Friendly Environmental Strategies to Recycle Zinc-Carbon Batteries for Excellent Gel Polymer Electrolyte (PVA-ZnSO4-H2SO4) and Carbon Materials for Symmetrical Solid-State Supercapacitors.

In this report, we introduce a novel idea to prepare a redox additive in a gel polymer electrolyte system of PVA-ZnSO4-H2SO4 based on zinc-carbon battery recycling. Here, zinc cans from spent zinc-carbon batteries are dissolved completely in 1 M H2SO4 to obtain a redox additive in an aqueous electrolyte of ZnSO4-H2SO4. Moreover, carbon nanoparticles and graphene nanosheets were synthesized from carbon rod and carbon powder from spent zinc-carbon batteries by only one step of washing and electrochemical exfoliation, respectively, which have good electrochemical capability. The three-electrode system using a ZnSO4-H2SO4 electrolyte with carbon nanoparticles and graphene nanosheets as working electrodes shows high electrochemical adaptability, which points out its promising application in supercapacitor devices. Thus, the symmetrical solid-state supercapacitor devices based on the sandwich structure of graphene nanosheets/PVA-ZnSO4-H2SO4/graphene nanosheets illustrated the highest energy density of 39.17 W h kg-1 at a power density of 1700 W kg-1. While symmetrical devices based on carbon nanoparticles/PVA-ZnSO4-H2SO4/carbon nanoparticles exhibited a maximum energy density of 35.65 W h kg-1 at a power density of 1700 W kg-1. Moreover, these devices illustrate strong durability after 5000 cycles, with approximately 90.2% and 73.1% remaining, respectively. These results provide a promising strategy for almost completely recycling zinc-carbon batteries, one of the most popular dry batteries.

Zinc-Carbon Battery Recycling for Investigating Carbon Materials for Supercapacitor Applications.

In this paper, carbon materials, including graphene nanosheets and carbon nanoparticles, were prepared from spent zinc-carbon batteries by the following two simple methods: electrochemical exfoliation and ultrasonication. Here, graphene nanosheets were synthesized by electrochemical exfoliation in 0.5 M H2SO4 by using a direct current power supply with two carbon rods from spent zinc-carbon batteries. Carbon nanoparticles were prepared by fast ultrasonication in a low-cost, green solution of DI water and ethanol. Graphene nanosheets in this study have high quality, large scale, and good electrochemical ability, while carbon nanoparticles have a unique nanosize and a good specific surface area. These carbon materials were applied for electrochemical measurements for supercapacitor studies and showed excellent stability at different temperatures. Moreover, electric double-layer capacitor devices based on graphene nanosheets and carbon nanoparticles were also used in electrochemical studies with strong stability and good electrochemical capability.

A mini review of current studies on metal-organic frameworks-incorporated composite solid polymer electrolytes in all-solid-state lithium batteries.

All-solid-state lithium batteries (ASSLBs) using solid polymer electrolytes (SPEs) are believed to be future next-generation batteries aiming to replace high-risk traditional batteries using liquid electrolytes, which have a wide application range in portable electronic devices, portable power supplies, and especially in electric vehicles. Moreover, the appearance of SPEs can overcome the electrolyte leakage and flammability problems in conventional lithium-ion batteries. Nevertheless, ASSLBs still face some limitations due to the low ionic conductivity of solid-state electrolytes (SSEs) at room temperature and the poor contact electrode/electrolyte interface, which can be solved by suitable strategies. Currently, the research strategies of metal-organic frameworks that can be incorporated into solid polymer electrolytes offer a remarkable method for producing uniform solid polymer electrolytes that have good electrode/electrolyte contact interfaces and high ionic conductivity. Herein, the updates of current studies about metal-organic framework-incorporated composite solid polymer electrolytes are discussed in this mini-review.

The current status of hydrogen energy: an overview.

Hydrogen is the most environmentally friendly and cleanest fuel that has the potential to supply most of the world's energy in the future, replacing the present fossil fuel-based energy infrastructure. Hydrogen is expected to solve the problem of energy shortages in the near future, especially in complex geographical areas (hills, arid plateaus, etc.) and harsh climates (desert, ice, etc.). Thus, in this report, we present a current status of achievable hydrogen fuel based on various scopes, including production methods, storage and transportation techniques, the global market, and the future outlook. Its objectives include analyzing the effectiveness of various hydrogen generation processes and their effects on the economy, society, and environment. These techniques are contrasted in terms of their effects on the environment, manufacturing costs, energy use, and energy efficiency. In addition, hydrogen energy market trends over the next decade are also discussed. According to numerous encouraging recent advancements in the field, this review offers an overview of hydrogen as the ideal renewable energy for the future society, its production methods, the most recent storage technologies, and transportation strategies, which suggest a potential breakthrough towards a hydrogen economy. All these changes show that this is really a profound revolution in the development process of human society and has been assessed as having the same significance as the previous industrial revolution.

Green and Facile Synthesis of Porous SiO2@C Adsorbents from Rice Husk: Preparation, Characterization, and Their Application in Removal of Reactive Red 120 in Aqueous Solution.

In this work, a green, novel, fast, and facile approach for synthesizing a SiO2/C nanocomposite series from rice husk (RH) through quenching and grinding techniques has been reported along with its application for the adsorptive removal of Reactive Red 120 (RR120) dye from an aqueous solution. The effect of carbonization temperature on the textural and interfacial features of RH was confirmed by scanning electron microscopy (SEM), while the structure and elemental composition of the as-synthesized RH were investigated via XRD, Brunauer-Emmett-Teller (BET), FT-IR, Raman, and X-ray photoelectron spectroscopy (XPS). The RH had a high surface area (521.35 m2 g-1), large micropores, mesopores, and total pore volumes of 0.5059, 3.9931, and 5.2196 cm3 g-1, while SiO2 and C were the two major components. In the batch adsorption test, the effects of pH, contact time, adsorbent mass, temperature, and initial RR120 concentration were investigated. The maximum adsorption capacity was fitted by Langmuir, Freundlich, Temkin, Dubinin-Radushkevich (D-R), Hasley, Harkins-Jura, and BET isotherm models, and Langmuir was the best-fitted model. In addition, the pseudo-first-order, pseudo-second-order, intraparticle diffusion, and Elovich chemisorption models were used to explain the adsorption kinetics. Additionally, the values of Gibbs free energy, enthalpy, and entropy thermodynamics suggested that the RR120 adsorption phenomenon by RH8-3 was endothermic and spontaneous. The adsorption process was controlled by a physical mechanism, and the maximum adsorption capacity was found to be 151.52 mg g-1 at pH 2, with a contact time of 90 min, adsorbent amount of 0.03 g, and temperature of 313 K. The adopted technique may open up a new alternative route for the mass utilization of RH for the removal of dyes in water and wastewater and also for various practical applications.

Ion accumulation-induced capacitance elevation in a microporous graphene-based supercapacitor.

High-performance porous 3D graphene-based supercapacitors are one of the most promising and challenging directions for future energy technologies. Microporous graphene has been synthesized by the pyrolysis method. The fabricated lightweight graphene with a few layers (FLG) has an ultra-high surface area of 2266 m2 g-1 along with various-sized micropores. The defect-induced morphology and pore size distribution of the fabricated graphene are examined, and the results show that the micropores vary from 0.85 to 1.9 nm and the 1.02 nm pores contribute 30% of the total surface area. The electrochemical behaviour of the electrode fabricated using this graphene has been studied with various concentrations of the KOH electrolyte. The highest specific capacitance of the graphene electrode of 540 F g-1 (close to the theoretical value, ∼550 F g-1) can be achieved by using the 1 M KOH electrolyte. This high specific capacitance contribution involves the counter ion adsorption, co-ion desorption, and ion permutation mechanisms. The formation of a Helmholtz layer, as well as the diffusion of the electrolyte ions, confirms this phenomenon. The symmetrical solid-state supercapacitor fabricated with the graphene electrodes and PVA-KOH gel as the electrolyte exhibits excellent energy and power densities of 18 W h kg-1 and 10.2 kW kg-1, respectively. This supercapacitor also shows a superior 100% coulombic efficiency after 6000 cycles.

Two-Dimensional NH4V3O8 Nanoflakes as Efficient Energy Conversion and Storage Materials for the Hydrogen Evolution Reaction and Supercapacitors.

Herein, for the first time, we present two-dimensional (2D) NH4V3O8 nanoflakes as an excellent material for both energy conversion of the hydrogen evolution reaction and storage of supercapacitors by a simple and fast two-step synthesis, which exhibit a completely sheet-like morphology, high crystallinity, good specific surface area, and also stability, as determined by thermogravimetric analysis. The 2D-NH4V3O8 flakes show an acceptable hydrogen evolution performance in 0.5 M H2SO4 on a glassy carbon electrode (GCE) coated with 2D-NH4V3O8, which results in a low overpotential of 314 mV at -10 mA cm-2 with an excellent Tafel slope as low as 90 mV dec-1. So far, with the main focus on energy storage, 2D-NH4V3O8 nanoflakes were found to be ideal for supercapacitor electrodes. The NH4V3O8 working electrode in 1 M Na2SO4 shows an excellent electrochemical capability of 274 F g-1 at 0.5 A g-1 for a maximum energy density of 38 W h kg-1 at a power density as high as 250 W kg-1. Moreover, the crystal structure of 2D-NH4V3O8 is demonstrated by density functional theory (DFT) computational simulation using three functionals, GGA, GGA + U, and HSE06. The simple preparation, low cost, and abundance of the NH4V3O8 material provide a promising candidate for not only energy conversion but also energy-storage applications.

Computation and Investigation of Two-Dimensional WO3·H2O Nanoflowers for Electrochemical Studies of Energy Conversion and Storage Applications.

The aim of this study is to prepare a two-dimensional (2D) WO3·H2O nanostructure assembly into a flower shape with good chemical stability for electrochemical studies of catalyst and energy storage applications. The 2D-WO3·H2O nanoflowers structure is created by a fast and simple process at room condition. This cost-effective and scalable technique to obtain 2D-WO3·H2O nanoflowers illustrates two attractive applications of electrochemical capacitor with an excellent energy density value of 25.33 W h kg-1 for high power density value of 1600 W kg-1 and good hydrogen evolution reaction results (low overpotential of 290 mV at a current density of 10 mA cm-2 with a low Tafel slope of 131 mV dec-1). A hydrogen evolution reaction (HER) study of WO3 in acidic media of 0.5 M H2SO4 and electrochemical capacitor (supercapacitors) in 1 M Na2SO4 aqueous electrolyte (three electrode system measurements) demonstrates highly desirable characteristics for practical applications. Our design for highly uniform 2D-WO3·H2O as catalyst material for HER and active material for electrochemical capacitor studies offers an excellent foundation for design and improvement of electrochemical catalyst based on 2D-transition metal oxide materials.

Multifunctional applications for waste zinc-carbon battery to synthesize carbon dots and symmetrical solid-state supercapacitors.

In this study, we provide a simple and green approach to recycle waste zinc carbon batteries for making carbon dots and porous carbon material. The carbon dots are easily synthesized by one green step, the hydrothermal treatment of a carbon rod in a mixture of DI water and pure ethanol to obtain a blue fluorescence under UV light, which can be used directly as a fluorescence ink. The as-prepared carbon dot process give typical dots with a uniform diameter from 3 to 8 nm with a strong slight blue fluorescent. The porous carbon material is also recycled from carbon powder in a waste battery via one green step annealing process without any chemical activation and with a hierarchically porous structure. This porous carbon material is demonstrated as an electrode for symmetrical solid state supercapacitors (SSCs) in a sandwich structure: porous carbon/PVA-KOH/porous carbon. The SSCs using recycled porous carbon electrodes exhibit a good energy density of 4.58 W h kg-1 at a power density of 375 W kg-1 and 97.6% retention after 2000 cycles. The facile one green step of hydrothermal and also that of calcination provide a promising strategy to recycle waste zinc carbon batteries, which transfers the excellent applications.

Food seasoning-derived gel polymer electrolyte and pulse-plasma exfoliated graphene nanosheet electrodes for symmetrical solid-state supercapacitors.

Kitchen sea salt or table salt is used every day by cooks as a food seasoning. Here, it is introduced into a gel polymer (poly(vinyl) alcohol (PVA)-table salt) for use as an electrolyte, and an electrode was constructed from graphene nanosheets for use as symmetrical solid-state supercapacitors. The graphene sheets are prepared by a pulse control plasma method and used as an electrode material, and were studied by X-ray diffraction (XRD), Raman spectroscopy, as well as scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). A specific capacitance of 117.6 F g-1 at 5 mV s-1 was obtained in a three electrode system with table sea salt as an aqueous electrolyte. For a symmetrical solid-state supercapacitor: graphene/PVA-table sea salt/graphene gave a good specific capacitance of 31.67 F g-1 at 0.25 A g-1 with an energy density of 6.33 W h kg-1 at a power density of 600 W kg-1, with good charge-discharge stability, which was 87% after 8000 cycles. Thus, the development of table sea salt as an environmentally friendly electrolyte has a good potential for use in energy storage applications.

Transparent Flexible Heteroepitaxy of NiO Coated AZO Nanorods Arrays on Muscovites for Enhanced Energy Storage Application.

Transparent flexible energy storage devices are considered as important chains in the next-generation, which are able to store and supply energy for electronic devices. Here, aluminum-doped zinc oxide (AZO) nanorods (NRs) and nickel oxide (NiO)-coated AZO NRs on muscovites are fabricated by a radio frequency (RF) magnetron sputtering deposition method. Interestingly, AZO NRs and AZO/NiO NRs are excellent electrodes for energy storage application with high optical transparency, high conductivity, large surface area, stability under compressive and tensile strain down to a bending radius of 5 mm with 1000 bending cycles. The obtained symmetric solid-state supercapacitors based on these electrodes exhibit good performance with a large areal specific capacitance of 3.4 mF cm-2 , long cycle life 1000 times, robust mechanical properties, and high chemical stability. Furthermore, an AZO/NiO//Zn battery based on these electrodes is demonstrated, yielding a discharge capacity of 195 mAh g-1 at a current rate of 8 A g-1 and a discharge capacity of over 1000 cycles with coulombic efficiency to 92%. These results deliver a concept of opening a new opportunity for future applications in transparent flexible energy storage.

Plasma-Induced Exfoliation Provides Onion-Like Graphene-Surrounded MoS2 Nanosheets for a Highly Efficient Hydrogen Evolution Reaction.

With the goal of obtaining sustainable earth-abundant electrocatalyst materials displaying high performance in the hydrogen evolution reaction (HER), here we propose a facile one-pot plasma-induced electrochemical process for the fabrication of new core-shell structures of ultrathin MoS2 nanosheets engulfed within onion-like graphene nanosheets (OGNs@MoS2). The resultant OGNs@MoS2 structures not only increased the number of active sites of the semiconducting MoS2 nanosheets but also enhanced their conductivity. Our OGNs@MoS2 composites exhibited high HER performance, characterized by a low overpotential of 118 mV at a current density of 10 mA cm-2, a Tafel slope of 73 mV dec-1, and long-time stability of 105 s without degradation; this performance is much better than that of the sheet-like graphene-wrapped MoS2 composite GNs@MoS2 (182 mV, 82 mV dec-1) and is among the best ever reported for composites involving MoS2 and graphene nanosheets prepared through a simple one-batch process and using a low temperature and a short time for the HER. This approach appears to be an effective and simple strategy for tuning the morphologies of composites of graphene and transition metal dichalcogenide materials for a broad range of energy applications.

Role of precursors mixing sequence on the properties of CoMn2O4 cathode materials and their application in pseudocapacitor.

In this study, the effect of oxygen vacancy in the CoMn2O4 on pseudocapacitive characteristics was examined, and two tetragonal CoMn2O4 spinel compounds with different oxygen vacancy concentrations and morphologies were synthesized by controlling the mixing sequence of the Co and Mn precursors. The mixing sequence was changed; thus, morphologies were changed from spherical nanoparticles to nanoflakes and oxygen vacancies were increased. Electrochemical studies have revealed that tetragonal CoMn2O4 spinels with a higher number of oxygen vacancies exhibit a higher specific capacitance of 1709 F g-1 than those with a lower number of oxygen vacancies, which have a higher specific capacitance of 990 F g-1. Oxygen vacancies create an active site for oxygen ion intercalation. Therefore, oxidation-reduction reactions occur because of the diffusion of oxygen ions at octahedral/tetrahedral crystal edges. The solid-state asymmetric pseudocapacitor exhibits a maximum energy density of 32 Wh-kg-1 and an excellent cyclic stability of nearly 100%.

New Simultaneous Exfoliation and Doping Process for Generating MX2 Nanosheets for Electrocatalytic Hydrogen Evolution Reaction.

Doping nonmetal atoms into layered transition metal dichalcogenide MX2 structures has emerged as a promising strategy for enhancing their catalytic activities for the hydrogen evolution reaction. In this study, we developed a new and efficient one-step approach that involves simultaneous plasma-induced doping and exfoliating of MX2 bulk into nanosheets-such as MoSe2, WSe2, MoS2, and WS2 nanosheets-within a short time and at a low temperature (ca. 80 °C). Specifically, by utilizing active plasma that is generated with an asymmetric electrical field during the electrochemical reaction at the surface of the submerged cathode tip, we are able to achieve doping of nitrogen atoms, from the electrolytes, into the semiconducting 2H-MX2 structures during their exfoliation process from the bulk states, forming N-doped MX2. We selected N-doped MoS2 nanosheets for demonstrating their catalytic hydrogen evolution potential. We modulated the electronic and transport properties of the MoS2 structure with the synergy of nitrogen doping and exfoliating for enhancing their catalytic activity. We found that the nitrogen concentration of 5.2 atom % at N-doped MoS2 nanosheets have an excellent catalytic hydrogen evolution reaction, where a low overpotential of 164 mV at a current density of 10 mA cm-2 and a small Tafel slope of 71 dec mV-1-much lower than those of exfoliated MoS2 nanosheets (207 mV, 82 dec mV-1) and bulk MoS2 (602 mV, 198 dec mV-1)-as well as an extraordinary long-term stability of >25 h in 0.5 M H2SO4 can be achieved.