碳化
催化作用
多孔性
化学工程
材料科学
碳纤维
电催化剂
化学
电化学
电极
有机化学
复合材料
复合数
扫描电子显微镜
工程类
物理化学
作者
Jingfei Kang,Can Sheng,Jiayi Wang,Han Xu,Bin Zhao,Sha Chen,Yan Qing,Yiqiang Wu
标识
DOI:10.1016/j.ijhydene.2022.11.210
摘要
Defect and interface engineering has been established as efficient methods for altering the electrical structure and improving the activity of electrocatalysts. Here, a rational design architecture consisting of Ni2P nanoparticles embedded in P-doped carbonized wood fibers (Ni2P/PCWF) is synthesized by simultaneous carbonization and phosphorization. A synergistic enhancement effect between electronic structure manipulation and interface regulation is observed in Ni2P/PCWF during the urea oxidation reaction (UOR). First, the P doping of carbon can optimize the electronic structure of Ni2P/PCWF. Second, the charge transport process is aided by the Ni2P nanoparticles embedded in the PCWF. Lastly, electron transfer can be accelerated by the in-situ formed heterogeneous interface between metal phosphides and metal hydroxides (hydroxyl oxides). Due to the synergy of the structural and electrical modulation, Ni2P/PCWF exhibits remarkable electrocatalytic properties toward the UOR under alkaline conditions. It only requires 1.34 V (vs. RHE) to achieve a current density of 50 mA cm−2, and the increase in potential at 10 mA cm−2 for 70 h is insignificant (≈2.9%). This work supports the development of new strategies using sustainable, renewable wood fibers to develop excellent UOR catalysts for energy-saving H2 generation.
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