Hydrogen energy production through photoelectrochemical (PEC) water splitting has great potential in the field of renewable energy. This study focuses on the hydration enthalpy difference of cations (Li+ , Na+ , and K+ ) in an aqueous solution for the chemical self-oxidation process without an external applied bias. The thickness of the cation/H2 O double layer is controlled. The starting materials are low-cost copper foil and the synthesis uses alkali cation-engineered chemical self-oxidation. Li+ ions are strongly attracted to water molecules. This forms a sufficient OH- layer on the Cu foil surface. By accelerating the oxidation reaction, a large surface area of Cu(OH)x nanowires (NWs) with high purity and a uniform shape are obtained. This optimal p-type Cu2 O NWs photocathode is CuO-free, has the highest conductivity, and is fabricated through phase transition using precise vacuum annealing. The other alkali cations produce the Cu2 O/CuO mixed or CuO phases that degrade the PEC performances with severe corrosive reactions. The Cu/Li : Cu2 O/AZO/TiO2 /Pt photocathode has a 50 h stability with a photocurrent density of 8.4 mA cm-2 at 0 VRHE . The fabricated photoelectrode did not structurally collapse after stability measurements during this period. The captured hydrogen production was in agreement with the calculated faradaic efficiency.
Keywords: hydrogen; nanowires; oxidation; photoelectrochemistry; water splitting.
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