We prepare group VI transitional metal dichalcogenides (TMDs, or MX 2 ) from the 1T phase with quantum-sized and monolayer features via a quasi-full electrochemical process. The resulting two-dimensional (2D) MX 2 (M = W, Mo; X = S, Se) quantum dots (QDs) are ca . 3.0–5.4 nm in size with a high 1T phase fraction of ca . 92%–97%. We attribute this to the high Li content intercalated in the 1T-MX 2 lattice (mole ratio of Li:M is over 2:1), which is achieved by an increased lithiation driving force and a reduced electrochemical lithiation rate (0.001 A/g). The high Li content not only promotes the 2H → 1T phase transition but also generates significant inner stress that facilitates lattice breaking for MX 2 crystals. Because of their high proportion of metallic 1T phase and sufficient active sites induced by the small lateral size, the 2D 1T-MoS 2 QDs show excellent hydrogen evolution reactivity (with a typical η 10 of 92 mV, Tafel slope of 44 mV/dec, and J 0 of 4.16 × 10 –4 A/cm 2 ). This electrochemical route toward 2D QDs might help boost the development of 2D materials in energy-related areas.
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Chen et al. (2017) studied this question.
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