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Multi-functional NiS_2/FeS_2/N-doped carbon nanorods derived from metal-organic frameworks with fast reaction kinetics for high performance overall water splitting and lithium-ion batteries

机译:源自金属-有机骨架的多功能NiS_2 / FeS_2 / N掺杂碳纳米棒,具有快速的反应动力学,可用于高性能整体水分解和锂离子电池

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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 parallel to 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.
机译:具有成本效益,高效和耐用的多功能电极材料的开发可以大大降低电化学装置的总体成本。我们在这里报告了通过Fe / Ni基双金属金属-有机骨架的碳化和硫化来控制包裹在N掺杂碳纳米棒(NiS2 / FeS2 / NC)中的NiS2 / FeS2纳米粒子的受控合成。得益于结构和成分特性,所得的NiS2 / FeS2 / NC纳米棒具有丰富的活性位,高电导率和快速的质量转移,从而以172 mV和231 mV的超电势输送10和20 mA cm(-2)。氢析出反应和氧析出反应分别在1.0 M KOH溶液中具有稳定的稳定性。当用作整体水分解的双功能电催化剂时,仅需1.58 V即可在1.0 M KOH中提供10 mA cm(-2)的电流密度,优于平行于RuO2的商用Pt / C的电流密度。此外,锂离子电池测试还显示出高可逆容量(在100 mA g(-1)时为718 mA h g(-1))以及出色的循环稳定性和倍率性能。本文的工作不仅为设计具有相似形貌和结构的高效多功能电极材料提供了一个有前途的策略,而且可以扩展到其他混合金属硫化物的合成以进行能量转换和存储。

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