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A bifunctional nanoporous Ni-Co-Se electrocatalyst with a superaerophobic surface for water and hydrazine oxidation

机译:一个双功能纳米多孔Ni-Co-Se electrocatalyst对水和superaerophobic表面联氨氧化

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摘要

The sluggish kinetics of the oxygen evolution reaction (OER) has severely hindered the energetic convenience of water splitting. Thus, developing a highly efficient catalyst for the OER and replacing the OER with hydrazine oxidation (HzOR) are effective strategies for water electrolysis to achieve sustainable hydrogen production. Herein, bifunctional nanosheet arrays Ni0.6Co0.4Se with a porous structure were fabricated on Ni foam (NF) by the bubble dynamic template method during electrodeposition. Compared with CoSe2 and NiSe2, Ni0.6Co0.4Se exhibits excellent electrocatalytic performance for both the OER and HzOR. A low overpotential of only 249 mV is required to drive 10 mA cm(-2), and a retention rate of nearly 100% after 24 h at 10 mA cm(-2) is observed for Ni0.6Co0.4Se towards the OER. By substituting the OER by HzOR, an extremely high current density of 300 mA cm(-2) at 0.4 V vs. RHE and a retention rate of 86.8% at 200 mA cm(-2) after 12 h can be achieved. Interestingly, the mechanistic reason for the enhanced catalytic ability of Ni0.6Co0.4Se was studied, which is associated with the synergistic effects of Ni and Co, large ECSA, high electrical conductivity and most importantly the superaerophobic nature induced by the porous structure of Ni0.6Co0.4Se. The non-noble metal bifunctional electrocatalyst demonstrates a promising potential for application in both the OER and HzOR.
机译:缓慢的进化动力学的氧气反应(OER)严重地阻碍了精力充沛的便利的水分裂。开发一种高效的催化剂OER与肼取代OER氧化(HzOR)是有效的策略水电解来实现可持续发展制氢。nanosheet数组Ni0.6Co0.4Se多孔结构组装在镍泡沫(NF)泡沫期间动态模板方法电沉积。Ni0.6Co0.4Se展览优秀electrocatalyticOER和HzOR的性能。过电压的只需要249 mV开车马10厘米(2)和保留率的近100%24小时后马10厘米(2)观察Ni0.6Co0.4Se OER。OER HzOR,一个非常高的电流密度马300 cm(2)为0.4 V和流值和保留马86.8%的速度在200 cm(2)后12 h实现。增强的催化能力Ni0.6Co0.4Se进行了研究,这是相关的倪的协同效应和有限公司大ECSA,发起高导电性和大多数重要的是superaerophobic性质引起的Ni0.6Co0.4Se的多孔结构。非贵金属双官能electrocatalyst演示了一个有前途的潜力应用程序在OER和HzOR。

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