Nickel pyrophosphate combined with graphene nanoribbon used as efficient catalyst for OER

被引:46
作者
Souza, Alan S. [1 ]
Bezerra, Leticia S. [1 ]
Cardoso, Eduardo S. F. [1 ]
Fortunato, Guilherme V. [1 ,2 ]
Maia, Gilberto [1 ]
机构
[1] Univ Fed Mato Grosso do Sul, Inst Chem, Ave Senador Filinto Muller 1555, BR-79074460 Campo Grande, MS, Brazil
[2] Univ Sao Paulo, Inst Chem Sao Carlos, Ave Trabalhador Sao Carlense 400, BR-13566590 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会; 瑞典研究理事会;
关键词
Catalysts;
D O I
10.1039/d1ta00817j
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
Although noble-metal based materials (IrO2 and RuO2) are regarded state-of-the-art catalysts for oxygen evolution reaction (OER), their high price, long-term instability, and scarcity have fueled the search for alternative materials that are relatively cheaper and highly abundant in nature and which can be used for the development of electrolyzers that are suitable for hydrogen production. The present work reports the development and application of a new hybrid catalyst derived from the thermal treatment of a mixture of graphene nanoribbons (GNR) and nickel pyrophosphate (beta-Ni2P2O7); the proposed hybrid material was found to present remarkably improved properties which include easy charge transfer, high electroactive surface area, high activity, and effective resistance to corrosion in OER in alkaline medium. The combination of highly dispersed beta-Ni2P2O7-30 wt% in direct contact with GNR-70 wt%, coupled with the application of thermal treatment - which ensured some enrichment of Ni in the GNiPy350N catalyst, contributed toward the production of an efficient material with excellent and stable OER activity in alkaline conditions. Compared to the state-of-the-art IrO2 (300 mV), the GNiPy350N catalyst required an overpotential of approximately 320 mV to reach the current density of 10 mA cm(-2) when immobilized on carbon paper electrode.
引用
收藏
页码:11255 / 11267
页数:13
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