Electrochemical Energy Storage Performance Research Articles

Pseudocapacitive Electrode Based on MnO2 Loaded Activated Charcoal on Graphite Paper for Sustainable Energy Storage

AbstractThe design of high‐performance electrode material without compromising energy and power density is critical for the advancement in hybrid electric vehicle technology. In this perspective, we have fabricated a MnO2 loaded activated charcoal‐based electrode on graphite paper as an endeavour to improve the energy storage capabilities. The electrode material is synthesized by employing a sustainable route and the structural, microstructural, and textural properties have been investigated. The electrochemical performance for energy storage is evaluated and the fabricated electrode on graphite paper exhibits remarkably high‐power density (811 W kg−1) maintaining high energy density (106 Wh kg−1) at the same time, along with high gravimetric specific capacitance value of 768 F g−1 at 2 mA cm−2. The obtained results demonstrate the excellent performance of the electrode material, suggesting MnO2 loaded activated charcoal as a prospective electrode material to meet the demand of hybrid electric vehicles as well as to contribute to our transitioning towards low‐to‐zero carbon emission technology.

Separating Cationic and Anionic Redox Activity in the Lithium-Rich Antiperovskite (Li2Fe)SO.

Lithium-rich antiperovskites promise to be a compelling class of high-capacity cathode materials due to the existence of both cationic and anionic redox activity. Little is however known about the effect of separating the electrochemical cationic process from the anionic process and the associated implications on the electrochemical performance. In this context, we report the electrochemical properties of the illustrative example of three different (Li2Fe)SO materials with a focus on separating cationic from anionic effects. With the high-voltage anionic process, an astonishing electrochemical capacity of around 400 mAh g-1 can initially be reached. Our results however identify the anionic process as the cause of poor cycling stability and demonstrate that the fading reported in previous literature is avoided by restricting to only the cationic processes. Following this path, our (Li2Fe)SO-BM500 shows strongly improved performance as indicated by constant electrochemical cycling over 100 cycles at a capacity of around 175 mAh g-1 at 1 C. Our approach also allows us to investigate the electrochemical performance of the bare antiperovskite phase excluding extrinsic activity from initial or cycling-induced impurity phases. Our results underscore that synthesis conditions are a critical determinant of electrochemical performance in lithium-rich antiperovskites, especially with regard to the amount of electrochemical secondary phases, while the particle size has not been found to be a crucial parameter. Overall, separating and understanding the effects of the cationic from the anionic redox activity in lithium-rich antiperovskites provides the route to further improve their performance in electrochemical energy storage.

Green synthesis of nanostructured 1T/2H-MoS2 hybrid phase with polyol solvents and microwave heating

Green synthesis approaches have attracted greatly of attention in recent years since they address the issues associated with sustainability than conventional synthesis methods. New research fields in green nanoscience are being developed as a result of the incorporation of green chemistry principles into nanoscience. In this paper, the successful microwave-assisted green synthesis of MoS2 nanoparticles in a single pot using polyol solvents such as ethylene glycol and glycerol is demonstrated. The coexistence of 1T and 2H phases in MoS2 nanomaterials was determined using advanced techniques such as XRD, Raman, XPS, and TEM images. The highest 1T proportion obtained was 84.5% when compared to the 2H phase. The reaction mechanism and the phase transition between 1T and 2H were described and illustrated. The role of polyol solvents in the practical synthesis of nano MoS2 under microwave heating is also evaluated and explained. Due to the ability of the metallic 1T phase to enhance electrical conductivity, it is believed that hybrid nanostructures exhibit superior electrochemical performance for energy storage and conversion applications.

NANOCARBONS-BASED TRIFUNCTIONAL ELECTROCATALYSTS FOR OVERALL WATER SPLITTING AND METAL-AIR BATTERIES: - METAL-FREE AND HYBRID ELECTROCATALYSTS.

Trifunctional electrocatalysts, an exciting class of materials that can simultaneously catalyze hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR), can significantly enhance the performance and economic viability of electrochemical energy storage and conversion technologies such as water-splitting electrolyzers, metal-air batteries, fuel cells and their integrated devices. Such multifunctional electrocatalysts encompass multiple active sites that can simultaneously catalyze two or more different electrochemical reactions and are feasible routes for addressing global energy and environmental challenges. This review accounts for nanocarbons-based trifunctional electrocatalysts reported for electrolyzers, metal-air batteries and integrated electrolyzer-battery systems, providing a practical perspective. Metal-free and hybrid (hybrids of nanocarbons and transition metals/compounds) trifunctional electrocatalysts are covered. Given the growing importance of green technologies, we discuss biomass-derived carbon-based trifunctional electrocatalysts separately. The collective information provided in the review could help researchers derive more effective and durable trifunctional electrocatalysts suitable for commercial use.

Enhanced energy storage performance of copper intercalated redox active 1, 2, 4, 5-benzene-tetracarboxylic Acid organic framework

Supercapattery being remarkable energy storage device combining the strength of supercapacitors and batteries can offer both high power and enhanced energy storage capabilities. In the realm of advanced materials, Metal-Organic Frameworks (MOFs) represent a unique category of porous materials formed through strong bonds between organic linkers and metal ions. Through meticulous ingredient selection, MOFs can exhibit extremely large surface areas, exceptional chemical stability, and significant pore volumes. In this study, we demonstrate the electrochemical energy storage performance of copper intercalated MOF (Cu-MOF) synthesized via a hydrothermal method for the application of supercapattery. Initially, we employed a three-electrode assembly to scrutinize the electrochemical characteristics of the synthesized material. To investigate the nature of the electrodes, electrochemical analysis including cyclic voltammetry (CV), galvanostatic charge discharge (GCD), and electrochemical impedance spectroscopy (EIS) were performed. The synthesized material exhibited excellent specific capacity of 403.5 C/g at 1.5 A/g, indicating its battery-grade quality. Due to its superior electrochemical performance, the supercapattery device was fabricated by coupling Cu-MOF with activated carbon (AC), Cu-MOF was subjected to positive and AC was employed as the negative electrode. The Cu-MOF//AC exhibited remarkable specific capacity of 165 C/g at 0.7 A/g. Furthermore, this device showcased impressive specific energy of 40 Wh/kg at specific power of 567 W/kg. The device demonstrated an impressive maximum specific power of 6336 W/kg, while its exceptional stability of 95.6 % was demonstrated through 5000 cycles at room temperature. The performance of fabricated device was also evaluated using a theoretical model to assess the diffusive and capacitive contribution. The hybrid characteristics of the devices were investigated using a power law.

Biomass Waste Utilization as Nanocomposite Anodes through Conductive Polymers Strengthened SiO2/C from Streblus asper Leaves for Sustainable Energy Storages.

Sustainable anode materials, including natural silica and biomass-derived carbon materials, are gaining increasing attention in emerging energy storage applications. In this research, we highlighted a silica/carbon (SiO2/C) derived from Streblus asper leaf wastes using a simple method. Dried Streblus asper leaves, which have plenty of biomass in Thailand, have a unique leaf texture due to their high SiO2 content. We can convert these worthless leaves into SiO2/C nanocomposites in one step, producing eco-materials with distinctive microstructures that influence electrochemical energy storage performance. Through nanostructured design, SiO2/C is thoroughly covered by a well-connected framework of conductive hybrid polymers based on the sodium alginate-polypyrrole (SA-PPy) network, exhibiting impressive morphology and performance. In addition, an excellent electrically conductive SA-PPy network binds to the SiO2/C particle surface through crosslinker bonding, creating a flexible porous space that effectively facilitates the SiO2 large volume expansion. At a current density of 0.3 C, this synthesized SA-PPy@Nano-SiO2/C anode provides a high specific capacity of 756 mAh g-1 over 350 cycles, accounting for 99.7% of the theoretical specific capacity. At the high current of 1 C (758 mA g-1), a superior sustained cycle life of over 500 cycles was evidenced, with over 93% capacity retention. The research also highlighted the potential for this approach to be scaled up for commercial production, which could have a significant impact on the sustainability of the lithium-ion battery industry. Overall, the development of green nanocomposites along with polymers having a distinctive structure is an exciting area of research that has the potential to address some of the key challenges associated with lithium-ion batteries, such as capacity degradation and safety concerns, while also promoting sustainability and reducing environmental impact.

Rational design of hierarchical porous reduced graphene oxide/9,10-phenanthraquinone/porous carbon nanocomposites for high-performance supercapacitors

The development of advanced electrode material is crucial for promoting the application of new high-performance green energy storage devices and remains a great challenge. Herein, by introducing porous carbon (PC) or carbon nanotubes (CNTs) to further modify the redox-active 9,10-phenanthrenequinone (PQ) molecule non-covalently functionalized reduced graphene oxide (RGO), we have designed and synthesized RGO/PQ/PCs (RPPs) and RGO/PQ/CNTs-10 (RPC-10) nanocomposites using a simple one-step solvothermal method. Benefiting from the optimization of the hierarchical porous nanostructures and each composition further strengthens their respective advantages in the novel synthesized nanocomposites (RPPs and RPC-10), the RPPs and RPC-10 electrodes demonstrated significantly superior electrochemical energy storage performance over the RGO and RGO/PQ (RP) electrodes, especially for the RPP-10 electrode with a high specific capacitance of 343.5 F g−1 at 0.5 A g−1 and good rate capability (69.23 %, 0.5 − 40 A g−1). Furthermore, both the symmetric supercapacitor assembled with the optimal RPP-10 electrode and the hybrid supercapacitor assembled with the RPP-10 negative electrode and the NCSRC-24 positive electrode previously reported show excellent energy densities and ultra-long cycling stabilities. This result demonstrates that the synthesized novel RPP-10 nanocomposite is a highly promising candidate for new light-weight, sustainable, high-flexible and high-performance energy storage devices.

Construction of rod-like micro/nano structure and its effects on the electrochemical energy storage performance of lithium-rich manganese-based cathode material

Construction of rod-like micro/nano structure and its effects on the electrochemical energy storage performance of lithium-rich manganese-based cathode material

Electrochemical charge storage performance of (Mn, Ni, Mo, Co, Fe)3O4 high entropy oxide nanoparticles produced via thermal plasma route

Highly complex high entropy metal oxides (HEOs) have several unique characteristics, such as more active sites and material stability that improve the electrochemical charge storage capacity. In this study, HEOs (Mn, Ni, Mo, Co, Fe)3O4 nanoparticles were synthesized using a thermal plasma route and its electrochemical energy storage performance was studied with two distinct electrolytes such as 1 M KOH and NaOH. The X-ray diffraction analysis revealed the phase pure spinel structured HEOs with crystalline size ranging from 13 to 29 nm. Scanning electron microscopy and electron dispersive X-ray spectroscopy results revealed the quasi-spherical morphology and uniform distribution of constitutional cations in the as-synthesized HEOs. The X-ray photoelectron spectroscopy results identified the oxidation states of cations in spinel HEOs. The charge/discharge studies of as-synthesized HEOs showed a specific capacitance of 215 F g-1 /26.9 mAh g-1 at a current density of 2 A g-1 in 1 M KOH electrolyte which is 156 % greater than 1 M NaOH electrolyte. Furthermore, a high capacitance retention of 91 % was achieved after completing 3000 cycles at 10 A g-1 current density which indicates that the HEOs have excellent charge/discharge reversibility. Electrochemical impedance spectroscopy revealed that the solution and charge transfer resistances of HEOs electrodes were 1.04 and 3.2 Ω, respectively. This novel synthesis strategy attempts to overcome the difficulties experienced by established methods for bulk manufacture of phase pure HEOs since thermal plasma method is a rapid and a single-step approach for the bulk production of nanomaterial.

Elucidating Electrochemical Energy Storage Performance of Unary, Binary, and Ternary Transition Metal Phosphates and their Composites with Carbonaceous Materials for Supercapacitor Applications

Transition metal compounds (TMCs) are being researched as promising electrode materials for electrochemical energy storage devices (supercapacitors). Among TMCs, transition metal phosphates (TMPs) have good, layered structures owing to open framework and protonic exchange capability among different layers, good surface area due to engrossed porosity, rich active redox reaction sites owing to octahedral structure and variable valance metallic ions. Hence TMPs become more ideal for supercapacitor electrode materials compared to other TMCs. However, TMPs have got some issues like low conductivity, rate performance, stability, energy, and power densities. But these problems can be addressed by making their composites with carbonaceous materials, e.g., carbon nanotubes (CNTs), graphene oxide (GO), graphitic carbon (GC), etc. A few factors like high surface area, excellent electrical conductivity of carbon materials and variable valence metal ions in TMPs caused great enhancement in their electrochemical performance. This article tries to discuss and compare the published data, majorly in last decade, regarding the electrochemical energy storage potential of pristine unary, binary, and ternary TMPs and their hybrid composites with carbonaceous materials (CNTs, GOs/rGOs, GC, etc.). The electrochemical performance of the hybrids has been reported to be higher than the pristine counterparts. It is hoped that the current review will open a new gateway to study and explore the high performance TMPs based supercapacitor materials.

Polymer Binder-Free aqueous spinning of biomimetic CNT based hierarchical hollow fiber for structural and energy storage application

Assembly of functional nanomaterials into structural–functional integrated materials, such as structural-energy storage materials, are highly desirable for lightweight, high-performance wearable electronics, automobiles, and aviation/aerospace vehicles, yet extremely challenging due to the paradox between functional properties and the maintenance of mechanical properties. Herein, inspired by wheat-straw structures, we reported a polymer binder-free aqueous spinning strategy to manufacture biomimetic hollow carbon nanotube-based fibers (H-CNTF), where two-dimensional graphene oxide (GO) nanosheets are employed as an alternative to polymer binder for assisting the formation of hollow structures by rapid interaction with cations in coagulation, forming strong interaction with CNTs and tunning rheological property of spinning dope. The hierarchical hollow structure consisting of micron-scale hollow tubular space and porous walls endows H-CNTF with large surface area and abundant loading sites for guest materials, and the good CNT orientation and the absence of polymer binder enable H-CNTF excellent electrical and mechanical properties. As a proof of concept, the resulting H-CNTF supercapacitor electrodes exhibit high electrochemical energy storage performance with a specific capacity of 163 F/cm3 and high tensile strength of 0.35 N/tex. In addition, the polymer composite based on H-CNTF is about 100 % stronger than that based on solid fiber owing to the more uniform composite structure. The combination of outstanding electrochemical and mechanical properties makes this hollow fiber a promising material for future structural and energy storage applications.

Synergistic Corrosion Engineering on Metallic Manganese Toward High‐Performance Electrochemical Energy Storage

AbstractMnO/rGO with enhanced electrochemical kinetic properties is widely investigated as electrode for high‐performance electrochemical energy storage (EES) devices. However, the synthesis of MnO/rGO via traditional methods suffers from low atomic utilization and complex techniques that are undesirable for practical implementation. Different from existing fabrication strategies, here using metallic manganese as Mn source, a novel, eco‐friendly, and corrosion engineering‐based approach to address the above issues is demonstrated. It is thermodynamically feasible as supported by the E‐pH analysis and for the first time, a significant synergetic effect is observed between NH4+ and GO in strengthening the metallic Mn corrosion reaction. Particularly, in the “ammonia circulation” process, the NH3 molecule, derived from NH4+, acts as a “carrier” for Mn2+ to facilitate its transfer by forming [Mn(NH3)2]2+, which effectively prevents “in situ corrosion”. The phase and structure evolution during the reaction are clarified, and the synergistic corrosion mechanism is also proposed. Benefiting from the efficient lithium‐ion evolution kinetics, Mn─O─C bond formed between MnO and rGO and outstanding structural integrity, the resultant MnO/rGO demonstrates exceptional EES performances in both lithium‐ion batteries and lithium‐ion capacitors. This finding will offer potential for mild, cost‐effective, and environmentally friendly fabrication of other graphene‐based metal oxide electrodes using corrosion engineering.

Enhanced electrochemical energy storage performance by mediating BaTiO3 nanoparticles into the multilayers of Ti3C2Tx MXene

MXenes belong to the family of two-dimensional (2D) transition metal carbides, have been identified as advanced energy materials with exceptional performance. In this paper, we employed a strategy to intercalate BaTiO3 (BTO) nanoparticles into the two-dimensional (2D) Ti3C2Tx MXene sheets and use as electrode materials for electrochemical performances. BTO intercalated MXenes prove more active areas for improved electrochemical performance. As a result, the BTO intercalated Ti3C2Tx MXene electrode exhibits a high specific capacitance of 254.28F/g at 1 A/g and a retention ratio 74% after 10,000 cycles. The electrochemical stability study confirms that restacking issues were resolved. Thus, the intercalation of BTO enhanced the reaction kinetics of the MXenes and facilitate the charge storage valuable mechanism for next-generation smart energy storage devices.

Sonochemically synthesized novel CNTs-PANI/CoNi(PO4)2 nanocomposites with enhanced electrochemical energy storage performance for asymmetric supercapacitor applications

Carbon nanotubes (CNTs) were polymerized with polyaniline (PANI) via an in-situ polymerization approach. These functionalized CNTs (PANI-CNTs) were added in various concentrations to the sono-chemically synthesized Co-Ni binary transition metals phosphate (CoNi(PO4)2) to ultimately have their nanocomposites. Electron microscopy (SEM & HRTEM) was employed to reveal the morphology and microscopic features. The structural evaluation of metal phosphate and PANI/CNTs was done by X-ray diffractometer analysis, whereas chemical grafting of cobalt nickel phosphate (CoNi(PO4)2) was done by Fourier transformed infrared spectroscopy and Raman spectroscopy. The hierarchical structured CoNi(PO4)2 with 40 mg PANI/CNTs mass (CNP40) presented enhanced specific capacity of 1268 Cg−1 (2136 F g−1 at 1.5 F g−1) with excellent diffusive behavior (b = 0.5). A resulted hybrid supercapacitor device consisting of CNP40 as +ve electrode and activated carbon AC) as −ve electrode, presented excellent energy density of ∼87 Whkg−1 with good power density of 680 W kg−1 maintained to 32.9 W kg−1 (@ 20,400 W kg−1) with 37% rate performance, and excellent cyclic performance (∼100%) after 5000 charge-discharge cycles. Furthermore, capacitive-diffusive analysis revealed that the device showed 55% diffusive and 45% capacitive behaviour. This improved electrochemical performance might be attributed mainly to the uniform and hierarchical chemical grafted morphology of the novel combination of binary phosphates and PANI functionalized CNTs in the nanocomposite obtained via a rather different sonochemical approach.

The fabrication of Ti3C2 and Ti3CN MXenes by electrochemical etching

2D MXenes are well-known for their outstanding performance in electrochemical energy storage and many other applications owing to their high conductivity and specific surface area. An obstacle to the wider...

Morphology-controlled synthesis of a NiCo-carbonate layered double hydroxide as an electrode material for solid-state asymmetric supercapacitors

NiCo-carbonate layered double hydroxides of diverse morphologies, such as nanorod, microcube, microplate and urchin-like, are synthesized by a single-step synthesis and their electrochemical energy storage performance is evaluated.

Enhanced hydrogen evolution and symmetric supercapacitor performance of a Ru-doped multiphase WS2 electrode

The metallic and semiconductive phase (1T/2H) coupling enhanced electrochemical energy generation and storage performance of the Ru-doped WS2 multifunctional electrode is reported here.

Element screening of metal sites in Fe-based Prussian blue framework materials for ammonium ion battery applications: a first-principles study.

Prussian blue framework materials are expected to be the next generation of electrode materials for commercial batteries because their three-dimensional framework structures facilitate the rapid transport and storage of ions and a variety of redox processes. This work compared the calculations of the model before and after the dispersion correction, and the model considering the effect of van der Waals force was more stable. In addition, the distances between H, C and N atoms were within the range of van der Waals force. Thus it was confirmed that NH4+ was adsorbed on the Ax site in the Prussian blue framework material (AxMa[Mb(CN)6]) by van der Waals interaction, and the charge transfer was mainly achieved by the interaction between the H atom in NH4+ and the N atom in the Prussian blue framework. On this basis, the properties of NH4+ batteries were theoretically screened for the Fe-based Prussian blue analogues (PBAs) with different Ma elements (Ma = Co, Cu, Fe, Mg, Mn, Ni, V or Zn). Considering the regulating effect of different metal elements on the electronic structures of PBAs, MgFe and ZnFe PBAs as the electrode materials of NH4+ batteries are expected to show excellent electrochemical energy storage performance in organic electrolytes.

Electrochemical energy storage performance of one-step laser written Cu-C composites

One-step laser written copper-carbon (Cu-C) composites are ideal for assembling supercapacitors, but their structuring-performance correlation remains unclear. In this study, the microstructure of written composites has been controlled by varying the laser power. Their electrochemical energy storage performance has been investigated and compared to reveal the contribution of each component. The porous carbon-rich (C-rich) structure, introduced by laser carbonization of the substrate, can provide abundant active sites for the Faraday reaction of the copper-rich (Cu-rich) structure. The continuous sintered Cu-rich structure, obtained by laser reduction of ionic precursor and in-situ joining, can ensure fast transfer of electrons in the composites. Owing to their synergistic effect, our optimal composite exhibits an excellent specific capacity of 107.2 C/cm2 at 1 mA/cm2. This study provides a theoretical reference for the development of high-performance supercapacitors.

Phosphorus-Doped Nickel Oxide Micro-Supercapacitor: Unleashing the Power of Energy Storage for Miniaturized Electronic Devices.

For an uninterrupted self-powered network, the requirement of miniaturized energy storage device is of utmost importance. This study explores the potential utilization of phosphorus-doped nickel oxide (P-NiO) to design highly efficient durable micro-supercapacitors. The introduction of P as a dopant serves to enhance the electrical conductivity of bare NiO, leading to 11-fold augmentation in volumetric capacitance to 841.92 Fcm-3 followed by significant enhancement of energy and power density from 6.71 to 42.096 mWhcm-3 and 0.47 to 1.046 Wcm-3, respectively. Theoretical calculations used to determine the adsorption energy of OH- ions, revealing higher in case of bare NiO (1.52eV) as compared to phosphorus-doped NiO (0.64eV) leading to high electrochemical energy storage performance. The as-designed micro-supercapacitor (MSC) device demonstrates a facile integration with the photovoltaic system for renewable energy storage and smooth transfer to external loads for enlightening the blue LED for ≈1min. The choice of P-NiO/Ni not only contributes to cost reduction but also ensures minimal lattice mismatch at the interface facilitating high durability up to 15 K cycles along with capacitive retention of ≈100% and coulombic efficiency of 93%. Thus, the heterostructure unveils the possibilities of exploring miniaturized energy storage devices for portable electronics.