过电位
电催化剂
双功能
二硫化钼
析氧
材料科学
催化作用
化学工程
纳米技术
纳米片
分解水
化学
电化学
冶金
电极
光催化
工程类
物理化学
生物化学
作者
Bo Chen,PingAn Hu,Fan Yang,Xing-Jiang Hua,Fairy Fan Yang,Fei Zhu,Ruiyan Sun,Ke Hao,Kuaishe Wang,Zongyou Yin
出处
期刊:Small
[Wiley]
日期:2023-01-26
卷期号:19 (14)
被引量:69
标识
DOI:10.1002/smll.202207177
摘要
Abstract 2D molybdenum disulfide (MoS 2 ) is developed as a potential alternative non‐precious metal electrocatalyst for energy conversion. It is well known that 2D MoS 2 has three main phases 2H, 1T, and 1T′. However, the most stable 2H‐phase shows poor electrocatalysis in its basal plane, compared with its edge sites. In this work, a facile one‐step hydrothermal‐driven in situ porousizing of MoS 2 into self‐supporting nano islands to maximally expose the edges of MoS 2 grains for efficient utilization of the active stable sites at the edges of MoS 2 is reported. The results show that such active, aggregation‐free nano islands greatly enhance MoS 2 's hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) bifunctional electrocatalytic activities. At a low overpotential of 248 and 300 mV, the porous MoS 2 nano islands can generate a current density of 10 mA cm −2 in HER and OER, which is much better than typical nanosheet morphology. Surprisingly, the porous MoS 2 nano islands even exhibit better performance than the current commercial RuO 2 catalyst in OER. This discovery will be another effective strategy to promote robust 2H‐phase, instead of 1T/1T′‐phase, MoS 2 to achieve efficient endurable bifunctional HER/OER, which is expected to further replace precious metal catalysts in industry.
科研通智能强力驱动
Strongly Powered by AbleSci AI