Gudal Chandan Chandru, Pan Uday Narayan, Paudel Dasu Ram, Kandel Mani Ram, Kim Nam Hoon, Lee Joong Hee
Department of Nano Convergence Engineering (BK21 Four), Jeonbuk National University, Jeonju, Jeonbuk 54896, Republic of Korea.
Carbon Composite Research Centre, Jeonbuk National University, Jeonju, Jeonbuk 54896, Republic of Korea.
ACS Appl Mater Interfaces. 2022 Mar 30;14(12):14492-14503. doi: 10.1021/acsami.2c00278. Epub 2022 Mar 18.
Metallic (1T) molybdenum disulfide (MoS) is a much better electrocatalyst than the semiconducting (2H) MoS because of its superior conductivity, presence of active basal planes, and bulky interlayers. However, the lack of thermodynamic stability has hindered its practical uses. The insertion of transition metals and nonmetals in the interlayers and the crystal is known to improve both the thermodynamic stability and the catalytic efficacy of 1T-MoS. In this study, for the first time we have developed an electrocatalyst for water splitting based on metallic copper molybdenum sulfide (1T-CMS). The present catalyst, P-doped and intercalated 1T-CMS ultrathin 2D nanosheets on carbon cloth (P-1T-CMS@CC), demonstrates excellent catalytic efficacy for both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). It required an overpotential of 95 mV for HER and of 284 mV for OER at a current density of 10 mA cm. The P-1T-CMS@CC(+ -) device also shows excellent performance, requiring a cell voltage of only 1.51 V at a current density of 10 mA cm.
金属性(1T)二硫化钼(MoS)由于其卓越的导电性、活性基面的存在以及较大的层间距,是一种比半导体性(2H)二硫化钼更好的电催化剂。然而,缺乏热力学稳定性阻碍了其实际应用。已知在层间和晶体中插入过渡金属和非金属可提高1T-MoS的热力学稳定性和催化效率。在本研究中,我们首次开发了一种基于金属性铜钼硫化物(1T-CMS)的析水电催化剂。目前的催化剂,即碳布上的P掺杂和插层的1T-CMS超薄二维纳米片(P-1T-CMS@CC),对析氢反应(HER)和析氧反应(OER)均表现出优异的催化效率。在电流密度为10 mA cm时,HER所需的过电位为95 mV,OER所需的过电位为284 mV。P-1T-CMS@CC(+ -)装置也表现出优异的性能,在电流密度为10 mA cm时,电池电压仅需1.51 V。