Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati781039, Assam, India.
ACS Appl Mater Interfaces. 2023 Feb 1;15(4):5336-5344. doi: 10.1021/acsami.2c21041. Epub 2023 Jan 18.
Rationally designing a noble metal-free electrocatalyst for OER and HER is pivotal for large-scale energy generation via water splitting. A multimetallic electrocatalyst FeVO(OH)/NiMoW(OH), aimed at tuning the electronic structure, is fabricated and shows considerable improvement in the water-splitting reaction kinetics, aided by low Tafel slope values of 24 mV/dec for OER and 67 mV/dec for HER, respectively. By taking advantage of (e̅-e̅) repulsions at the t level, we introduced high-valency Mo and W to provide a viable path for π-electron donation from oxygen 2p orbitals to vacant Mo and W orbitals for a dynamic electronic structure and an interfacial synergistic effect, which optimized the bond lengths for reaction intermediates to facilitate water splitting. The hybrid catalyst FeVO(OH)/NiMoW(OH) shows intrinsic activity and durability toward OER and HER tested for 48 h at a current density of 20 mA/cm and a cell voltage of 1.65 V @ 20 mA/cm.
理性设计用于 OER 和 HER 的无贵金属电催化剂对于通过水分解大规模发电至关重要。我们制备了一种多金属电催化剂 FeVO(OH)/NiMoW(OH),旨在通过调整电子结构,来提高水分解反应动力学。该电催化剂的 OER 和 HER 的 Tafel 斜率值分别低至 24 mV/dec 和 67 mV/dec,这表明其具有很大的改进。通过利用 t 能级上的(e̅-e̅)排斥作用,我们引入了高价 Mo 和 W,为氧 2p 轨道上的π电子向空的 Mo 和 W 轨道捐赠提供了可行的途径,从而形成动态电子结构和界面协同效应,优化了反应中间体的键长,促进了水分解。在电流密度为 20 mA/cm 和电池电压为 1.65 V@20 mA/cm 的条件下,测试了 48 小时后,混合催化剂 FeVO(OH)/NiMoW(OH) 对 OER 和 HER 表现出内在的活性和耐久性。