Simple Co-precipitation Method Research Articles

Adsorption and photocatalytic degradation of 2,4-dicholrophenol using surgical mask derived SMAC-Fe2O3 composite; adsorption isotherms, kinetics, thermodynamics.

Hybrid material of surgical mask activated carbon (SMAC) and Fe2O3 (SMAC-Fe2O3) composite was prepared by simple co-precipitation method and used as potential material for the remediation of 2,4-dicholrophenol (2,4-DCP). The XRD patterns exhibited the presence of SMAC and Fe2O3, FTIR spectrum showed the FeO-carbon stretching at the wavenumber from 400 to 550cm-1. UV-Vis DRS results showed the band gap was 1.97eV and 2.05eV for SMAC-Fe2O3 and Fe2O3, respectively. The SEM images revealed that the Fe2O3 doped onto the fiber morphology of SMAC. The outcomes of the BET examination exhibited a surface area of 195 m2/g and a pore volume of 0.2062 cm3/g for the SMAC/Fe2O3 composite. The batch mode study shows the maximum adsorption and photocatalytic degradation efficacies which were 97% and 78%, respectively. The experimental data was studied with both linear and nonlinear adsorption isotherm and kinetics models. The nonlinear Langmuir isotherm and pseudo-second-order kinetics (PSOK) models have well fit compared with other models. The Langmuir maximum adsorption capacity (qmax) was found 161.60mg/g. Thermodynamic analysis shows that the 2,4-DCP adsorption onto SMAC-Fe2O3 was a spontaneous and exothermic process. The PSOK assumes that the adsorption process was chemisorption. The photocatalytic degradation rate constant of 2,4-DCP was calculated using pseudo-first-order kinetics (PFOK) and the rate constant for SMAC-Fe2O3 and Fe2O3 were 0.859 × 10-2min-1 and 0.616 × 10-2min-1, correspondingly. In addition, the obtained composite exhibited good reusability after a few cycles. These results confirmed that SMAC-Fe2O3 composite is an effective adsorbent and photocatalyst for removing 2,4-DCP pollutants.

Biodegradable Acid-Based Fe2MnO4 Nanoparticles for Water Remediation.

This study demonstrated the synthesis of Fe2MnO4 modified by citric acid, a biodegradable acid, using a simple co-precipitation method. Characterization was performed using qualitative analysis techniques such as Fourier-transformed infrared spectroscopy, scanning electron microscopy equipped with energy-dispersive X-ray spectroscopy, X-ray diffraction, selected-area electron diffraction, N2 adsorption-desorption, and zero-point charge. The prepared nanoparticles had a rough and porous surface, and contained oxygenous (-OH, -COOH, etc.) functional groups. The specific surface area and average pore size distribution were 83 m2/g and 5.17 nm, respectively. Net zero charge on the surface of the prepared nanoparticles was observed at pH 7.5. The prepared nanoparticles were used as an adsorbent to remove methylene blue dye from water under various conditions. Using small amounts of the adsorbent (2.0 g/L), even a high concentration of MB dye (60 mg/L) could be reduced by about ~58%. Exothermic, spontaneous, feasible, and monolayer adsorption was identified based on thermodynamics and isotherm analysis. Reusability testing verified the stability of the adsorbent and found that the reused adsorbent performed well for up to three thermal cycles. Comparative analysis revealed that the modified adsorbent outperformed previously reported adsorbents and unmodified Fe2MnO4 in terms of its partition coefficient and equilibrium adsorption capacity under different experimental conditions.

Fabrication of Cu3Mo2O9 doped MWCNT nanocomposites as efficient photocatalyst for malachite green dye degradation

In the present work, Cu3Mo2O9@MWCNT was synthesised by a simple co-precipitation method followed by ultrasonication. The synthesised nanocomposite was analysed by spectral and analytical characterization techniques, such as FT-IR, XRD, PL, FESEM, XPS, HRTEM, BET and LCMS. The Cu3Mo2O9@MWCNT nanocomposites achieved photocatalytic degradation efficiency of 96 % for malachite green dye under visible light in 180 min. Furthermore, scavenger tests were carried out to identify the role of reactive species aided in the degradation process. Cu3Mo2O9@MWCNT shows stable photocatalytic performance until the fourth cycle. The constructed nanocomposites exhibited excellent stability and reusability features that were suitable for its practical application.

Interlayer-spacing regulation of NiFe LDH nanosheets cathode with high rate performance for chloride ion battery

Chloride ion batteries (CIBs) possess the multiple advantages of high theoretical volumetric energy density, abundant precursor resources and high safety due to the dendrit-free characteristic, which provide more choices and opportunities for electrochemical energy storage. In this work, NiFe LDH nanosheets with different interlayer spacing are prepared using a simple co-precipitation method with the interlayer spacing of LDH nanosheets extended from 7.695 Å to 24.114 Å. Expanding interlayer space of LDHs nanoplates helps to the promote ion diffusion and enhance their action kinetics. Additionally, the increased oleophobicity between NiFe LDH nanosheets cathode with increased interlayer spacing and solvent PC is beneficial for the structural stability of the materials during cycling. Compared with typical chloride ion-intercalated NiFe LDH nanosheets, the NiFe-C17H25O3 LDH with the maximum interlayer spacing demonstrates a performance improvement of about 213 % (with a discharge specific capacity of 64.2 mAh/g after 200 cycles) at high current density and good rate performance. This work provides a simple and effective interlayer spacing control strategy for the design of CIBs cathodes under high current density.

Effect of doping on the morphology of cerium molybdate: A mechanistic approach towards efficient energy storage and sustainable environmental mitigation through heterogeneous photocatalysis

In this paper, we describe the synthesis of cerium molybdate (Ce2(MoO4)3) and different compositions of Bi-doped cerium molybdate (Ce2-xBix(MoO4)3) where x = 0.01, 0.03, 0.05, 0.07, and 0.09, through simple co-precipitation method. The synthesized materials were optically, structurally, and morphologically characterized by various sophisticated techniques, including UV–visible, FTIR, Raman, PXRD, BET, and SEM-EDX. Upon addition of bismuth, the optical band gaps are reduced from 3.35 eV (Ce2(MoO4)3) to 2.83 eV Ce1.93Bi0.07(MoO4)3. The charge storage potential and AC conductivity of the synthesized materials were investigated through dielectric studies where the dielectric constant increased by increasing dopant concentration up to 7 %. At 20 Hz, Ce1.93Bi0.07(MoO4)3 showed a significantly greater dielectric constant (3.597 × 106) compared to undoped Ce2(MoO4)3 (3.262 × 105). Similarly, the AC conductivity of Ce1.93Bi0.07(MoO4)3 increased up to 4.758 S m−1 compared to the undoped Ce2(MoO4)3 (2.270 S m−1) at 20 MHz. The photocatalytic efficiency was investigated against diclofenac potassium, which also considerably improved by increasing bismuth content. The maximum photodegradation efficiency of 87.9 % was observed for Ce1.93Bi0.07(MoO4)3 in 180 min under UV light irradiation at optimized conditions (pH = 4, catalyst dosage = 20 mg, and initial concentration of drug = 5 mg L−1). The photocatalytic reaction followed pseudo-first-order kinetics with a rate constant of 0.0108 min−1 with stability up to five successive runs of photocatalytic activity indicating its good recyclability. These findings suggest that Bi-doped cerium molybdate could be used as a promising material for photocatalysis and energy storage devices.

Photoelectrochemical sensor for nitrite determination based on the etching of BiOCl/Zn0.5Cd0.5S

A rapid photoelectrochemical (PEC) sensor was constructed for nitrite detection in food based on the one-step chemical etching strategy of BiOCl/Zn0.5Cd0.5S (BOC/ZCS) nanocomposites by nitrite. BOC/ZCS heterojunction was prepared by a simple coprecipitation method, and it was found that BOC/ZCS showed significant photoelectrochemical (PEC) activity. The results of this study confirmed that the decrease in the photocurrent of the sensor was linked to the etching of ZCS by nitrite under acidic conditions. Under optimized conditions, the BOC/ZCS-based PEC sensor showed good analytical properties for detecting nitrite, with linear ranges of 1–100 μM and 100–600 μM. The detection limit of the sensor was 0.41 μM (S/N = 3). Excellent repeatability, reproducibility, low background noise, and immunity to interference were demonstrated using the proposed system, and satisfactory results were achieved for the nitrite assay using real samples. These results demonstrate a new method for nitrite detection developed using the proposed PEC sensor.

Terbium (III) and salicylamide doped nickel ferrite (NiFe2O4) nanoparticles synthesized from Olea europaea L. plant extracts via eco-friendly green synthesis approach and co-precipitation method

An eco-friendly and cost-effective NiFe2O4 nanoparticles and its derivatives NiFe2O4:salicylamide, NiFe2O4:salicylamide:Tb3+ and NiFe2O4:salicylamide:Tb3+:Olea europaea L. extracts have been successfully synthesized using a simple and refluxed-assisted chemical co-precipitation method and green route approach followed by thermal treatment steps. In this report, the structural, morphological, optical characteristics and biological activities of the nanoparticles were characterized by using XRD, SEM, FTIR, UV-Vis, PL, BET analysis, antibacterial assays and antioxidant activities. The results from XRD revealed that NiFe2O4 has a crystalline structure and EDX elemental mapping confirmed the uniform distributed of all the elements in the matrix. The incorporation of salicylamide, Tb3+ and Olea europaea L. extracts into NiFe2O significantly enriched the luminescence intensities and changed the emission colour coordinates. Colour tunability was achieved with luminescence ranging from bright blue emission to reddish orange light, which makes nanoparticles important candidates for solid-state lighting technologies. Combining olive leaf extracts with NiFe2O4 nanoparticles provided effective antioxidant and antibacterial activity by reducing and stabilizing of nanoparticles. Moreover, all experimental results reveal new ideas for the design and optimization of multifunctional nanomaterials with higher sensitivity and pave the way for the production of new functional nanomaterials.

MnO2@Al‐BDC nanocomposite as adsorbent of remarkable high efficiency toward iron remediation from wastewaters

Global environmental problems, especially those related to water contamination brought on by rapid industrialization and economic growth, are among the most dangerous threats facing humanity today. In this research work, Al3+ based metal–organic framework with 1,4‐benzenedicarboxylic acid (H2BDC) linker has been synthesized by a simple and economic coprecipitation method. The obtained Al‐BDC MOF was utilized as an adsorbent for sequestering iron from wastewater, but only 54.0% of iron concentration was eliminated after 120 min. To boost the removal efficiency, modification of the Al‐BDC MOF was carried out. MnO2@Al‐BDC nanocomposite was prepared and applied as a nanoadsorbent for iron remediation from water. The adsorption capability of Al‐BDC MOF was greatly enhanced by facile modification. The adsorption efficiency reached 97.0% using 35.0 mg of the nanocomposite after 120 min compared to 54.0% iron removal using the un‐modified MOF. The effect of pH of the medium was then studied using MnO2@Al‐BDC nanocomposite. The best elimination efficacy of iron was accomplished at pH ~ 2.2. The adsorption of iron on the surface of MnO2@Al‐BDC nanocomposite attains 97.0% (120 min) using a 35.0 mg dose of adsorbent and reaches 98.7% utilizing a 50.0 mg dose of adsorbent. In contrast, at pH = 9.2, the removal efficiency drops to 90.0% (after 120 min, 35.0 mg adsorbent). The adsorption capability was examined also using a variety of iron concentrations, i.e., 2.5, 5.0, and 7.5 mg/L where the adsorption efficiency dropped notably upon increasing the concentration. It dropped from 96.3% to 87.0% using 35.0 mg of MnO2@Al‐BDC nanocomposite at 90 min. The newly developed adsorbent showed a pronounced efficiency for Fe3+ removal against real samples collected from different water sources. Ultimately, this research introduces a novel MnO2@Al‐BDC nanocomposite, synthesized through a simple and economical coprecipitation method, to address water contamination by iron. The innovation lies in the significant enhancement of iron elimination efficiency, from 54.0% with unmodified Al‐BDC MOF to 97.0% with the MnO2@Al‐BDC nanocomposite.

Controllable morphology, excellent stability and non-equivalent doping-induced optical properties of Mn4+-activated K2NaScF6 red phosphor for high-quality warm WLED

Currently, Mn4+ activated fluoride red phosphor has been widely studied to improve the optical performance of white light-emitting diode (WLED) in the field of high-efficiency lighting and wide color gamut backlight display. In this paper, a series of red-emitting K2NaScF6:Mn4+ phosphors are synthesized by a simple co-precipitation method with a non-equivalent substitution of Mn4+ for Sc3+ at room temperature. The crystal structure, morphology and elemental composition of K2NaScF6:Mn4+ phosphors prepared using different reaction conditions are systematically investigated. Interestingly, the K2NaScF6:Mn4+ phosphors exhibit narrowband red emission with low correlated color temperature (CCT), high color purity and short fluorescence lifetime. Compared to equivalent doping, the mechanism of short fluorescence lifetime caused by non-equivalent doping has also been systematically discussed. The optimal doping concentration is determined by setting a series of Mn4+ doping concentrations and the concentration quenching mechanism is analyzed. The crystal field strength (Dq), Racah parameters (B and C) and nephelauxetic ratio (β1) are calculated in detail to evaluate the crystal field environment of Mn4+ in K2NaScF6. The good water resistance of the as-prepared sample K2NaScF6:Mn4+ is verified by comparing with the commercially available phosphor K2SiF6:Mn4+. Moreover, the thermal stability is also analyzed by calculating the activation energy (Ea), chromaticity shift (ΔE) and chromaticity coordinate variation (CCV). Importantly, the as-packaged warm WLED (InGaN chip + YAG:Ce3+ + K2NaScF6:Mn4+) has excellent optical properties (CCT = 4082 K, color rendering index (CRI, Ra = 91.2) and luminous efficiency (LE) = 78.86 lm/W), and it exhibits good output stability at high drive currents. In summary, our work demonstrates that K2NaScF6:Mn4+ red phosphors possess a great potential application in warm WLED for the indoor lighting.

Surfactant assisted wet chemical synthesis of Cu doped NiO@CNF nanocomposites and their photocatalytic behaviour in degrading brilliant green dye under UV light irradiation

This manuscript details the synthesis of pure NiO and various concentrations of Cu-doped NiO using a simple co-precipitation method, with particular amount of carbon nanoflake (CNF) loading. The prepared materials were initially characterized using X-ray diffraction, scanning electron microscopy with EDAX, transmission electron microscopy, energy dispersive X-ray. Further, UV-diffusion reflectance spectra studies were conducted to explore the optical properties of the prepared nanocomposites. XPS was utilized to explore the surface chemical states and interactions. The XRD pattern analysis revealed that both pure NiO and Cu-doped NiO nanoparticles (NPs) exhibited a face-centered cubic structure. Subsequently, the photocatalytic efficiency of the synthesized samples was evaluated for the degradation of the organic pollutant like brilliant green (BG) under UV light irradiation. Significantly, 30 mol % Cu-doped NiO@CNF nanocomposite demonstrated an enhanced photocatalytic efficiency (97 %) in degrading BG dye when compared to doped oxide materials under UV light. Moreover, the stability of the catalyst was outstanding, and it was effectively reused for five consecutive cycles.

Investigation of the efficacy of Zn/Ce-CuO nanoparticles for enhanced photocatalytic, antibacterial, and antioxidant activities.

The world is dealing with unprecedented environmental challenges, leading to a growing urgency to limit environmental damage. So, this study focuses on the synthesis of pure CuO, Zn, Ce, and Zn/Ce dual-doped CuO nanoparticles (NPs)using extract of Citrus limon leaves as reductant via simple co-precipitation method. The X-ray diffraction (XRD) characterization was employed to analyze structural characteristics of synthesized samples which confirm influence of Zn or Ce doping on crystallite size, dislocation density, and strain. The role of functional groups, changes in force constant, and bond length on addition of dopants was indicated by FTIR results. The SEM and TEM results showed variation in morphology from irregular to spherical. The zeta-potential and BET analysis confirmed surface potential as well as surface area characteristics. The change in energy gap values from 1.81 to 1.45eV of Zn/Ce-doped CuO NPscomputed from UV-vis analysis elevated its photocatalytic performance and reduced the chances of recombination of electron-hole pair due to presence of trapping levels between valence and conduction bands. The enhanced photo-degradation of Congo red (CR) and rhodamine B (RhB) with 91 and 94%, respectively, for Zn/Ce-doped CuO NPswas observed. The so-obtained samples have also exhibited good antibacterial and antioxidant activities.

Physicochemical characteristics of DyFeO3 perovskite nanoparticles synthesized by a simple co-precipitation method at room temperature

Physicochemical characteristics of DyFeO3 perovskite nanoparticles synthesized by a simple co-precipitation method at room temperature

A Minimalist Iron Oxide Nanoprobe for the High-Resolution Depiction of Stroke by Susceptibility-Weighted Imaging.

The precise mapping of collateral circulation and ischemic penumbra is crucial for diagnosing and treating acute ischemic stroke (AIS). Unfortunately, there exists a significant shortage of high-sensitivity and high-resolution in vivo imaging techniques to fulfill this requirement. Herein, a contrast enhanced susceptibility-weighted imaging (CE-SWI) using the minimalist dextran-modified Fe3O4 nanoparticles (Fe3O4@Dextran NPs) are introduced for the highly sensitive and high-resolution AIS depiction under 9.4 T for the first time. The Fe3O4@Dextran NPs are synthesized via a simple one-pot coprecipitation method using commercial reagents under room temperature. It shows merits of small size (hydrodynamic size 25.8nm), good solubility, high transverse relaxivity (r2) of 51.3 mM-1s-1 at 9.4 T, and superior biocompatibility. The Fe3O4@Dextran NPs-enhanced SWI can highlight the cerebral vessels readily with significantly improved contrast and ultrahigh resolution of 0.1mm under 9.4 T MR scanner, enabling the clear spatial identification of collateral circulation in the middle cerebral artery occlusion (MCAO) rat model. Furthermore, Fe3O4@Dextran NPs-enhanced SWI facilitates the precise depiction of ischemia core, collaterals, and ischemic penumbra post AIS through matching analysis with other multimodal MR sequences. The proposed Fe3O4@Dextran NPs-enhanced SWI offers a high-sensitivity and high-resolution imaging tool for individualized characterization and personally precise theranostics of stroke patients.

Intercalation of decanoate anions (C10) in layered double hydroxide Mg[sbnd]Al and its application as controlled-release corrosion inhibitor of steel

This study focuses on the preparation and characterization of a novel anticorrosion pigment based on decanoate anions (C10‐) intercalated within layered double hydroxide (LDH) MgAl. The LDH-NO3, LDH-C10 were synthesized by a simple co-precipitation method and analyzed by XRD, infrared spectroscopy, thermogravimetry and electronic microscopy. The LDH-C10 pigment with a basal distance of about 20 Å was consistent with the arrangement of C10 anions in bilayer. The inhibition efficiency of the LDH-C10 pigment in electrolyte and in alkyd resin paint was studied by electrochemical impedance spectroscopy and potentiodynamic techniques. The pigments act as a C10− nanocontainer, which release the C10− anions in contact with chloride ions that lead to the formation of a passive layer on steel. In alkyd resin, the LDH-C10-enriched organic coating exhibit very interesting anticorrosive performance in NaCl electrolyte during 40 days of immersion.

Tuning of structural, magnetic, and optical properties of ZnO nanoparticles by Co and Cu doping

Undoped, Cu, and Co-doped ZnO nanoparticles were synthesized by a simple co-precipitation method. We studied the structural, chemical, magnetic, and optical properties of synthesized nanoparticles by using X-ray Diffraction, Fourier Transform Infrared, Scanning Electron Microscopy, Vibrating-Sample Magnetometer, and UV–VIS spectroscopy. The X-ray Diffraction analysis discovers the crystalline hexagonal wurtzite structure and confirms the incorporation of Cu2+ and Co2+ in the ZnO lattice. The SEM photographs show that the nanoparticles are agglomerated, and the grain size of pure ZnO is decreased upon doping, showing inhibition of grain growth through doping. From VSM the coercivity and saturation magnetization of Co-doped (0.0189 emu/g and 84.044Oe) is higher as compared to pure and Cu-doped ZnO. The energy gap of doped and un-doped nanoparticles determined from the absorption spectrum indicates that it increases by doping of Copper and cobalt.

Sensitive detection of cardiac glycoside digoxin based on sheet like structured cerium manganese oxide electrocatalyst

Digoxin (DGN), a widely used cardiac glycoside steroid for treating heart diseases. The prescription dosage range of digoxin is 0.5 – 2.0 ng/mL and concentration above 2 ng/mL can lead to intoxication. To monitor and detect digoxin in blood level is essential to minimize the endanger toxicity of human health. Addressing this concern, here we prepare a cerium manganese oxide (CMO) catalyst by a simple chemical coprecipitation method followed by heat treatment. The CMO morphological and structural characteristics were investigated by various spectroscopic techniques. The electrochemical properties of CMO catalyst were evaluated using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques, which also determined its electrochemical performance. Due to the high conductivity and large surface area with abundant active sites, CMO catalyst was used as a modified electrode material for detecting DGN in biological samples. The CMO sensor exhibits excellent electrocatalytic performance, with a dynamic linear range of 7.81 ×10–6 pg/L to 430 ×10–6 pg/L. The limit of detection and limit of quantification (LOD and LOQ) were found to be 1.99 ×10–6 pg/L and 6.05 ×10–6 pg/L, respectively. Furthermore, the sensor’s efficiency was validated through selectivity test and analysis of biological samples such as human blood and urine.

Tailoring CuOx loading on CoFe2O4 nanocubes photocatalyst for superior photocatalytic degradation of triclosan pollutants under VL irradiation and toxicological evaluation

In this study, we report the development of a novel CuOx(3 wt%)/CoFe2O4 nanocubes (NCs) photocatalyst through simple co-precipitation and wet impregnation methods for the efficient photocatalytic degradation of triclosan (TCS) pollutants. Initially, rod-shaped bare CoFe2O4 was synthesized using a simple co-precipitation technique. Subsequently, CuOx was loaded in various percentages (1, 2, and 3 wt%) onto the surface of bare CoFe2O4 nanorods (NRs) via the wet impregnation method. The synthesized materials were systematically characterized to evaluate their composition, structural and electrical characteristics. The CuOx(3 wt%)/CoFe2O4 NCs photocatalyst exhibited superior photocatalytic degradation efficiency of TCS (89.9%) compared to bare CoFe2O4 NRs (62.1 %), CuOx(1 wt%)/CoFe2O4 (80.1 %), CuOx(2 wt%)/CoFe2O4 (87.0 %) under visible light (VL) irradiation (λ ≥ 420 nm), respectively. This enhanced performance was attributed to the improved separation effectiveness of photogenerated electron (e−) and hole (h+) in CuOx(3 wt%)/CoFe2O4 NCs. Furthermore, the optimized CuOx(3 wt%)/CoFe2O4 NCs exhibited strong stability and reusability in TCS degradation, as demonstrated by three successive cycles. Genetic screening on Caenorhabditis elegans showed that CuOx(3 wt%)/CoFe2O4 NCs reduced ROS-induced oxidative stress during TCS photocatalytic degradation. ROS levels decreased at 30, 60, and 120-min intervals during TCS degradation, accompanied by improved egg hatching rates. Additionally, expression levels of stress-responsible antioxidant proteins like SOD-3GFP and HSP-16.2GFP were significantly normalized. This study demonstrates the efficiency of CuOx(3 wt%)/CoFe2O4 NCs in degrading TCS pollutants, offers insights into toxicity dynamics, and recommends its use for future environmental remediation.

NiO/MnO2 nanocomposite in addition of layered Reduced Graphene oxide (RGO) electrode for accountable supercapacitor application

Reduced Graphene oxide/Nickel oxide/Magnesium dioxide) RGO/NiO/MnO2 nanocomposite electrode was successfully prepared by simple co-precipitation method. The synthesised nanocomposite was characterised by XRD, FESEM, EDAX, FTIR, UV, CV, GCD, EIS. The RGO/NiO/MnO2 nanocomposite was pretreated by ultrasonication, followed by thermal annealing at 350 oC. The crystalline face and size of nanocomposite were analysed by X-Ray Diffraction (XRD). The sandwich-like structure of RGO/NiO/MnO2 was analysed by Scanning Electron Microscope (SEM). This structure promoted an efficient contact between electrolyte and active materials, and the distinct architecture could offer fast transfer channels of ion and electrons. The nanocomposite exhibited high conductivity owing to the presence of RGO. The electrochemical performance of prepared nanocomposite was done by Cyclic Voltammetry (CV), Galvanostatic charge discharge (GCD), Electrical Impedance Spectroscopy (EIS). The synthesised RGO/NiO/MnO2 nanocomposite acquired high specific capacitance of 1167F/g at current density of 1 A/g. The low cost, low temperature RGO/NiO/MnO2 nanocomposite electrode could be the promising electrode for Energy storage devices.

Zn doped CeO2 supporting Ni–Pt catalysts toward robust hydrogen generation from hydrous hydrazine

Ni-based bimetallic catalysts with noble metals exhibit high activity and selectivity for hydrogen generation from hydrazine monohydrate. However, their poor service durability remains a critical challenge. This study investigated the use of Zn-doped CeO2 as a support for Ni–Pt catalysts to improve their long-term stability. A series of Ni–Pt/Zn-doped-CeO2 catalysts were prepared via a simple co-precipitation and reduction method. Compared to the pristine Ni50Pt50/CeO2 catalyst, the Zn doping can improve the stability of CeO2 support in the alkaline condition, and the X-ray photoelectron spectroscopy (XPS) analysis clearly indicates that Zn doping leads to a negative shift in the binding energy of connected Ni and thus enhances the stability of the electronic structure in the catalysts. The findings in this work suggest that Zn-modified CeO2 supporting Ni–Pt catalyst offer a promising approach to achieving a better balance between activity and durability for hydrogen generation catalysts.

Constructing low-cost stable zinc-ion batteries with sodium-rich monoclinic manganese hexacyanoferrate cathode

Manganese-based Prussian blue analogues are ideal candidate cathode materials for constructing high-voltage zinc-ion batteries. However, challenges have persisted in realizing envisioned highly stable electrochemical cycling systems due to manganese dissolution under aqueous conditions and self-corrosion of zinc metal anodes. Considering practical application demands and cost-effectiveness, non-aqueous organic zinc-ion batteries have shown significant development potential by avoiding interference from active hydrogen and offering a stable wide voltage window. Herein, a sodium-rich monoclinic structured manganese hexacyanoferrate (m-MnHCF) was synthesized via a simple coprecipitation method, achieving a stable high-voltage zinc-ion battery energy storage system in a diluted 0.2 M Zn(CF3SO3)2 electrolyte in acetonitrile, a non-protonic polar solvent. The battery exhibited a discharge specific capacity of 77 mAh g−1 at the current density of 1 A g−1 after 620 cycles. Furthermore, by circumventing interference from active hydrogen, a cost-advantaged zinc powder anode (Zn-P) was successfully introduced into the energy storage system. Assembled Zn-P||m-MnHCF cells exhibited stable cycling for 100 cycles at a current density of 0.5 A g−1 with close to 100 % coulombic efficiency, showcasing limitless possibilities for the future, as demonstrated by illuminated LED arrays.