Comprehensive Electrochemical Impedance Spectroscopy Study of Flow-Electrode Capacitive Deionization Cells.

Flow-electrode capacitive deionization (FCDI) offers infinite ion adsorption for continuous desalination of high-concentration saline water by supplying a flow-electrode to the cell. Although extensive efforts have been made to maximize the desalination rate and efficiency of FCDI cells, the electrochemical properties of these cells are not fully understood. This study investigated the factors affecting the electrochemical properties of FCDI cells containing activated carbon (AC; 1-20 wt %) and various flow rates (6-24 mL/min) for the flow-electrode using electrochemical impedance spectroscopy before and after desalination. Examination of the impedance spectra using the distribution of relaxation time and equivalent circuit fitting analysis revealed three distinctive resistances such as internal, charge transfer, and ion adsorption resistances. The overall impedance decreased significantly after the desalination experiment due to increased ion concentrations in the flow-electrode. The three resistances decreased with increasing concentrations of AC in the flow-electrode due to the extension of electrically connected AC particles that participated in the electrochemical desalination reaction. The ion adsorption resistance decreased significantly due to the flow rate dependence of the impedance spectra. In contrast, the internal and charge transfer resistances were invariant.

New Luminescent Pyridine-based Disc type Molecules: Synthesis, Photophysical, Electrochemical, and DFT studies.

The design and synthesis of new conjugated luminescent molecules have attracted the attention of researchers because of their various applications, especially in the field of optoelectronic devices. Most of the applications were mainly based on the intramolecular charge transfer (ICT). For this purpose, we designed and synthesized a series of new donor-acceptor based disc type molecules i.e. 2,4,6-tris(4-(alkyloxy)phenyl)pyridines carrying variable alkoxy chains [i.e. n = 2, 4, 6, 8, 10, 12, 14, 16]. Further, the structures of all the synthesized compounds were confirmed by using ATR-IR, 1H-NMR, 13C-NMR, and ESI-MS analysis. Moreover, the photophysical property study indicated that all the molecules are blue light emitting materials, however the change of alkoxy chain length in phenyl arms does not affect their absorption, emission, and energy levels. Besides, the thermal study revealed that core is stable up to 350 °C. Also, the DFT study showed that the photo induced electron transfer caused by HOMO-LUMO excitation in the studied molecules. Therefore, all the molecules have potential applications in optoelectronic applications.

Treatment of phenolic wastewater by anaerobic fluidized bed microbial fuel cell using carbon brush as anode: microbial community analysis and m-cresol degradation mechanism.

Anaerobic fluidized bed microbial fuel cell (AFB-MFC) is a technology that combines fluidized bed reactor and microbial fuel cell to treat organic wastewater and generate electricity. The performance and the mechanism of treating m-cresol wastewater in AFB-MFC using carbon brush as biofilm anode were studied. After 48 h of operation, the m-cresol removal efficiency of AFB-MFC, MAR-AFB (fluidized bed bioreactor with acclimated anaerobic sludge), MAR-FB (ordinary fluidized bed reactor with only macroporous adsorptive resin) and AST (traditional anaerobic sludge treatment) were 95.29 ± 0.67%, 85.78 ± 1.81%, 71.24 ± 1.86% and 70.41 ± 0.32% respectively. The maximum output voltage and the maximum power density of AFB-MFC using carbon brush as biofilm anode were 679.7 mV and 166.6 mW/m2 respectively. The results of high-throughput sequencing analysis indicated the relative abundance of dominant electroactive bacteria, such as Trichococcus, Geobacter, and Pseudomonas, on the anode carbon brushes was higher than that of AST, and also identified such superior m-cresol-degrading bacteria as Bdellovibrio, Thermomonas, Hydrogenophaga, etc. Based on the determination of m-cresol metabolites detected by Gas Chromatography-Mass Spectrometry (GC-MS), the possible biodegradation pathway of m-cresol under anaerobic and aerobic conditions in AFB-MFC was speculated. The results showed that m-cresol was decomposed into formic acid-acetic anhydride and 3-methylpropionic acid under the action of electrochemistry, which is a simple degradation pathway without peripheral metabolism in AFB-MFC.

A Composite of Two Dimensional GeSe2 /Nitrogen-Doped Reduced Graphene Oxide for Enhanced Capacitive Lithium-Ion Storage.

A composite of two-dimensional (2D) GeSe2 nanosheets dispersed on N-doped reduced graphene oxide (GeSe2 /N-rGO) is fabricated via a simple hydrothermal method combined with post-selenization process. The high electronic conductivity and the substantial void spaces of the wrinkled N-rGO can improve the electrical conductivity of the active material and accommodate the volume evolution of GeSe2 nanosheets during the (de)lithiation processes, while GeSe2 nanosheets can reduce ion diffusion length effectively. Meanwhile, the unique layered structure is beneficial to the contact of the active material and electrolyte, and the reversibility of conversion reaction has also been improved. Furthermore, kinetics analysis reveals a pseudocapacitance-dominated Li+ -storage mechanism at high rates. In-situ X-ray diffraction analysis discloses that the conversion reaction has played a certain part in Li+ -storage. Thus, the GeSe2 /N-rGO composite delivers excellent rate capability and good long-term stability with a high reversible capacity of 711.0 mA h g-1 after 2000 cycles at 1 A g-1 .

Characterization of electrodes modified with sludge-derived biochar and its performance of electrocatalytic oxidation of azo dyes.

Pyrolysis of waste sludge in sewage treatment can achieve a substantial reduction in solid waste and obtain sludge-based biochars with multiple functions. However, the electrochemical properties of sludge-derived biochar as electrode modification material and the electrocatalytic ability of biochar-modified electrodes are still unclear. In this study, sludge-based biochars were prepared at various pyrolysis temperatures (400 °C, 500 °C, 600 °C, 700 °C, and 800 °C) and then were cast on glassy carbon electrodes to fabricate composite biochar-electrodes (GC400, GC500, GC600, GC700, and GC800). The results of elemental analysis and Raman spectra showed that sludge-based biochar prepared at higher temperatures exhibited higher aromaticity and degree of defect structures. And the results of cyclic voltammetry and electrochemical impedance spectra confirmed that biochar-modified electrodes prepared at higher temperatures (>600 °C) possessed better electrocatalytic activity and electrochemical stability, and their higher oxygen evolution potential than control test could improve the electrocatalytic efficiency. In the electrocatalytic oxidation of methyl orange, the removal rate with GC800 was the highest, reaching 94.49% within 240 min, and the removal rates with other composite electrodes were 90.61% (GC700) > 86.96% (GC600) > 80.32% (GC). The free radical quenching experiment revealed that the electrocatalytic degradation of methyl orange mainly depended on the indirect oxidation of hydroxyl radicals generated by electrocatalysis, accounting for 81.3% of the removal rate. The biochar-modified electrode not only greatly improved the electrocatalytic ability of the electrode for the degradation of azo dyes, but also achieved the recycling application of products after pyrolysis of sludge waste.

Enhanced tensile and electrochemical performance of MXene/CNT hierarchical film.

Nowadays, it is highly desirable to achieve high strength, flexibility and electrochemical performance for supercapacitor electrodes simultaneously. Herein, few-layer MXene flakes are assembled into free-standing films by facile vacuum-filtration method, in which hydrophilic-functionalized carbon nanotubes (CNTs) are further incorporated. The morphology of MXene/CNT composite films evolves from compact to 'CNT in MXene' to laminar to 'MXene in CNT' and finally to separate structures when increasing the CNT weight percentage. Among them, the laminar structure in which thin MXene and CNT layers are stacked alternately is demonstrated to be the best. The laminar MXene/CNT film possesses much higher strength, elongation and specific capacitance than MXene film due to the engineered porosity, good interaction between MXene flakes and CNTs, and proper CNTs' distribution. As a result, high specific capacitance of 423.4 F g-1at 1 A g-1and capacitance retention of nearly 60% at 10 A g-1are accomplished. Moreover, the composite film is flexible and withstands bending up to 180°, indicating that the proposed laminar MXene/CNT composite film is a superb candidate for flexible supercapacitors.

Synthesis of novel Co3O4 nanocubes-NiO octahedral hybrids for electrochemical energy storage supercapacitors.

Fabrication of novel metal oxide nanostructured composites is a proficient approach to develop efficient energy storage devices and development of cost-free and eco-friendly metal oxide nanostructures for supercapacitor applications received considerable attention in recent years. The Co3O4 nanocubes-NiO octahedral structured composite was constructed using facile and one-step calcination process. Cyclic voltammetry, charge-discharge, and electrochemical impedance spectral techniques have been employed to analyze the specific capacitance of the synthesized nanostructures and the composites. Specific capacitance and cycling stability of the composites were evaluated with the pristine Co3O4 and NiO nanostructures. The composite showed a specific capacitance of 832 F g-1 at a current density of 0.25 A g-1, which was ~1.5 and ~1.9-times higher than pristine Co3O4 nanocubes and NiO octahedral structure, respectively. On the other hand, electrode showed approximately 50 % capacity retention at a higher current density (5 Ag-1) because of the uniform morphology of Co3O4 and NiO. The charge-discharge stability measurements of the composite showed an admirable specific capacitance retention capability, which was 94.5 % after 2000 continuous charge-discharge cycles at a current density of 5 A g-1. The superior electrochemical performance of the nano-composite was ascribed to synergistic effects and uniform morphology. Efficient nanostructure development using facile and one-step calcination process and electrochemical performance make the synthesized composite a promising device for supercapacitor applications.

Multidimensional Integrated Chalcogenides Nanoarchitecture Achieves Highly Stable and Ultrafast Potassium-Ion Storage.

Potassium-ion batteries (KIBs) have come into the spotlight in large-scale energy storage systems because of cost-effective and abundant potassium resources. However, the poor rate performance and problematic cycle life of existing electrode materials are the main bottlenecks to future potential applications. Here, the first example of preparing 3D hierarchical nanoboxes multidimensionally assembled from interlayer-expanded nano-2D MoS2 @dot-like Co9 S8 embedded into a nitrogen and sulfur codoped porous carbon matrix (Co9 S8 /NSC@MoS2 @NSC) for greatly boosting the electrochemical properties of KIBs in terms of reversible capacity, rate capability, and cycling lifespan, is reported. Benefiting from the synergistic effects, Co9 S8 /NSC@MoS2 @NSC manifest a very high reversible capacity of 403 mAh g-1 at 100 mA g-1 after 100 cycles, an unprecedented rate capability of 141 mAh g-1 at 3000 mA g-1 over 800 cycles, and a negligible capacity decay of 0.02% cycle-1 , boosting promising applications in high-performance KIBs. Density functional theory calculations demonstrate that Co9 S8 /NSC@MoS2 @NSC nanoboxes have large adsorption energy and low diffusion barriers during K-ion storage reactions, implying fast K-ion diffusion capability. This work may enlighten the design and construction of advanced electrode materials combined with strong chemical bonding and integrated functional advantages for future large-scale stationary energy storage.

Nitrogen-doped lignin-derived electrode materials for supercapacitors were prepared using the domain-limited effect.

Supercapacitors, pivotal in mitigating the energy crisis stemming from dwindling fossil fuel reservoirs, necessitate meticulous consideration of electrode material preparation. While lignin-derived carbon materials sourced sustainably exhibit commendable potential as electrode materials, their intrinsic low capacitance limits widespread utilization. Herein, nitrogen atom doping of lignin (CNL) was accomplished employing a chemical modification technique employing cyanuric chloride as a dopant. The resultant nitrogen content measured at 2.85 %. Subsequent to CNL carbonation, the generated C3N4 was selectively confined to the internal surface of the CNLMS-800 through a domain-limited activation method, thereby rendering it suitable for deployment as a supercapacitor electrode material. CNLMS-800 manifests a substantial specific surface area of 1778.0 m2 g-1 and a concomitantly diminutive pore size of 2.6 nm. Noteworthy, the specific capacitance of CNLMS-800 attains 473.0 F g-1 at a current density of 0.5 A g-1 in a 6 M KOH electrolyte. The resultant energy density reaches 39.0 Wh kg-1 at a power density of 338.0 W kg-1. Crucially, even after 20,000 charge/discharge cycles at a current density of 10 A g-1, the capacitance retention attains an impressive 87.5 % in the KOH electrolyte. This innovative utilization of sustainable resources for electrode fabrication epitomizes a seminal advancement in the field of energy technology.

Epoxy-based multifunctional solid polymer electrolytes for structural batteries and supercapacitors. a short review.

The potential applications of epoxy-based solid polymer electrolytes are continually expanding because of their versatile characteristics. These characteristics include mechanical rigidity, nonvolatility, nonflammability, and electrochemical stability. However, it is worth noting that pure epoxy-based solid polymer electrolytes inherently exhibit lower ion transport capabilities when compared to traditional liquid electrolytes. Striking a balance between high mechanical integrity and superior ionic conductivity at room temperature poses a significant challenge. In light of this challenge, this review is dedicated to elucidating the fundamental concepts of epoxy-based solid polymer electrolytes. It will explore various preparation techniques, the incorporation of different nanomaterials into epoxy-based solid polymer electrolytes, and an evaluation of their multifunctional properties. This comprehensive evaluation will cover both mechanical and electrical properties with a specific focus on their potential applications in batteries and structural supercapacitors.

Study on the Effect of Polyamine Water Treatment Agent on Metal Corrosion Inhibition in Boiler Steam-Water System.

A polyamine water treatment agent was prepared with the film-forming amine (N-oleyl-1,3-propylenediamine) and the neutralizing amine (cyclohexanamine) under optimal conditions. The copper sulfate liquid drop experiment showed that a protective film was formed by the polyamine water treatment agent on carbon steel. The analyses of the polarization curve and electrochemical impedance spectroscopy of carbon steel indicated that the polyamine water treatment agent exhibited geometric effects, which could inhibit both anode and cathode reactions of carbon steel, and the corrosion inhibition effect of the polyamine water treatment agent showed an extreme-concentration phenomenon. A metal corrosion experiment in a simulated boiler steam-water system indicated that the polyamine water treatment agent mitigated the corrosion of carbon steel at different temperatures, and the corrosion inhibition rates of the polyamine water treatment agent in liquid and gas environments at 150 °C were 53.84% and 67.43%, respectively, better than that at 350 °C. SEM-EDS characterization indicated that the formation of the corrosion product, iron oxide, on the carbon steel was reduced with the addition of the polyamine water treatment agent in the simulated boiler steam-water system.

Synthesis, characterization, and electrochemical evaluation of SnFe2O4@MWCNTS nanocomposite as a potential hydrogen storage material.

The widespread use of hydrogen as a vehicle fuel has prompted us to develop a new nanocomposite by immobilizing of tin ferrite nanoparticles (SnFe2O4) on the surface of multi-walled carbon nanotubes (abbreviated as MWCNTS) for the first time. The prepared nanocomposite powder (SnFe2O4@MWCNTS) was investigated utilizing various microscopy and spectroscopy methods, such as FT-IR, XRD, SEM, EDX, and BET techniques. Moreover, the electrochemical property of SnFe2O4@MWCNTS nanocomposite was investigated by cyclic voltammogram (CV) and charge-discharge chronopotentiometry (CHP) techniques. A variety of factors on the hydrogen storage capacity, such as current density, surface area of the copper foam, and the influence of repeated hydrogen adsorption-desorption cycles were assessed. The electrochemical results indicated that the SnFe2O4@MWCNTS has high capability and excellent reversibility compared to SnFe2O4 nanoparticles (NPs) for hydrogen storage. The highest hydrogen discharge capability of SnFe2O4@MWCNTs was achieved ∼ 365 mAh/g during the 1st cycle, and the storage capacity enhanced to ∼ 2350 mAh/g at the end of 20 cycles using a current of 2 mA. Consequently, the SnFe2O4@MWCNTS illustrated great capacity as a prospective active material for hydrogen storage systems.

Enhancing the photoinduced via a novel nano-combination of terbium oxide and nickel oxide on graphene oxide surface: Cytotoxicity and water treatment.

The target is a novel nano-combination membrane (NCM) via Terbium oxide nanoparticles (Tb2O3 NPs) and nickel oxide (NiO NPs) which integrates on the graphene oxide (GO) surface. The NCM is characterized by different tools such as X-ray diffraction (XRD), UV-visible spectrophotometer (UV-vis), and Scanning electron microscopy (SEM)for removing organic pollutants. The precipitation method has been applied for fabricating the selected metal oxides (MOs), where the terbium chloride and nickel chloride are used as precursors for fabricating the metal oxides (MOs) NPs that formed with potassium hydroxide in the solution. The photocatalytic activity of fabricated NCM has been noticed with the quenching of mixed Rhodamine B (RhB) and methyl orange (MO) dyes at various times for water treatment. UV-vis spectra confirmed the excellent efficiency against organic pollution degradation. After exposure to the light for 100 min, the photodegradation efficacy of MB and RhB appeared at 46.88 % and 16.4 %, with GO@Tb2O3, by GO@Tb2O3.NiO the efficiency was 54.8 % and 32.3 % after 100 min, while GO@NiO has degradation efficiency at 43 % and 17.3 % for MB and RhB respectively. The cytotoxicity of NCM is detected with hepatocellular carcinoma (HepG2) and breast adenocarcinoma (MCF-7), the result illustrated that the fabricated NCM does not affect the cancer cells with the 10 µL, but with the higher concentration of 100 µL, the cell lysis was observed. The results of photocatalytic and cytotoxicity are recommended using these fabricated NCM in water treatment.

Exploring Microstructure, Wear Resistance, and Electrochemical Properties of AlSi10Mg Alloy Fabricated Using Spark Plasma Sintering.

Al-Si-Mg alloy has excellent casting performance due to its high silicon content, but the coarse eutectic silicon phase can lead to a decrease in its mechanical properties. Samples of AlSi10Mg alloy were prepared by using a spark plasma sintering method, and it was found that sintering temperature has a significant impact on the grain size, eutectic silicon size and wear and corrosion properties after heat treatment. At a sintering temperature of 525 °C, the alloy exhibits the best wear performance with an average friction coefficient of 0.29. This is attributed to the uniform precipitation of fine eutectic silicon phases, significantly improving wear resistance and establishing adhesive wear as the wear mechanism of AlSi10Mg alloy at room temperature. The electrochemical performance of AlSi10Mg sintered at 500 °C is the best, with Icorr and Ecorr being 1.33 × 10-6 A·cm-2 and -0.57 V, respectively. This is attributed to the refinement of grain size and eutectic silicon size, as well as the appropriate Si volume fraction. Therefore, optimizing the sintering temperature can effectively improve the performance of AlSi10Mg alloy.

Effect of ion structure on the nanostructure and electrochemistry of surface active ionic liquids.

HYPOTHESIS: The ion structure of surface active ionic liquids (SAILs), i.e. ion charge group and alkyl chain structure, controls their bulk and interfacial nanostructure and the electrochemical properties near an electrode. EXPERIMENTS: The structures in the bulk and at the interface were investigated by small and wide-angle X-ray scattering (SAXS) and atomic force microscopy (AFM), respectively. An investigation was performed using cyclic voltammetry. FINDINGS: All SAILs show pronounced sponge-like bulk nanostructure. For the first time, the bulk nanostructures of SAILs are found to change from anion bilayer structures to cation-anion interdigitated structures as the ion structures change from short alkyl chain cations and linear alkyl chain anions to long alkyl chain cations and branched alkyl chain anions. The bulk nanostructure packs more compactly at a higher temperature, likely due to the conformational change and enhanced interdigitations of alkyl chains. The thicknesses of SAIL interfacial layers align with the repeat distances of the bulk nanostructure, similar to conventional ILs with long cation alkyl chains. All SAILs have wide electrochemical windows >4 V, which are not affected by the alkyl chain structure and cation charge groups.

F-doped TiO2(B)/reduced graphene for enhanced capacitive lithium-ion storage.

A composite of F-doped TiO2(B) and reduced graphene oxide (F-TiO2(B)/rGO) was successfully synthesized via a one-step hydrothermal route. It was found that the introduction of F ions in the synthetic process has led to the uniform dispersion of TiO2(B) on rGO nanosheets. The F ions have also been doped into the lattice of TiO2(B), which greatly improved the conductivity of the materials. Consequently, this composite delivered a large capacity of 249.4 mA h g-1 at 0.2 A/g. It also demonstrated a capacity of 203.1 mA h g-1 and an excellent capacity retention of 96% after 500 cycles even at a high current density of 2 A/g.

Zinc-Bromine Rechargeable Batteries: From Device Configuration, Electrochemistry, Material to Performance Evaluation.

Zinc-bromine rechargeable batteries (ZBRBs) are one of the most powerful candidates for next-generation energy storage due to their potentially lower material cost, deep discharge capability, non-flammable electrolytes, relatively long lifetime and good reversibility. However, many opportunities remain to improve the efficiency and stability of these batteries for long-life operation. Here, we discuss the device configurations, working mechanisms and performance evaluation of ZBRBs. Both non-flow (static) and flow-type cells are highlighted in detail in this review. The fundamental electrochemical aspects, including the key challenges and promising solutions, are discussed, with particular attention paid to zinc and bromine half-cells, as their performance plays a critical role in determining the electrochemical performance of the battery system. The following sections examine the key performance metrics of ZBRBs and assessment methods using various ex situ and in situ/operando techniques. The review concludes with insights into future developments and prospects for high-performance ZBRBs.

Carbon-Coated CuNb13O33 as A New Anode Material for Lithium Storage.

Niobates are very promising anode materials for Li+-storage rooted in their good safety and high capacities. However, the exploration of niobate anode materials is still insufficient. In this work, we explore ~1 wt% carbon-coated CuNb13O33 microparticles (C-CuNb13O33) with a stable shear ReO3 structure as a new anode material to store Li+. C-CuNb13O33 delivers a safe operation potential (~1.54 V), high reversible capacity of 244 mAh g-1, and high initial-cycle Coulombic efficiency of 90.4% at 0.1C. Its fast Li+ transport is systematically confirmed through galvanostatic intermittent titration technique and cyclic voltammetry, which reveal an ultra-high average Li+ diffusion coefficient (~5 × 10-11 cm2 s-1), significantly contributing to its excellent rate capability with capacity retention of 69.4%/59.9% at 10C/20C relative to 0.5C. An in-situ XRD test is performed to analyze crystal-structural evolutions of C-CuNb13O33 during lithiation/delithiation, demonstrating its intercalation-type Li+-storage mechanism with small unit-cell-volume variations, which results in its capacity retention of 86.2%/92.3% at 10C/20C after 3000 cycles. These comprehensively good electrochemical properties indicate that C-CuNb13O33 is a practical anode material for high-performance energy-storage applications.

Synthesis and electrochemical properties of Mn-doped Li2Mn0.1Ti1.9(PO4)3 materials.

The hunt for a higher power storage, relatively inexpensive, non-polluting battery technology is currently a pressing issue because of the rapid growth of the worldwide economic and the progressively significant environmental pollution. Among the possible nanomaterials for rechargeable batteries that can have heteroatoms applied to it in order to improve its electrochemical behavior is LixTiy(PO4)3. Carbon-coated Mn-doped Li2Mn0.1Ti1.9(PO4)3 materials was synthesized by spray drying method. The material was characterized by XRD, SEM, TEM, BET, TGA et al. Crystal data refinement results by Rietveld method showed that the symmetry space group is Pbcn.The lattice parameters of Li2Mn0.1Ti1.9(PO4)3 are a = 11.9372 Å, b = 8.5409 Å, c = 8.5979 Å, α = ß = γ = 90°, V = 876.59 Å3 and Z = 4). Rietveld refinement was performed, and the confidence factors are Rwp = 11.79%, Rp = 9.14%, and χ2 = 1.425. It was exhibited that LMTP0.1/CA-700 material has good crystallinity. Testing the cells with LAND test procedure (200 mA/g current density for 200 cycles), the LMTP0.1/CA-700 material has a discharge specific capacity of about 65 mAh/g. The capacity decayed by only 3% during the cycle. It has some potential application values as cathode of lithium ion battery in the future.

Thickness Dependency of Battery Anode Properties in Multilayer Graphene.

With the development of practical thin-film batteries, multilayer graphene (MLG) is being actively investigated as an anode material. Therefore, research on determining a technique to fabricate thick MLG on arbitrary substrates at low temperatures is essential. In this study, we formed an MLG with controlled thickness at low temperatures using a layer exchange (LE) technique and evaluated its anode properties. The LE technique enabled the formation of a uniform MLG with a wide range of thicknesses (25-500 nm) on Ta foil. The charge/discharge characterization using coin-type cells revealed that the total capacity, which corresponded to Li intercalation into the MLG interlayer, increased with increasing MLG thickness. In contrast, cross-sectional transmission electron microscopy showed a metal oxide formed at the MLG/Ta interface during annealing, which had small Li capacity. MLG with sufficient thickness (500 nm) exhibited an excellent Coulombic efficiency and capacity retention compared to bulk graphite formed at high temperatures. These results have led to the development of inexpensive and reliable rechargeable thin-film batteries.