MOE Laboratory of Bioinorganic and Synthetic Chemistry, The Key Lab of Low-Carbon Chemistry and Energy Conservation of Guangdong Province, School of Chemistry, Sun Yat-sen University , Guangzhou 510275, China.
J Am Chem Soc. 2018 Jan 17;140(2):610-617. doi: 10.1021/jacs.7b08521. Epub 2018 Jan 2.
Low-cost transition-metal dichalcogenides (MS) have attracted great interest as alternative catalysts for hydrogen evolution. However, a significant challenge is the formation of sulfur-hydrogen bonds on MS (S-H), which will severely suppress hydrogen evolution reaction (HER). Here we report Cu nanodots (NDs)-decorated NiS nanotubes (NTs) supported on carbon fibers (CFs) (Cu NDs/NiS NTs-CFs) as efficient electrocatalysts for HER in alkaline media. The electronic interactions between Cu and NiS result in Cu NDs that are positively charged and can promote water adsorption and activation. Meanwhile, NiS NTs are negatively charged and can weaken S-H bonds formed on catalyst surfaces. Therefore, the Cu/NiS hybrids can optimize H adsorption and desorption on electrocatalysts and can promote both Volmer and Heyrovsky steps of HER. The strong interactions between Cu and NiS cause the Cu NDs/NiS NTs-CFs electrocatalysts to exhibit the outstanding HER catalytic performance with low onset potential, high catalytic activity, and excellent stability.
廉价的过渡金属二硫属化物 (MS) 作为析氢反应的替代催化剂引起了极大的兴趣。然而,一个重大的挑战是 MS (S-H) 上形成硫氢键,这将严重抑制析氢反应 (HER)。在这里,我们报告了在碳纤维 (CF) 上负载铜纳米点 (NDs) 修饰的 NiS 纳米管 (NTs) 的 Cu NDs/NiS NTs-CFs 作为碱性介质中 HER 的高效电催化剂。Cu 和 NiS 之间的电子相互作用导致带正电荷的 Cu NDs,从而可以促进水的吸附和活化。同时,NiS NTs 带负电荷,可以削弱催化剂表面形成的 S-H 键。因此,Cu/NiS 杂化物可以优化电催化剂上 H 的吸附和解吸,并促进 HER 的 Volmer 和 Heyrovsky 步骤。Cu 和 NiS 之间的强相互作用导致 Cu NDs/NiS NTs-CFs 电催化剂表现出优异的 HER 催化性能,具有低起始电位、高催化活性和优异的稳定性。