Electrochemical Energy Storage Materials

Flexible electronic products, with their characteristics of flexibility and wearability, have attracted significant attention and have become an important direction in the research and development of the electronics industry. Planar micro-supercapacitors (MSCs) with flexible composite electrodes can provide reliable energy support for these products, propelling their further development. The research employed a quick, effective, and environmentally friendly method of laser scribing to create shape-controllable flexible composite electrodes on composite films of Poly(3,4-ethylenedioxythiophene) and graphene oxide (PEDOT/GO), which were subsequently assembled into MSCs. An analysis of the composite electrode morphology, structure, and elemental distribution was conducted through the utilization of SEM, TEM, and XPS techniques. Following this, a comprehensive evaluation of the electrochemical performance of the flexible MSCs was carried out, which included cyclic voltammetry (CV), galvanostatic charge/discharge (GCD), and assessment of cyclic stability. The analysis of the CV results indicated that the MSCs achieved the areal capacitance of 5.78 mF/cm² at 5 mV/s. After 5000 cycles at a current density of 0.05 mA/cm², the capacitance retention rate was 85.4%. The high areal capacitance and strong cycle stability of MSCs highlight the potential of PEDOT/reduced graphene oxide (PEDOT/rGO) electrodes in electrode applications. Full article

Manganese-based layered oxides are promising cathode materials for potassium-ion batteries (PIBs) due to their low cost and high theoretical energy density. However, the Jahn-Teller effect of Mn³⁺ and sluggish diffusion kinetics lead to rapid electrode deterioration and a poor rate performance, greatly limiting their practical application. Here, we report a Co/Al co-substitution strategy to construct a P3-type K_0.45Mn_0.7Co_0.2Al_0.1O₂ cathode material, where Co³⁺ and Al³⁺ ions occupy Mn³⁺ sites. This effectively suppresses the Jahn-Teller distortion and alleviates the severe phase transition during K⁺ intercalation/de-intercalation processes. In addition, the Co element contributes to K⁺ diffusion, while Al stabilizes the layer structure through strong Al-O bonds. As a result, the K_0.45Mn_0.7Co_0.2Al_0.1O₂ cathode exhibits high capacities of 111 mAh g⁻¹ and 81 mAh g⁻¹ at 0.05 A g⁻¹ and 1 A g⁻¹, respectively. It also demonstrates a capacity retention of 71.6% after 500 cycles at 1 A g⁻¹. Compared to the pristine K_0.45MnO₂, the K_0.45Mn_0.7Co_0.2Al_0.1O₂ significantly alleviates severe phase transition, providing a more stable and effective pathway for K⁺ transport, as investigated by in situ X-ray diffraction. The synergistic effect of Co/Al co-substitution significantly enhances the structural stability and electrochemical performance, contributing to the development of new Mn-based cathode materials for PIBs. Full article

Composite solid electrolytes (CSEs), often incorporating succinonitrile (SCN), offer promi I confirm sing solutions for improving the performance of all-solid-state batteries. These electrolytes are typically made of ceramics such as Li₇La₃Zr₂O₁₂ (LLZO) and polymers such as poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP). Garnet-applied polymer–ceramic electrolyte (g-PCE) is composed of PVDF-HFP, SCN, and LLZO. However, the interface between SCN and LLZO is reportedly unstable owing to the polymerization of SCN. This polymerization could cause two serious problems: (1) gelation during the mixing of LLZO and SCN and (2) degradation of ionic performance during charge and discharge. To prevent this catalytic reaction, polyacrylonitrile (PAN) can be added to the g-PCE (g-PPCE). PAN blocks the polymerization of SCN through a cyclization process involving La ions which occurs more rapidly than SCN polymerization. In this study, the enhanced chemical stability of the garnet-applied PAN-added polymer ceramic electrolyte (g-PPCE) was achieved by using an impregnation process which added SCN with 5 wt.% of PAN. The resulting CSE has an ionic conductivity of ~10^-⁴ S/cm at room temperature. Coin-type cells assembled with LFP (LiFePO₄) and LNCM (LiNi₀.₆Co₀.₂Mn₀.₂O₂) cathodes with Li-metal anodes show specific discharge capacities of 150 and 167 mAh/g at 0.1 C, respectively, and stable cycle performance. Additionally, a pouch-type cell with a discharge capacity of 5 mAh also exhibits potential electrochemical performance. Full article

Silicon is a promising anode material and can already be found in commercially available lithium-ion cells. Reliable modeling and simulations of new active materials for lithium-ion batteries are becoming more and more important, especially regarding cost-efficient cell design. Because literature lacks an electrochemical model for silicon-dominant electrodes, this work aims to close the gap. To this end, a Newman p2D model for a lithium-ion cell with a silicon-dominant anode and a nickel-cobalt-aluminum-oxide cathode is parametrized. The micrometer silicon particles are partially lithiated to 1200 mAh ${\mathrm{g}}_{\mathrm{Si}}^{-1}$. The parametrization is based on values from the electrode manufacturing process, measured values using lab cells, and literature data. Charge and discharge tests at six different C-rates up to 2C serve as validation data, showing a root-mean-squared error of about 21 mV and a deviation in discharge capacity of about 1.3%, both during a 1 C constant current discharge. Overall, a validated parametrization for a silicon-dominant anode is presented, which, to the best of our knowledge, is not yet available in literature. For future work, more in-depth studies should investigate the material parameters for silicon to expand the data available in the literature and facilitate further simulation work. Full article

In the recent rechargeable battery industry, lithium sulfur batteries (LSBs) have demonstrated to be a promising candidate battery to serve as the next-generation secondary battery, owing to its enhanced theoretical specific energy, economy, and environmental friendliness. Its inferior cyclability, however, which is primarily due to electrode deterioration caused by the lithium polysulfide shuttle effect, is still a major problem for the real industrial usage of LSBs. The optimization of the separator and functional barrier layer is an effective strategy for remedying these issues. In this article, the current progress based on the classification and modification of functional separators is summarized. We will also describe their working mechanisms as well as the resulting LSB electrochemical properties. In addition, necessary performance for separators will also be mentioned in order to gain optimized LSB performance. Full article

High-voltage spinel LiNi_0.5Mn_1.5O₄ (LNMO) is a promising candidate as a lithium-ion battery cathode material to fulfill the high-energy density demands of the electric vehicle industry. In this work, the design of the experiment’s methodology has been used to analyze the influence of the ratio of the different components in the electrode preparation feasibility of laboratory-scale coatings and their electrochemical response. Different outputs were defined to evaluate the formulations studied, and Derringer–Suich’s methodology was applied to obtain an equation that is usable to predict the desirability of the electrodes depending on the selected formulation. Afterward, Solver’s method was used to figure out the formulation that provides the highest desirability. This formulation was validated at a laboratory scale and upscaled to a semi-industrial coating line. High-voltage 1 Ah lithium-ion pouch cells were assembled with LNMO cathodes and graphite-based anodes and subjected to rate-capability tests and galvanostatic cycling. 1 C was determined as the highest C-rate usable with these cells, and 321 and 181 cycles above 80% SOH were obtained in galvanostatic cycling tests performed at 0.5 C and 1 C, respectively. Furthermore, it was observed that the LNMO cathode required an activation period to become fully electrochemically active, which was shorter when cycled at a lower C-rate. Full article

Porous carbon materials (PCs) were prepared via hydrothermal carbonization from calcium lignosulfonate (CL) based on enzymatic hydrolysis and alkali activation. The effects of enzymatic hydrolysis and different KOH feeding ratios on the structure and electrochemical properties of enzymatic hydrolysis CL (EHCL)-derived PCs were evaluated in detail. The results showed that the EHCL-derived PCs showed a higher SSA than that of CL. When the mass ratio of KOH/EHCL was 3/2, the PCs exhibited a honeycomb-like microscopic morphology with a specific surface area of up to 1771 m²/g and a 3D hierarchical porous structure composed of abundant micropores, mesopores, and macropores. As an electrode in a supercapacitor, the highest specific capacitance was 147 F/g at a current density of 0.25 A/g, and it maintained 78% of the initial value at a high current density of 10 A/g. The excellent electrochemical cycle and structural stability were confirmed on the condition of a higher capacitance retention of 95.2% after 5000 times of galvanostatic charge/discharge. This work provides a potential application of CL in high-performance supercapacitors. Full article

The dissolution of active material in aqueous batteries can lead to a rapid deterioration in capacity, and the presence of free water can also accelerate the dissolution and trigger some side reactions that affect the service life of aqueous batteries. In this study, a MnWO₄ cathode electrolyte interphase (CEI) layer is constructed on a δ-MnO₂ cathode by cyclic voltammetry, which is effective in inhibiting the dissolution of Mn and improving the reaction kinetics. As a result, the CEI layer enables the δ-MnO₂ cathode to produce a better cycling performance, with the capacity maintained at 98.2% (vs. activated capacity at 500 cycles) after 2000 cycles at 10 A g⁻¹. In comparison, the capacity retention rate is merely 33.4% for pristine samples in the same state, indicating that this MnWO₄ CEI layer constructed by using a simple and general electrochemical method can promote the development of MnO₂ cathodes for aqueous zinc ion batteries. Full article

Activated carbons (ACs) have been the most widespread carbon materials used in supercapacitors (SCs) due to their easy processing methods, good electrical conductivity, and abundant porosity. For the manufacture of electrodes, the obtained activated carbon based on sawdust (karagash and pine) was mixed with conductive carbon and polyvinylidene fluoride as a binder, in ratios of 75% activated carbon, 10% conductive carbon black, and 15% polyvinylidene fluoride (PVDF) in an N-methyl pyrrolidinone solution, to form a slurry and applied to a titanium foil. The total mass of each electrode was limited to vary from 2.0 to 4.0 mg. After that, the electrodes fitted with the separator and electrolyte solution were symmetrically assembled into sandwich-type cell construction. The carbon’s electrochemical properties were evaluated using cyclic voltammetry (CV) and galvanostatic charge–discharge (CGD) studies in a two-electrode cell in 6M KOH. The CV and CGD measurements were realized at different scan rates (5–160 mV s⁻¹) and current densities (0.1–2.0 A g⁻¹) in the potential window of 1 V. ACs from KOH activation showed a high specific capacitance of 202 F g⁻¹ for karagash sawdust and 161 F g⁻¹ for pine sawdust at low mass loading of 1.15 mg cm⁻² and scan rate of 5 mV s⁻¹ in cyclic voltammetry test and 193 and 159 F g⁻¹ at a gravimetric current density of 0.1 A g⁻¹ in the galvanostatic charge–discharge test. The specific discharge capacitance is 177 and 131 F g⁻¹ at a current density of 2 A g⁻¹. Even at a relatively high scan rate of 160 mV s⁻¹, a decent specific capacitance of 147 F g⁻¹ and 114 F g⁻¹ was obtained, leading to high energy densities of 26.0 and 22.1 W h kg⁻¹ based on averaged electrode mass. Surface properties and the porous structure of the ACs were studied by scanning electron microscopy, energy-dispersive X-ray analysis, Raman spectroscopy, and the Brunauer–Emmett–Teller method. Full article

As wearable electronic devices are becoming an integral part of modern life, there is a vast demand for safe and efficient energy storage devices to power them. While the research and development of microbatteries and supercapacitors (SCs) have significantly progressed, the latter has attracted much attention due to their excellent power density, longevity, and safety. Furthermore, SCs with a 1D fiber shape are preferred because of their ease of integration into today’s smart garments and other wearable devices. Fiber supercapacitors based on carbon nanotubes (CNT) are promising candidates with a unique 1D structure, high electrical and thermal conductivity, outstanding flexibility, excellent mechanical strength, and low gravimetric density. This review aims to serve as a comprehensive publication presenting the fundamentals and recent developments on CNT-fiber-based SCs. The first section gives a general overview of the supercapacitor types based on the charge storage mechanisms and electrode configuration, followed by the various fiber fabrication methods. The next section explores the different strategies used to enhance the electrochemical performance of these SCs, followed by a broad study on their stretchability and multifunctionality. Finally, the review presents the current performance and scalability challenges affecting the CNT-based SCs, highlighting their prospects. Full article

Aqueous zinc-ion batteries (ZIBS) are becoming more popular as the use of energy storage devices grows, owing to advantages such as safety and an abundant zinc supply. In this study, molybdenum powder was loaded directly on carbon fiber cloth (CFC) via multi-arc ion plating to obtain Mo@CFC, which was then oxidatively heated in a muffle furnace for 20 min at 600 °C to produce high mass loading α-MoO₃@CFC (α-MoO₃ of 12–15 mg cm⁻²). The cells were assembled with α-MoO₃@CFC as the cathode and showed an outstanding Zn²⁺ storage capacity of 200.8 mAh g⁻¹ at 200 mA g⁻¹ current density. The capacity retention rate was 92.4 % after 100 cycles, along with an excellent cycling performance of 109.8 mAh g⁻¹ following 500 cycles at 1000 mA g⁻¹ current density. Subsequently, it was shown that CFC-loaded α-MoO₃ cathode material possessed significantly improved electrochemical performance when compared to a cell constructed from commercial MoO₃ using conventional slurry-based electrode methods. This work presents a novel yet simple method for preparing highly loaded and binder-free cathodic materials for aqueous ZIBs. The results suggest that the highly loaded cathode material with a high charge density may be potentially employed for future flexible device assembly and applications. Full article

Aqueous zinc-ion batteries offer the greatest promise as an alternative technology for low-cost and high-safety energy storage. However, the development of high-performance cathode materials and their compatibility with aqueous electrolytes are major obstacles to their practical applications. Herein, we report the synthesis of orthorhombic V₂O₅·nH₂O nanorods as cathodes for aqueous zinc batteries. As a result, the electrode delivers a reversible capacity as high as 320 mAh g⁻¹ at 1.0 A g⁻¹ and long-term cycling stability in a wide window of 0.2 to 1.8 V using a mild ZnSO₄ aqueous electrolyte. The superior performance can be attributed to the improved stability of materials, inhibited electrolyte decomposition and facilitated charge transfer kinetics of such materials for aqueous zinc storage. Furthermore, a full cell using microsized Zn powder as an anode within capacity-balancing design exhibits high capacity and stable cycling performance, proving the feasibility of these materials for practical application. Full article

The electrode concept of graphite and silicon blending has recently been utilized as the anode in the current lithium-ion batteries (LIBs) industry, accompanying trials of improvement of cycling life in the commercial levels of electrode conditions, such as the areal capacity of approximately 3.3 mAh/cm² and volumetric capacity of approximately 570 mAh/cm³. However, the blending concept has not been widely explored in the academic reports, which focused mainly on how much volume expansion of electrodes could be mitigated. Moreover, the limitations of the blending electrodes have not been studied in detail. Therefore, herein we investigate the graphite blending electrode with micron-sized SiO_x anode material which is one of the most broadly used Si anode materials in the industry, to approach the commercial and practical view. Compared to the silicon micron particle blending electrode, the SiO_x blending electrode showed superior cycling performance in the full cell test. To elucidate the cause of the relatively less degradation of the SiO_x blending electrode as the cycling progressed in full-cell, the electrode level expansion and the solid electrolyte interphase (SEI) thickening were analyzed with various techniques, such as SEM, TEM, XPS, and STEM-EDS. We believe that this work will reveal the electrochemical insight of practical SiO_x-graphite electrodes and offer the key factors to reducing the gap between industry and academic demands for the next anode materials. Full article