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A solar-driven photoelectrochemical (PEC) cell is emerging as one of the promising clean hydrogen generation systems. Engineering of semiconductor heterojunctions and surface morphologies of photoelectrodes in a PEC cell has been a primitive approach to boost its performance. This study presents that a molybdenum disulfide (MoS2) nanoflakes photoanode on 3-dimensional (3D) porous carbon spun fabric (CSF) as a substrate effectively enhances hydrogen generations due to sufficiently enlarged surface area. MoS2 is grown on CSFs utilizing a hydrothermal method. Among three different MoS2 coating morphologies depending on the amount of MoS2 precursor and hydrothermal growth time, film shape MoS2 on CSFs had the largest surface area, exhibiting the highest photocurrent density of 26.48 mA/cm2 and the highest applied bias photon-to-current efficiency (ABPE) efficiency of 5.32% at 0.43 VRHE. Furthermore, with a two-step growth method of sputtering and a subsequent hydrothermal coating, continuous TiO2/MoS2 heterojunctions on a porous CSF further promoted the photoelectrochemical performances due to their optimized bandgap alignments. Enlarged surface area, enhanced charge transfer, and utilization of visible light enable a highly efficient MoS2/TiO2/CSF photoanode with a photocurrent density of 33.81 mA/cm2 and an ABPE of 6.97 % at 0.87 VRHE. The hydrogen generation amount of the PEC cell with MoS2/TiO2/CSF photoanode is 225.4 μmol/L after light irradiation of 60 s.

Abstract Background No previous studies have quantified tear glucose (TG) levels in dogs or compared changes in TG and blood glucose (BG) concentrations. Objective To quantify TG concentration and evaluate its correlation with BG level in dogs. Methods Twenty repetitive tests were performed in alternate eyes of four dogs, with a minimum washout period of 1 week. Tears and blood were collected at 30‐min intervals with successive glucose injections (1 g/kg) every 30 min. Cross‐correlations of BG and TG levels were assessed. The delay and association between TG and corresponding BG levels were analysed for each dog; samples were collected at 5‐min intervals. The tears were collected using microcapillary tubes. Collected tears and blood were analysed for glucose concentration using a colorimetric assay and commercially available glucometer, respectively. Results The average baseline BG and TG levels were 4.76 ± 0.58 and 0.39 ± 0.04 mmol/L, respectively. Even with highly fluctuating BG levels, a significant cross‐correlation coefficient (r = 0.86, p

The aggregation of zinc oxide nanoparticles leads to an increased absorbance in the ultraviolet-visible region by an induced light scattering effect. Herein, we demonstrate the inhibition of photoconversion activity in ZnO-graphene core-shell quantum dots (QD) (ZGQDs) agglomerated by 4-aminophenol (4-AP) used as a linker. The ZnO-graphene quantum dots (QD) aggregates (ZGAs) were synthesized using a facile solvothermal process. The ZGAs revealed an increased absorbance in the wavelengths between 350 and 750 nm as compared with the ZGQDs. Against expectation, the calculated average photoluminescence lifetime of ZGAs was 7.37 ns, which was 4.65 ns longer than that of ZGQDs and was mainly due to the high contribution of a slow (τ2, τ3) component by trapped carriers in the functional groups of graphene shells and 4-AP. The photoelectrochemical (PEC) cells and photodetectors (PDs) were fabricated to investigate the influence of ZGAs on the photoconversion activity. The photocurrent density of PEC cells with ZGAs was obtained as 0.04 mA/cm2 at 0.6 V, which was approximately 3.25 times lower than that of the ZGQDs. The rate constant value of the photodegradation value of rhodamine B was also decreased by around 1.4 times. Furthermore, the photoresponsivity of the PDs with ZGAs (1.54 μA·mW−1) was about 2.5 times as low as that of the PDs with ZGQDs (3.85 μA·mW−1). Consequently, it suggests that the device performances could be degraded by the inhibition phenomenon of the photoconversion activity in the ZGAs due to an increase of trap sites.