纳米棒
塔菲尔方程
过电位
材料科学
化学工程
交换电流密度
杂原子
碳纤维
分解水
聚合
兴奋剂
纳米技术
电化学
催化作用
化学
复合数
电极
聚合物
有机化学
物理化学
复合材料
光催化
光电子学
工程类
戒指(化学)
作者
Xiaohong Wang,Long Xia,Chuanluan Guo,Lili Luo,Juguo Dai,Xiaohui Liu,He Liu,Chunying Yang,Yiting Xu,Birong Zeng,Lizong Dai
标识
DOI:10.1016/j.apsusc.2022.156276
摘要
Interfacial engineering of cost-effective non-noble materials is attractive for synthesizing advanced electrocatalysts toward hydrogen evolution reaction (HER). Herein, we prepare N, S-doped Mo2C-Mo/C heterogeneous nanorods (NSMB-1.25) with abundant active heterointerfaces and defect sites via in situ polymerization and carburization strategy. The polyaniline-derived heteroatom-doped carbon acts not only as a matrix but also as a carbon source for Mo2C formation. The phase transition of Mo2C-Mo heterostructure is accurately regulated by delicately varying the dosage of the polymerization initiator and calcine temperature. The synergistic effects of Mo2C, metallic Mo and N, S doping carbon significantly enhance the HER activity and durability of nanorods. Benefiting from the plentiful active sites of the Mo2C-Mo heterointerfaces, fast charge and mass transfer channels, heteroatomic doping and large surface area, the as-prepared NSMB-1.25 nanorods deliver only 118 mV overpotential at 10 mA cm−2 current density, small Tafel slopes of 74 mV dec-1, high exchange current density of 25.84 × 10-2 mA cm−2 and excellent stability in 1.0 M KOH solution. This work may support a feasible strategy for reasonably designing highly active heterogeneous interfaces to achieve efficient energy conversion and storage.
科研通智能强力驱动
Strongly Powered by AbleSci AI