Co2Ni1O4/不锈钢复合材料的制备及其电催化析氧性能 |
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引用本文: | 曾庆乐,刘小超,刘超,漆小鹏.Co2Ni1O4/不锈钢复合材料的制备及其电催化析氧性能[J].复合材料学报,2021,38(11):3764-3774. |
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作者姓名: | 曾庆乐 刘小超 刘超 漆小鹏 |
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作者单位: | 江西理工大学 材料冶金化学学部,赣州 341000 |
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基金项目: | 江西省重点研发计划(20202BBEL53023);国家自然科学基金(22065015) |
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摘 要: | 电解水包括析氢反应(HER)与析氧反应(OER),由于OER是复杂的4电子转移过程,制作出具有优异耐久性的高活性的非贵金属OER电催化剂对于电解水至关重要。为了降低成本,选择304型不锈钢网(SS)作为基体,使用电沉积的方法制备钴-镍双氢氧化物,利用真空煅烧的方法制备钴-镍氧化物。使用XRD、SEM、TEM、XPS和电化学工作站对Co2Ni1O4/SS复合材料的晶体结构、形貌和电催化OER性能进行了研究。结果表明:电沉积制备的钴-镍双氢氧化物煅烧之后转变成尖晶石结构的钴-镍氧化物;在不锈钢表面成功合成了大量密集的层状结构;在1.0 mol/L KOH电解液中,Co2Ni1O4/SS电极表现出优异的OER电催化性能,达到10 mA·cm?2电流密度时所需要的过电位仅为240 mV,Tafel斜率为53.92 mV·dec?1,并且表现出优异的稳定性。
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关 键 词: | 电沉积 不锈钢 尖晶石化合物Co2Ni1O4 水分解 析氧反应 |
收稿时间: | 2020-11-16 |
Synthesis and electrocatalytic oxygen evolution performances of Co2Ni1O4/stainless steel composites |
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Affiliation: | Faculty of Materials Metallurgy and Chemistry, Jiangxi University of Science and Technology, Ganzhou 341000, China |
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Abstract: | Electrolytic water includes hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), because OER is a complex 4-electron transfer process, developing highly active non-precious OER electrocatalysts with superior durability is crucial to electrolytic water. In order to reduce the cost, 304 stainless steel mesh (SS) was selected as the matrix, Co-Ni double hydroxides was prepared by electrodeposition, Co-Ni oxides were produced by vacuum calcination. The crystal structure, morphology and electrocatalytic OER performance of Co2Ni1O4/ SS composite were studied by XRD, SEM, TEM, XPS and electrochemical workstation. As a result, the Co-Ni double hydroxides prepared by electrodeposition are transformed into Co-Ni oxides with spinel structure after vacuum calcination; successfully synthesized a large number of dense layered structures on the surface of stainless steel;the Co2Ni1O4/SS electrode exhibits an outstanding OER catalytic activity with an overpotentials of 240 mV at 10 mA·cm?2 and a Tafel slop as low as 53.92 mV·dec?1 in 1.0 mol/L KOH. In addition, the Co2Ni1O4/SS composites shows excellent stability in the alkaline electrolyte. |
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