
The development of strategies for water-electrolysis half-cell-reaction catalysts without the use of precious metals/metal oxides and the synergistic compilation of catalysts for the full-cell fabrication are receiving tremendous scientific attention. Here, alkaline water-electrolysis full cells are developed with novel spongy catalysts for both anode and cathode reactions, such as Co3O4 nitrogen-doped reduced graphene oxide (Co3O4/NrGO) composite sponge for oxygen evolution reaction (OER) and nickel nitrogen-doped reduced graphene oxide (NiNrGO) for hydrogen evolution reaction (HER). The performance of the developed OER catalyst, Co3O4/NrGO, is compared with that of the commercial one (IrO2) in alkaline medium with a common benchmark cathode catalyst (Pt) and an augmented full-cell performance is shown from this novel combination (320mAcm(-2) at an operating voltage of 1.9V for Co3O4/NrGO, with 199mAcm(-2) for IrO2). A water-electrolysis full cell is developed without the use of HER catalyst Pt, but rather using a porous spongy catalyst, NiNrGO, having a low operating potential with a high stability (270mAcm(-2) at an operating voltage of 1.9V with a stability tested for more than 9h). This work opens up the possibilities of designing lightweight water-electrolysis cells without the use of commercial benchmark precious-metal catalysts.
引用
收藏
页码:4295 / 4300
页数:6
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