PBA derived FeCoP nanoparticles decorated on NCNFs as efficient electrocatalyst for water splitting

过电位 双功能 电催化剂 材料科学 分解水 化学工程 普鲁士蓝 纳米颗粒 纳米纤维 催化作用 析氧 碳化 碳纳米纤维 阳极 纳米技术 无机化学 电化学 化学 电极 复合材料 碳纳米管 物理化学 有机化学 扫描电子显微镜 光催化 工程类
作者
Bei Wei,Guan‐Cheng Xu,Jincheng Hei,Li Zhang,Tingting Huang
出处
期刊:International Journal of Hydrogen Energy [Elsevier BV]
卷期号:46 (2): 2225-2235 被引量:44
标识
DOI:10.1016/j.ijhydene.2020.10.150
摘要

Transition metal phosphides have been known as promising electrocatalysts for hydrogen evolution and oxygen evolution reactions (HER and OER) due to their high catalytic activity. In this work, the FeCoP nanoparticles decorated on N-doped electrospun carbon nanofibers ([email protected]) was successfully synthesized through depositing Fe, Co-based Prussian blue analogue Co3[Fe(CN)6]2·10H2O (FeCo-PBA) onto the electrospun PVP/PAN nanofibers via layer-by-layer approach, followed by carbonization and phosphorization treatments. Benefiting from the high electrical conductivity, abundant catalytic active sites and the synergistic effect between FeCoP nanoparticles and N-doped carbon nanofibers network, the obtained [email protected] displays good bifunctional electrocatalytic activity. In 1 M KOH, the [email protected] achieves 10 mA cm−2 at an overpotential of 290, 226 mV for OER and HER, respectively. Moreover, it demands overpotential of 196 mV to achieve 10 mA cm−2 for HER in 0.5 M H2SO4. The [email protected] is used as both anode and cathode for overall water splitting, it requires a low voltage of 1.65 V to achieve a current density of 10 mA cm−2 and maintains outstanding stability over 10 h. Herein, a strategy for preparing bifunctional electrocatalysts of compositing transition metal phosphides with carbon nanofibers is proposed, and the application of metal-organic framework in electrocatalytic field is further extended.
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