Unexpected High-Performance Photocatalytic Hydrogen Evolution in Co@NCNT@ZnIn2 S4 Triggered by Directional Charge Separation and Transfer.

The structural design of photocatalysts is highly related to the separation and transfer of photogenerated carriers, which is essential for the improvement of photocatalytic hydrogen evolution performance. Here, the hybrid photocatalyst M@NCNT@ZIS (M: Fe, Co, Ni; NCNT: nitrogen-doped carbon nanotube; ZIS: ZnIn2 S4 ) with a hierarchical structure is rationally designed and precisely synthesized. The unique hollow structure with a large specific surface area offers abundant reactive sites, thus increasing the adsorption of reactants. Importantly, the properly positioned metal nanoparticles realize the directional charge migration from ZIS to M@NCNT, which significantly improves the efficiency of charge separation. Furthermore, the intimate interface between M@NCNT and ZIS effectively facilitates charge migration by shortening the transfer distance and providing numerous transport channels. As a result, the optimized Co@NCNT@ZIS exhibits a remarkable photocatalytic hydrogen evolution efficiency (43.73 mmol g-1 h-1 ) without Pt as cocatalyst. Experimental characterizations and density functional theory calculations demonstrate that the synergistic effect between hydrogen adsorption and interfacial charge transport is of great significance for improving photocatalytic hydrogen production performance.

Ultrahigh piezocatalytic capability in eco-friendly BaTiO3 nanosheets promoted by 2D morphology engineering.

Piezocatalysis, converting mechanical vibration into chemical energy, is an emerging technology to address environmental issues. In this work, we propose an efficient method to significantly improve the piezocatalytic activity by morphology engineering rather than composition design. The catalytic property in BaTiO3 nanocrystallites with diverse morphologies is investigated by dye degradation and hydrogen production under ultrasonic vibration. The BaTiO3 nanosheets exhibit an excellent piezocatalytic activity with a degradation rate of 0.1279 min-1 for Rhodamine B, far beyond those in previous piezocatalytic literature and even comparable to excellent photocatalysts, and also a high hydrogen production rate of 92 µmol g-1 h-1. Compared with nanowires and nanoparticles, the 2D morphology greatly enhances the piezocatalytic activity in nanosheets owing to much larger piezoelectric potential. This proves that the piezocatalytic property is dominated by the morphology-dependent piezoelectricity, rather than specific surface area as other catalysis. Dominated by bending vibrating mode, the piezocatalytic activity reaches a maximum at the piezoelectric resonating frequency, and it increases with the ultrasonic power. Moreover, it has good reusability and wide versatility for catalytic degradation. This work gives an in-depth understanding of piezocatalytic mechanism and provides a way to develop high performance and eco-friendly piezocatalysts.