Madasu Sreenivasulu, Ghada A. Khouqeer, Ranjan S. Shetti, Naglaa AbdelAll, Abdullah N. Alodhayb and Nagaraj P. Shetti*,
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Related to further catalysts, the carbon material synthesized at 600 °C (Co-SPC600) displays superior electrochemical performance. At a 10 mA cm<sup>–2</sup> of current density in 1 M KOH, the electroactive catalyst Co-SPC600 requires an overpotential of 260 mV (119 mV dec<sup>–1</sup>) for the OER and 111 mV (111 mV dec<sup>–1</sup>) for the HER. The active catalyst Co-SPC600 demonstrates a current degradation of less than 4.2% for OER and less than 4.6% for HER, indicating sustained durability over 60 h. For overall water splitting, Co-SPC600/NF//Co-SPC600/NF operates at 1.50 V with constant progression of H<sub>2</sub> and O<sub>2</sub> at the cathode and anode, correspondingly, exhibiting a current reduction of less than 4.8% over 80 h. 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引用次数: 0
摘要
为析氢反应(HER)、尿素氧化反应(UOR)和析氧反应(OER)开发高效、稳健、经济的三功能电催化剂,对电化学能量转换过程至关重要。这项工作展示了用一种简单、可持续、经济上可行和可扩展的方法,在掺有硫的极多孔石墨碳上合成稳定实用的钴纳米颗粒。催化剂在不同温度下通过直接热解和富氮气氛炭化进行强化。对于进一步的催化剂,在600℃下合成的碳材料(Co-SPC600)表现出优异的电化学性能。在电流密度为10 mA cm-2、1mkoh的情况下,电活性催化剂Co-SPC600对OER和HER的过电位要求分别为260 mV (119 mV dec1)和111 mV (111 mV dec1)。活性催化剂Co-SPC600演示了不到4.2%的电流退化为她OER和不到4.6%,表明持续耐久性超过60 h。整体水分裂,Co-SPC600 / NF在1.50 V / / Co-SPC600 / NF经营不断发展的氢气和氧气在阴极和阳极,相应地,展示当前减少不到4.8%超过80 h。此外,Co-SPC600 / NF促进尿素氧化在1.37 V 0.33 M尿素和1米KOH溶液。
Co-Incorporated S-Doped Graphitic Carbon Derived from Orange Peel Biowaste: An Efficient Electrocatalyst for Sustainable Water Splitting and Urea Oxidation
The advancement of effective, robust, and cost-effective trifunctional electrocatalysts for the hydrogen evolution reaction (HER), urea oxidation reaction (UOR), and oxygen evolution reaction (OER), is essential for electrochemical energy conversion processes. This work demonstrates the synthesis of steady and practical cobalt nanoparticles on extremely porous graphitic carbon doped with sulfur using a straightforward, sustainable, economically viable, and scalable approach. The catalysts were strengthened at varying temperatures via direct pyrolysis followed by carbonization in a nitrogen-rich atmosphere. Related to further catalysts, the carbon material synthesized at 600 °C (Co-SPC600) displays superior electrochemical performance. At a 10 mA cm–2 of current density in 1 M KOH, the electroactive catalyst Co-SPC600 requires an overpotential of 260 mV (119 mV dec–1) for the OER and 111 mV (111 mV dec–1) for the HER. The active catalyst Co-SPC600 demonstrates a current degradation of less than 4.2% for OER and less than 4.6% for HER, indicating sustained durability over 60 h. For overall water splitting, Co-SPC600/NF//Co-SPC600/NF operates at 1.50 V with constant progression of H2 and O2 at the cathode and anode, correspondingly, exhibiting a current reduction of less than 4.8% over 80 h. Furthermore, Co-SPC600/NF facilitates urea oxidation at 1.37 V in a solution of 0.33 M urea and 1 M KOH.
期刊介绍:
Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.