4.7 Article

Carbon nanospheres supported bimetallic Pt-Co as an efficient catalyst for NaBH 4 hydrolysis

Journal

APPLIED SURFACE SCIENCE
Volume 540, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apsusc.2020.148296

Keywords

Sodium borohydride; Hydrogen; Pt-Co nanoparticles; Efficient catalyst; Isotopic tracer method

Funding

  1. National Natural Science Foundation of China [51971197, 51771164, 51701175]
  2. Natural Science Foundation of Hebei Province [E2019203161, E2018203117]
  3. Linus Pauling Distinguished Postdoctoral Fellowship program

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A highly efficient catalyst composed of carbon nanospheres supporting ultrafine bimetallic Pt-Co nanoparticles was successfully synthesized for hydrogen evolution from NaBH4 hydrolysis in this study. The catalyst exhibited outstanding performance in kinetic and thermodynamic tests, with high hydrogen generation rate and low activation energy. The hydrolytic mechanism was investigated using isotopic tracer method and mass spectrometric analysis, showing that the catalyst maintained high catalytic activity even after five cycles of performance tests.
Sodium borohydride (NaBH4) is widely identified as a promising hydrogen storage material, therefore, developing a catalyst with high efficiency for hydrogen production is an important subject for development and utilization of hydrogen energy. Meanwhile the hydrolytic mechanism of NaBH4 needs further study which is helpful for hydrolysis researches. In this study, an efficient catalyst comprising of carbon nanospheres (CNSs) supporting ultrafine bimetallic Pt-Co nanoparticles (CNSs@Pt0.1Co0.9) has been successfully synthesized for hydrogen evolution from NaBH4 hydrolysis. The growth of the Pt-Co nanoparticles on the surface of CNSs is regulated by adjustment of solvent during the preparation. The as-prepared CNSs@Pt0.1Co0.9 catalyst exhibits an outstanding performance in the kinetic and thermodynamic tests with the highest hydrogen generation rate (HGR) of 8943 mL(H2).min(-1).g(M)(-1), initial turnover frequency (TOF) value of 280.1 moL(H2).min(-1).molPt(-1), and a low activation energy (E-a) of 38.0 kJ.mol(-1). The hydrolytic mechanism has been surveyed simultaneously by the isotopic tracer method through the mass spectrometric analysis. The catalyst retains extremely high catalytic activity value and the hydrogen generation conversion is still 100% even after five cycles in the catalytic performance tests.

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