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October 9, 2025Langmuir1 citations

Boosting Electrocatalytic Hydrogen Evolution Reaction by a Cellulose-Derived Nitrogen-Doped Order Carbon Matrix Decorated with Ni Nanoparticles

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GSGaojie ShiWDWenbin DingBYBochao Yan

Key Points

  • The electrocatalyst shows a high HER performance with an overpotential of 172 mV at 10 mA cm-2 in alkaline media.
  • High graphitization degree and homogeneously dispersed Ni nanoparticles significantly enhance catalytic activity.
  • A self-assembly strategy using oxidized cellulose and Ni2+ ions successfully retains the ordered structure of the catalyst.
  • The addition of urea increases metal loading and further boosts the performance of the biomass-derived electrocatalysts.

Abstract

Biomass-derived catalysts have been broadly developed for the hydrogen evolution reaction (HER) from water electrolysis because of their natural structure. However, loading metal on this kind of catalyst to improve HER performance may damage the ordered structure of the carbon matrix due to the weak interaction between the biomass base and metal ions. Herein, a facile self-assembly strategy is proposed to fabricate a cellulose-derived high graphitization degree electrocatalyst embedded with nickel nanoparticles (NPs). Based on the pore structure analysis and powder X-ray diffraction (XRD) pattern, the highly dispersed metal sites and high graphitization degree can be ascribed to the interaction between Ni2+ ions and oxidized cellulose. The addition of urea can increase the metal loading amount to further improve the activity. Benefiting from the highly ordered carbon structure and the homogeneously dispersed Ni NPs, Ni NPs/N-doped carbon (Ni-BCN) demonstrates a high HER performance in alkaline media, with an overpotential of 172 mV to reach a current density of 10 mA cm-2 and long-term durability. This research introduces a novel strategy to design excellent HER electrocatalysts from biomass recourse.

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Cite This Study

Shi et al. (2025) studied this question.

synapsesocial.com/papers/68e7d631bd66d359be626533https://doi.org/10.1021/acs.langmuir.5c03812
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