The mono-dispersed cubic siegenite CuNi2 S4 ultra-fine (≈5 nm) nanocrystals are fabricated through crystallization engineering under hot injection. The strong hydroxylation on mostly exposed CuNi2 S4 (220) surface leads to the formation of multi-valence (Cu+ , Cu2+ , Ni2+ , Ni3+ ) species with unsaturated hybridization and coordination micro-environments, which can induce rich redox reactions to optimize interfacial kinetics for the adsorbed reaction intermediates. The as-synthesized CuNi2 S4 nanocrystals with ultra-small particle size and the characteristics of being highly dispersed can increase specific surface area and hydroxylated active sites, which considerably contribute to the improvement of photocatalytic activities. Experimental and theoretical studies indicate that the CuNi2 S4 with unique surface condition can properly modulate the charge density distribution and the electronic band structure, thus achieving an optimal band gap for enhancing visible light absorption. Additionally, the strong hydroxylation on CuNi2 S4 (220) surface can not only make the photocatalytic process stable in alkaline environment but also bring about an impurity level between conduction and valence band, which facilitates the separation of photo-induced charge carriers by suppressing the rapid re-combination of exited electrons and holes. The optimization of band structure should be the intrinsic reason for the efficient photocatalytic pollutant degradation and hydrogen production under visible light illumination.
Keywords: band structure modulation; crystalline engineering; hydrogen production; photocatalytic degradation; ultra-fine bi-metal sulfide nanocrystals.
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