transition metal dichalcogenides (TMDs), MoS 2 as a HER catalyst has attracted considerable attention because of its high intrinsic activity at the edge sites comparable to Pt as predicted by density functional theory (DFT) calculation. [3] However, the practical application of 2H-MoS 2 is impeded largely due to the low density of edge sites and also its high electron transfer resistance originated from its semiconductor nature. [4] To increase the density of edge sites, a nanoengineering strategy is to reduce the lateral size of TMDs flakes. [5] Besides, a metallic character of 2D TMDs increases the electron transfer efficiency. [6] Moreover, a reduction of the layered TMD thickness could significantly enhance the electron transfer in the direction perpendicular to the basal plane. [7] As a result, the utilization of these active sites in the layers away from the electrode substrate could be maximized.As a member of TMDs, 1T-TiS 2 owns metallic phase. Additionally, it is predicted to possess more active edge sites than 2H-MoS 2 .[8] But the bulk 1T-TiS 2 still exhibits deficient HER performance due to low density of accessible active sites and sluggish electron transfer kinetics across the interlayer. [9] Here, we nanoengineered 1T-TiS 2 into quantum dots (QDs) with atomic layer thickness in order to simultaneously enhance the density of edge sites and facilitate the electron transfer from the substrate to the edge sites. [5a,10] The TiS 2 QDs were preparedThe overall electrocatalytic activity toward hydrogen evolution reaction for layered transition metal dichalcogenides is governed by their intrinsic activity, the corresponding density of active sites, and the electron transfer resistance. Here, nanoengineering strategies to scale down both the lateral size and thickness of layered 1T-TiS 2 powder to quantum dots ( ).
Electrocatalysis