Construction of a high-performance photocatalytic fuel cell (PFC) based on plasmonic silver modified Cr-BiOCl nanosheets for simultaneous electricity production and pollutant removal.

The development of high-performance photocatalytic fuel cells (PFCs) is seriously hampered by poor light utilization rates and low charge carrier transfer efficiency. Herein, we have experimentally obtained plasmonic Ag modified Cr-BiOCl (Cr-BOC/Ag) with high visible light photocatalytic activity and provided direct evidence for the substantially enhanced catalytic activity in metal-semiconductor photocatalysts. The experimental results revealed that the Cr doping and Ag modification could not only extend the photo absorption of BiOCl from the UV to the visible light region but could also greatly increase the generation and transfer rate of charge carriers because of its narrowed band gap and the localized surface plasmon resonance (LSPR) effect of metallic Ag. Under visible light irradiation, the Cr-BOC/Ag showed a remarkable enhancement in the PFC performance when the optimum contents of Cr doping and Ag loading was 14.4% and 4%, respectively. The trapping experiments and multiple characterizations demonstrated that the advantageous combination of the Cr doping effect and SPR effect induced by the Ag nanoparticles is responsible for the high generation rate of oxidative species and effective charge carrier transfer. By using RhB as fuel, approximately 75.1% color removal efficiency and 8.38% coulombic efficiency were obtained under visible light irradiation for 240 min, which are higher than those of MO and TC. In addition, the Jsc and Voc of the Cr-BOC/Ag photoanode were measured to be 0.0073 mA cm-2 and 0.543 V.

Ultrathin BiOCl Single-Crystalline Nanosheets with Large Reactive Facets Area and High Electron Mobility Efficiency: A Superior Candidate for High-Performance Dye Self-Photosensitization Photocatalytic Fuel Cell.

Strong dye adsorption and fast electron transfer are of crucial importance to achieve high conversion efficiency of dye self-photosensitization photocatalytic fuel cells (DSPFCs). In this study, we have experimentally achieved the enhanced cell performance in ultrathin BiOCl{010} (BOC(010)-U) nanosheets and provide an idea to investigate the relationship between the physical structure and the chemical performance of semiconductor materials. Experimental phenomenon showed that the exposed areas of highly active {010} facets were remarkably enhanced with the decrease of the BiOCl thickness. The large area of {010} facets with abundant active sites and open channel characteristic were exposed to facilitate photosensitization process, and the atomically thin structure was designed to speed up electron transfer. By employing 40 mL of 5 mg/L rhodamine B as fuel, it was found that the BOC(010)-U photoanode exhibited superior photovoltaic performance and photocatalytic degradation activity than other materials in the DSPFC system, whose Jsc and Voc were measured to be 0.00865 mA/cm2 and 0.731 V, respectively. Besides, about 72% color removal efficiency and 10.77% Coulombic efficiency were obtained under visible light irradiation for 240 min. The experimental results and multiple characterizations demonstrated that the strong dye adsorption ability and efficient charge migration were responsible for the sustaining generation of photocurrent and enhancement of pollutants degradation activity.

Enhanced photocatalytic activity of CdS/SnS2 nanocomposite with highly-efficient charge transfer and visible light utilization for selective reduction of 4-nitroaniline.

Photocatalytic reduction can be an effective and promising technology for the selective reduction of aromatic nitro organics. In this paper, a novel Z-scheme CdS/SnS2 photocatalyst was well-designed and fabricated via simple in-site reaction process containing thioacetamide as a sulfur sources and cubic CdSnO3 as template. The resulting CdS/SnS2 composite has well-constructed cubic nanostructure of strong adhesion between CdS and SnS2, presenting high absorption to visible light. Importantly, strong charge transfer between the contacting regions of CdS and SnS2 through the intermediate sulfur atoms combined with both metals was generated, which speeds up separation of photogenerated electron and hole. The advantageous combination of high light-harvesting and effective charge transfer is responsible for the excellent photocatalytic activity at the CdS/SnS2 heterointerface. Resultantly, the prepared CdS/SnS2 composites exhibit high conversion efficiency and selectivity on 4-nitroaniline (4-NA) reduction in the aqueous solution containing ammonium formate under visible light irradiation, which can reduce almost all 4-NA within 12 min. Trapping experiments and ESR analysis demonstrated that ammonium formate not only can effectively decrease recombination of photogenerated charge carriers but also react with holes to generate CO2- radicals possessing strong reduction ability. The 4-NA are effectively photo-reduced by the synergistic effect of electrons and CO2- radicals. According to the experimental results, a possible Z-scheme charge transfer mechanism was proposed. Besides, the photo-reduction of aromatic nitro organics possessed different para-groups (p-nitrophenol, nitrobenzene, and p-nitrobenzaldehyde) was also investigated. It is found that the electron-drawing group can decrease the electron density of its para-position nitryl, which quickens the nitro reduction.

A facile strategy to fabricate hollow cadmium sulfide nanospheres with nanoparticles-textured surface for hexavalent chromium reduction and bacterial inactivation.

Exploring morphology and surface structure of semiconductor photocatalyst is crucial for researching their photocatalytic performance. In this paper, hollow CdS nanospheres (CdS-HSs) were successfully fabricated via simple template self-removal strategy. The prepared CdS-HSs were characterized by XRD, SEM, HR-TEM, UV-vis diffuse reflectance spectra (DRS), XPS, photocurrent response (I-T), photoluminescence (PL) and electrochemistry impedance spectroscopy (EIS). It was found that the prepared CdS-HSs have nanoparticles-textured surface composed of ultra-small CdS nanoparticles (∼20 nm) and large surface areas. DRS result demonstrated that the CdS-HSs exhibit strong visible light absorption capacity. The results of photocurrent response, photoluminescence and EIS revealed that hollow structure and nanoparticles-textured surface can effectively increase light reflection effect and decrease recombination rate of electrons and holes. Compared to the traditional CdS, the hollow CdS nanospheres exhibit higher photocatalytic activity on Cr(VI) reduction under visible light irradiation, which are primarily attributed to its rapid separation of electron-hole pairs and improved visible light absorption. Moreover, CdS-HSs was also demonstrated as an effective and potential material on photocatalytic disinfection. The result of mechanism experiments proved that h+, e- and O2- play important roles on the bacteria inactivation.