| Literature DB >> 29333655 |
Chaoliang Tan1, Zhimin Luo1, Apoorva Chaturvedi1, Yongqing Cai2, Yonghua Du3, Yue Gong4, Ying Huang1, Zhuangchai Lai1, Xiao Zhang1, Lirong Zheng5, Xiaoying Qi6, Min Hao Goh6, Jie Wang1, Shikui Han1, Xue-Jun Wu1, Lin Gu4, Christian Kloc1, Hua Zhang1.
Abstract
Nanostructured transition metal dichalcogenides (TMDs) are proven to be efficient and robust earth-abundant electrocatalysts to potentially replace precious platinum-based catalysts for the hydrogen evolution reaction (HER). However, the catalytic efficiency of reported TMD catalysts is still limited by their low-density active sites, low conductivity, and/or uncleaned surface. Herein, a general and facile method is reported for high-yield, large-scale production of water-dispersed, ultrasmall-sized, high-percentage 1T-phase, single-layer TMD nanodots with high-density active edge sites and clean surface, including MoS2 , WS2 , MoSe2 , Mo0.5 W0.5 S2 , and MoSSe, which exhibit much enhanced electrochemical HER performances as compared to their corresponding nanosheets. Impressively, the obtained MoSSe nanodots achieve a low overpotential of -140 mV at current density of 10 mA cm-2 , a Tafel slope of 40 mV dec-1 , and excellent long-term durability. The experimental and theoretical results suggest that the excellent catalytic activity of MoSSe nanodots is attributed to the high-density active edge sites, high-percentage metallic 1T phase, alloying effect and basal-plane Se-vacancy. This work provides a universal and effective way toward the synthesis of TMD nanostructures with abundant active sites for electrocatalysis, which can also be used for other applications such as batteries, sensors, and bioimaging.Entities:
Keywords: MoS2, MoSSe; hydrogen evolution; metallic 1T phase; nanodots; transition metal dichalcogenides
Year: 2018 PMID: 29333655 DOI: 10.1002/adma.201705509
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849