材料科学
析氧
合金
纳米纤维
碳纳米纤维
化学工程
氧还原反应
氮气
纳米颗粒
氧气
碳纤维
兴奋剂
无机化学
纳米技术
电化学
电极
冶金
碳纳米管
复合材料
物理化学
有机化学
化学
复合数
工程类
光电子学
作者
Peng Wei,Xueping Sun,Qirui Liang,Xiaogang Li,Zhimin He,Xiangsheng Hu,Jinxu Zhang,Min Hui Wang,Qing Li,Hui Yang,Jiantao Han,Yunhui Huang
标识
DOI:10.1021/acsami.0c08271
摘要
The rational design and exploration of the oxygen evolution reaction (OER) electrocatalysts with high efficiency, low cost, and long-term durability are extremely important for overall water splitting. Recently, numerous studies have shown that the OER reaction kinetics can be modified by optimizing components, introducing carbon matrix, and regulating porous nanostructures. Herein, a flexible and controllable electrospinning strategy is proposed to construct porous nitrogen (N)-doped carbon (C) nanofibers (NFs) with nickel–iron (NiFe) alloy nanoparticles encapsulated inside (NiFe@NCNFs) as an OER electrocatalyst. Benefiting from the strong synergistic effects that stem from the one-dimensional mesoporous structures with optimized binary metal components encapsulated in the N-doped carbon nanofibers, the NiFe@NCNFs exhibits enhanced OER performance with a low overpotential (294 mV at 10 mA cm–2) and excellent durability (over 10 h at 10 mA cm–2) in alkaline solution. Both experimental characterizations and density functional theory (DFT) calculations validate that a suitable binary metal ratio can lead to the optimal catalytic activity. Moreover, a two-electrode electrolyzer is assembled by using NiFe@NCNFs anode and Pt/C cathode in 1.0 M KOH media for the overall water splitting, which delivers an initial cell voltage of only 1.531 V at 10 mA cm–2, as well as long-term stability up to 20 h. This study sheds light on the design and large-scale production of low-cost and high-performance electrocatalysts toward different energy applications in the future.
科研通智能强力驱动
Strongly Powered by AbleSci AI