4.6 Article

Removing the barrier to water dissociation on single-atom Pt sites decorated with a CoP mesoporous nanosheet array to achieve improved hydrogen evolution

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 8, 期 22, 页码 11246-11254

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ta02936j

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资金

  1. Shenzhen Basic Research Project [JCYJ20170818092720054, JCYJ20190808145203535, JCYJ20190808144413257]
  2. National Natural Science Foundation of China [21671136]
  3. Postdoctoral Science Foundation of China [2019M663085]
  4. Major Programs for Science and Technology Development of Shenzhen [JSGG20160328151657828, XCL201110060]
  5. Major Industrial Projects of Shenzhen [s2017001850011]
  6. Project of Natural Science Foundation of Guangdong Province [2020A1515010380, 2014A030311028]

向作者/读者索取更多资源

The hydrogen evolution reaction (HER) in alkaline solution has attracted considerable interest, but it is limited by the kinetically sluggish water dissociation step. Herein, we report single-atom Pt immobilized in the lattice of CoP mesoporous nanosheets (MNSs) grown on carbon fiber cloth (CFC) (Pt-at-CoP MNSs/CFC) with ultralow Pt loading (0.7 wt% relative to CoP, 5.89 mu g cm(geo)(-2)) as a high-performance electrocatalyst for the HER in alkaline solution. Assisted by the strong interaction between Pt(at)and CoP, water dissociation becomes spontaneous, providing Pt-at-CoP MNSs/CFC with a low HER kinetic barrier. Accordingly, Pt-at-CoP MNSs/CFC exhibits outstanding HER performance with negligible onset potential, super high catalytic activity, and excellent durability that is even superior to the commercial 20 wt% Pt/C catalyst. Moreover, Pt-at-CoP MNSs/CFC exhibits excellent catalytic activity and stability toward seawater electrolysis.

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