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In this work, sodium cholate (NaC) was used as novel green reducing agent for graphene oxide (GO) reduction at 90 °C and short synthesis time using a continuous segmented flow reaction system. As a comparison, we had used the common reducing agent which is glucose to study its chemical and electrochemical properties. The morphologies of GO and reduced-graphene oxide (rGO) were characterized with X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscope (FESEM), Fourier transformed infrared (FTIR), Raman and Ultraviolet–Visible (UV–Vis) spectroscopy analysis demonstrated that reduction of GO occurred. For electrochemical measurements, the rGO was cast on carbon cloth to investigate the electrochemical performance with cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) measurements. NaC assisted rGO (rGO–NaC) was able to achieve a specific capacitance up to 94 F g−1 at 0.1 A g−1 and remarkable capacitance retention of 103% after 10,000 cycles. A flexible test shows that rGO–NaC bendable at 0°–60°. These results demonstrate that rGO–NaC is promising as flexible supercapacitors electrodes.

Carbon dots (CDs) were successfully derived from water hyacinth leaves and the binary composite was achieved by incorporating CDs with g-C3N4 through hydrothermal treatment. The average particle size of CDs was found to be 3.1 nm and a blue-green fluorescence was emitted under the UV light irradiation. Both of the composites loaded with 20 wt.% (20CDs/g-C3N4) and 40 wt.% (40CDs/g-C3N4) of CDs achieved the highest degradation efficiency of 2,4-dichlorophenol (2,4-DCP) with 1.7 times higher than that of pure g-C3N4. This work successfully improved the properties of g-C3N4 by elongating the lifetime of photogenerated electrons and widening the visible light response. Both of 20CDs/g-C3N4 and 40CDs/g-C3N4 recorded the highest photocatalytic performance in degrading 2,4-DCP with degradation rate constant of 0.0194, and 0.0186 min−1, respectively. This is contributed by the prolonged charge carrier lifetime in 20CDs/g-C3N4; good visible light absorption and high specific surface area in 40CDs/g-C3N4. For the scavenger test, hole (h+) and superoxide radical (·O2−) were acknowledged as the key active species in photocatalysis.

Incorporating cadmium sulfide quantum dots (CdS QDs) onto ZnO nanorod (ZNRs) has been investigated to be an efficient approach to enhance the photovoltaic performance of the inverted organic solar cell (IOSC) devices based on ZNRs/poly (3-hexylthiophene) (P3HT). To synthesize CdS/ZNRs, different durations of deposition per cycle from 1 to 9 min were used to deposit CdS via SILAR technique onto ZNRs surface grown via hydrothermal method at low temperature on FTO substrate. In typical procedures, P3HT as donor polymer were spun-coating onto CdS/ZNRs to fabricate IOSC devices, followed by Ag deposition as anode by magnetron sputtering technique. Incorporation of CdS QDs has modified the morphological, structural, and optical properties of ZNRs. Incorporation of CdS QDs onto ZNRs also led to higher open circuit voltage (Voc) and short circuit current density (Jsc) of optimum ZNRs/CdS QDs devices due to the increased interfacial area between ZNRs and P3HT for more efficient exciton dissociation, reduced interfacial charge carrier recombination as a result of lower number of oxygen defects which act as electron traps in ZnO and prolonged carrier recombination lifetime. Therefore, the ZNRs/CdS QDs/P3HT device exhibited threefold higher PCE (0.55%) at 5 min in comparison to pristine ZNR constructed device (0.16%). Overall, our study highlights the potential of ZNRs/CdS QDs to be excellent electron acceptors for high efficiency hybrid optoelectronic devices.

In this article, a simple new technique has been developed for the preparation of ZnO/ZnAl2O4-mixed metal oxide (MMO) as anode materials for visible light dye-sensitized (DS) photodetector using Zn/Al-layered double hydroxide (LDH) as precursor. Subsequently, a detailed correlation between the structural properties of the prepared samples and the photo-responsive behavior of the fabricated DS photodetectors was elucidated. Specifically, it is evidenced that a high surface area of the prepared mesoporous MMO anode materials exhibit excellent dye absorptivity and thus facilitate free electron transfer and increase the photocurrent in the fabricated DS photodetector. A significant bathochromic shift was observed in the optical energy of the prepared MMO samples under the increment of molar ratio, providing a short electron transfer pathway in the optimized Z7A DS photodetector, which in turn demonstrated photo-responsivity and photo-detectivity of 6 mA/W and 1.7 × 10+10 Jones, respectively. This work presents an alternative approach for the design of an eco-friendly MMO-based DS photodetector.