Electrochemical Energy Storage Performance Research Articles

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

Elucidating electrochemical energy storage performance of unary, binary, and ternary transition metal phosphates and their composites with carbonaceous materials for supercapacitor applications

Elucidating electrochemical energy storage performance of unary, binary, and ternary transition metal phosphates and their composites with carbonaceous materials for supercapacitor applications

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.

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.

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.

Facile synthesis of free-binder (NiCo)x(CuZn)1-xMoO4 (x = 0, 0.25, 0.5, 0.75, and 1)/nickel foam electrodes for supercapacitor application

In this work, free-binder (NiCo)x(CuZn)1-xMoO4 (x = 0, 0.25, 0.5, 0.75, and 1)/nickel foam electrodes were prepared by cetyltrimethylammonium bromide (CTAB)-assisted hydrothermal synthesis method. The composition modulated the morphology of material deposited on the nickel foam due to the different interactions between various cations and MoO42− species. With the increase of the Ni and Co contents, the morphology of molybdates transformed from agglomerated spherical particles to the flower-like hierarchal 2D flakes. Therefore, the application of multicomponent can be improved the electrochemical performance via tuning the morphology and physicochemical properties. The (NiCo)0.5(CuZn)0.5MoO4/nickel foam electrode with flower-like morphology showed the highest specific capacitance of 1176 F g−1 at a current density of 1 A g−1 and significant rate capability of 83 % (980 F g−1 up to 5 A g−1). The hierarchal flower-like (NiCo)0.5(CuZn)0.5MoO4//activated carbon asymmetric capacitor offered the rather high performance for electrochemical energy storage including energy density of 41.5 Wh kg−1 at power density of 1450 W kg−1.

Hollow Polyaniline Helical Nanobelts toward Efficient Electrochemical Energy Storage and Adsorption Performance

Hollow Polyaniline Helical Nanobelts toward Efficient Electrochemical Energy Storage and Adsorption Performance

Redox-active 9,10-phenanthrenequinone non-covalently modify reduced graphene oxide for high-performance asymmetric supercapacitor and zinc-ion hybrid capacitors

Redox-active organic molecules show great potential in novel renewable energy storage devices by modifying carbon-based materials in covalent or non-covalent forms due to their light-weight, rich structural diversity, good designability and abundance. Herein, we synthesized redox-active 9,10-phenanthrenequinone (PQ) molecules non-covalently modified reduced graphene oxide (RGO) nanocomposites by an improved simple one-step solvothermal method and explored their application as advanced electrode in aqueous energy storage devices. Benefiting from the rich redox-active sites brought by the anchored PQ molecules and the formation of the hierarchical porous network nanostructures with the RGO substrates that facilitates the charge transport and ion diffusion kinetics, the synthesized RGO/PQs nanocomposites exhibit significantly enhanced electrochemical energy storage performance. The optimal RGO/PQ-1.5 electrode has a high specific capacitance of 383.3 F g−1 at 0.5 A g−1 and good rate capability. And the asymmetric supercapacitor (ASC) assembled with the N-RGO negative electrode exhibits significantly better energy density than pure carbon electrode ASCs. More surprisingly, the assembled RGO/PQ-1.5//Zn zinc-ion hybrid capacitor exhibits an attractive specific capacity of 139.4 mAh g−1, a high energy density of 134.6 Wh kg−1, and an ultra-long cycling stability with 95.3 % capacity retention after 14,000 cycles, demonstrating excellent zinc-ion energy storage performance.

Surface‐amorphized nickel sulfide with boosted electrochemical performance for aqueous energy storage

AbstractThe ingenious structural design of electrode materials has a great influence on boosting the integrated conductivity and improving the electrochemical behavior of energy storage equipment. In this work, a surface‐amorphized sandwich‐type Ni3S2 nanosheet is synthesized by an easy hydrothermal and solution treatment technique. Because of the in‐built defect‐rich feature of the amorphous Ni3S2 layer, the constructed crystalline/amorphous heterointerface as well as dual nanopore structure of Ni3S2 nanosheet, the electron/ion transport and interfacial charge transfer is boosted, which contribute to high ionic conductivity and low resistance of the SA‐Ni3S2 electrode. The SA‐Ni3S2 electrode shows high specific capacitance (1767.6 F g−1 at 0.5 A g−1); the SA‐Ni3S2//AC device delivers high specific capacitance (131.2 F g−1 at 0.2 A g−1) and outstanding cycle stability (75% capacitance retention after 10000 cycles). In Ni‐Zn battery measurement, the SA‐Ni3S2//Zn exhibits satisfying specific capacity (211.2 mAh g−1 at 0.5 A g−1) and cycle durability (68% capacity decay after 2000 cycles). The results imply that the rational design of surface‐amorphized heterostructure is helpful for fabrication of electrode materials with high electrochemical performance in energy storage applications.

Defect engineering on BiFeO3 through Na and V codoping for aqueous Na-ion capacitors

Sodium with low cost and high abundance is considered as a substitute element of lithium for batteries and supercapacitors, which need the appropriate host materials to accommodate the relatively large Na+ ions. Compared to Li+ storage, Na+ storage makes higher demands on the structural optimization of perovskite bismuth ferrite (BiFeO3). We propose a novel strategy of defect engineering on BiFeO3 through Na and V codoping for high-efficiency Na+ storage, to reveal the roles of oxygen vacancies and V ions played in the enhanced electrochemical energy storage performances of Na-ion capacitors. The formation of the oxygen vacancies in the Na and V codoped BiFeO3 (denoted as NV-BFO), is promoted by Na doping and suppressed by V doping, which can be demonstrated by XPS and EPR spectra. By the first-principles calculations, the oxygen vacancies and V ions in NV-BFO are confirmed to substantially lower the Na+ migration energy barriers through the space and electric field effects, to effectively promote the Na+ transport in the crystals. Electrochemical kinetic analysis of the NV-BFO//NV-BFO capacitors indicates the dominant capacitive-controlled capacity, which depends on fast Na+ deintercalation-intercalation process in the NV-BFO electrode. The NV-BFO//NV-BFO capacitors open up a new avenue for developing high-performance Na-ion capacitors.

ZIF-derived hollow cattail-shaped composites with hierarchical channels towards enhanced electrochemical properties for supercapacitors

Despite the achievement in generating various hollow architectures, designing hollow composites with hierarchical channels remains challenging to achieve excellent electrochemical energy storage performance. To address this issue, we developed an in situ self-assembly strategy to prepare hollow composites using zeolitic-imidazolate frameworks and carbon nanotubes (ZIF@CNT). These ZIF@CNT architectures with different appearances are prepared by adjusting the stirring rate during the reaction. Subsequently, the sulfurization strategy is applied to convert ZIF-67 to cobalt sulfide (CoS), resulting in the hollow CoS@CNT hybrids. These hierarchical channels include the hollow CoS cavities and CNT channels. The unique hollow composites with different dimensions played a synergistic effect between subunits, thus giving excellent electrochemical properties. The impact of particle cavity channel size on electrochemical properties was evaluated systematically. As expected, CoS@CNT with hollow cattail-shape structures (HCCoS@CNT) resulted in the optimal specific capacitance (1250 F/g) and cyclic stability (90.4 % for over 10,000 times of cycling at 10 A/g). The designed hybrid supercapacitor, HCCoS@CNT//active carbon (AC), delivered an exceptional energy density of 40 Wh kg−1 at 800 W kg−1 of the power density. Together, these findings provide a reference for preparing complex hollow structures as high-performance electrodes, clarifying the optimization of composites for improved electrochemical properties.