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Black phosphorus (BP) has gained great attention as a potential candidate in the photocatalytic field due to its tunable bandgap and high-mobility features, however, poor stability behavior and the high charge recombination of BP limit its practical application. In the present work, a liquid phase exfoliation method is employed to prepare layered BP. The as-prepared layered BP is decorated on TiO2 nanosheets to form a TiO2 nanosheets@BP composite, which stabilizes BP existence under a hydro-oxygen environment. Whereafter, the photocatalytic properties of the TiO2 nanosheets@BP composite towards the degradation of Rhodamine B (RhB) are proven to be greatly enhanced compared to those of pure layered BP and TiO2 nanosheets, and the photodegradation rate reached 98% after 120 minutes irradiation under UV-Vis light. It is worth mentioning that the photocatalytic cycling performance of the TiO2 nanosheets@BP composite remained at 92.5% under the irradiation of UV-Vis light after three cycles. The main reason for this lies in the fact that the formation of the TiO2 nanosheets@BP composite may favor light absorption and effectively reduce the recombination of electron–hole pairs. more...

Black phosphorus (BP) has gained great attention as a potential candidate in the photocatalytic field due to its tunable bandgap and high-mobility features, however, poor stability behavior and the high charge recombination of BP limit its practical application. In the present work, a liquid phase exfoliation method is employed to prepare layered BP. The as-prepared layered BP is decorated on TiO2 nanosheets to form a TiO2 nanosheets@BP composite, which stabilizes BP existence under a hydro-oxygen environment. Whereafter, the photocatalytic properties of the TiO2 nanosheets@BP composite towards the degradation of Rhodamine B (RhB) are proven to be greatly enhanced compared to those of pure layered BP and TiO2 nanosheets, and the photodegradation rate reached 98% after 120 minutes irradiation under UV-Vis light. It is worth mentioning that the photocatalytic cycling performance of the TiO2 nanosheets@BP composite remained at 92.5% under the irradiation of UV-Vis light after three cycles. The main reason for this lies in the fact that the formation of the TiO2 nanosheets@BP composite may favor light absorption and effectively reduce the recombination of electron-hole pairs. more...

Multinary copper-based metal sulfide (Cu-M-S) nanocrystals (NCs) usually have high absorption coefficients and near-optimum direct band gaps, which have been considered as novel photo-absorption materials for quantum dot-sensitized solar cells (QDSCs) and hole-transport materials for perovskite solar cells (PSCs). However, the formation and phase transformation mechanisms of Cu-M-S NCs during the solution-based preparing approaches are complicated. Herein, Cu-M-S NCs, including Cu2ZnSnS4 (CZTS), Cu2SnS3 (CTS), CuInS2 (CIS), and CuSbS2 (CAS), have been synthesized through solution-based hot-injection methods. Their formation and phase transformation mechanisms have been studied in terms of the growth kinetics. An effective method has been proposed to investigate the formation mechanisms of Cu-M-S NCs. The results suggest that CZTS, CTS, and CIS NCs are formed through an inter-reaction between metal sulfides rather than the classical cation exchange reactions, and CAS NCs are formed based on the CuxS structure; these findings provide new insights into the formation of Cu-M-S NCs. In addition, the anisotropic or isotropic growth processes during the growth stage have been found to be the key issues in the formation of a zinc blende or wurtzite structure NCs, respectively, which can be controlled by tuning the relative reactivity of metal precursors. more...

Until now, it is a great challenge for the controllable synthesis of copper antimony sulfide (CAS) nanocrystals (NCs), as the reactivity of precursors is quite difficult to be controlled during the synthesis process. In the present work, a novel solution-based method is proposed to synthesize CAS NCs by choosing N,N′-diphenylthiourea as the sulfide precursor, which is favorable for balancing the relative reactivity of Cu and Sb ions. It is found that three phases (CuSbS2, Cu12Sb4S13 and Cu3SbS4) of CAS NCs with size tunability were successfully synthesized for the first time. To the best of our knowledge, the lowest reaction temperature of 110 °C and the highest yield over 90% for CAS NCs were also achieved for the first time, which may be considered to be a green synthesis route compared with other conventional methods. Optical properties indicate that the as-prepared CAS NCs have strong optical absorption in the visible light region of the solar spectrum, and we also observed the band gap tunability of CuSbS2 and Cu3SbS4 materials for the first time. more...

Few-layer graphene/TiO2 nanocrystal composites are successfully in situ synthesized at a low temperature of 400 °C using C28H16Br2 as the precursor. Raman mapping images show that the TiO2 nanocrystals are very uniformly dispersed in the composite films, and the in situ coating during the thermal decomposition process will favor the formation of a good interface combination between the few-layered graphene and the TiO2 nanocrystals. The few-layer graphene/TiO2 nanocrystal composites are used as photoanodes in dye-sensitized solar cells (DSSCs), and the conversion efficiency of 8.25% is obtained under full sun irradiation (AM 1.5), which increases by 65% compared with that of the pure TiO2 nanocrystal DSSCs (5.01%). It is found that the good interface combination between few-layered graphene and TiO2 nanocrystals may improve the electric conductivity and lifetime of photoinduced electrons in DSSCs. Moreover, some carbon atoms are doped into the crystal structure of the TiO2 nanocrystals during the thermal decomposition process, which will enhance the light absorption by narrowing the band gap and favor the improvement of the photovoltaic efficiency. more...