High Conductivity Research Articles

An electrochemical sensor based on electrochemically activated carbon cloth and poly (o-aminothiophenol) cross-linked nanogold imprinted layer for the determination of tert-butylhydroquinone

In this study, an electrochemical sensor based on MoS2 with enhanced electrochemical signals from electrochemically activated carbon cloth (EACC) electrodes and cross-linked o-aminothiophenol functionalized AuNPs (o-ATP@AuNPs) was developed for the detection of the unsaturated vegetable oil antioxidant tert-butylhydroquinone (TBHQ). In this approach, carbon cloth is activated through the implementation of electrochemical methods, thereby effectively increasing its specific surface area. The resulting EACC, serving as an electrode substrate, enables the growth of additional nanomaterials and enhances conductivity. The incorporation of MoS2 effectively augments the sensitivity of the electrochemical sensor. Subsequently, MIP/MoS2/EMCC is formed via electropolymerization, utilizing TBHQ as the template molecule and o-ATP@AuNPs as the functional monomer. The SS bond of o-ATP ensures a strong and stable connection between MoS2 and o-ATP@AuNPs, thereby facilitating the immobilization of MIP. In addition, the high conductivity possessed by o-ATP@AuNPs could effectively improve the sensitivity of the electrochemical sensor. Under the optimal conditions, MIP/MoS2/EMCC could determine TBHQ in the range of 1 × 10−3 μM to 120 μM by differential pulse voltammetry (DPV) with a detection line of 0.72 nM. The proposed MIP/MoS2/EMCC is expected to be applied in the future for the selective and sensitive detection of TBHQ in vegetable oils.

Bioinspired Robust Gas-Permeable On-Skin Electronics: Armor-Designed Nanoporous Flash Graphene Assembly Enhancing Mechanical Resilience.

Soft on-skin electrodes play an important role in wearable technologies, requiring attributes such as wearing comfort, high conductivity, and gas permeability. However, conventional fabrication methods often compromise simplicity, cost-effectiveness, or mechanical resilience. In this study, a mechanically robust and gas-permeable on-skin electrode is presented that incorporates Flash Graphene (FG) integrated with a bioinspired armor design. FG, synthesized through Flash Joule Heating process, offers a small-sized and turbostratic arrangement that is ideal for the assembly of a conductive network with nanopore structures. Screen-printing is used to embed the FG assembly into the framework of polypropylene melt-blown nonwoven fabrics (PPMF), forming a soft on-skin electrode with low sheet resistance (125.2 ± 4.7 Ω/□) and high gas permeability (≈10.08mg cm⁻2 h⁻¹). The "armor" framework ensures enduring mechanical stability through adhesion, washability, and 10,000 cycles of mechanical contact friction tests. Demonstrating capabilities in electrocardiogram (ECG) and electromyogram (EMG) monitoring, along with serving as a self-powered triboelectric sensor, the FG/PPMF electrode holds promise for scalable, high-performance flexible sensing applications, thereby enriching the landscape of integrated wearable technologies.

Multi-heterostructured MXene/NiS2/Co3S4 with S-Vacancies to Promote Polysulfide Conversion in Lithium-Sulfur Batteries.

The severe shuttle effect of polysulfides (LiPSs) and the slow liquid-solid phase conversion are the main obstacles hindering the practical application of lithium-sulfur (Li-S) batteries. Separator modification with a high-activity catalyst can boost LiPSs conversion and suppress their shuttle effect. In this work, multi-heterostructured MXene/NiS2/Co3S4 with rich S-vacancies was constructed facilely with a hydrothermal and high-temperature annealing strategy for separator modification. The MXene sheet not only provides a physical barrier but also ensures a high conductivity and adsorption capacity of the catalyst; the dual active centers of NiS2 and Co3S4 catalyze LiPSs conversion. In addition, the vacancies and heterostructures can modulate the electronic structure of the catalyst, improve its intrinsic activity, and reduce the polysulfides reaction barrier, thus facilitating ion/electron transport and inhibiting the shuttle effect. Benefiting from these advantages, the Li-S battery with MXene/NiS2/Co3S4 modified separator exhibits exciting discharge capacities (1495.4 mAh g-1 at 0.1C and 549.0 mAh g-1 at 6C) and an excellent ultra-long cycle life (average capacity decay rate of 0.026% for 2000 cycles at 2C); at a high sulfur loading of 10.0 mg cm-2, the battery operates for nearly 80 cycles at 0.2C, giving a capacity retention rate of 75.76%. This work provides a high-activity catalyst for Li-S batteries.

Sustainable chitosan derived 3D hierarchically porous carbon aerogel toward advanced infrared-radar compatibility

Simultaneously achieving infrared-radar compatibility in one material is an important challenge for multi-spectral compatible stealth technology. Chitosan-derived three-dimensional (3D) hierarchically porous carbon aerogel can effectively solve the problem. Inspired by floors-pillars concept, this work elaborately designed and successfully fabricated 3D skeletons consisted of two-dimensional (2D) sheets and one-dimensional (1D) struts. Benefiting from esterification and directional freeze drying method, the entire network could provide sufficient space for reducing thermal conductivity and motivating dipole polarization sites. Thanks to the facile calcination process, conductive components could be obtained, which guarantee low infrared (IR) emissivity and high conduction loss performance. In this work, the as-prepared carbon aerogel with ultra-low density of 0.005 g cm−3 exhibits superb infrared stealth property. It shows a low thermal conductivity coefficient of only 0.0933 W m−1 K−1. In addition, the heating rate of the upper surface is slow when placed on a heating platform of 60 °C. The relevant IR emissivity value is as low as 0.563 in 3–5 μm band and 0.432 in 8–14 μm band. Under relatively thin thicknesses, the prominent radar stealth performance including the optimum reflection loss value of −75.90 dB, the maximum effective bandwidth of 3.93 GHz, and the simulated radar cross section reduction value of 27.66 dB m2, can be obtained. This study not only introduces innovative design ideas but also offers technical approaches, facilitating further development in the realm of infrared-radar compatible stealth.

Peculiarities in XPS spectra of Sn/SiO2 layers as an effect of surface charge

X-ray photoelectron spectroscopy based on synchrotron radiation was used to investigate the composition of the observed SnO2-x/Sn:SiO2-x thin layer grown by organometallic chemical vapour deposition on single-crystalline silicon wafer with additional argon ions etching treatment. Due to the formation of a thermodynamic anomaly during in situ layer growth, an efficient oxygen exchange between silicon and tin oxide phases occurs. The present study addresses the effect of localized surface charging and its influence on the obtained XPS core level spectra. We found that due to the high electrical conductivity of metallic tin and the direct coupling of tin particles to the silicon wafer, the XPS Sn 3d5/2 core level spectrum is not affected by the surface charge compared to the highly charged dielectric silicon oxide matrix, as observed for the XPS O 1 s and Si 2p core level spectra. Our results show that the core level spectra of Si 2p and O 1 s are shifted up to 3 eV due to the presence of uncompensated positive charge on the surface of the silica matrix. These results provide insight into the influence of surface charge effects on the analysis of conductor/insulator composite materials and contribute to the application of Sn-based materials in various application concepts related to energy and surface functionalization.

Discovering the Order-Disorder Transition in Quinoline Intercalated Vanadium Oxide with Superior Calcium Storage via Polyhedral Distortion.

Calcium-ion batteries (CIBs) are considered as potential next-generation energy storage systems due to their abundant reserves and relatively low cost. However, irreversible structural changes and weak conductivity still hinder in current CIBs cathode materials. Herein, an organic molecular intercalation strategy is proposed, in which V2O5 regulated with quinoline, pyridine, and water molecules are studied as cathode material to provide fast ion diffusion channels, large storage host, and high conductivity for Ca ions. Among them, V2O5-quinoline (QVO) owns the largest interplanar spacing of 1.25 nm and the V-O chains are connected with organic molecular by hydrogen bond, which stabilizes the crystal structure. As a result, QVO exhibits a specific capacity of 168 mAh g-1 at 1 A g-1 and capacity retention of 80% after 500 cycles at 5 A g-1 than the other materials. Furthermore, X-Ray diffraction and X-ray absorption spectroscopy results reveal a reversible order-disorder transformation mechanism of Ca2+ for QVO, which can make full use of the abundant active sites for high capacity and simultaneously achieve fast reaction kinetics for excellent rate performance. These results demonstrate that QVO is a promising cathode material for CIBs, providing more choices for the development of high-performance CIBs.

High-performance flexible planner device featuring WS2 electrode and non-aqueous polymeric ionic electrolytes incorporated with ionic liquid and dual redox additives

Introducing redox-active species to enhance redox-activity at electrode–electrolyte interfaces, and designing the rational architecture of flexible supercapacitors comprising high-performance active materials and electrolytes with a wide potential window would be a key strategy to boost energy and power density. Herein, for the first time, we prepared an ionic liquid-based polymer electrolyte (IL/PE) by entrapping ionic liquid N-methyl-N-butyl pyrrolidinium bis (trifluoromethane sulfonyl) imide (P14TFSI)) in a polymer electrolyte Poly (diallyl dimethylammonium bis (trifluoromethane sulfonyl) imide (PDADMATFSI)) and blended with dual redox-additives (potassium iodide, KI and diphenylamine, DPA). The IL/PE with dual redox additives, demonstrates spectacular flexibility, high ionic conductivity (∼23.8 × 10−4 S cm−1), and stability in a wide potential window (∼5.9 V). A symmetrical interdigitated planner device is fabricated using dual redox-active IL/PE and flower-like WS2 electrode material. Benefiting from the synergistic effect of dual redox-active additive, the highest energy density of 47.86 µWh cm−2 at a power density of 3509 µW cm−2, and a high working potential (3 V) with excellent cycling stability upto 20,000 cycles has been achieved.

Poly(ethylene oxide)- and Polyzwitterion-Based Thermoplastic Elastomers for Solid Electrolytes.

In this article, ABA triblock copolymer (tri-BCP) thermoplastic elastomers with poly(ethylene oxide) (PEO) middle block and polyzwitterionic poly(4-vinylpyridine) propane-1-sulfonate (PVPS) outer blocks were synthesized. The PVPS-b-PEO-b-PVPS tri-BCPs were doped with lithium bis-(trifluoromethane-sulfonyl) imide (LiTFSI) and used as solid polyelectrolytes (SPEs). The thermal properties and microphase separation behavior of the tri-BCP/LiTFSI hybrids were studied. Small-angle X-ray scattering (SAXS) results revealed that all tri-BCPs formed asymmetric lamellar structures in the range of PVPS volume fractions from 12.9% to 26.1%. The microphase separation strength was enhanced with increasing the PVPS fraction (fPVPS) but was weakened as the doping ratio increased, which affected the thermal properties of the hybrids, such as melting temperature and glass transition temperature, to some extent. As compared with the PEO/LiTFSI hybrids, the PVPS-b-PEO-b-PVPS/LiTFSI hybrids could achieve both higher modulus and higher ionic conductivity, which were attributed to the physical crosslinking and the assistance in dissociation of Li+ ions by the PVPS blocks, respectively. On the basis of excellent electrical and mechanical performances, the PVPS-b-PEO-b-PVPS/LiTFSI hybrids can potentially be used as solid electrolytes in lithium-ion batteries.

Facile and rapid synthesis method of dielectric nanocomposite for simultaneous enhancement of electromagnetic wave absorbing/shielding characteristics

The present study involves the fabrication of poly[4-(2-thiophene)aniline] (PTA) nanocomposite for absorption-dependent shielding applications, demonstrating enhanced absorption and small reflection properties. The Microwave absorption characteristics of the fabricated polymer were studied at different loading ratios, resulting in a minimum reflection loss (RLmini) of − 44 dB for the 8 wt % loading ratio. The macromolecular architecture of the PTA material offers higher dielectric loss resulting from higher conduction and interfacial loss. Additionally, the shielding performance is also evaluated, and the sample containing 8 wt % filler demonstrates an impressive − 36.5 dB shielding efficacy. The performance of polymers is significantly impacted by their unit periodic order arrangement. Conducting polymers with linear structure and special π-orbitals angles possess unique characteristics in comparison to their branched and the random copolymer, making them highly sought after as efficient organic conductors, magnetic substances, electrochromic materials, and high dielectric agents. Monomer units contained two periodical cyclic structures and the creation of the inductive effects of heteroatoms elongates the conjugation and reduces the energy bandgap difference between the HOMO and LUMO levels, enabling smoother electron flow and enhancing absorption capacity. The findings indicate that PTA nanocomposite is a promising radar-absorbing coating material due to its superior absorption ability and outstanding shielding performance.

Development of Al-25Si-xCe Alloy with High Conductivity and Low Expansivity for Thermal Management Purpose

Development of Al-25Si-xCe Alloy with High Conductivity and Low Expansivity for Thermal Management Purpose

Manipulating the mechanical strength and thermal conductivity of a Mg–4Zn-0.6Zr alloy through Ca addition

In this study, the microstructure, mechanical properties, and thermal conductivity of as-extruded Mg–4Zn-0.6Zr-xCa (x = 0, 0.3, 0.6, 0.9 wt%) alloys were investigated. The results revealed a bimodal grain size distribution in all the alloys due to incomplete dynamic recrystallization (DRX), characterized by the coexistence of elongated deformed grains and equiaxed DRX grains. The bimodal grain size distribution enhanced the mechanical properties of the studied alloys. Furthermore, Ca alloying facilitated the formation of Ca2Mg6Zn3 phases, through which the DRX extent was also enhanced. The precipitation of secondary phases, along with the increased DRX induced by Ca addition, was beneficial in eliminating the lattice distortion of the alloys, resulting in improved thermal conductivity compared to the Ca-free Mg–4Zn-0.6Zr alloy. The optimum combination of mechanical properties and thermal conductivity was achieved in the Mg–4Zn-0.6Zr-0.6Ca alloy, with yielding strength, ultimate tensile strength, tensile fracture elongation, and thermal conductivity values of 271 MPa, 318 MPa, 17.6 %, and 123.9 W/(m‧K), respectively. This work demonstrates that Mg–Zn–Zr–Ca-based alloys can be developed with high strength and high thermal conductivity, significantly expanding the industrial application of magnesium alloys.

Effect of electrical modes on dielectric and insulation properties of plasma electrolytic oxidation ceramic films on Al

The preparation of insulating ceramic films on the surface of Al wires using plasma electrolytic oxidation technology can effectively achieve high temperature resistance and high thermal conductivity of ceramic insulated wires. The current study is not clear about the key factors and intrinsic influence mechanism which affect the dielectric and insulation properties of ceramic film. In this paper, the effects of different electrical modes and parameters on the microstructure, phase composition, dielectric and insulation properties of ceramic films are investigated. The results indicated that the effect of electrical modes on the dielectric property had no significant regularity. Among the three electrical modes, the effect of the current density mode is the most significant. When the current density increased from 8 A/dm2 to 20 A/dm2, the film thickness increased from 15.4 μm to 52.9 μm; the porosity increased from 2.74 % to 15.89 %; the breakdown voltage increased from 215 V to 345 V, and the breakdown strength decreased from 14 V/μm to 6.5 V/μm. Changing the electrical modes can change the microdischarge characteristics and realize the regulation of the microstructure, phase composition and content of the ceramic film, which in turn affects ceramic film's dielectric and insulation properties. The key factors to improve the dielectric and insulation properties of ceramic films are the increase of crystallinity and the reduction of defects and porosity.

Electrochemical detection of tryptophan in pineapple fruit using a green and chemically synthesized PANI/CuO nanocomposite modified electrode

This study investigated the electrochemical detection of Tryptophan (Trp) in pineapple using a glassy carbon electrode (GCE) modified with nanocomposites of green and chemically synthesized copper oxide-polyaniline (PANI/CuOgrn and PANI/CuOchm). Given the properties of PANI/CuOgrn and PANI/CuOchm that have never been applied in the detection of Trp, it indicates that the development of a highly sensitive and selective sensing platform for Trp-is necessary. Such a platform would take advantage of high electric conductivity, larger surface area, and improved catalytic activity of the nanocomposites. PANI/CuOgrn and PANI/CuOchm nanocomposites were formed by doping polyaniline (PANI) with green and chemically synthesized copper oxide (CuO) nanoparticles. Using Debye-Scherrer the particle sizes of PANI/CuOgrn and PANI/CuOchm were found to be 15 nm and 13 nm, respectively. Through cyclic voltammetry (CV) and square wave voltammetry (SWV), the electrochemical behaviour of CuOch, CuOgrn, PANI/CuOchm, and PANI/CuOgrn electrodes was studied, with the focus on comparing the nanocomposites for tryptophan (Trp) catalysis. GCE-PANI/CuOchm showed a higher current response of 3.2 μA than GCE-PANI/CuOgrn. SWV was used to determine Trp, with the linear range of 5.11 μM to 25.85 μM and limit of detection (LOD) values of 3.947 and 2.037 μM for GCE-PANI/CuOchm, and 3.434 and 2.427 μM for GCE-PANI/CuOgrn. The GCE-PANI/CuOchm electrode achieved a recovered percentage of 96 % to 109 %, with an average RSD value of 18.3 (n=3), while the GCE-PANI/CuOchm electrode achieved a percentage recovery of 85 % to 103 % with an RSD value of 12.7 (n=3). The high recovery percentages for both electrodes confirm their dependability in detecting Trp. The high concentration of Trp-in the fruit and the electrode's sensitivity to identifying Trp-in actual sample analysis may account for the high recovery percentage observed.

Design of hybrid Ag–Au nanostructure based fully elastomeric nanocomposite electrodes for soft integrated electronics

Recent advancements in stretchable devices have opened new avenues for constructing soft electronics for use in applications such as health-monitoring wearables, advanced integrated circuits, and soft robotics. Meeting the increasing demand for enhanced functionality in soft electronics requires the development of soft conductors with high electrical conductivity, mechanical durability, and cost-effectiveness. Researchers have addressed this challenge by creating percolated networks within the elastomer as a nanocomposite using low-dimensional conducting nanomaterials to endow non-stretchable metallic materials with mechanical stretchability. For example, silver nanowires (AgNWs) have found wide application as essential fillers in soft conductor nanocomposites owing to their remarkable aspect ratio and cost-efficiency. However, their application is limited by their susceptibility to environmental degradation and poor compatibility with semiconducting materials. In this work, the hybrid Ag–Au based nanomaterials as a filler nanomaterial within an elastomer in a nanocomposite format was generated, as it exploits the strengths of each material while mitigating their respective weaknesses. Specifically, the work introduces the merit of the hybrid elastomeric electrodes that consist of AgNWs decorated with Au nanoparticles (AANWs), and Au nanosheets (AuNSs) embedded in a polydimethylsiloxane (PDMS) elastomer. These electrodes exhibit remarkable mechanical resilience and electrical conductivity, making them suitable for application in transistors, logic gates, integrated electronics, and soft displays. The work explores the synthesis and properties of hybrid materials comprising AgNWs and AuNSs, highlighting the promising potential of these materials for future research and development.

Vertically aligned and conformal BN-coated carbon fiber to achieve enhanced thermal conductivity and electrical insulation of a thermal interface material

Due to excellent thermal conductivity, high aspect ratio, and low density, mesophase pitch-based carbon fibers (MPCFs) are highly desired in electronic packaging. However, their thermal conductivity is hard to present in the polymer matrix because of the disordered stacking and low filling. Moreover, few researches are focused on the enhancement of the electrical insulation performance for MPCFs. Herein, we report vertically aligned and insulating boron nitride (BN) coated carbon fiber (CF) powders as significant fillers for polymer composites, endowing markedly improved thermal conductivity and electrical insulation. The high-quality BN coating layer on the surface of the CF is produced by a cooling precipitation method and high-temperature treatment with ingenious use of solubility properties, exhibiting a conformal, dense, and highly crystalline structure. This preparation method overcomes the limitations of coating thickness and particle agglomeration, resulting in a 31-fold enhancement of the electrical resistivity of the CF powders. After orientation treatment in a silicone rubber matrix, such CF@BN-filled pads exhibit good thermal conductivity, significantly improved insulation performance, and excellent mechanical properties. Among them, the optimized pad achieves a thermal conductivity of 12.06 W m−1 K−1, a volume resistivity of 50 × 108 Ω cm and a breakdown voltage of 3100 V mm−1, exceptional flexibility, and a favorable compression ratio (@45 psi) of 41.7 %. This work provides unique insights into constructing carbon fiber fillers as well as the preparation of high thermal conductivity composites, thereby expanding the application scenarios of carbon fiber powder in electronic packaging.

Study of structural, dynamical stability, electronic magnetic and optical properties of RbSnO3 oxide perovskite compound using the density functional theory approach

This study investigates the structural, phonon, elastic, electronic, magnetic and optical properties of cubic perovskite RbSnO3. The calculations are based on the linearized augmented plane wave method with total potential (FP-LAPW), implemented in the Wien2k code; two approximations are used for calculate properties, PBE-GGA and TB-mBJ . The values of the tolerance factor and the formation energy of this material indicate that it is stable in the cubic structure of Pm3̅m symmetry. The Born criteria for the compound under study confirm its mechanical stability, while its phonon dispersion curves confirm its dynamic stability. The results of the electronic and magnetic properties show that the compound is ferromagnetic (FM) semi-metallic (DM) with semiconductor behavior in the majority spin channel and with an indirect gap in the M → Γ direction and having a total magnetic moment equal to 1 μB and a Curie temperature equal to 527 K. Optical spectra of the compound show high optical conductivity in the infrared region and towards the end of the spectrum at around 6 eV, high reflection in the infrared region with a maximum at 0.25 eV, and high absorption in the ultraviolet region at 6 eV. In view of these results, the RbSnO3 perovskite can be a promising candidate for spintronics applications as it can be used in optical devices working in the ultraviolet (UV) light region.

Investigating the Wear Mechanism of TiAlN/TiN PVD-Coated WC Inserts in End Milling of Incoloy 925 Under Synergy of Bio-Degradable Fatty Acids and Nano-Metallic Solid Lubricant

Abstract Rapid tool wear in machining difficult-to-cut material is a significant challenge since it is related to tool cost, surface integrity of machined components, and power consumption. The reduction in tool wear may be accomplished by cutting fluids, especially in modern biodegradable fatty acids. Because of its high lubricity, coconut oil is the best choice for lubricating fatty acids. However, this oil has poor heat transfer properties. Hence, to further improve its properties, copper (Cu) nanoparticles (NPs), which have a high thermal conductivity to cost ratio compared to other nanoparticles in addition to anti-frictional and anti-wear properties (due to self-repairing properties caused by their low shear strength and easy deposition on contacting surfaces), have been dispersed in coconut oil, thus creating a nano-lubricant (nanofluid). It is found that synthesized nano-lubricants perform better in thermo-physics and tribology than pure coconut oil. Further, research has been carried out on the combined effects of coconut oil and 0.3 vol% Cu-NPs on Incoloy 925's end milling performance and tool wear mechanism (viz., coating delamination, adhesion, abrasion, and oxidation). It is found that tool wear-rate is reduced, which in turn increases tool life, due to effective cooling and lubrication when nanofluid-based minimum quantity lubrication (NMQL)-assisted machining is performed rather than dry and pure oil-based minimum quantity lubrication (MQL) conditions. Consequently, energy consumption in machining and surface quality of machined components are improved.

Development of Superior Nickel Oxide Layer for Boosted Hole‐Transport Performance in Perovskite Solar Cells

Although revolutionary power conversion efficiency progress has been realized for inverted perovskite solar cells (PSCs), the selection and optimization of the hole‐transporting materials (HTMs) are still crucial for fabricating high‐efficiency, stable, and low‐cost PSCs. Nickel oxide (NiOx) is widely used in the PSCs community for material design and modification. However, various NiOx synthesis processes lead to kinds of NiOx, and it is difficult to determine which NiOx is suitable for application in PSCs. Herein, two kinds of NiOx HTMs are synthesized using sol–gel processed and chemical‐calcination‐processed (CCP) routes for the preparation of PSCs. Based on the physical properties of two kinds of NiOx HTMs as well as the corresponding photovoltaic parameters of PSCs, it is demonstrated that superior NiOx HTMs is obtained by the CCP method with the following properties: high transmittance to ensure sufficient sunlight capture of perovskite, appropriate energy levels to promote hole extraction and transfer, high conductivity to support charge transfer, and a good wetting surface to boost perovskite spreading and film formation. Thus, in this study, the direction for the reasonable selection of HTMs is pointed out to prepare efficient PSCs.

Liquid Metal Electrode Ink for Printable Lithium‐Ion Batteries

Recent advancements have significantly improved the flexibility of lithium‐ion batteries (LIBs). The battery electrode contains a reaction layer and a current collector layer. Flexible battery electrodes, in which these layers are integrated, are fabricated in a single process, simplifying the electrode fabrication process. However, to date, integrated electrodes have lower conductivity than conventional two‐layer electrodes, and the process that maintains conductivity has not been simplified. This study proposes a liquid metal electrode ink that simultaneously plays the role of the reaction and current collector layers with high conductivity and can be formed in a single process via printing. It employs a gallium‐based liquid metal as a liquid current collector, embedded with Li4Ti5O12 or Li2TiS3 as active materials. These liquid metal electrodes exhibit a high electronic conductivity of 104 S cm−1 and can be fabricated without requiring the lengthy postprocessing time associated with conventional inks. Moreover, the ink can be applied directly to various insulating and nonflat curved substrates, demonstrating its charge–discharge performance, even when bent to a 1 mm radius to maintain flexibility. Liquid metal‐based electrode inks simplify the LIB fabrication process, contributing to efficient production methods for electrodes in future LIBs.

In situ high‐quality LiF/Li3N inorganic and phenyl‐based organic solid electrolyte interphases for advanced lithium–oxygen batteries

AbstractLithium metal shows a great advantage as the most promising anode for its unparalleled theoretical specific capacity and extremely low electrochemical potential. However, uncontrolled lithium dendrite growth and severe side reactions of the reactive intermediates and organic electrolytes still limit the broad application of lithium metal batteries. Herein, we propose 4‐nitrobenzenesulfonyl fluoride (NBSF) as an electrolyte additive for forming a stable organic–inorganic hybrid solid electrolyte interphase (SEI) layer on the lithium surface. The abundance of lithium fluoride and lithium nitride can guarantee the SEI layer's toughness and high ionic conductivity, achieving dendrite‐free lithium deposition. Meanwhile, the phenyl group of NBSF significantly contributes to both the chemical stability of the SEI layer and the good adaptation to volume changes of the lithium anode. The lithium–oxygen batteries with NBSF exhibit prolonged cycle lives and excellent cycling stability. This simple approach is hoped to improve the development of the organic–inorganic SEI layer to stabilize the lithium anodes for lithium–oxygen batteries.