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首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >NiCoP self-supporting electrode with the sea urchin-like microstructure for the synchronous reaction of hydrogen evolution and contaminant degradation
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NiCoP self-supporting electrode with the sea urchin-like microstructure for the synchronous reaction of hydrogen evolution and contaminant degradation

机译:Nicop自支撑电极与海胆相似的微观结构,用于氢进化和污染物降解的同步反应

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The development of an earth-rich and efficient and stable electrocatalyst is the key to achieving efficient hydrogen production from electrolysis of water. In energy-saving hydrogen production, the oxygen evolution reaction in the electrolysis of water is often another important factor that restricts efficient hydrogen production. Therefore, in this study, we used carbon cloth as the base of the self-supporting electrode. Nickel and cobalt, rich non-noble metals, were introduced to the carbon cloth through a simple hydrothermal reaction. The composite phosphides of nickel and cobalt were obtained by low-temperature phosphating. The prepared materials possess a sea urchin-like microstructure which is composed of microspheres in center and nanospines on its surface. Based on this unique sea urchin-like structure, NiCoP/CC self-supporting electrode exhibits a good hydrogen evolution performance in acidic solutions. The required overpotentials were only 178 mV and 395 mV vs RHE at 10 and 100 mA cm-2, respectively. We used this NiCoP/CC self-supporting electrode as the cathode and the pure CC as the anode. Under the condition of a constant current density of 2 mA cm-2, the degradation efficiency of methylene blue at 90 min was 88% and hydrogen was produced constantly on the NiCoP/CC self-supporting electrode, which provided an idea for the combination of hydrogen evolution reaction and organic matter degradation.
机译:开发一种富土高效稳定的电催化剂是实现水电解高效制氢的关键。在节能制氢中,水电解过程中的析氧反应往往是制约高效制氢的另一个重要因素。因此,在本研究中,我们使用碳布作为自支撑电极的基础。镍和钴是丰富的非贵金属,通过简单的水热反应被引入碳布中。采用低温磷化法制备了镍钴复合磷化膜。所制备的材料具有海胆状的微观结构,由中心的微球和表面的纳米松组成。基于这种独特的海胆状结构,NiCoP/CC自支撑电极在酸性溶液中表现出良好的析氢性能。在10和100 mA cm-2时,与RHE相比,所需的过电位分别仅为178 mV和395 mV。我们使用这种NiCoP/CC自支撑电极作为阴极,纯CC作为阳极。在恒定电流密度为2macm-2的条件下,90min时亚甲基蓝的降解效率为88%,并且在NiCoP/CC自支撑电极上不断产生氢气,这为析氢反应与有机物降解的结合提供了思路。

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