Top-down nanostructured multilayer MoS2 with atomically sharp edges for electrochemical hydrogen evolution reaction

Abstract

Cost-efficient and readily scalable platinum-free electrocatalysts are crucial for a smooth transition to future renewable energy systems. Top-down activation of MoS2 promises the production of sustainable hydrogen evolution electrocatalysts from the Earth-abundant molybdenite ore. Here, the deterministic nanopatterning of multilayer MoS2 with numerous zigzag edges is explored as a pathway to enhance hydrogen evolution reaction (HER). Nanopatterned single-nanosheet MoS2 electrodes are assessed by two highly localized electrochemical techniques: selected area voltammetry (with lithography-defined regions of electrode-electrolyte contact) and Scanning ElectroChemical Microscopy (SECM). The nanopatterning effect is the most pronounced after prolonged electrochemical cycling in an acidic electrolyte. The electrocatalytic hydrogen evolution activity of edge-enriched electrodes is dramatically enhanced: the maximum electrochemical current density (jmax) achieved at -510 mV vs. reversible hydrogen electrode (mVRHE) is increased by two orders of magnitude, reaching >300 mA⋅cm−2. Both the η10 and η100 overpotentials are significantly reduced as well. Meanwhile, pristine MoS2 shows just ≈6 times jmax increase (≈30 mA⋅cm−2) after the very same cycling. The increased electrocatalytic activity comes with electrode morphology degradation, evidenced by ex-situ scanning electron microscopy. SECM directly visualizes stronger HER activity in the regions with densely located zigzag edges. Intense white light illumination significantly boosts HER on MoS2 electrodes due to the photo-enhanced MoS2 conductivity. These results improve the understanding and reveal the limitations of MoS2-based electrocatalytic water splitting.