Fangyuan Fan, Chunlin Teng, Rongjin Zhu, Lina Zhu, Lingfei Xu and Yeshuang Du
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引用次数: 0
摘要
电化学水分解是一种潜在的“绿色”方法来产生大量的氢。但其半反应——析氧反应(OER)动力学缓慢,过电位大。这阻碍了电能到氢能的能量转换效率,导致成本增加。此外,稀有金属催化剂如RuO2和IrO2具有较高的OER催化活性,但储量低且价格昂贵。因此,探索高效、稳定、廉价的过渡金属基电催化剂来加快OER速率是一种合理的途径。本文采用简单的一锅水热法合成了泡沫镍负载的s掺杂NiFe2O4@NiSe2纳米球。由于独特的结构、大的表面积、众多的活性位点、s -阴离子原子的掺入以及不同组分之间的协同作用,s掺杂NiFe2O4@NiSe2纳米球在碱性介质中对OER表现出非常高效的电催化活性。当电流密度为10 mA cm−2时,OER过电位为190 mV。同时,它表现出优异的长期稳定性,并在时间电位测定试验中保持在10 mA cm−2≥94 h。
Heterogeneous S-NiFe2O4@NiSe2 nanospheres for the oxygen evolution reaction with long-term stability†
Electrochemical water-splitting is a potential “green” approach to produce a large amount of hydrogen. However, its half reaction, the oxygen evolution reaction (OER), suffers sluggish dynamics and huge overpotential. This encumbers the energy conversion efficiency from electric energy to hydrogen energy, resulting in cost increases. Besides, rare metal catalysts such as RuO2 and IrO2 have high OER catalytic activity but they are low in reserve and expensive. Hence, exploration of highly efficient, stable and cheap transition metal-based electrocatalysts to speed up the OER rate is a rational approach. Herein, S-doped NiFe2O4@NiSe2 nanospheres supported on nickel foam were synthesized through a simple one-pot hydrothermal method. Thanks to the unique structure, large surface area, numerous active sites, incorporation of S-anion atoms and synergistic effect between different components, S-doped NiFe2O4@NiSe2 nanospheres showed extraordinarily efficient electrocatalytic activity towards the OER in alkaline medium. When the current density was 10 mA cm−2, the OER overpotential was 190 mV. Meanwhile, it exhibited excellent long-term stability and was maintained at 10 mA cm−2 for ≥94 h in a chronopotentiometry test.