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Study of the catalytic activity of 3D macroporous Ni and NiMo cathodes for hydrogen production by alkaline water electrolysis

机译:3D大孔Ni和NiMo阴极对碱性水电解制氢的催化活性研究。

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Platinum is the electrode material with the highest catalytic activity for the hydrogen evolution reaction (HER). However, its high cost and scarcity are the two major barriers for its usage in the industrial alkaline water electrolysis, which requires searching for other cheaper and more available materials with good catalytic activity. Ni-based materials have attracted more and more attention due to their good activity for the HER and sufficient corrosion resistance in alkaline solutions at considerable low cost. According to the Brewer intermetallic bonding theory, molybdenum alloyed with nickel (hypo-hyper-d-electronic transition metal) could improve the intrinsic catalytic activity for the HER. In this work, Ni and NiMo metallic coatings were galvanostatically electrodeposited on a stainless steel AISI 304 substrate by means of the double-template electrochemical process. The evaluation of these electrodes as H-2-evolving cathodes was done in 30 % wt. KOH by pseudo-steady-state polarization curves and electrochemical impedance spectroscopy (EIS) at different temperatures. From Tafel curves results, it is shown that the NiMo electrodes have higher catalytic activity than Ni. On the other hand, from EIS results, it is possible to conclude that the NiMo electrodes showed higher intrinsic catalytic activity for HER than the pure Ni electrode as a consequence of alloying hypo-hyper-d-electronic transition metals.
机译:铂是对氢释放反应(HER)具有最高催化活性的电极材料。然而,其高成本和稀缺性是其在工业碱性水电解中使用的两个主要障碍,这需要寻找其他更便宜,更易获得且具有良好催化活性的材料。镍基材料因其对HER的良好活性和在碱溶液中的足够低的耐蚀性而以相当低的成本引起了越来越多的关注。根据布鲁尔金属间键合理论,钼与镍(次-高-d-电子过渡金属)合金化可提高HER的固有催化活性。在这项工作中,通过双模板电化学工艺将Ni和NiMo金属涂层恒电流电镀在不锈钢AISI 304基底上。这些电极作为H-2演化的阴极的评估是在30%wt。 KOH通过伪稳态极化曲线和电化学阻抗谱(EIS)在不同温度下进行。从Tafel曲线结果可知,NiMo电极比Ni具有更高的催化活性。另一方面,从EIS结果可以得出结论,由于合金化了高d电子过渡金属,NiMo电极对HER的固有催化活性要比纯Ni电极高。

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