Application Of Electrode Research Articles

Application of Electrodes for Degradation of Reactive Dyes in the Case of Textile Industry Wastewater

Application of Electrodes for Degradation of Reactive Dyes in the Case of Textile Industry Wastewater

Microfabrication through Self‐Ordering of Cracks: Mechanism, Upscaling and Application for Transparent Electrodes

AbstractWhen drying a colloidal solution, cracks appear in the resulting colloidal film. In certain cases, spontaneous order is observed, and cracks form arrays of periodic patterns. Although this phenomenon might be envisioned as a patterning method, overcoming practical challenges is necessary to transform it into a technological tool for microfabrication. This study explores various technological aspects aimed at leveraging the self‐assembly of cracks as a scalable microfabrication tool for large‐scale device production. Through a series of analyses, including time‐resolved Grazing‐Incidence Small‐Angle X‐Ray Scattering (GISAXS), it is offered novel insights into controlling the crack self‐ordering mechanism, minimizing defects, and implementing strategies for large‐scale patterning and pattern transfer. The process proves to be surprisingly robust, maintaining its efficacy with the same colloidal solution even after two years. By introducing biphasic dip‐coating, large‐scale crack patterns up to 100 cm2, while preserving their periodicity and ordering is achieved. As a proof of concept, the use of crack‐patterned colloidal films as masks for fabricating metallic sub‐micrometer objects, that serve as transparent electrodes with adjustable transparency and conductivity is showcased. Overall, this method presents significant advantages over conventional lithography, being cost‐effective, versatile, environmentally friendly, and scalable, thereby offering new perspectives for diverse applications requiring cost‐effective and large‐scale patterning.

Supercapacitors and triboelectric nanogenerators based on electrodes of greener iron nanoparticles/carbon nanotubes composites

The development of supporting materials based on carbon nanotubes (CNTs) impregnated with iron nanoparticles via a sustainable and green synthesis employing plant extract of Punica granatum L. leaves was carried out for the iron nanoparticle modification and the following impregnation into the carbon nanotubes composites (CNT-Fe) that were also coated with polypyrrole (CNT-Fe + PPy) for use as electrode for supercapacitor and triboelectric nanogenerators. The electrochemical characterization of the materials by cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) assays revealed that the CNT-Fe + PPy gave rise to better performance due to the association of double-layer capacitance behavior of carbon derivative in association with the pseudocapacitance contribution of PPy resulting in an areal capacitance value 202 mF/ cm2 for the overall composite. In terms of the application of electrodes in triboelectric nanogenerators, the best performance for the composite of CNT-Fe + PPy was 60 V for output voltage and power density of 6 μW/cm2. The integrated system showed that the supercapacitors can be charged directly by the nanogenerator from 0 to 42 mV in 300 s. The successful green synthesis of iron nanoparticles on CNT and further PPy coating provides a feasible method for the design and synthesis of high-performance SCs and TENGs electrode materials. This work provides a systematic approach that moves the research front forward by generating data that underpins further research in self-powered electronic devices.

Novel sol-gel route for expanding the glass forming region of tin phosphate glass for secondary battery electrode applications

In this paper, tin-phosphate amorphous glass and nano-crystallized ceramic materials were synthesized by sol-gel methods and heat treated at 400 °C with the composition of xSnO2− (100-x)P2O5 (xSnP: ‘x’ from 40 to 90 mol%). The electrical and thermal properties of tin-phosphate materials were investigated by electrical impedance spectroscopy (EIS) and thermogravimetry – differential thermal analysis – mass spectroscopy (TG–DTA–MS). Moreover, the local structure of xSnP was characterized by 119Sn-Mössbauer and magic angle spinning (MAS) 31P NMR spectroscopies. Homogeneous glasses were obtained for xSnP with ‘x’ from 50 to 80, while Sn(HPO4), SnO2, and Sn3(PO4)2 nanoparticles formed in 40SnP and 90SnP compositions, respectively. The nano-crystallized 40SnP and 90SnP samples showed large electrical conductivity (σ) of 2.02×10−5 and 1.04×10−4S cm−1 due to the conductive crystalline phases of SnP2O7 and defective SnO2, respectively. The lower σ of about 10−8S cm−1 were recorded for xSnP with ‘x’ from 50 to 80 owing to the decomposition of the 3D network built by phosphate tetrahedrons. 119Sn-Mössbauer spectra proved the growing number of SnIVO6 units, which do not contribute to the rise of electrical conductivity. On the other hand, larger σ values of 1.79×10−4 and 6.4×10−3S cm−1 were confirmed for 40SnP and 90SnP samples after heat treatment, resulting in partial reduction of SnIV to SnII and growing of the 3D network structure by PO43−. It is concluded that highly electrically conductive xSnP samples can be synthesized by the sol-gel method followed by slow heat treatment. In addition, the battery evaluation was performed of xSnP samples as cathode and anode in a sodium-ion battery. The highest initial capacity recorded for 90SnP nano-crystallized ceramic at 37.97 mAh g−1 under a current rate of 20 mA g−1 with capacity retention (%) of 48.15% after 100 cycles as a cathode material. The anode test showed that the 40SnP nano-crystallized ceramic has the largest initial capacity of 375 mAh g−1 and after heat treatment 50SnP glass significantly increased to 425 mAh g−1 compared with 186 mAh g−1 before heat treatment. Also, the heat treatment effect on the initial capacity of 90SnP nano-crystallized ceramic with observation largest value of 470 mAh g−1. These results open the way to maybe applying these glass and nano-crystallized ceramic materials in all-solid-state batteries.

Fabrication of Activated Carbon Derived from Glycerin Pitch for Desulfurization of Model Fuel Oil and Electrode Application.

One of the world's challenging energy issues is introducing practical and affordable technology for organosulfur removal in fuel. Adsorptive desulfurization (ADS) can address this issue if highly effective activated carbon (AC) derived from industrial waste with excellent textural properties is used. In this study, the derived ACs from glycerin pitch loaded with P and Fe (AC/P and AC/Fe) were used as adsorbents for the ADS of model fuel oils, such as dibenzothiophene (DBT) at mild operating conditions. Under the optimized experimental conditions, 0.3 g of adsorbent dosage, 60 min reaction time, 30 °C temperature, and pH 4, the maximal DBT removal of 96.28 and 43.64%, respectively, for AC/P and AC/Fe was realized. The results indicated that the phosphorus-doped AC/P increases the selectivity of the ADS mechanism for DBT removal. Kinetic investigations disclosed that the adsorption process follows second-pseudo-order kinetics and the Langmuir adsorption isotherm model. The adsorbents remained active for five successive reuses, indicating their robust real-world applications. The electrochemical properties of the fabricated carbon electrodes were analyzed via cyclic voltammetry by coating the ACs with polytetrafluoroethylene (PTFE) as a binder. The transition-metal-doped AC/Fe, though exhibiting 5 times lower surface area, showed the highest specific capacitance at a scan rate of 5 mVs-1 (0.65 μF cm-2). Similarly, the extended AC:PTFE capacitor at a 10% binder ratio offered the maximum capacitance value (1.13 μF cm-2). The synthesized ACs demonstrated potential application as an electrode material, and hence glycerin pitch could be a low-cost precursor to improve the feasibility of commercial production of AC.

Precycling Strategy in Suitable Voltage to Improve the Stability of Interfacial Film and Suppress the Decline of LiNi0.6Mn0.2Co0.2O2 Cathode at Elevated Temperatures.

Layered ternary oxide LiNixMnyCo1-x-yO2 is a promising cathode candidate for high-energy lithium-ion batteries (LIBs). However, the capacity of LIBs is significantly restricted by several factors, including the repeated dissolution-regeneration of the interfacial film at high temperatures, the dissolution of transition metals, and the increase of impedance. Herein, a new precycling strategy in suitable voltage scope at room temperature is proposed to construct a uniform, thermally stable, and insoluble cathode-electrolyte interface (CEI), which helps to maintain stable cycling performances at high temperatures. Specifically, after 5 precycles in the range of 3.85-4.3 V at room temperature, a CEI layer containing numerous inorganic components and oligomers is formed on the surface of LiNi0.6Mn0.2Co0.2O2. Subsequently, the harmful side reactions are effectively suppressed, endowing the cell with an excellent capacity retention of 84.67% after 50 cycles at 0.5C and 55 °C, much higher than that of 65.61% under the conventional film-forming process conditions. This work emphasizes the crucial role of the precycling strategy in regulating the characteristics of CEI layer on the surface of cathode electrode, opening up a new avenue for the high-temperature application of positive electrodes of LIBs.

Self-encapsulated hydrogel bioelectrode for arrhythmic management

Encapsulation is crucial for constructing hydrogel bioelectronics for detecting bioelectric signals and applying electrical stimulation. However, introducing an extra encapsulating layer in bioelectrodes can lead to complex fabrication processes, reduced conductivity, and compromised mechanical performance. Here, we develop a one-step strategy of controllable construction for self-encapsulated hydrogel bioelectrodes (SHBs) for arrhythmic management. By utilizing the nonsolvent-induced phase separation-like (NIPS-like) method, acrylamide facilitates the phase separation of the poly(3,4-ethylenedioxythiophene) (PEDOT) chains and the poly(styrene sulfonic acid) (PSS) chains, leading to the formation of SHBs with a conducting layer coated by an encapsulating layer. SHBs exhibit high conductivity (309.73 ± 15.05 S m−1), bright stretchability (exceeding 300%), and tissue-like Young's modulus (16.33 ± 1.58 kPa), simultaneously. Therefore, SHBs can record the different components of atrial and ventricular excitation in vivo without filtering, and keep a smooth baseline in long-time electrocardiogram of the rat. Moreover, SHBs can stimulate the arrhythmic heart, restoring it to a normal rhythm. Our finding provides a way to promote the detection and modulation application of hydrogel electrodes in bioelectronics.

High loading electrode with superior electron/ion transport network for high performance lithium-ion batteries

High loading electrode design is beneficial to increase the energy density of lithium ion batteries. Two obstacles for the high loading electrode application should be removed, including the limitation on ion/electron transport within high loading electrode and the structure stability. Here, the electron conduction on LiNi0.8Co0.1Mn0.1O2 cathodes is enhanced with evenly and tightly Ketjen Black coating via high-speed dry mixing, while carbon nanotube is added to enhance the electron conduction between LiNi0.8Co0.1Mn0.1O2 particles, thus to construct three-dimensional electron migration channel. In addition, the large amount of electrolyte adsorbed by porous Ketjen Black and carbon nanotube enhances the Li+ ion diffusivity in this network. As a result, LiNi0.8Co0.1Mn0.1O2 electrode with only 1 % Ketjen Black and 3 % carbon nanotube can achieve both high electron/Li+ ion diffusivity and high parking density (2.2 g cm−3). A thick electrode with an areal mass loading of 20 mg cm−2 shows a high specific capacity of 111.2 mA h g−1 at 4 C and capacity retention rate of 98.2 % after 100 cycles at 2 C.

Recent Trends in Therapeutic and Electroanalytical Applications of Boron-Doped Diamond Sensors

Abstract:: In recent years, research and development efforts have been heavily focused on conductive diamond electrodes for electrochemical applications. Such initiatives may have been spurred by their broad potential window, low background current, chemical inertness, and mechanical robustness. Compared to other carbon-based materials, conducting diamond can oxidize several analytes before the breakdown of water in aqueous electrolytes. Since the evolution of oxygen and hydrogen does not obstruct the analysis, this is significant for the detection and/or identification of species in solution. As a result, conductive diamond electrodes expand the application of electrochemical detection and make it possible to use them for analytes that are incompatible with traditional electrode materials. Fabricating boron-doped diamond films via chemical vapor deposition on different substrates is of special interest. This article highlights the therapeutic and electroanalytical applications of boron-doped diamond electrodes in various aspects in addition to the synthetic strategies to obtain Boron Doped Diamond Electrodes (BDDE), the cost-effectiveness of BDD and its in-vivo compatibility that will help the analytical researchers to learn almost everything about the previous studies done on BDDE and encourage them to work more efficiently in this research field.

Development of cost-efficient BaMnO3/rGO nanocomposite as electrode for energy storage applications in supercapacitor

The excessive fossil fuels utilization leads to environment contamination along with energy loss and is becoming a serious issue in these days. Therefore, to handle these energy issues, alternative sources and energy-storing devices like supercapacitors are in demand in the modern era. Many perovskites have been used in supercapacitors as electrode material but because of its less cyclic stability and poor conductivity, rGO mixed to enhance the electrochemical properties of perovskite. Therefore, we used rGO with BaMnO3 to fabricate BaMnO3/rGO nanocomposite through hydrothermal method for supercapacitor electrodes. After different physical analyses, BaMnO3/rGO nanocomposite showed remarkable electrode applications having distinct nanostructure with increased surface area, conductivity, crystallinity and improved morphology. The electrode material demonstrated a substantial surface area (54.32 m2 g−1) measured by Brunner–Emmett–Teller analysis, while scanning electron microscopy results showed that BaMnO3 dispersed tightly on rGO. The fabricated electrode material demonstrated a specific capacitance of 1359.85 F g−1, energy density of 78.62 Wh kg−1 and power density of 322.6 W kg−1 at 1 A g−1 current density. Furthermore, the Nyquist plot revealed a low value of Rct (0.04 Ω), indicating good electrical conductivity, while the material displayed stability even after 5000th cycle. This work revealed that, such extraordinary and outstanding qualities of BaMnO3/rGO nanocomposite provide a viable option for use in next-generation supercapacitor applications along with high stability and cost effectiveness.

Manufacturing Shape-Controllable Flexible PEDOT/rGO Composite Electrodes for Planar Micro-Supercapacitors.

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.

Fabrication and characterization of a novel multilayer heterojunction Si3N4-PbO2 nanocomposite electrode and its application on electrocatalysis degradation of sulfathiazole

To lengthen the lifetime and extend the potential commercial applications of lead dioxide electrode, herein, a novel multilayer heterojunction Ti/ SnO2-Sb2O3/ graphene oxide/ carbon nanotube/ Si3N4-PbO2 electrode (Si3N4-PbO2 electrode) was fabricated by co-electrodeposition process that doping Si3N4 nanoparticles in eletroplating solution. Various spectroscopic and microscopic techniques, including scanning electron microscopy (SEM) equipped with energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS), were employed to characterize the surface of the fabricated electrode. The EDS analysis confirmed the successful attachment of 5.49 %wt Si and 2.46 %wt N elements from Si3N4 nanoparticles onto the PbO2 surface, while the XRD results indicated a shift in the preferred orientation of PbO2 grains from β(110) to β(101). The water adsorption energy and ·OH desorption energy in the electrocatalysis process were determined to be 0.71 eV and 0.241 eV through theoretical calculating. Subsequently, the Si3N4-PbO2 electrode was employed as an anode for the electrocatalytic degradation of sulfathiazole-simulated wastewater and real sulfonamides wastewater. Under optimized conditions determined via response surface methodology (RSM), the COD degradation efficiency reached 69.37 % for sulfathiazole and 62.35 % for real sulfonamides wastewater. The final COD concentration of the real sulfonamides wastewater was reduced to 77.05 mg/L, under the national urban sewage discharge standard. Finally, the degradation mechanism and pathway of sulfathiazole has been arranged based on the electron spin resonance (ESR), cyclic voltammetry (CV), while the intermediates were detected by Gas Chromatography-Mass Spectrometer (GC-MS) and the reactive sites of sulfathiazole were predicted by using Fukui function.

Highly Stable Polyaniline-Based Cathode Material Enabled by Phosphorene for Zinc-Ion Batteries with Superior Specific Capacity and Cycle Life.

Aqueous zinc-ion batteries (ZIBs) are regarded as a type of promising energy-storage device because of their high safety and low cost, and polyaniline (PANI) is normally employed as a cathode material for ZIBs owing to its unique electrochemical properties and high environmental stability. However, a low specific capacity and a short cycle life limit the development and applications of PANI-based electrodes. Herein, we have developed a novel type of highly stable PANI-based cathode material enabled by phosphene (PR) for aqueous Zn-PANI batteries through in situ chemical oxidative polymerization. The introduction of PR nanoflakes not only inhibits the degradation of PANI and generates more active sites for Zn2+ storage but also enables a synergistic effect of the Zn2+ insertion/extraction and P-Zn alloying reaction. This promotes a high reversible specific capacity of 240.2 mAh g-1 at 0.2 A g-1 and excellent rate performance for the PR/PANI nanocomposite cathode material. Compared to the pristine PANI cathode material, the PR/PANI nanocomposite cathode material is more suitable for the Zn-PANI battery, thanks to its higher specific capacity and better cycle stability. This study provides an innovative approach for developing the next generation of reliable PR-based electrode materials for aqueous energy-storage devices.

Incorporating pre-stretching into electroless copper plating for conductivity improvement of elastic nylon fabric: application in ECG electrode

Incorporating pre-stretching into electroless copper plating for conductivity improvement of elastic nylon fabric: application in ECG electrode

Morphology modification of LiNi0.5Co0.2Mn0.3O2 by incorporating cotton textiles in lithium-ion capacitors

To address the alerting issue of energy demand, lithium-ion capacitors (LICs) have been widely studied as promising electrochemical energy storage devices, which can deliver higher energy density than supercapacitors (SCs), and have higher power density with longer cycling life than lithium-ion batteries (LIBs). In this work, the active material lithium nickel cobalt manganese oxide LiNi0.5Co0.2Mn0.3O2 (NCM523) is grown on a cotton textile template and building a 3-dimensional (3D) integrity to improve capacitance and energy density of LICs by enhancing the interfacial ion-exchange process. With the 3D structure, the specific discharge capacitance is increased to 718.67 F g−1 at 0.1 A g−1 from that of non-textile NCM523 (265.97 F g−1), and remains a high capacitance of 254.48 Fg−1 at 10 A g−1 in the half-cell capacitors. In addition, the energy density can achieve up to 36.17 Wh kg−1 at the power density of 1,200 W kg−1 in the full-cell capacitor. The textile NCM can maintain an energy density of 28.26 Wh kg−1 at the current density of 10 A g−1 and power density of 6,000 W kg−1. Our results present promising applications of electrodes with the 3D porous structure for high energy density LICs.

Synthesis and Investigation of Electrochemical Studies on Thulium Tellurite (TmTeO3) for Supercapacitor Electrode Application

Thulium tellurite ([Formula: see text]) is synthesized by hydrothermal method. It exhibits nearly cuboid-shaped particles along with triangular particles. [Formula: see text] is found to be monoclinic. The energy gap is 5.87[Formula: see text]eV, the Urbach energy value is 0.287[Formula: see text]eV and the refractive index is 1.881. The size of the particle is determined as 107[Formula: see text]nm. Optical transitions between energy levels assign absorption and emission peaks. Tm, was found in the oxide matrix as Tellurite. Magnetic susceptibility between 20[Formula: see text]K and 300[Formula: see text]K decreases with temperature, reaches saturation and aligns all Thulium spins. M–H curve confirms paramagnetic nature at 300[Formula: see text]K and feeble ferromagnetic nature at 77[Formula: see text]K. Cyclic voltammogram and chronopotentiometry analysis exhibit pseudo-capacitive behavior. The potential window is 0.82. Specific capacitance is found to be 87[Formula: see text]F/g. Chronopotentiometry analysis shows 55[Formula: see text]F/g specific capacitance. Impedance analysis shows a pseudo-capacitive nature. [Formula: see text] symmetrical supercapacitor device is fabricated with potential window of 1.52[Formula: see text]V. A specific capacitance of 37.75[Formula: see text]F/g at 1 A/g, energy density 6.055[Formula: see text]Wh kg[Formula: see text] and power density 760.99[Formula: see text]W kg[Formula: see text] was achieved. Impedance analysis shows low series resistance of 2.567[Formula: see text][Formula: see text] and charge transfer resistance of 0.473[Formula: see text][Formula: see text]. Cyclic performance with 80% specific capacitance retention is observed after 5000 cycles. The [Formula: see text] symmetric supercapacitor electrodes possess good electrochemical properties due to wider potential window, long cycle stability and notable energy density.

Non-invasive electroarthrography measures cartilage in live horses and correlates to direct measurements of cartilage streaming potentials in weight bearing regions of equine metacarpophalangeal joints

ObjectiveTo perform non-invasive Electroarthrography (EAG) on live horses and establish relationships between EAG and direct measurements of cartilage streaming potentials in weight bearing areas of the equine metacarpophalangeal joint. DesignEAG was performed bilaterally on the metacarpophalangeal joints of live horses (n=3). Separate experiments used metacarpophalangeal joint explants (n=11) to measure EAG obtained during simulated loading followed by direct measurements of cartilage streaming potentials on joint surfaces using the Arthro-BST probe. Joints were assigned to relatively normal (n=5) and mildly degraded (n=6) groups based on histological scoring of Safranin-O/Fast Green stained sections. ResultsEAG, involving application of electrodes to skin surrounding the joint and repeated weight shifting, was well-tolerated in live horses. One pair of distal forelimbs were available for analogous ex vivo EAG testing and measurements were strongly correlated to in vivo EAG measurements obtained on the same joints (r=0.804, p=0.016, n=8). Both indirect (EAG) and direct (Arthro-BST) measurements of cartilage streaming potentials distinguished between normal and mildly degraded cartilage with statistically significant differences at 5 of 6 and 4 of 6 electrodes during simulated standing and walking, respectively. Strong and moderate correlations for weight bearing regions on the dorsal phalanx and central metacarpus were detected during both standing and walking. At the metacarpus/sesamoid interface a moderate correlation occurred during walking. ConclusionNon-invasive EAG was used successfully in a clinical scenario and correlated to direct measurements of streaming potentials in weight bearing cartilage. These data support the potential of EAG to contribute to the diagnosis and treatment of degenerative joint diseases.

Growth of Atomic layer-deposited Monoclinic Molybdenum Dioxide Films Stabilized by Tin Oxide Doping for DRAM Capacitor Electrode Applications.

Dynamic random-access memory (DRAM) capacitor electrodes, exemplified by TiN, face performance limitations owing to their relatively low work functions in addition to the formation of a low-k interfacial layer caused by their insufficient chemical stability. With recent advances in device scaling, these issues have become increasingly problematic, prompting the exploration of alternative electrode materials to replace TiN. Molybdenum dioxide (MoO2) has emerged as a promising candidate for this application, outperforming TiN due to its low resistivity, high work function (>5 eV), and excellent chemical stability. Moreover, monoclinic MoO2 exhibits a distorted rutile structure, enabling the in situ growth of high-k rutile TiO2 on MoO2 at low deposition temperatures. However, MoO2 deposition poses challenges because of its metastable nature compared to the more stable molybdenum oxide (MoOx) phases, such as MoO3 and Mo4O11. In this work, we successfully fabricated Sn-doped MoOx (TMO) films by atomic layer deposition (ALD) at 300 °C. A stabilized monoclinic MoO2 phase was achieved using ALD by incorporating SnOx into MoOx on both SiO2 and TiN substrates. The ALD TMO process comprised MoOx and SnOx subcycles, and the MoOx:SnOx subcycle ratio was varied from 100:1 to 20:1. High growth rates ranging from 0.19 to 0.34 nm/cycle were achieved for ALD TMO with varying the MoOx:SnOx subcycle ratio from 20:1 to 100:0. After post-deposition annealing at 500 °C, polycrystalline TMO films were obtained with smooth surface morphology. ALD TMO exhibited excellent interface quality with ALD TiO2, possessing a negligible low-k interfacial layer. Moreover, a rutile TiO2 film with a high dielectric constant of 136 was successfully grown on a 20% Sn-TMO electrode. Overall, this study provides a strategy to stabilize metastable MoO2 films using ALD, and it demonstrates the superiority of ALD TMO as a promising DRAM capacitor electrode material.

Elucidating the Reductive Decomposition Mechanism in Sulfide Solid Electrolyte Li4SnS4.

The sulfide solid electrolyte Li4SnS4 has garnered considerable interest due to its exceptional moisture durability, which is attributed to its stable hydrated state. However, a major limitation of certain sulfide solid electrolytes, including Li4SnS4, is their low reduction durability, which limits their application in the negative electrodes of all-solid-state batteries and impedes qualitative material development assessments. In this study, we introduced a quantitative and straightforward method for evaluating the reductive decomposition of Li4SnS4 to better understand its degradation mechanism. The configuration of the electrochemical evaluation cell was modified from SUS|Li4SnS4|Li to SUS|Li4SnS4|Li3PS4|Li, allowing for stabilization of the reference potential of the counter electrode. The reductive decomposition potential of Li4SnS4 was quantitatively assessed by using cyclic voltammetry in a two-layer electrochemical evaluation cell. We observed a minor irreversible reduction current below +1.2 V and a pronounced decomposition peak at +1.0 V. Notably, reductive decomposition continued below 0 V, which is typically the onset point for Li electrodeposition. Postreduction, the solid electrolyte was comprehensively analyzed through optical microscopy, X-ray diffraction, and X-ray absorption spectroscopy. These analyzes revealed the following: (i) The SnS44- unit in Li4SnS4 initially decomposes into Li2S and β-Sn with the dissociation of the Sn-S bond; (ii) the resulting β-Sn forms LixSn alloys such as Li0.4Sn; and (iii) the ongoing reductive decomposition reaction is facilitated by the electronic conductivity of these LixSn alloys. These findings offer crucial methodological and mechanistic insights into the development of higher-performance solid electrolyte materials.

Laser shock-enabled optical–thermal–mechanical coupled welding method for silver nanowires

Silver nanowires (AgNWs) are recognized as highly promising materials for flexible and transparent electrode applications. However, existing material-processing methods fail to achieve uniform and reliable AgNWs junctions. In this study, we propose a new method using the laser shock effect combined with the laser heating effect, for creating AgNW junctions within thin films. We explored the welding mechanism of AgNWs through optic-thermal welding, laser shock-enabled mechanical welding, and laser-shock-enabled optical-thermal-mechanical (LS-OTM) experiments, as well as numerical simulations, and the results demonstrate that the innovative mechanism of the LS-OTM process lies in its utilization of laser shock to adjust the gap between the nanowire junctions, which in turn achieves a fine control of the thermal effect of the heating laser localised surface plasmon resonance, and the atomic diffusion in the solid state at intermediate temperature under the action of the impact force is the mechanism of the formation of high-quality junctions. We prepared flexible transparent conductive films and studied their transmittance, conductivity, and thermal properties, the results show that the flexible transparent conductive films prepared by LS-OTM welding method have excellent transmittance, conductivity, and thermal properties, this verifies the feasibility and effectiveness of this processing strategy. The LS-OTM method is a viable solution for manufacturing transparent, conductive films from AgNWs for emerging applications such as flexible heated films, flexible displays, and wearable medical devices.