Improved charge transfer and photoelectrochemical performance of CuI/Sb2S3/TiO2 heterostructure nanotube arrays.

Charge transfer is important for the performance of a photoelectrochemical cell. Understanding photogenerated charge accumulation and separation is mandatory for the design and optimisation of photoelectrochemical cells. Unique stacked and embedded heterostructure of Sb2S3/TiO2 nanotube arrays (NTAs) was fabricated through anodic oxidation with the hydrothermal method. Surface photovoltage spectroscopy, phase spectra and photoluminescence measurements were performed to explore the mechanism by which the inorganic hole transport material CuI affects the charge transfer and photoelectrochemical properties of Sb2S3/TiO2 heterostructure NTAs. The interfacial separation and transport of photoinduced charge carriers were also examined by applying current-voltage characteristics (J-V), incident-photon-to-current conversion efficiency (IPCE) and Mott-Schottky techniques. Results show that CuI acts not only as a hole-conducting and electron-blocking material but also as a light-absorbing material in the ultraviolet range. Efficient charge transfer processes exist in CuI/Sb2S3/TiO2 heterostructure NTAs. The photoelectrochemical performance of CuI/Sb2S3/TiO2 heterostructure NTAs is dramatically improved. Under AM 1.5G illumination at 100mW/cm(2), the short-circuit current density and open-circuit voltage are 3.51mA/cm(2) and 0.87V, respectively. The photoelectric conversion efficiency of CuI/Sb2S3/TiO2 heterostructure NTAs (0.95%) is 36% higher than that of Sb2S3/TiO2 heterostructure NTAs (0.66%).

PbS sensitized TiO2 nanotube arrays with different sizes and filling degrees for enhancing photoelectrochemical properties.

PbS nanoparticles (PbS NPs), an efficient sensitizer for TiO2 nanotube arrays (TiO2 NAs), were fabricated by the method of sonication-assisted successive ionic layer adsorption and reaction (SILAR). The filling degree and size of PbS NPs can be tuned by changing the repeated cycles (N) of the SILAR process. TiO2 NAs can be fully covered with PbS NPs with a size ranging from less than 4 nm to 25 nm and large aggregates inside and outside the nanotubes when N reaches 15. The growth mechanism of PbS NPs in TiO2 NAs was expounded in great detail in this work. Ultraviolet-visible diffuse-reflectance spectra and surface photovoltage spectroscopy were used to investigate the light absorption properties and the transfer behavior of photogenerated charges in PbS-modified TiO2 NA heterostructures. Results show that the absorption range of TiO2 NAs is extended from the ultraviolet to the visible region by PbS NPs modification. A heterojunction is formed between PbS NPs and TiO2 NAs, facilitating the separation of photogenerated charge carriers. This PbS NPs fully-covered TiO2 NA electrode exhibits the best photoelectrochemical performance in all PbS-sensitized TiO2 NA electrodes, due to a larger number of small PbS NPs (<4 nm). With AM 1.5G illumination at 100 mW cm(-2), its short-circuit current density, open-circuit voltage and photoelectric conversion efficiency are 9.55 mA cm(-2), 0.95 V and 2.83%, respectively.

[Isolation and degrading characters of pendimethalin degrading bacteria].

Microbial degradation of pendimethalin and the effects of culture conditions in vitro are studied. Twenty-nine strains are isolated by enrichment from soil and sludge. 3 strains can degrade more than 80% of pendimethalin of 100 mg x L(-l) in 3 days in culture fluid. 2 bacteria are considered as efficiently degrading strains identified as Pseudomonas, Mirococcus luteus. The efficiency of degradation is affected by culture conditions such as pH, temperature and the concentration of sucrose and pendimethanlin. The optimal conditions are proposed.