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One-dimensional ZnO nanorods (ZnO NRs) have the edge over other nanostructures due to their unique properties. Current work fabricated ZnO NRs on pre-seeded ITO glass substrate through hydrothermal synthesis using customized hydrothermal set-up. The sources of Zn2+ and OH− ions were supplied continuously from zinc nitrate hexahydrate and hexamethylenetetramine (HMTA), respectively whereby the concentration of both precursors and the temperature of growth solution varied from 0.01 M to 0.05 M and from 80 °C to 120 °C, respectively. The impact of concentration and temperature variation on hydrothermal reaction and corresponding PEC cell performance is discussed. Field emission scanning electron microscopy (FESEM) results revealed that the morphology of prepared ZnO NRs arrays is concentration- and temperature-dependent. X-ray diffraction (XRD) reflected strong orientation along (002) direction for the hexagonal wurtzite ZnO NRs, and the film crystallinity greatly improved when the temperature increased. At optimal concentration and hydrothermal temperature, the ZnO NRs photoanode exhibited a bandgap value of 3.22 eV and achieved an impressive photocurrent density of 0.483 mA/cm2 that was attributed to the ordered rods alignment and improved optical properties. In addition, the electrochemical impedance spectroscopy (EIS) demonstrated optimized one-dimensional (1D) NRs sample showed better charge separation and transfer rate, which was two times larger than ZnO nanoparticles. The present work exhibited better photoelectrochemical performance than the other reported literature showing the high quality of ZnO NRs produced.

Noble metal nanostructures have been widely explored as an effective method to increase photon absorption and charge separation in plasmonic photocatalysis. In this study, we integrated two differe...

In this project, crystalline silver nanowires (AgNWs) are successfully grown using a continuous segmented flow process. The robust relationship among the structural, electrical and optical properties of the AgNWs in the function of the polyvinylpyrrolidone (PVP) chain length is elaborated. A concise carrier transport and a density mechanism are also discussed using a localized conductive atomic force microscopy analysis. The obtained results proved that the AgNWs synthesized using PVP with a chain length of 1.3 M exhibit excellent electrical and optical properties in the form of flexible transparent film with a sheet resistance of 90% at various bending angles. These findings present an alternative approach for production of AgNWs and fabrication of a high flexible transparent electrode.

Crystallinity and band offset alignment of inorganic electron acceptor play a vital role in enhancing the device performance of inverted organic solar cell (IOSC). In this report, homogenous and vertically-aligned chemical treated ZnO nanorods (ZNR) were successfully grown on fluorine-doped tin oxide (FTO) substrate via a fully-solution method. It was found that the morphology of ZnO was fine-tuned from truncated surface to tubular structure under both of the anionic (KOH) and protonic (HCl) treatment. An extraordinary defect quenching phenomenon and hyperchromic energy band edge shift were observed in 0.1 M KOH-treated ZNR proven by the highest (0 0 2) peak detection and the lowest defect density. Compared with the pristine sample, the 0.1 M KOH-treated ZNR device showed a remarkable improvement in power conversion efficiency (PCE) up to 0.32%, signifying the effectiveness of anodic treatment. The robust correlation between the dependency of chemical treated ZNR and the device performance was established. This work elucidates a feasible method towards efficient IOSC devices development.

Charge transport dynamics in ZnO based inverted organic solar cell (IOSC) has been characterized with transient photocurrent spectroscopy and localised photocurrent mapping-atomic force microscopy. The value of maximum exciton generation rate was found to vary from 2.6 × 1027 m−3s−1 (Jsat = 79.7 A m−2) to 2.9 × 1027 m−3s−1 (Jsat = 90.8 A m−2) for devices with power conversion efficiency ranging from 2.03 to 2.51%. These results suggest that nanorods served as an excellent electron transporting layer that provides efficient charge transport and enhances IOSC device performance. The photovoltaic performance of OSCs with various growth times of ZnO nanorods have been analysed for a comparison between AM1.5G spectrum and local solar spectrum. The simulated PCE of all devices operating under local spectrum exhibited extensive improvement with the gain of 13.3–13.7% in which the ZnO nanorods grown at 15 min possess the highest PCE under local solar with the value of 2.82%.

In this work, the photocatalytic performance of Ag3PO4, Nb2O5 and Ag3PO4/Nb2O5 hybrid photocatalysts to degrade methyl orange dye, MO, in an aqueous solution under visible light irradiation was evaluated. The Ag3PO4 and Ag3PO4/Nb2O5 photocatalysts, with various Ag to Nb molar ratios, were prepared using a facile precipitation method. The photocatalysts were characterized by X-ray diffraction, UV–Visible, X-ray Photoelectron, and Photoluminescence spectroscopies. Upon the addition of Ag3PO4, the band gap energy of Nb2O5 decreased from 3.0 eV to 2.7 eV, indicating the possible use of the Ag3PO4/Nb2O5 hybrid photocatalysts under visible light irradiation. All of the prepared Ag3PO4/Nb2O5 catalysts exhibited higher photocatalytic performance than Ag3PO4 in degrading methyl orange dye under 23-watt visible light irradiation. The Ag3PO4/Nb2O5 catalyst, with a mole ratio of 2:1, exhibited the fastest MO degradation rate of 7.3 × 10−2 min−1, which is twice faster than that of Ag3PO4. The catalyst also shows better stability, as it is reusable for up to six experimental cycles while maintaining its photocatalytic activity above 60%.

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.

Metal oxide based optical absorbance gas sensor (MOAGS) exhibits underlying potential to be the most promising energy-saving device with long-term stability and excellent sensing performance. In this work, a self-customized automated MOAGS setup was employed to study the carbon monoxide (CO) gas sensing performance between the hydrothermal synthesized ZnO nanorod (ZNR) and Indium-doped ZnO nanorod (IZNR) operating at room temperature of (25 ± 1)°C. Specifically, it was found that the In 3+ was evenly doped into ZnO lattice which in turn increased the defect density and generated an impurity state within the energy band structure of ZnO. The results showed that 0.04 mol% IZNR exhibited an optimum sensing performance with absolute optical absorbance change (OAC) of 0.067 a.u. under the 10 ppm of CO gas testing environment with fastest respond and recovery time. The dependency of sensing performances to the optical band gap energy alteration and the defect state was evaluated. This work provides a simple and feasible route to develop the room temperate operating MOAGS for hazardous gas detection.

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.

The present study reports a facile method to prepare carbon quantum dots (CQDs) via hydrothermal treatment using human fingernails as a green precursor. Fingernails derived CQDs (FN-CQDs) could selectively detect copper ions (Cu2+) at the concentration as low as 1 nM. Different weightage of FN-CQDs (30 wt%, 40 wt% and 50 wt%) were coupled with pure graphitic carbon nitride (g-C3N4) to remove 2,4-dicholorophenol (2,4-DCP) under sunlight irradiation. The composite loaded with 50 wt% of FN-CQD removed 100 % of 2,4-DCP in 75 min, which was almost 2 times higher than g-C3N4. The photocatalytic performance was in agreement with ultraviolet–visible diffuse reflectance spectra (UV–vis DRS) in which the photosensitizing effect was significantly exerted by 50 wt% of CQDs. In the presence of FN-CQDs, g-C3N4 was sensitized by sunlight with an average light intensity of ∼ 937 × 100 lx to donate more electrons for the generation of oxidizing radicals. Excessive loading of FN-CQDs (up to 50 wt%) created trap state that decreased the charge carrier transport in FN-CQDs/g-C3N4(50). Such drawbacks did not affect the overall performance of FN-CQDs/g-C3N4(50). The higher loading of FN-CQDs exerted stronger photosensitizing effects to overcome the limitation of high recombination rate of charge carriers and lower surface area. FN-CQDs could act as photosensitizer to increase the light absorption range to generate more electron and holes. It also served as electron reservoir for the reduction of oxygen molecule to produce superoxide anion radical ( O2−). Scavenging tests identified that O2− was the most active radical in the photodegradation of 2,4-DCP.

Highly oriented ZnO nanorod was successfully synthesised on Ag nanoseed coated FTO substrate via a microwave hydrolysis approach. It was found that the morphology and the optical properties of the ZnO nanorod are strongly influenced by the power of the microwave irradiation used during the growth process. The aspect ratio of the nanorods changed from high to low with the increasing of microwave power. It was also found that the optical band gap of the ZnO nanorod red shifted with the increasing of the microwave power, reflecting an excellent tune ability of the optical properties of ZnO nanorods. The photocatalytic activity of these unique nanorod was evaluated by a dehydrogenation process of isopropanol to acetone in the presence of ZnO nanorod. It was found that the ZnO nanorod exhibited an excellent catalytic performance by showing an ability to accelerate the production of 0.031 mol L−1 of acetone within only 35 min or 0.9 mmol L−1 min−1 from isopropyl alcohol dehydrogenation. It was almost no conversion from isopropyl alcohol when ZnO nanorods was absence during the reaction. In this report, a detailed mechanism of ZnO nanorod formation and the relationship between morphology and optical energy band gap are described.

Surface modification in nanostructures enables a thorough control on intrinsic properties, surface activity and enhancement of their usefulness in several device applications. The crystal growth and design in a low temperature regime (

The controllable growth of metal sulfide–metal oxide based nanomaterials with a tunable band gap structure is vital in the fabrication of new generation optoelectronic devices. In this paper, two-dimensional hierarchical CdS/ZnO nanorod arrays were successfully grown via a low temperature hydrothermal-SILAR method. A concise mechanism related to the surface and band gap modification on the CdS/ZnO nanorods was investigated under various CdS deposition cycles (N). The diameter and surface roughness properties of the sample were found to be linearly dependent on the value of N. A bathochromic shift in the optical energy band gap revealed the quantum size effects of the CdS/ZnO nanorods, as well as the induced interface band state and energy band split in the ZnO band state. An impressive improvement in the crystallinity of the sample was also observed under the CdS treatment. The correlation between the optical band gap and photovoltaic efficiency was evaluated. The results proved that the ZnO nanorod/CdS devices exhibited a threefold higher power conversion efficiency in comparison to a pristine ZnO nanorod device.

A simple low-temperature solution processed bismuth-doped ZnO nanorods (NRs) and poly(3-hexylthiophene) (P3HT) were used as electron acceptor and donor, respectively, in a hybrid inorganic–organic photovoltaic system. Controlling Bi precursor concentration via solution processing (hydrothermal method) plays an important role in altering the morphology, structure, and intrinsic defects of ZnO NRs. Interstitial doping of Bi–Bi2O3 into ZnO (BiZO) NRs results in simultaneous improvement of the open circuit voltage and short circuit current density primarily due to prolonged charge carrier recombination lifetime, increased donor–acceptor interfacial areas with efficient exciton dissociation, and charge carrier mobility. As a result, the power conversion efficiency of the 2 wt % BiZO NRs-P3HT device was significantly enhanced by 55% compared with that of the pristine device. Overall, our study highlighted the immense potential of BiZO NRs as an excellent electron acceptor for fabrication of hybrid optoelectroni...

Anion passivation effect on metal-oxide nano-architecture offers a highly controllable platform for improving charge selectivity and extraction, with direct relevance to their implementation in hybrid solar cells. In current work, we demonstrated the incorporation of fluorine (F) as an anion dopant to address the defect-rich nature of ZnO nanorods (ZNR) and improve the feasibility of its role as electron acceptor. The detailed morphology evolution and defect engineering on ZNR were studied as a function of F-doping concentration (x). Specifically, the rod-shaped arrays of ZnO were transformed into taper-shaped arrays at high x. A hypsochromic shift was observed in optical energy band gap due to the Burstein-Moss effect. A substantial suppression on intrinsic defects in ZnO lattice directly epitomized the novel role of fluorine as an oxygen defect quencher. The results show that 10-FZNR/P3HT device exhibited two-fold higher power conversion efficiency than the pristine ZNR/P3HT device, primarily due to the reduced Schottky defects and charge transfer barrier. Essentially, the reported findings yielded insights on the functions of fluorine on (i) surface –OH passivation, (ii) oxygen vacancies (Vo) occupation and (iii) lattice oxygen substitution, thereby enhancing the photo-physical processes, carrier mobility and concentration of FZNR based device.