摘要
Curved carbon structure can modulate the interaction between the catalyst and the reaction intermediates and enhance the intrinsic activity of the catalyst. However, it remains a significant challenge to prepare curved carbon without surfactants or templates. Herein, we report a facile strategy to prepare curved carbon via mechanical shaking process with polydopamine (PDA) as a precursor. Then, uniformly dispersed Pt nanoparticles (Pt NPs) are planted in situ on the curved carbon structure from free-standing TiO 2 nanosheets (C-rPDA-Pt/TiO 2 NSs) to prepare ultralow Pt loading (13.4 μg cm −2 ) catalysts for acidic hydrogen evolution reaction (HER). The mass activity of C-rPDA-Pt/TiO 2 NSs is tenfold higher than that of the planar carbon supported Pt catalyst (C-sPDA-Pt/TiO 2 NSs) and four times higher than that of 40 % commercial Pt/C catalyst at an applied voltage of −0.1 V. DFT calculations suggest that curved carbon structure effectively adjusts the electronic structure of Pt active sites, thereby achieving optimal Gibbs free energy for hydrogen evolution and enhancing HER performance.
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