Cracked monolayer 1T MoS2 with abundant active sites for enhanced electrocatalytic hydrogen evolution

被引:90
作者
Li, Yue [1 ]
Wang, Longlu [2 ]
Zhang, Shuqu [2 ]
Dong, Xueru [1 ]
Song, Yuze [1 ]
Cai, Tao [3 ]
Liu, Yutang [3 ]
机构
[1] Henan Inst Engn, Sch Mat & Chem Engn, Zhengzhou 451191, Henan, Peoples R China
[2] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[3] Hunan Univ, Coll Environm Sci & Engn, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
METALLIC PHASE-TRANSITION; MOLYBDENUM-DISULFIDE; ULTRATHIN NANOSHEETS; EDGE SITES; MECHANISM; NANOBELTS; GRAPHENE; FILMS;
D O I
10.1039/c6cy02649d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Molybdenum disulfide (MoS2) is a promising non-precious-metal catalyst, but its performance is limited by its density of active sites and poor electrical transport. Here, we report the design and preparation of cracked monolayer 1T MoS2 with a porous structure through the ultrasonication enhanced lithium intercalation of hydrothermally synthesized MoS2 nanosheets. The unique resulting catalyst can have more active sites introduced via the formation of porosity within the monolayer nanosheet, and the electrical transport ability can be increased through the change in electronic states from semiconducting in the 2H phase to metallic in the 1T phase. As is expected, the cracked monolayer 1T MoS2 exhibited good durability and an excellent hydrogen evolution reaction performance with a low overpotential (at 10 mA cm(-2)) of 156 mV (V vs. RHE) in acid media and a small Tafel slope of 42.7 mV dec(-1). This work will provide an intriguing and effective approach to designing electrocatalysts based on MoS2 or other layered materials with enhanced HER performance.
引用
收藏
页码:718 / 724
页数:7
相关论文
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