Tekalgne Mahider Asmare, Do Ha Huu, Nguyen Tuan Van, Le Quyet Van, Hong Sung Hyun, Ahn Sang Hyun, Kim Soo Young
Department of Materials Science and Engineering, Institute of Green Manufacturing Technology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, Republic of Korea.
VKTech Research Center, NTT Hi-Tech Institute, Nguyen Tat Thanh University, Ho Chi Minh City 700000, Vietnam.
ACS Omega. 2023 Oct 23;8(44):41802-41808. doi: 10.1021/acsomega.3c06403. eCollection 2023 Nov 7.
Designing low-cost hybrid electrocatalysts for hydrogen production is of significant importance. Recently, MXene-based materials are being increasingly employed in energy storage devices owing to their layered structure and high electrical conductivity. In this study, we propose a facile hydrothermal strategy for producing WS/TiC nanosheets that function as electrocatalysts in the hydrogen evolution reaction (HER). WS provides a high surface area and active sites for electrocatalytic activity, whereas MXene TiC facilitates charge transfer. As a result, the synthesized WS/TiC offers an increased surface area and exhibits an enhanced electrocatalytic activity in acidic media. The WS/TiC (10%) catalyst exhibited a low onset potential of -150 mV versus RHE for the HER and a low Tafel slope of ∼62 mV dec. Moreover, WS/TiC (10%) exhibited a double-layer capacitance of 1.2 mF/cm, which is 3 and 6 times greater than those of bare WS and TiC, respectively. This catalyst also maintained a steady catalytic activity for the HER for over 1000 cycles.
设计用于制氢的低成本混合电催化剂具有重要意义。最近,基于MXene的材料因其层状结构和高电导率而越来越多地应用于储能设备。在本研究中,我们提出了一种简便的水热策略来制备WS/TiC纳米片,其在析氢反应(HER)中用作电催化剂。WS为电催化活性提供了高表面积和活性位点,而MXene TiC则促进电荷转移。因此,合成的WS/TiC具有更大的表面积,并在酸性介质中表现出增强的电催化活性。WS/TiC(10%)催化剂在HER中相对于可逆氢电极(RHE)的起始电位为-150 mV,塔菲尔斜率约为62 mV/dec。此外,WS/TiC(10%)的双层电容为1.2 mF/cm²,分别是裸WS和TiC的3倍和6倍。该催化剂在HER中还能保持超过1000次循环的稳定催化活性。