Low‐Energy Hydrogen Ions Enable Efficient Room‐Temperature and Rapid Plasma Hydrogenation of TiO₂ Nanorods for Enhanced Photoelectrochemical Activity

Abstract Hydrogenation is a promising technique to prepare black TiO₂ (H‐TiO₂) for solar water splitting, however, there remain limitations such as severe preparation conditions and underexplored hydrogenation mechanisms to inefficient hydrogenation and poor photoelectrochemical (PEC) performance to be overcome for practical applications. Here, a room‐temperature and rapid plasma hydrogenation (RRPH) strategy that realizes low‐energy hydrogen ions of below 250 eV to fabricate H‐TiO₂ nanorods with controllable disordered shell, outperforming incumbent hydrogenations, is reported. The mechanisms of efficient RRPH and enhanced PEC activity are experimentally and theoretically unraveled. It is discovered that low‐energy hydrogen ions with fast subsurface transport kinetics and shallow penetration depth features, enable them to directly penetrate TiO₂ via unique multiple penetration pathways to form controllable disordered shell and suppress bulk defects, ultimately leading to improved PEC performance. Furthermore, the hydrogenation‐property experiments reveal that the enhanced PEC activity is mainly ascribed to increasing band bending and bulk defect suppression, compared to reported H‐TiO₂, a superior photocurrent density of 2.55 mA cm⁻² at 1.23 V_RHE is achieved. These findings demonstrate a sustainable strategy which offers great promise of TiO₂ and other oxides to achieve further‐improved material properties for broad practical applications.