Ha Thanh Duy Cam, Do Ha Huu, Lee Heehyeon, Ha Nguyen Ngoc, Ha Nguyen Thi Thu, Ahn Sang Hyun, Oh Youngtak, Kim Soo Young, Kim Myung-Gil
School of Advanced Materials Science and Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
School of Chemical Engineering and Materials Science, Chung-Ang University, Seoul 06974, Republic of Korea.
Nanoscale. 2022 Jul 7;14(26):9331-9340. doi: 10.1039/d2nr01800d.
Molybdenum disulfide (MoS)-based materials are extensively studied as promising hydrogen evolution reaction (HER) catalysts. In order to bring out the full potential of chalcogenide chemistry, precise control over the active sulfur sites and enhancement of electronic conductivity need to be achieved. This study develops a highly active HER catalyst with an optimized active site-controlled cobalt molybdenum sulfide (CoMoS) chalcogel/graphene oxide aerogel heterostructure. The highly active CoMoS chalcogel catalyst was achieved by the synergetic catalytic sites of [MoS] and the Mo-S-Co bridge. The optimized GO/CoMoS chalcogel heterostructure catalyst exhibited high catalytic HER performance with an overvoltage of 130 mV, a current density of 10 mA cm, a small Tafel slope of 40.1 mV dec, and remarkable stability after 12 h of testing. This study presents a successful example of a synergistic heterostructure exploiting both the appealing electrical functionality of GO and catalytically active [MoS] sites.
基于二硫化钼(MoS)的材料作为有前景的析氢反应(HER)催化剂受到广泛研究。为了充分发挥硫族化物化学的潜力,需要实现对活性硫位点的精确控制并提高电子导电性。本研究开发了一种具有优化的活性位点控制的硫化钴钼(CoMoS)硫属凝胶/氧化石墨烯气凝胶异质结构的高活性HER催化剂。高活性的CoMoS硫属凝胶催化剂是通过[MoS]的协同催化位点和Mo-S-Co桥实现的。优化后的GO/CoMoS硫属凝胶异质结构催化剂表现出高催化HER性能,过电压为130 mV,电流密度为10 mA cm,塔菲尔斜率小至40.1 mV dec,并且在测试12小时后具有显著的稳定性。本研究展示了一个成功的协同异质结构的例子,该异质结构利用了GO吸引人的电学功能和催化活性的[MoS]位点。