Suppr超能文献

挖掘多金属 FeVO(OH)/Ni(OH)中高价 Mo 和 W 金属中心在动态电子结构方面的潜力以实现超稳定和高效的全水分解。

Tapping the Potential of High-Valent Mo and W Metal Centers for Dynamic Electronic Structures in Multimetallic FeVO(OH)/Ni(OH) for Ultrastable and Efficient Overall Water Splitting.

机构信息

Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati781039, Assam, India.

出版信息

ACS Appl Mater Interfaces. 2023 Feb 1;15(4):5336-5344. doi: 10.1021/acsami.2c21041. Epub 2023 Jan 18.

Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验