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Electronically Double‐Layered Metal Boride Hollow Nanoprism as an Excellent and Robust Water Oxidation Electrocatalysts
Authors:HyukSu Han  Yu‐Rim Hong  Jungwook Woo  Sungwook Mhin  Kang Min Kim  Jiseok Kwon  Heechae Choi  Yong‐Chae Chung  Taeseup Song
Institution:1. Korea Institute of Industrial Technology, 137‐41 Gwahakdanji‐ro, Gangneung‐si, Gangwon, 25440 Republic of Korea;2. Department of Chemistry, Seoul Women's University, Seoul, 01797 Republic of Korea;3. Division of Materials Science and Engineering, Hanyang University, 222 Wangsimni‐ro, Seongdong‐gu, Seoul, 04763 Republic of Korea;4. Korea Institute of Industrial Technology, 156 Gaetbeol‐ro, Yeonsu‐gu, Incheon, 406‐840 Republic of Korea;5. Department of Energy Engineering, Hanyang University, Seoul, 04763 Republic of Korea;6. Korea Institute of Science and Technology, Center for Computational Science, 5 Hwarang‐ro 14‐gil, Seongbuk‐gu, Seoul, 02792 Republic of Korea;7. Institute of Inorganic Chemistry, University of Cologne, Greinstr. 6, 50939 Cologne, GermanyE‐mail: ,;8. Division of Materials Science and Engineering, Hanyang University, 222 Wangsimni‐ro, Seongdong‐gu, Seoul, 04763 Republic of KoreaE‐mail: ,;9.
Abstract:Metal–metalloid compounds have been paid much attention as new high‐performance water oxidation catalysts due to their exceptional durability for water oxidation in alkaline media originating from the multi‐dimensional covalent bonding of the metalloid with the surrounding metal atoms. However, compared to the excellent stability, a relatively low catalytic activity of metal‐metalloids often limits their practical application as high‐performance water oxidation catalysts. Here, for the first time, disclosed is a novel self‐templating strategy combined with atomic layer deposition (ALD) to design the electrochemically active and stable quaternary metal boride (vanadium‐doped cobalt nickel boride, VCNB), hollow nanoprism by inducing electronic double layers on the surface. The incorporation of V in a double‐layered structure can substantially increase the number of surface active sites with unsaturated electronic structure. Furthermore, the induced electronic double layers of V can effectively protect the dissolution of the surface active sites. In addition, density functional theory (DFT) calculations reveal that the impressive water oxidation properties of VCNB originate from the synergetic physicochemical effects of the different metal elements, Co and B as active sites, Ni as a surface electronic structure modifier, and V as a charge carrier transporter and supplier.
Keywords:electrocatalysts  metal boride  oxygen evolution reaction  water splitting
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