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A new homojunction is developed by in situ decorating g-C3N4 (CN) nanosheets with a C–N compound broken by s-triazine units (BST). The BST fragments rapidly transfer photogenerated electrons from the CN conduction band to generate hydrogen.

SSZ-13 has been commercialized as a catalyst in diesel engines for the selectivity catalytic reduction of nitrogen oxides (NO

TiNb2O7 (TNO) as a promising candidate anode for lithium-ion batteries (LIBs) shows obvious advantages in terms of specific capacity and safety, but which undergoes the intrinsic poor electrical and ionic conductivity. Herein, we propose a simple synthesis strategy of mesoporous TNO via a polymeric surfactant-mediated evaporation-induced sol-gel method, using polyvinylpyrrolidone (PVP) with different molecular weights (average Mw: 10000/58000/1300000) as the regulating agent, which greatly affects the lithium storage performance of the as-prepared TNO. The optimized TNO (i.e., PVP of 58000) delivers a high reversible capacity of 303.1 mAh/g at 1 C, with a retention rate of 73.4% (222.5 mAh/g) after 300 cycles. Even at 5 C, a high reversible capacity of 185.6 mAh/g can be achieved, with a retention rate of 72.3% after 1000 cycles. The superior lithium storage behavior is attributed to the fine mesoporous framework consisting of interconnected TNO nanocrystallites with high specific surface area and high mesoporosity, which greatly increases the active sites, improves the Li+ diffusion kinetics and alleviates volume fluctuation induced by the repetitive Li+ insertion-extraction processes.

Photocatalytic hydrogen evolution from water splitting presents an attractive prospect in dealing with the energy crisis, but the low efficiency of charge separation and migration still seriously hinders its further practical application. Here, an acidified boron-doped g-C

Introducing co-catalyst and constructing heterostructure are two of the most promising strategies in improving the photocatalytic H2 evolution performance of semiconductors. However, it has always been a great challenge to develop a facile and low-cost system to facilitate the highly efficient synergistic effect between co-catalyst and heterostructure. Herein, co-catalyst NiS decorated ZnS/CdS heterostructure (CdS/ZnS-NiS) has been fabricated by using a facile one-pot hydrothermal procedure for the photocatalytic H2 evolution from water splitting. As a result, CdS, ZnS and NiS contact closely with each other at nano scale to assemble into fluffy porous nanocomposite, the optimized CdS/ZnS-NiS exhibits a high hydrogen evolution rate of 60.44 mmol·h-1g-1 without the addition of extra noble metal co-catalyst, which is about 22.3 times higher than that of pure CdS and much higher than that of 1% wt Pt decorated CdS/ZnS (52.36 mmol·h-1g-1). One-pot fabrication process allows the formation of intimate contacted interface between different components, contributing to the sufficient exposure of active reaction sites. Moreover, noble-metal-free co-catalyst NiS distributes uniformly in both surface and inner region of porous nanocomposite. The synergistic effect between the intimately contacted heterostructure and co-catalyst boosts the separation and utilization of photogenerated charge carriers, resulting in a dramatically enhanced H2 evolution ability. This work provides a facile pathway to uniformly introduce noble-metal-free co-catalyst in heterostructure and gives out a paradigm in constructing high active solar energy conversion system.

A new photocatalyst, the tri-arm CdS/ZnS core–shell nanorod, is carefully designed for the first time, where tri-arm CdS nanorods are decorated by dodecylamine (DDA) molecules and then wrapped in an intermittent ZnS shell. The resultant photocatalyst with a CdS/ZnS mole ratio of 0.5 (CZS0.5) presents a significantly improved H2 evolution rate of 726.0 μmol/h (3 mg of catalysts, equal to 242.0 mmol/g/h) in the absence of co-catalysts, which is currently the highest value in CdS-based catalysts. The apparent quantum efficiency of CZS0.5 reaches 50.61% at 380 nm. The significantly enhanced photocatalytic performance can be attributed to a win–win situation between the analogous type-II mechanism formed in the CdS/ZnS heterojunction and the H+ adsorption resulting from the DDA molecules. Due to the analogous type-II mechanism, photogenerated electrons are transferred from the ZnS shell to the CdS nanorod. Owing to the decoration of DDA, many H+ ions are adsorbed on CdS. Thus, the photogenerated electrons gathered in CdS can be captured quickly and in a timely manner by the adsorbed proton H+ to produce hydrogen, which effectively suppresses the recombination of photogenerated electrons and holes. This study may bring new insights for developing other photocatalysts with high performance by using small organic molecules.