过电位
材料科学
碳化
电催化剂
纳米棒
化学工程
析氧
催化作用
双功能
分解水
双金属片
塔菲尔方程
电化学
锂(药物)
金属有机骨架
碳纤维
纳米技术
电极
化学
金属
复合材料
复合数
有机化学
冶金
物理化学
吸附
内分泌学
工程类
医学
光催化
扫描电子显微镜
作者
Shangdai Wang,Ping Ning,Shoushuang Huang,Wenwen Wang,Siming Fei,Qingquan He,Jiantao Zai,Yong Jiang,Zhangjun Hu,Xuefeng Qian,Zhiwen Chen
标识
DOI:10.1016/j.jpowsour.2019.226857
摘要
The development of cost-effective, highly efficient and robust multi-functional electrode materials can dramatically reduce the overall cost of electrochemical devices. We here report the controlled synthesis of NiS2/FeS2 nanoparticles encapsulated in N-doped carbon nanorods (NiS2/FeS2/NC) through carbonization and sulfurization of Fe/Ni-based bimetallic metal-organic frameworks. Benefiting from both structural and compositional characteristics, the resulting NiS2/FeS2/NC nanorods possess abundant active sites, high electrical conductivity and rapid mass transfer, thereby delivering 10 and 20 mA cm−2 at overpotential of 172 mV and 231 mV towards the hydrogen evolution reaction and oxygen evolution reaction with robust stability in 1.0 M KOH solution, respectively. When employed as a bifunctional electrocatalyst for overall water splitting, it requires only 1.58 V to deliver a current density of 10 mA cm−2 in 1.0 M KOH, outperforming that of the commercial Pt/C || RuO2. Additionally, lithium-ion batteries tests also show high reversible capacity (718 mA h g−1 at 100 mA g−1) and excellent cycling stability and rate performance. The work in this paper not only provides a promising strategy for designing efficient multi-functional electrode materials with similar morphology and structure, but also can be extended to the synthesis of other mixed metal sulfides for energy conversion and storage.
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