Research & Development Institute of Northwestern Polytechnical University in Shenzhen, Shenzhen, 518057, P. R. China.
Xi'an Key Laboratory of Functional Organic Porous Materials, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an, 710129, P. R. China.
Small. 2022 Jun;18(24):e2201306. doi: 10.1002/smll.202201306. Epub 2022 May 16.
The intrinsic sluggish kinetics of the oxygen evolution reaction (OER) limit the improvement of hydrogen evolution reaction (HER) performance, and substituting the anodic oxidation of biomass materials is an alternative approach, given its lower oxidation potential and higher added value compared to those of OER. In this study, a Ni S -MoS nanoheterojunction catalyst with strong electronic interactions is prepared. It exhibits high efficiency for both the HER and the electrooxidation of 5-hydroxymethylfurfural (HMF). In a two-electrode cell with Ni S -MoS serving as both the anode and cathode, the potential is only 1.44 V at a current density of 10 mA cm , which is much lower than that of pure water splitting. Density functional theory calculations confirm that the strong chemisorption of H and HMF at the interface leads to outstanding electrocatalytic activity. The findings not only provide a strategy for developing efficient electrocatalysts, but also provide an approach for the continuous production of high value-added products and H .
氧析出反应(OER)的固有缓慢动力学限制了析氢反应(HER)性能的提升,而生物质材料的阳极氧化替代方法由于其氧化势较低和附加值较高,是一种替代方法。本研究制备了具有强电子相互作用的 Ni S-MoS 纳米异质结催化剂。它对 HER 和 5-羟甲基糠醛(HMF)的电氧化均具有高效性。在以 Ni S-MoS 作为阳极和阴极的两电极电池中,在 10 mA cm 的电流密度下,其电位仅为 1.44 V,远低于纯水分解的电位。密度泛函理论计算证实,界面处 H 和 HMF 的强化学吸附导致了出色的电催化活性。这些发现不仅为开发高效电催化剂提供了一种策略,也为连续生产高附加值产品和 H 提供了一种途径。