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Self-Supporting Electrocatalyst Film Based on Self-Assembly of Heterogeneous Bottlebrush and Polyoxometalate for Efficient Hydrogen Evolution Reaction.

Yayu LinYoulong ZhuQian MaXianlan KePengwei MaRongfeng LiaoShaohong LiuDingcai Wu
Published in: Macromolecular rapid communications (2022)
Developing efficient electrocatalysts to promote the hydrogen evolution reaction (HER) is essential for a green and sustainable future energy supply. For practical applications, it is a challenge to achieve the self-assembly of electrocatalyst from microscopic to macroscopic scales. Herein, a facile strategy is proposed to fabricate a self-supporting electrocatalyst film (CNT-g-PSSCo/PW 12 ) for HER by electrostatic interaction-induced self-assembly of cobalt polystyrene sulfonate-grafted carbon nanotube heterogeneous bottlebrush (CNT-g-PSSCo) and polyoxometalate (PW 12 ). Co 2+ ions of CNT-g-PSSCo can function as junctions for interconnecting neighboring bottlebrushes to form the 3D nanonetwork structure and enable electrostatic capture of negatively charged PW 12 nanodots. Moreover, CNT backbones can provide highly conductive pathways to CNT-g-PSSCo/PW 12 . Such a self-assembled CNT-g-PSSCo/PW 12 displays a low overpotential of 31 mV at a current density of 10 mA cm -2 and a small Tafel slope of 25 mV dec -1 , showing high efficiency toward HER. Furthermore, CNT-g-PSSCo/PW 12 with a stable self-supporting film morphology exhibits long-term electrocatalytic stability over 1000 CV cycles without noticeable overpotential change in acidic media. The findings may provide a new avenue for constructing self-assembled functional nanonetwork materials with well-orchestrated structural hierarchy for many applications in energy, environment, catalysis, medicine, and others.
Keyphrases
  • reduced graphene oxide
  • metal organic framework
  • carbon nanotubes
  • high efficiency
  • gold nanoparticles
  • quantum dots
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