4.6 Article

Metal organic frameworks derived hierarchical hollow Ni0.85 Se|P composites for high-performance hybrid supercapacitor and efficient hydrogen evolution

Journal

ELECTROCHIMICA ACTA
Volume 303, Issue -, Pages 94-104

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2019.02.069

Keywords

Metal organic framework; Ni0.85S vertical bar P; Hollow yolk-shell; Battery-type electrode; Hybrid supercapacitor; Hydrogen evolution reaction

Funding

  1. National Natural Science Foundation of China [11474151, 11774156]
  2. National Key Project for Basic Research [2012CB932304]
  3. PAPD, People's Republic of China

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Hollow nano-/micromaterials with tunable shell architectures and compositions are becoming increasingly important and attractive for electrochemical energy conversion and storage. Here, we report carbon-incorporated mixed anionic nickel phosphorus-selenium (Ni0.85Se vertical bar P ) hollow yolk-shell micro-spheres synthesized by simultaneous selenization and phosphatization of Ni-based metal organic framework (Ni-MOF). Our experimental results indicated that P-doping reduces the synthesis temperature of the system and enhances the crystallinity of Ni0.85Se. As a result, this unique structure (Ni-0.85 Se vertical bar P) with better crystallinity and higher Ni2+/Ni3+ ratio shows outstanding specific capacity of 506 C g(-1) at 1 A g(-1). And the assembled Ni-0.85 Se vertical bar P//AC hybrid supercapacitor shows high power density of 20.7 Wh kg(-1) at energy density of 798.7 W kg(-1). Meanwhile, Ni-0.85 Se vertical bar P exhibits smaller Tafel slope of 90 mV dec(-1) and lower onset overpotential of 179 mV versus reversible hydrogen electrode (RHE) for hydrogen evolution reaction (HER) than that of NiP2 and Ni0.85Se, which demonstrates the modulated electronic structure of Ni-0.85 Se vertical bar P. Our study will provide a new strategy for combining P-doped induced high crystallinity mixed anion transition metal complexes with MOF of hollow structures for energy storage device and HER. (C) 2019 Elsevier Ltd. All rights reserved.

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