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首页> 外文期刊>Journal of Catalysis >High catalytic performance of nickel foam supported Co-2 P-Ni2P for overall water splitting and its structural evolutions during hydrogen/oxygen evolution reactions in alkaline solutions
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High catalytic performance of nickel foam supported Co-2 P-Ni2P for overall water splitting and its structural evolutions during hydrogen/oxygen evolution reactions in alkaline solutions

机译:镍泡沫的高催化性能负载CO-2 P-Ni2P,用于总水分裂及其在碱性溶液中的氢气/氧气进化反应期间的结构演变

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Understanding of the structure changes of the catalysts during hydrogen (HER) and oxygen (OER) evolution reactions is of paramount importance for design of catalysts with enhanced performance. This work reports the structure change investigations of phosphide-based catalysts in both HER and OER. Specifically, nickel foam supported Co2P-Ni2P (Co2P-Ni2P/NF) is synthesized by in-situ growth of Co2P-Ni2P on the current collector, i.e. nickel foam, and then used for the investigation of the structure changes during HER and OER. This method avoids the use of polymer binders, allowing for the systematic analysis of the structure changes of the catalysts after HER and OER. The obtained Co2P-Ni2P/NIF shows an excellent catalytic bifunctionality for HER and OER in alkaline solutions. It only needs an overpotential of 90 mV vs RHE to offer a current density of 10 mA cm(-2) for HER and needs an overpotential of 230 mV vs RHE to offer a current density of 50 mA cm(-2) for OER. Both HER and OER activities of Co2P-Ni2P/NF are higher than those of most bifunctional catalysts reported. Post-analysis shows the occurrence of the surface roughening and the formation of M-P-O (M=Co and Ni) at the surface in its initial period of the HER, and the surface roughening and the formation of a thin layer of amorphous MOOH (Mo and Ni) at the surface in its initial period of OER. The surface roughening and formation of M-P-O and amorphous hydroxide layer can be attributed to the main reason responsible for its high performance for HER and OER. Additionally, the Co2P-Ni2P/NF is also usable as both the cathode and anode for an electrolyzer for overall water splitting and shows high performance. (C) 2019 Elsevier Inc. All rights reserved.
机译:理解氢气(她)和氧气(oer)进化反应期间催化剂的结构变化对于具有增强性能的催化剂的设计至关重要。这项工作报告了她和伊尔透明剂中磷化磷酸酯催化剂的结构改变研究。具体地,通过在集电体上的CO 2 P-Ni2P的原位生长,即镍泡沫,然后用于调查她在她和伊尔的结构变化的研究中,合成了CO 2P-Ni2P(CO2P-NI2P / NF)。该方法避免使用聚合物粘合剂,从而允许系统分析她和伊尔之后的催化剂的结构变化。所得CO 2-Ni2P / NIF显示出优异的碱性溶液中的优异催化双官能度。它仅需要90 mV VS RHE的过电位,为她提供10 mA cm(-2)的电流密度,并且需要230 mV Vs RHE的过电位,为OER提供50 mA cm(-2)的电流密度。 CO 2P-NI2P / NF的她和OER活性高于报道的大多数双官能催化剂的活动。后分析显示其初始时段的表面粗糙化和形成MPO(m = Co和Ni)的发生,以及表面粗糙化和形成无定形Mooh的薄层(Mo和ni)在其初始oer的表面。 M-P-O和无定形氢氧化物层的表面粗糙化和形成可归因于负责她和伊尔的高性能的主要原因。另外,CO 2P-NI2P / NF也可用作用于电解槽的阴极和阳极,用于整体水分裂并显示出高性能。 (c)2019 Elsevier Inc.保留所有权利。

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