Advancement toward dye-sensitized photoelectrochemical cells to produce solar fuels by solar-driven water splitting requires a photosensitizer that is firmly attached to the semiconducting photoelectrodes. Covalent binding enhances the efficiency of electron injection from the photoexcited dye into the metal oxide. Optimization of charge transfer, efficient electron injection, and minimal electron-hole recombination are mandatory for achieving high efficiencies.
View Article and Find Full Text PDFPhotocatalytic plastic waste upcycling into value-added feedstock is a promising way to mitigate the environmental issues caused by the nondegradable nature of plastic waste. Here, we developed a MoS/g-CN photocatalyst that can efficiently upcycle poly(ethylene terephthalate) (PET) into valuable organic chemicals. Interestingly, the conversion mechanism is concentration-dependent.
View Article and Find Full Text PDFCovalent attachment of molecules to metal oxide surfaces typically demands the presence of an anchoring group that in turn requires synthetic steps to introduce. BODIPY (4,4-difluoro-4-bora-3a,4a-diaza--indacene) chromophores have long been used in dye-sensitized solar cells, but carboxylic acid groups typically had to be installed to act as surface anchors. We now find that even without the introduction of such anchors, the unmodified BODIPY can bind to TiO surfaces its BF group through boron-oxygen surface bonds.
View Article and Find Full Text PDFMolybdenum disulfide (MoS) has been extensively studied in its commonly occurring semiconducting 2H phase. Recent synthetic advances have enabled the bulk synthesis of the catalytically promising metallic 1T phase. However, the conductivity of bulk 1T-MoS has not been well characterized to ascertain the carrier transport properties.
View Article and Find Full Text PDFGraphitic carbon nitride (g-CN) and its doped analogues have been studied over the past decade in part due to their promising applications in heterogeneous photocatalysis; however, the effect of doping on the photoconductivity is poorly understood. Herein, we investigate Cu doped g-CN (Cu-g-CN) and demonstrate via extended X-ray absorption fine structure that Cu incorporates as an individual ion. Time-resolved optical pump terahertz probe spectroscopy was utilized to measure the ultrafast photoconductivity in response to a 400 nm pump pulse and showed that the Cu dopant significantly enhances photoconductivity of the as-prepared powdered sample, which decays within 10 ps.
View Article and Find Full Text PDF