摘要
Designing efficient and scalable electrocatalysts for the hydrogen evolution reaction (HER) remains critical to advancing sustainable hydrogen production. Here, we report tunable phase engineering and interfacial coupling in 3D hierarchical WO3 - x@1T-WS2/1T(2H)-WSe2 nanoscrew heterostructures synthesized via glancing angle deposition (GLAD), followed by sequential plasma-assisted sulfurization and selenization processes. This hierarchical 3D heterostructure integrates a conductive WO3-x core with sequential 1T-WS2 and WSe2 shells, enabling an enlarged electrochemically accessible surface area and enhanced accessibility to edge/defect-rich catalytic regions, along with favorable phase interfaces and charge-transport pathways. The resulting electrocatalyst demonstrates excellent HER performance in both acidic and alkaline media, with low onset potentials (-86 and -194 mV at 2 mA cm- 2 in 0.5 m H2SO4 and 0.5 m KOH, respectively), small Tafel slopes (46 mV dec- 1 in acid, 73.3 mV dec- 1 in base), and remarkable operational stability over 24 h. Electrochemical analyses reveal that synergistic interfacial interactions and an optimized shell-phase composition are pivotal for facilitating fast reaction kinetics and achieving similar to 100% faradaic efficiency for the HER. These findings establish WO3-x@1T-WS2/WSe2 nanoscrew heterostructures as a promising platform for next-generation water-splitting technologies, highlighting the potential of phase-tuned heterostructures for efficient production of green hydrogen.