过电位
碳纤维
催化作用
化学工程
析氧
材料科学
分解水
镍
气凝胶
热解
过渡金属
无机化学
复合数
化学
纳米技术
电化学
复合材料
冶金
光催化
有机化学
物理化学
工程类
电极
作者
Lu Shan,Yang Liu,Yang Chen,Xinjie Zhang,Hongjie Dai,Dahai Xu,Bingzhe Yu,Yi Zhang,Shaowei Chen,Ting He,Xiaoping Ouyang
标识
DOI:10.1021/acssuschemeng.4c07297
摘要
Carbon-based nanocomposites with atomically dispersed transition metals have been found to exhibit excellent electrocatalytic activity toward the oxygen evolution reaction (OER). Yet, the low metal loads and severe electrooxidation of carbon greatly limit the activity and stability. Reducing the pyrolysis temperature can weaken the aggregation of metal atoms, and using carbon aerogel as a 3D scaffold can maximize accessible metal sites. Simultaneously, a lower pyrolysis temperature can provide a higher oxygen content for the carbon substrate and enhance resistance against electrooxidation. Herein, carbon aerogels embedded with Fe–Ni dual atom centers (NCA/FeNi-500) are synthesized by controlled pyrolysis at 500 °C of a chitosan hydrogel composite along with FeCl3 and NiCl2. With an atomically dispersed metal loading of 4.35 wt %, NCA/FeNi-500 exhibits a remarkable OER catalytic activity in both alkaline water and simulated alkaline seawater, featuring a low overpotential of only +294 and +306 mV to reach the current density of 10 mA cm–2, respectively, along with excellent long-term stability during overall water splitting, a performance much better than those with commercial RuO2. First-principles calculations show that adjacent NiN4 sites effectively promote the OER kinetics at FeN4 sites by reducing the energy barrier of O–O formation. This is also manifested in alkaline saline water splitting.
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