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In this study, we have prepared cobalt selenide (CoSe2) due to its useful aspects from a catalysis point of view such as abundant active sites from Se edges, and significant stability in alkaline conditions. CoSe2, however, has yet to prove its functionality, so we doped palladium oxide (PdO) onto CoSe2 nanostructures using ultraviolet (UV) light, resulting in an efficient and stable water oxidation composite. The crystal arrays, morphology, and chemical composition of the surface were studied using a variety of characterization techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared (FTIR) spectroscopy. It was also demonstrated that the composite systems were heterogeneous in their morphology, undergoing a shift in their diffraction patterns, suffering from a variety of metal oxidation states and surface defects. The water oxidation was verified by a low overpotential of 260 mV at a current density of 20 mA cm(-2) with a Tafel Slope value of 57 mV dec(-1). The presence of multi metal oxidation states, rich surface edges of Se and favorable charge transport played a leading role towards water oxidation with a low energy demand. Furthermore, 48 h of durability is associated with the composite system. With the use of PdO and CoSe2, new, low efficiency, simple electrocatalysts for water catalysis have been developed, enabling the development of practical energy conversion and storage systems. This is an excellent alternative approach for fostering growth in the field. Funding Agencies|Ajman University [2022-IRG-HBS-5]; National Natural Science Foundation of China [NSFC 51402065, 51603053]

In this study, we have used cotton silk as a source of abundant hydroxyl groups for the fast nucleation/growth of cobalt oxide (Co3O4) nanowires via a hydrothermal method. The crystal planes of the Co3O4 nanowires well matched the cubic phase. The as-synthesized Co3O4 nanowires mainly contained cobalt and oxygen elements and were found to be highly sensitive towards uric acid in 0.01 M phosphate buffer solution at pH 7.4. Importantly, the Co3O4 nanowires exhibited a large surface area, which was heavily utilized during the immobilization of the enzyme uricase via a physical adsorption method. The potentiometric response of the uricase-immobilizing Co3O4 nanowires was measured in the presence of uric acid (UA) against a silver/silver chloride (Ag/AgCl) reference electrode. The newly fabricated uric acid biosensor possessed a low limit of detection of 1.0 +/- 0.2 nM with a wide linear range of 5 nM to 10 mM and sensitivity of 30.6 mV dec(-1). Additionally, several related parameters of the developed uric acid biosensor were investigated, such as the repeatability, reproducibility, storage stability, selectivity, and dynamic response time, and these were found to be satisfactory. The good performance of the Co3O4 nanowires was verified based on the fast charge-transfer kinetics, as confirmed via electrochemical impedance spectroscopy. The successful practical use of the uric acid biosensor was demonstrated based on the recovery method. The observed performance of the uricase-immobilizing Co3O4 nanowires revealed that they could be considered as a promising and alternative tool for the detection of uric acid under both in vitro and in vivo conditions. Also, the use of cotton silk as a source of abundant hydroxyl groups may be considered for the remarkably fast nucleation/growth of other metal-oxide nanostructures, thereby facilitating the fabrication of functional electrochemical devices, such as batteries, water-splitting devices, and supercapacitors. Funding Agencies|King Saud University, Riyadh, Saudi Arabia [RSP-2022/79]

The present study is focused on yogurt as a simple, inexpensive, abundant, and green source for the preparation of luminescent carbon material for enhancing the photodegradation of methylene blue (MB). It introduces an ecological and sustainable approach for the large-scale production of carbon material using the direct thermal annealing of yogurt in a muffle furnace. The size of the as-prepared carbon material is about 200-300 nm, with average particle size distribution of 355 nm. The material exhibits clear luminescence under illumination with ultraviolet light. The synthesized carbon material shows an outstanding degradation functionality of MB under the irradiation of ultraviolet (UV) light in aqueous media. Various dye degradation parameters such as initial dye concentration, catalyst dose, pH of dye solution, and scavenger effects have been investigated. The optimum MB concentration was found to be 2.3 × 10

In this study, we have used a mild pyrolytic process for the synthesis of luminescent carbon material from phalsa (Grewia asiatica Linn) and utilized it for the photodegradation of methylene blue (MB) in aqueous solution under the irradiation of ultraviolet (UV) light. The carbon material was found to be graphitic in nature and with carbon dot-like properties as demonstrated by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), dynamic light scattering (DLS), and UV-visible techniques. The prepared carbon material was further studied for the elucidation of functional groups through Fourier transform infra-red (FTIR) spectroscopy. The carbon material exhibits the nanostructured phase which makes it a high surface area material for useful surface reactions. Different photodegradation aspects were investigated, such as initial dye concentration, catalyst dose, effect of pH of dye solution, reusability, electrochemical active surface area (ECSA), and charge transfer and scavenger. Optimum conditions of 15 mg carbon material, initial dye concentration of 2.3 × 10−5 M solution, and pH 5 of dye solution gave the highest outperformance degradation efficiency. The degradation mechanism of MB in aqueous solution was dominated by the hydroxyl radicals as verified by the scavenger study. The reaction kinetics of MB degradation was followed by the pseudo first order kinetics and highest values of rate constants in the low initial dye concentration and the acidic pH of the MB solution. Significantly, the carbon material prepared from phalsa was found to be highly stable, as proven by the reusability experiments. Furthermore, the high ECSA and low charge transfer resistance of carbon material enabled it to have better performance. The use of mild pyrolytic process for the preparation of high performance luminescent carbon material from the biomass could be a great roadmap for the synthesis of a new generation of carbon materials for a wide range of applications including bio-imaging, catalysis, energy conversion and environmental applications.

The present study describes the effect of hydrolysis of polyethyleneimines in water/ethanol mixture on the morphology of the cobalt oxide (Co3O4), used as the main sensor component. The structure of the generated Co3O4 nanocrystals is consistent with a well-defined cubic phase crystallography, having only cobalt and oxygen elements. Developing simple, low-cost, sensitive, and selective cholesterol biosensors is essential for accurate monitoring of cholesterol to avoid cardiovascular diseases. These nanocrystals exhibit large surfaces suitable for facile and high loading of cholesterol oxidase enzyme through the physical adsorption method. Then, the fabricated cholesterol oxidase/ Co3O4 nanocrystals composite was implemented for potentiometric detection of cholesterol in 10 mM phosphate buffer of pH 7.3. Importantly, the presented cholesterol biosensor revealed a wide linear range of 0.005 mM to 3.0 mM with a limit of detection (LOD) of 0.001 mM. Additionally, the sensitivity of biosensor was estimated around 60 mVdec−1. The selectivity, stability, reproducibility, and repeatability were also observed as satisfactory. The dynamic response of the proposed method demonstrated a fast response time of less than 1 s. Furthermore, the successive addition method confirmed a remarkably stable response towards various cholesterol concentrations. Thus, the developed cholesterol oxidase/ Co3O4 nanocomposite may be used as an efficient alternative method to monitor low cholesterol concentrations form real samples.

The gout is mainly found due to accumulation of uric acid crystals into the joints which produces the inflammatory symptoms. Thus, it is highly demanded to detect uric acid from our body. Herein, we prepare a composite material of cobalt oxide (Co3O4) with hydroxide functionalized multi-walled carbon nanotubes (MWCNTs) by hydrothermal method. The composite material is used for the modification of glassy carbon electrode (GCE) and investigated for the electrochemical determination of uric acid (UA). The analytical techniques such as scanning electron microscopy (SEM), powder X-ray diffraction (XRD), energy dispersive spectroscopy (EDS) and Fourier Infra-red spectroscopy (FTIR) are used to characterize the composite material. The Co3O4 exhibits a dendrite morphology and very well chemically coupled with MWCNTs. The elemental analysis confirms the presence of cobalt (Co), oxygen (O) and carbon (C) as main constituent of the composite material. The Co3O4 exhibitsa cubic unit cell crystallography in the composite system. The FTIR study reveals the characteristic bands of Co–O bands in the composite material. The cyclic voltammetry isused to study the electrochemical properties of prepared materials. The composite sample with highest percentage of MWCNTs shows an excellent electrochemical activity towards the oxidation of uric acid in phosphate buffer solution pH 7.3. The enzyme free uric acid sensor possesses a linear range of 0.1 mM to 3 mM with a quantified limit of detection of 0.005 ± 0.0023 mM. The modified electrode is stable, selective, and very sensitive towards uric acid, therefore it may be used for the monitoring of uric acid from clinical samples. The proposed composite material can be of great interest for energy and biomedical fields.

In this study, we synthesized hybrid systems based on manganese oxide@zinc oxide (Mn

The successful monitoring of the anticancer drugs using nanostructured materials is very important but very challenging task. The uniform and controlled synthesis of metal oxide nanoparticles is highly needed in order to enhance the catalytic activity which could result into the development of sensitive and selective electrochemical devices. For this purpose, we have used a simple approach by involving polyaniline (PANI) as a sacrificing template for the growth of uniform and controlled Co3O4 nanoparticles by hydrothermal method. The structure, shape, composition and phase purity were studied by scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), X-ray diffraction (XRD) and Fourier transform Infrared (FTIR) techniques. The average size of Co3O4 nanoparticles was found below 50 nm. The cubic crystallography is confirmed for the Co3O4 nanoparticles. The electrochemical properties of PANI-assisted Co3O4 nanoparticles for methotrexate MTX drug were evaluated by cyclic voltammetry (CV) and linear sweep voltammetry (LSV) in Britton–Robinson buffer (BRB) of pH 3.5. The PANI-assisted Co3O4 nanoparticles were found highly sensitive for the MTX drug and exhibited a linear range from 5 to 75 µM of MTX and limit of detection for the modified electrode was estimated 1.98 µM. The proposed electrochemical sensor is low cost, simple, highly sensitive and selective towards MTX detection. The synthetic methodology of using the conducting polymer as a sacrificing template for the growth of controlled Co3O4 nanoparticles can be utilized for the wide range of electrochemical applications.

We have fabricated ZnO nano rods by hydrothermal method and successively doped them with tin (Sn) using different concentrations of 25, 50, 75 and 100 mg of tin chloride. XRD of the fabricated structures showed that ZnO possess hexagonal wurtzite phase. Scanning electron microscopy (SEM) was used to explore the morphology and it shows nanorod like morphology for all samples and no considerable change in the structural features were found. The dimension of nanorod is 200 to 300 nm. The doped materials were then investigated for their photo catalytic degradation of environmental pollutant Rhodamine B. The performance of doped ZnO is compared with the pristine ZnO. Scanning electron microscopy (SEM) was used to explore the morphology and it shows nanorod like morphology for all samples and no considerable change in the structural features were found. The dimension of nanorod is 200 to 300 nm. XRD of the fabricated structures showed that ZnO possess hexagonal wurtzite phase. Photo catalytic activity of rhodamine B was investigated under UV light and a maximum degradation efficiency of 85% was obtained. The optical property reveals the reduction in band gap of upto 17.14% for 100 mg Sn doped ZnO. The degradation is followed by the pseudo order kinetics. The produced results are unique in terms of facile synthesis of Sn doped ZnO and excellent photo degradation efficiency, therefore these materials can be used for other environmental applications.

Herein, we describe a cost-effective, efficient, sustainable, and environmentally friendly pyrolytic method for the synthesis of highly active carbon materials from Carica papaya fruit juice for the photodegradation of various pollutants, such as methylene blue (MB), in aqueous solutions using ultraviolet (UV) light. Various analytical techniques were used to examine the morphology, crystal quality, functional group chemistry, particle size distribution, and optical properties of the materials. For evaluating the performance of the newly prepared carbon material, various photocatalyst parameters were investigated, including initial dye concentration, catalyst dose, pH of dye solution, cyclic stability, and scavenger studies. The obtained findings attest that the optimal degradation efficiency of carbon material for high MB concentrations (2.3 × 10−5 M) is around 98.08%, whereas at low concentrations of MB (1.5 × 10−5 M) it reaches 99.67%. Degradation kinetics indicate that MB degrades in a first-order manner. Importantly, as the pH of the dye solution was adjusted to ~11, the degradation rate increased significantly. The scavenger study indicated that hydroxyl radicals were the predominant species involved in the degradation of MB. In addition, active surface site exposure and charge transfer were strongly associated with efficient MB degradation. On the basis of its performance, this newly developed carbon material may prove to be an excellent alternative and promising photocatalyst for wastewater treatment. Furthermore, the synthetic approach used to produce carbon material from Carica papaya fruit juice may prove useful for the development of a new generation of photoactive materials for environmentally friendly applications, as well as for the production of hydrogen from solar energy.

The chemical coupling of NiO nanostructures with thermally treated multiwall carbon nanotubes (MWCNTs) is not reported as it provides an enhanced dispersion of composite material in water. The dispersion of MWCNTs has been considered a big challenge. For this purpose, we first thermally treated MWCNTs at 1000°C in air for 30 min. Then, thermally treated MWCNTs were chemically coupled with NiO nanostructures by a hydrothermal method. The material characterization in terms of structure, morphology, and composition is well studied by different analytical techniques. The NiO composite (sample 2) with highest weight of MWCNTs had a leaf-like morphology and it exhibits a cubic phase of NiO. Cyclic voltammetry (CV) was used to study the electrochemical activity of prepared composite material towards the oxidation of uric acid in the phosphate buffer solution of pH 7.0. Sample 2 showed a well-behaved anodic peak with enhanced peak current and exhibited a linear range from 0.01 mM to 2.5 mM for uric acid with a low limit of detection 0.001mM. Sample 2 was found to be very selective under the environment of competing interferents such as urea, glucose, lactic acid and ethanol. This sample exhibits significant stability, thus it is a potential protocol for the monitoring of uric acid from real samples. This study provides a low-cost platform for the fabrication of efficient materials for various applications such as batteries, fuel cells and water splitting.

In this study, simple, new and functional silky nanostructures of Co3O4 are prepared by hydrothermal method. These nanostructures are successfully used for the enzyme free sensing of uric acid in 0.1 M phosphate buffer solution of pH 7.3. Physical characterization experiments were carried out to explore the morphology, composition and crystalline phase of the newly prepared Co3O4 nanostructures. Scanning electron microscopy (SEM) shows a silk like morphology and energy dispersive spectroscopy (EDS) revealed the presence of Co and O as the main elements. Powder X-ray diffraction (XRD) demonstrates a cubic crystallography with well resolved diffraction patterns. The electrochemical activity of these silky Co3O4 nanostructures was evaluated by cyclic voltammetry (CV) in a 0.1 M phosphate buffer solution at pH 7.3. The high purity and unique morphology of Co3O4 shows a highly sensitive and selective response towards the non-enzymatic sensing of uric acid. This uric acid sensor exhibits a linear range of 0.5 mM to 3.5 mM uric acid and a 0.1 mM limit of detection. The anti-interference capability of this uric acid sensor was monitored in the presence of common interfering species. Furthermore, electrochemical impedance spectroscopy confirms a low charge transfer resistance value of 5.11 K Ω cm2 for silky Co3O4 nanostructures which significantly supported the CV results. The proposed modified electrode is stable, selective and reproducible which confirms its possible practical use. Silky Co3O4 nanostructures can be of great importance for diverse electrochemical applications due to their excellent electrochemical activity and large surface area.

In this study, a wet chemical method was used to produce iron-doped CuO nanostructures. Cyclic voltammetry was employed to record sensor signals in a saline phosphate buffer solution of pH 7.3. Iron added into CuO nanostructures contributed electrons to the conduction band of CuO, showing a well-resolved electro-oxidation peak for uric acid. The developed sensor exhibits a wide linear range of uric acid concentrations from 0.05 mM to 4 mM. The limit of detection for the sensor was found to be 0.01 mM. The sensor is highly selective, sensitive, and stable. The results of the in vitro analysis of uric acid motivated the researchers to measure the uric acid from the marine shellfish Perna viridis and razor clam Solen dactylus. The obtained results reveal that the proposed sensor will help to avoid the gout and could be used as an early safeguard of human health.

International audience; In this study, we have successfully doped sulfide (S-2) and chloride (Cl-1) simultaneously into ZnO by hydrothermal method. The structure, morphology, composition and optical properties of the prepared S-Cl doped ZnO nanostructures were investigated by x-ray diffraction (XRD), scanning electron microscopy (SEM), scanning transmission electron microcopy (STEM), energy dispersive spectroscopy(EDX) and UV-visible (UV-Vis) spectroscopy techniques. After, doping of both S and Cl into ZnO no significant alteration in the nanorod morphology was noticed. The wurtizite crystal structure of ZnO was retained with a red shift in the 2Ɵ towards high angle. The XRD results are supported by the high resolution transmission electron microscopy. The elemental analysis revealed a successful doping of S and Cl into ZnO structure. Importantly, the optical band gap of ZnO was decreased 2.9 eV upon doping of S and Cl ions. Thus, the nonmetal doping via S and Cl has significantly enhanced the photocatalytic properties of ZnO towards methylene blue (MB) due to high density of active sites and decreased charge recombination rate of electron-hole pairs. The photo-degradation efficiency towards MB reached 99.64% upon using S and Cl doped ZnO photocatalyst using optimum dose of 15 mg and initial dye concentration of 1.87×10-6M. The use of simultaneous nonmetal doping concept could of great importance for the preparation of other nanostructured materials and their use in potential applications like solar cells, and photoelectrochemical water splitting.

In this study, cupric oxide–polyaniline (CuO–PANI) composite was prepared by two-step methodology. First step was involved in the synthesis of PANI by the chemical oxidative polymerization of aniline in the presence of (NH4)2S2O8 as an oxidizing agent. In the second step, 25 mg of PANI was used as template for making a composite with CuO by hydrothermal method. The crystalline phase, morphology and composition of composite material were investigated by the powder X-ray diffraction and scanning electron microscopy techniques. The composite material contained the monoclinic phase of CuO and some poor diffraction patterns of PANI. The composite material exhibits a flower-like morphology. The CuO–PANI composite was deposited on the glassy carbon electrode and used for the electrochemical determination of hydrochlorothiazide (HCT) in Britton–Robinson (B–R) buffer pH 4.0 by the cyclic voltammetry. The HCT has shown a well resolved anodic peak at 1.20 V against Ag/AgCl reference electrode. The electrode kinetics was diffusion controlled and irreversible in nature. The CuO–PANI composite possessed a linear from 8 to 52 µM HCT concentration with a regression coefficient of 0.99. The limit of detection of the CuO–PANI composite was obtained as 0.8 µM for the HCT. The CuO–PANI composite is highly selective, stable and sensitive for the HCT. Therefore, we believe that the newly prepared CuO–PANI composite material can be useful for the different electrochemical applications.

Developing highly active nonprecious metal and binder free bifunctional electrocatalysts for water splitting is a challenging task. In this study, we used a simple strategy to deposit a nickel iron layered double hydroxide (NiFeLDH) onto cobalt oxide (Co3O4) nanowires. The cobalt oxide nanowires are covered with thin nanosheets of NiFeLDH forming a core shell structure. The Co3O4 nanowires contain the mixed oxidation states of Co2+ and Co3+, and the surface modification of Co3O4 nanowires has shown synergetic effects due to there being more oxygen defects, catalytic sites, and enhanced electronic conductivity. Further, the core shell structure of Co3O4 nanowires demonstrated a bifunctional activity for water splitting in 1 M KOH aqueous solution. From the hydrogen evolution reaction (HER), a current density of 10 mA cm - 2 is achieved at a potential of - 0.303 V vs. reversible hydrogen electrode (RHE). Meanwhile for the case of the oxygen evolution reaction (OER), a current density of 40 mA cm - 2 is measured at a potential of 1.49 V vs. RHE. Also, this electrocatalyst has shown a considerable long- term stability of 15 h for both the HER and the OER. Importantly, electrochemical impedance spectroscopy has shown that the NiFeLDH integration onto cobalt oxide exhibited around 3 fold decrease of charge transfer resistance for both the HER and the OER in comparison with pristine cobalt oxide films, which reveals an excellent electrocatalytic activity for both faradaic processes. All these results confirm that the proposed electrocatalyst can be integrated into an efficient water splitting system.

The design of efficient nonprecious catalysts for the hydrogen evolution reaction (HER) or the oxygen evolution reaction (OER) is a necessary, but very challenging task to uplift the water-based economy. In this study, we developed a facile approach to produce porous carbon from the dehydration of sucrose and use it for the preparation of nanocomposites with cobalt oxide (Co3O4). The nanocomposites were studied by the powder X-ray diffraction and scanning electron microscopy techniques, and they exhibited the cubic phase of cobalt oxide and porous structure of carbon. The nanocomposites showed significant OER activity in alkaline media, and the current densities of 10 and 20 mA cm(-2) could be obtained at 1.49 and 1.51 V versus reversible hydrogen electrode (RHE), respectively. The impedance study confirms favorable OER activity on the surface of the prepared nanocomposites. The nanocomposite is cost-effective and can be capitalized in various energy storage technologies.

In this study, a simple approach was used to produce nonprecious, earth abundant, stable and environmentally friendly NiCo2O4/CuO composites for the oxygen evolution reaction (OER) in alkaline media. The nanocomposites were prepared by a low temperature aqueous chemical growth method. The morphology of the nanostructures was changed from nanowires to porous structures with the addition of CuO. The NiCo2O4/CuO composite was loaded onto a glassy carbon electrode by the drop casting method. The addition of CuO into NiCo2O4 led to reduction in the onset potential of the OER. Among the composites, 0.5 grams of CuO anchored with NiCo2O4 (sample 2) demonstrated a low onset potential of 1.46 V vs. a reversible hydrogen electrode (RHE). A current density of 10 mA cm−2 was achieved at an over-potential of 230 mV and sample 2 was found to be durable for 35 hours in alkaline media. Electrochemical impedance spectroscopy (EIS) indicated a small charge transfer resistance of 77.46 ohms for sample 2, which further strengthened the OER polarization curves and indicates the favorable OER kinetics. All of the obtained results could encourage the application of sample 2 in water splitting batteries and other energy related applications.

Herein, we propose for the first time visible light photodetector based on n-type ZnO nanorods decorated with p-type Co3O4 nanowires. The heterojunction was fabricated on fluorine doped tin oxide (FTO) glass substrate by low temperature aqueous chemical growth method. ZnO exhibits nanorod morphology and cobalt oxide possesses nanowire shape with sharp tail. Energy dispersive spectroscopy (EDS) confirmed the presence of Zn, O, and Co elements in the heterojunction. ZnO and Co3O4 have hexagonal and cubic phases, respectively, as confirmed by XRD. The dense and perpendicular ZnO nanorods are acting as a scattering layer for visible light, while Co3O4 nanowires act as a visible-light absorber. The all oxide p-n junction can operate as visible light photodetector. Furthermore, the heterojunction also shows a reproducible and fast response for the detection of visible light. Optimization of the device is needed (presence of buffer layers, tuning a thickness of the optical absorber) to improve its functionalities.

The successful monitoring of the anticancer drugs using nanostructured materials is very important but very challenging task. Beside this, uniform and ultra-small size of metal oxide nanoparticles is highly needed in order to enhance the catalytic activity which could result into the development of sensitive and selective electrochemical sensors for methotrexate (MTX). For this purpose, we have used a simple approach involving the polyaniline (PANI) as a sacrificing template for the growth of uniform and ultra-small Co3O4 nanoparticles by hydrothermal method. The structure, shape, composition and phase purity were studied by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD) and Fourier transform Infrared (FTIR) techniques. The average size of Co3O4 nanoparticles was below 50 nm. The cubic crystallography is confirmed for the Co3O4 nanoparticles. The electrochemical properties of PANI assisted Co3O4 nanoparticles for MTX drug was evaluated by cyclic voltammetry (CV) and linear sweep voltammetry (LSV) in Britton–Robinson buffer (BRB) of pH 3.5. The PANI assisted Co3O4 nanoparticles were found highly sensitive for the MTX drug and exhibited a linear range from 5-75µM of MTX and limit of detection for the modified electrode was estimated 1.98µM. The proposed electrochemical sensor is low cost, simple, highly sensitive and selective towards MTX detection. The synthetic methodology using the conducting polymer as a sacrificing template for the growth of controlled and ultra-small Co3O4 nanoparticles can be utilized for the wide range of electrochemical applications.

Herein, we propose for the first time visible light photodetector based on n-type ZnO nanorods decorated with p-type Co3O4 nanowires. The heterojunction was fabricated on fluorine doped tin oxide (FTO) glass substrate by low temperature aqueous chemical growth method. ZnO exhibits nanorod morphology and cobalt oxide possesses nanowire shape with sharp tail. Energy dispersive spectroscopy confirmed the presence of Zn, O, and Co elements in the heterojunction. ZnO and Co3O4 have hexagonal and cubic phases, respectively, as confirmed by XRD. The dense and perpendicular ZnO nanorods are acting as a scattering layer for visible light, while Co3O4 nanowires act as a visible-light absorber. The all oxide p–n junction can operate as visible light photodetector. Furthermore, the heterojunction also shows a reproducible and fast response for the detection of visible light. Optimization of the device is needed (presence of buffer layers, tuning a thickness of the optical absorber) to improve its functionalities.

The design of the earth‐abundant, nonprecious, efficient, and stable electrocatalysts for efficient hydrogen evolution reaction (HER) in alkaline media is a hot research topic in the field of renewable energies. A heterostructured system composed of MoSx deposited on NiO nanostructures (MoSx@NiO) as a robust catalyst for water splitting is proposed here. NiO nanosponges are applied as cocatalyst for MoS2 in alkaline media. Both NiO and MoS2@NiO composites are prepared by a hydrothermal method. The NiO nanostructures exhibit sponge‐like morphology and are completely covered by the sheet‐like MoS2. The NiO and MoS2 exhibit cubic and hexagonal phases, respectively. In the MoSx@NiO composite, the HER experiment in 1 m KOH electrolyte results in a low overpotential (406 mV) to produce 10 mA cm−2 current density. The Tafel slope for that case is 43 mV per decade, which is the lowest ever achieved for MoS2‐based electrocatalyst in alkaline media. The catalyst is highly stable for at least 13 h, with no decrease in the current density. This simple, cost‐effective, and environmentally friendly methodology can pave the way for exploitation of MoSx@NiO composite catalysts not only for water splitting, but also for other applications such as lithium ion batteries, and fuel cells., A.V. and Z.H.I. acknowledge Knut and Alice Wallenberg Foundation, the Kempe Foundation, and the LTU Lab fund program for partial funding. J.A. and P.Y.T. acknowledge funding from Generalitat de Catalunya 2017 SGR 327 and JRM 2017 SGR 1246. J.A., P.Y.T., and J.R.M. acknowledge the Spanish MINECO project ENE2017‐85087‐C3. ICN2 acknowledges support from the Severo Ochoa Programme (MINECO, Grant no. SEV‐2013‐0295‐17‐1). ICN2 and IREC are funded by the CERCA Programme/Generalitat de Catalunya. Part of the present work was performed in the framework of Universitat Autònoma de Barcelona Materials Science PhD program.

In this research work, we have produced a composite material consisting titanium dioxide (TiO2) and zinc oxide (ZnO) nanostructures via precipitation method. Scanning electron microscopy (SEM) study has shown the mixture of nanostructures consisting nanorods and nano flower. Energy dispersive spectroscopy (EDS) study has confirmed the presence of Ti, Zn and O as main elements in the composite. X-ray diffraction (XID) study has revealed that the successful presence of TiO2 and ZnO in the composite. The composite material exhibits small optical energy band gap which led to reduction of the charge recombination rate of electron-hole pairs. The band gap for the composite TiO2/ZnO samples namely 1, 2, 3 and 4 is 3.18, 3.00, 2.97 and 2.83 eV respectively. Small optical bandgap gives less relaxation time for the recombination of electron and hole pairs, thus favorable photodegradation is found. The degradation efficiency for the TiO2/ZnO samples for methylene blue in order of 55.03%, 75.7%, 85.14% and 90.08% is found for the samples 1, 2, 3 and 4 respectively. The proposed study of titanium dioxide addition into ZnO is facile and inexpensive for the development of efficient photocatalysts. This can be capitalized at large scale for the energy and environmental applications. Funding Agencies|King Saud University, Riyadh, Saudi ArabiaKing Saud University [RSP-2020/79]

In this study, simple, new and functional silky nanostructures of Co

The occurrence of available energy reservoirs is decreasing steeply, therefore we are looking for an alternative and sustainable renewable energy resources. Among them, hydrogen is considered as gr ...

There are many challenges associated with the fabrication of efficient, inexpensive, durable and very stable nonprecious metal catalysts for the hydrogen evolution reaction (HER). In this study, we have designed a facile strategy by tailoring the concentration of precursors to successfully obtain nickel-cobalt bimetallic sulfide (NiCo

Designing a facile and low-cost methodology to fabricate earth-abundant catalysts is very much needed for a wide range of applications. Herein, a simple and straightforward approach was developed to tune the electronic properties of cobalt oxide nanostructures by doping them with nickel and then using them to catalyze the oxygen evolution reaction (OER) in an aqueous solution of 1.0 M KOH. The addition of a nickel impurity improved the conductivity of the cobalt oxide, and further increased its activity towards the OER. Analytical techniques such as scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and powder X-ray diffraction (XRD) were used to investigate, respectively, the morphology, composition and crystalline structure of the materials used. The nickel-doped cobalt oxide material showed randomly oriented nanowires and a high density of nanoparticles, exhibited the cubic phase, and contained cobalt, nickel and oxygen as its main elements. The nickel-doped cobalt oxide also yielded a Tafel slope of 82 mV dec

Designing a facile and low-cost methodology to fabricate earth-abundant catalysts is very much needed for a wide range of applications. Herein, a simple and straightforward approach was developed to tune the electronic properties of cobalt oxide nanostructures by doping them with nickel and then using them to catalyze the oxygen evolution reaction (OER) in an aqueous solution of 1.0 M KOH. The addition of a nickel impurity improved the conductivity of the cobalt oxide, and further increased its activity towards the OER. Analytical techniques such as scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and powder X-ray diffraction (XRD) were used to investigate, respectively, the morphology, composition and crystalline structure of the materials used. The nickel-doped cobalt oxide material showed randomly oriented nanowires and a high density of nanoparticles, exhibited the cubic phase, and contained cobalt, nickel and oxygen as its main elements. The nickel-doped cobalt oxide also yielded a Tafel slope of 82 mV dec(-1) and required an overpotential of 300 mV to reach a current density of 10 mA cm(-2). As an OER catalyst, it was shown to be durable for 40 h. Electrochemical impedance spectroscopy (EIS) analysis showed a low charge-transfer resistance of 177.5 ohms for the nickel-doped cobalt oxide, which provided a further example of its excellent OER performance. These results taken together indicated that nickel doping of cobalt oxide can be accomplished via a facile approach and that the product of this doping can be used for energy and environmental applications.

In this study, zinc oxide (ZnO) nanorods are doped with copper by low temperature aqueous chemical growth method using different concentrations of copper 5 mg, 10 mg, 15 mg and 20 mg and labeled as sample 1, 2, 3 and 4 respectively. The morphology and phase purity of nanostructures was investigated by scanning electron microscopy, and powder X-ray diffraction techniques. The optical characterization was carried out through UV–Vis spectrophotometer. The band gap of coper doped ZnO has brought reduction at 250–600 nm and it indicates the fewer time for the recombination of electron and hole pairs, thus enhanced photo degradation efficiency is found. ZnO exhibits nanorods like shape even after the doping of copper. The photo degradation efficiency for the two chronic dyes such as methyl orange MO and methylene blue MB was found to be 57.5% and 60% respectively for a time of 180 mints. This study suggests that the copper impurity in ZnO can tailor its photocatalytic activity at considerable rate. The proposed photo catalysts are promising and can be used for the waste water treatment and other environmental applications.

There are many challenges associated with the fabrication of efficient, inexpensive, durable and very stable nonprecious metal catalysts for the hydrogen evolution reaction (HER). In this study, we have designed a facile strategy by tailoring the concentration of precursors to successfully obtain nickel–cobalt bimetallic sulfide (NiCo2S4) using a simple hydrothermal method. The morphology of the newly prepared NiCo2S4 comprised a mixture of microparticles and nanorods, which were few microns in dimension. The crystallinity of the composite sample was found to be excellent with a cubic phase. The sample that contained a higher amount of cobalt compared to nickel and produced single-phase NiCo2S4 exhibited considerably improved HER performance. The variation in the salt precursor concentration during the synthesis of a material is a simple methodology to produce a scalable platinum-free catalyst for HER. The advantageous features of the multiple active sites of cobalt in the CN-21 sample as compared to that for pristine CoS and NiS laid the foundation for the provision of abundant active edges for HER. The composite sample produced a current density of 10 mA cm−2 at an overpotential of 345 mV. Also, it exhibited a Tafel value of 60 mV dec−1, which predominantly ensured rapid charge transfer kinetics during HER. CN-21 was highly durable and stable for 30 hours. Electrochemical impedance spectroscopy showed that the charge transfer resistance was 21.88 ohms, which further validated the HER polarization curves and Tafel results. CN-21 exhibited a double layer capacitance of 4.69 μF cm−2 and a significant electrochemically active surface area of 134.0 cm2, which again supported the robust efficiency for HER. The obtained results reveal that our developed NiCo2S4 catalyst has a high density of active edges, and it is a non-noble metal catalyst for the hydrogen evolution reaction. The present findings provide an alternative strategy and an active nonprecious material for the development of energy-related applications.

CuO microstructures are produced in the presence of water-soluble amino acids by hydrothermal method. The used amino acids include isoleucine, alpha alanine, and arginine as a soft template and are ...