ISSN: 2155-983X
+44 1300 500008
Junyuan Xu
Hydrogen (H2 ) has been proposed to be a clean and carbon-neutral energy carrier that can be used as next-generation fuel to fulfill both stationary and transportation needs. Compared to steam reforming, electro-catalytic water splitting represents a greener and more sustainable way for H2 generation and has been intensively investigated in recent years. The Oxygen Evolution Reaction (OER) has been a bottleneck to improve water splitting efficiency. It involves four concerted proton-coupled electron transfer steps and is both thermodynamically and kinetically demanding. Without a catalyst, the OER usually takes place at a high over-potential leading to a large energy loss. Compared to the OER, the H2 Evolution Reaction (HER) can be accomplished comparatively easily, but efficient electro-catalysts are still needed to reduce the over-potential for HER and enable the reaction to take place at a practically high rate. Lately, earth-abundant transition metal based electrocatalysts have been demonstrated to be highly active for both HER and OER and are proposed to be promising alternatives to Platinum Group Metal (PGM) catalysts for use in water electrolysers. In this study, we showed our recent efforts to developing efficient and durable transition metal based electrocatalysts, including transition metal phosphides obtained by wet chemical reduction followed by post-phosphorization treatment and cobalt ultrafine clusters prepared by cluster beam deposition. We have demonstrated that all these catalysts show electro-catalytic performance favorably compared to PGM based electrocatalysts for HER or OER and therefore hold substantial promise for use as low-cost catalysts in water electrolysers.
Electrocatalytic water splitting is a promising approach to generating hydrogen from water. In order to enhance water splitting efficiency, it is essential to promote gas revolution from catalysts surface, reduce the over-potential of oxygen evolution (OER), and inhibit the production of the hydrogen peroxide by-product. To realize them, in this work, we take a cue from nature to promote water splitting activity of hollow porous Fe3O4 microspheres (M−Fe3O4) with the aids of hemoglobin. Hemoglobin monolayer was self-assembled on the surface of M−Fe3O4 catalysts. It transported newly-generated oxygen molecules away from catalysts surface and exhibited chiral-induced spin selectivity (CISS) effect during OER reaction. Owing to the “helping hand” of hemoglobin, the OER onset potential of hollow porous Fe3O4 microspheres reduced by 100 mV and the current density was enhanced 2 folds. The results indicate a new strategy for designing earth-abundant catalysts which combine the merits of oxygen transferring and CISS effect for electrocatalytic water splitting.
Published Date: 2020-11-23; Received Date: 2020-11-14