A direct Z-scheme NiCo2O4/ZnIn2S4 heterojunction for highly efficient visible-light-driven H2 evolution.

Abstract

Exploiting efficient and stable photocatalysts is the primary goal of photocatalytic water splitting for H2 production. In this work, a sea urchin-like bimetallic NiCo2O4-decorated ZnIn2S4 heterojunction was fabricated via a solvent evaporation method. Investigation shows that the introduction NiCo2O4 can expand the UV-vis absorption range, enhance the absorption intensity, promote the charge separation, decrease the charge transfer resistance, induce more active sites, and decrease the H2 evolution overpotential of the composite. Besides, the charge transfer between NiCo2O4 and ZnIn2S4 follows a Z-scheme route based on the ˙OH radical capture experiments; this can preserve the strong oxidation-reduction reaction ability of photogenerated electrons and holes, leading to a faster H2 evolution rate, which reaches 17.28 mmol g-1 h-1 over the 4.8%-NiCo2O4/ZnIn2S4 composite under 300 W Xe lamp irradiation in 20 vol% triethanolamine (TEOA) solution and is 3.0 times higher than that of ZnIn2S4. In addition, NiCo2O4/ZnIn2S4 also has excellent stability during 5 consecutive cycles. This work provides an effective method for constructing a highly effective Z-scheme heterojunction system for photocatalytic H2 production.