High Conductivity Research Articles

Entropy-Assisted Anion-Reinforced Solvation Structure for Fast-Charging Sodium-Ion Full Batteries.

Anion-reinforced solvation structure favors the formation of inorganic-rich robust electrode-electrolyte interface, which endows fast ion transport and high strength modulus to enable improved electrochemical performance. However, such a unique solvation structure inevitably injures the ionic conductivity of electrolytes and limits the fast-charging performance. Herein, a trade-off in tuning anion-reinforced solvation structure and high ionic conductivity is realized by the entropy-assisted hybrid ester-ether electrolyte. Anion-reinforced solvation sheath with more anions occupying the inner Na+ shell is constructed by introducing the weakly coordinated ether tetrahydrofuran into the commonly used ester-based electrolyte, which merits the accelerated desolvation energy and gradient inorganic-rich electrode-electrolyte interface. The improved ionic conductivity is attributed to the weakly diverse solvation structures induced by entropy effect. These enable the enhanced rate performance and cycling stability of Prussian blue||hard carbon full cells with high electrode mass loading. More importantly, the practical application of the designed electrolyte was further demonstrated by industry-level 18650 cylindrical cells.

Synergistic Enhancement of Biaxial Stretching and Multilayer Composites in All-Solid-State Polymer Electrolytes.

As an important component of lithium-ion batteries, all-solid-state electrolytes should possess high ionic conductivity, excellent flexibility, and relatively high mechanical strength. All-solid-state polymer electrolytes (ASSPEs) based on polymers seem to be able to meet these requirements. However, pure ASSPEs have relatively low ionic conductivity, and the addition of inorganic fillers such as lithium salts will reduce their flexibility and mechanical strength. To address the above issues, in this paper, the solvent-free method was used to prepare a poly(vinylidenefluoride-co-hexafluoropropylene)/lithium bis(trifluoromethanesulfonyl) imide/poly(ethylene oxide) all-solid-state polymer electrolyte, which was then subjected to 4 × 4 magnification synchronous bidirectional stretching. Subsequently, it was multilayered with PEO-based composite polymer electrolytes to obtain multilayered composite polymer electrolytes (MCPEs). Bidirectional stretching provides superior in-plane and out-of-plane mechanical properties to MCPEs by inducing molecular chain orientation, which suppresses the growth of lithium dendrites. Concurrently, it facilitates the formation of the β-crystal form of PVDF-HFP, thereby weakening the ion solvation effect and reducing the lithium-ion migration energy barrier. Multilayered compounding improves the interfacial contact between MCPEs and electrodes, thereby reducing the interfacial impedance. Experiments have demonstrated that the MCPEs prepared in this paper exhibit high ionic conductivity at room temperature (1.83 × 10-4 S cm-1), low interfacial resistance (547 Ω cm-2), excellent mechanical properties (26 MPa), and excellent cycling rate performance (a capacity retention rate of 90% after 110 cycles at 0.1 C), which can meet the performance requirements of lithium-ion batteries for ASSPEs.

Sea Cucumber-Inspired Polyurethane Demonstrating Record-Breaking Mechanical Properties in Room-Temperature Self-Healing Ionogels.

Practical applications of existing self-healing ionogels are often hindered by the trade-off between their mechanical robustness, ionic conductivity, and temperature requirements for their self-healing ability. Herein, this challenge is addressed by drawing inspiration from sea cucumber. A polyurethane containing multiple hydrogen-bond donors and acceptors is synthesized and used to fabricate room-temperature self-healing ionogels with excellent mechanical properties, high ionic conductivity, puncture resistance, and impact resistance. The hard segments of polyurethane, driven by multiple hydrogen bonds, coalesce into hard phase regions, which can efficiently dissipate energy through the reversible disruption and reformation of multiple hydrogen bonds. Consequently, the resulting ionogels exhibit record-high tensile strength and toughness compared to other room-temperature self-healing ionogels. Furthermore, the inherent reversibility of multiple hydrogen bonds within the hard phase regions allows the ionogels to spontaneously and efficiently self-heal damaged mechanical properties and ionic conductivity multiple times at room temperature. To underscore their application potential, these ionogels are employed as electrolytes in the fabrication of electrochromic devices, which exhibit excellent and stable electrochromic performance, repeatable healing ability, and satisfactory impact resistance. This study presents a novel strategy for the fabrication of ionogels with exceptional mechanical properties and room-temperature self-healing capability.

Superior initiator reactivity and electrochemical properties of In(OTf)3 over Sn(OTf)2 for 1,3-dioxolane based solid polymer electrolyte

The in-situ polymerization of 1,3-dioxolane (PDOL) in battery cells has attracted extensive attention, however, the differences of Lewis acid initiators on the DOL monomer conversion (C%) and electrochemical properties has been ignored. Here, it is demonstrated that compare with Sn(OTf)2 Lewis acid initiator, the gelation of DOL is achieved at the lower addition of In(OTf)3. By optimizing their content in the gelation process, their C% are comparable which are 95.7 % and 93.5 % for In(OTf)3 and Sn(OTf)2, respectively. However, the higher ionic conductivity (7.1 × 10−4 S cm−1 at room temperature), electrochemical window (~4.5 V) and Li+ transference number (0.42) are obtained for DOL initiated with In(OTf)3, due to its lower molecular weight which is helpful to the intermolecular Li+ transport along PDOL main chain; In addition, the Li/Li symmetrical cell of In(OTf)3 can be stably cycled for >500 h at 3 mA cm−2, with an over-potential of 178mv. The storage and cycling impedances of half cells further proves the stable interface of In(OTf)3 initiated DOL toward to lithium metal in comparison with those of Sn(OTf)2. Scanning electron microscopy results show a denser and thinner interface in the DOL catalyzed by In(OTf)3. Finally, the assembled Li/LiFePO4 battery delivers specific discharge capacity and capacity retention rates of 115.5mAh g−1 and 85 %, respectively after 300 cycles at 1C. Through the initiator selection, the DOL synthesis and electrochemical properties can be tuned, which further broadens the design idea of PDOL based solid polymer electrolyte.

Exploring the mechanism of infrared emissivity control in YSZ-based ceramics doped with Yb2O3

Due to its exceptional thermal stability and high conductivity, Yttrium stabilized zirconia (YSZ) has become an essential material in the field of infrared camouflage. Although YSZ exhibits relatively low emissivity within the 3–5 μm wavelength range, the increasing operating temperatures of aircraft necessitate further reduction in infrared emissivity within this specific band, in accordance with the Wien displacement law. This study focuses on the preparation of ceramic samples of YSZ doped with varying concentrations of Yb2O3 through a high-temperature solid-state reaction. It aims to investigate the influence of different doping concentrations on the microstructure, crystal structure, and infrared radiation characteristics of YSZ ceramic blocks. The experimental results demonstrated that the addition of Yb2O3 induces changes in the grain size and phase content of YSZ. Notably, as the amount of Yb2O3 doping increases, the infrared emissivity of YSZ samples in the 3–5 μm wavelength range exhibits a pattern of initial decrease followed by an increase. Remarkably, at a doping amount of 3 % mol, YSZ ceramics demonstrated the lowest emissivity, with the average emissivity of the 3–5 μm wavelength range decreasing from 0.41 to 0.38.

Stretchable supramolecular hydrogel with instantaneous self-healing for electromagnetic interference shielding control and sensing

Conductive hydrogels possess instantaneous self-healing and adhesive properties have generated great excitement in the fields of sensing and electromagnetic interference (EMI) shielding. In this study, we ingeniously designed hydrogel-based soft materials with high conductivity by using poly(vinyl alcohol) (PVA), positively charged Ti3C2Tx MXene and thioctic acid (TA) as source materials. Through concentration-induced ring-opening polymerization of TA monomers in an aqueous solution of potassium hydroxide (KOH), supramolecular poly(potassium thioctate) (poly(PT)) was obtained. Then, the multifunctional poly(PT)/PVA/p-MXene hydrogel with exceptional stretchability, substrate-adhesion and self-healing capability was achieved through abundant dynamic bonds, including disulfide bonds, hydrogen bonds, coordination bonds and electrostatic interactions. The hydrophobic main chains within poly(PT) provide robust protection against the oxidative degradation of MXene. This hydrogel shows outstanding strain sensing and extraordinary EMI shielding effectiveness (SE) of 48.56 dB caused by the inner structure, conductivity, and water content. Interestingly, the EMI SE can be regulated by reabsorbing moisture from the air, thereby enabling the reuse of dried hydrogel. Furthermore, the EMI SE can be dynamically modulated through controlled deformations, confirming the potential application for electromagnetic waves (EMWs) sensing. This innovative approach not only simplifies the fabrication of multifunctional materials but also expands the applications of adhesive hydrogels with conductivity.

Exploring Protonation State, Ion Binding, and Photoactivated Channel Opening of an Anion Channelrhodopsin by Molecular Simulations.

Channelrhodopsins are light-gated ion channels with a retinal chromophore found in microbes and are widely used in optogenetics, a field of neuroscience that utilizes light to regulate neuronal activity. GtACR1, an anion conducting channelrhodopsin derived from Guillardia theta, has attracted attention for its application as a neuronal silencer in optogenetics because of its high conductivity and selectivity. However, atomistic mechanisms of channel photoactivation and ion conduction have not yet been elucidated. In the present study, we investigated the molecular characteristics of GtACR1 and its photoactivation processes by molecular simulations. The QM/MM RWFE-SCF method which combines highly accurate quantum chemistry calculations with long-time molecular dynamics (MD) simulations were used to model protein structures of the wild-type and mutants with different protonation states of key groups and to calculate absorption energies for verification of the models. The QM/MM modeling together with MD simulations of free-energy calculations favors protonation of a key counterion carboxyl group of Asp234 with a strong binding of a chloride ion in the extracellular pocket in the dark state. A channel open state was also successfully modeled by the QM/MM RWFE-SCF free-energy optimizations, providing atomistic insights into the channel activation mechanism.

High toughness, flexible and thermally conductive fluorine rubber composite films reinforced by hexagonal boron nitride flakes for thermal management

The rapid advancement of electronic information technology has generated a substantial demand for polymer-based thermal management materials. In order to address the challenges of heat dissipation and avoid signal interference, it is essential to develop polymer-based thermal management materials with both high thermal conductivity and low dielectric properties. Herein, hexagonal boron nitride flakes (h-BNFs) with a high aspect ratio and some hydroxyl groups were prepared using the high pressure homogenization technique. Subsequently, h-BNF/fluorine rubber (h-BNF/FKM) composite films were fabricated through a simple and scalable blade coating method. During the blade coating process, most of the h-BNFs can align with their (002) crystal planes paralleling to the horizontal direction. In addition, the rest of the h-BNFs will randomly distribute and overlap with each other, combining with the horizontally aligned h-BNFs to form a distinctive three-dimensional packing network. This unique network structure enables the h-BNF/FKM composite films to have thermal conductivities of up to 0.44 W/(m·K). Moreover, the introduction of h-BNFs can effectively reduce the dielectric constants and dielectric losses of FKM films. More importantly, the h-BNF/FKM composite films also exhibit outstanding mechanical toughness, excellent flexibility, good adhesion and improved flame-retardancy, providing promising applications in the electronic device thermal management.

Flexible electrospun carbon nanofibers - Nickel disulfide@carbon nanofibers - Carbon nanofibers sandwich structure as binder-free anode for high performance lithium-ion batteries

People have recently shown increasing interest in wearable and flexible electronics. Due to their high electrical conductivity and flexibility, carbon nanofibers can be utilized for various flexible applications. However, pure carbon nanofibers have low capacity, which makes it challenging to achieve high capacity for flexible applications. Herein, sandwich-like nanofibers - nickel disulfide@carbon nanofibers - carbon nanofibers are obtained through a multi-step electrospinning process to serve as a flexible binder-free anode for lithium-ion batteries. This strategy stabilizes the structure well with two layers of carbon nanofibers, effectively accelerating the Li+diffusion and promoting the electrolyte infiltration. Accordingly, the electrode exhibits a discharge capacity of 551.8 mAh g-1 at 0.1 A g-1 after 100 cycles and achieves a discharge capacity of 523.8 mAh g-1 at 1 A g-1 after 1000 cycles, demonstrating excellent cyclic stability and high capacity for Li+ storage. The kinetic analysis also reveals that the sandwich structure provides a higher capacity contribution. This work introduces a novel approach for creating flexible binder-free anodes with high performance, effectively expanding the application of sulfides through electrospinning.

Saturation degree in dopant monolayers as modulator of Al-doping of ZnO by the Atomic Layer Deposition-supercycle approach

Transparent conductive oxides are trending topic in science and technology due to counterintuitive properties: optical transparency and high electrical conductivity. ZnO is a promising example with optoelectronic properties enhanced by supervalent doping. Al-doped ZnO (AZO) has emerged as leading candidate to replace environmentally hazardous In-doped SnO2. However, an ongoing debate exists regarding whether Al-doping improves its optoelectronic properties by substitutional doping or by promoting active defects. Here, we focused on Al-doping of ZnO by atomic layer deposition (ALD) applying the supercycle approach, showing that, decreasing Zn precursor dosing during dopant cycles, the decreasing saturation degree of Zn-species monolayers leads to morphological and microstructural changes that negatively impact optoelectronic properties, whereas Al content remains invariant. Our results demonstrate that unsaturated surfaces after decreasing Zn precursor dosing play a crucial role in Al incorporation, suggesting that, to maximize the effect of doping, complete oxide substitution reactions rather than those of conventional ALD must control growth, while crystallinity must remain. These findings could impact strategy designing for optimization of optoelectronic properties of AZO films deposited by ALD by inclining the debate towards the hypothesis that electrical properties are determined by Al substitutional doping together with active defects formed due to substitutional doping itself.

Trapping Ions to Enhance High-Field Energy Harvesting Performance by Filling Polar Macromolecular Dielectrics.

In the quest for sustainable and renewable energy sources, researchers and engineers have explored innovative technologies to harvest energy from various environmental sources. Dielectric elastomer generators (DEGs) with high energy harvesting performance have been proven to be promising energy collectors, but achieving a high dielectric constant (ε') and low electrical conductivity (EC) under high electric fields of dielectric elastomer (DE) simultaneously is a struggle, which poses significant challenges. In this study, high-content carboxyl group-grafted liquid polybutadiene (HCPB) is synthesized and then adopted as an organic dielectric filler to blend and cocross-link with a butadiene rubber (BR) matrix to prepare DE composites with high energy harvesting performance. The introduction of carboxyl groups enhances polarization while trapping free Al3+ in the matrix, which revolutionarily achieves a significant increase in ε' under extremely low EC. Ultimately, the contradiction between increased ε' and decreased EC under high electric fields is reconciled, resulting in a 30 HCPB/BR composite with high energy density (w = 91.9 mJ/cm3) and fine power conversion efficiency (PCE = 24.1%). This advancement paves the way for the development of HCPB/BR composite-based DEGs with enhanced ε' and energy harvesting performance.

Laser Powder Bed Fusion of Multifunctional Bio-inspired Vertical Honeycomb Sandwich Structures: For the Application of Lightweight Bipolar Plates of Proton Exchange Membrane Fuel Cells

The bipolar plate (BPP) is a crucial component of proton exchange membrane fuel cells (PEMFC). However, the weight of BPPs can account for around 80% of a PEMFC stack, posing a hindrance to the commercialization of PEMFCs. Therefore, the lightweight design of BPPs should be considered as a priority. Honeycomb sandwich structures meet some requirements for bipolar plates, such as high mechanical strength and lightweight. Animals and plants in nature provide many excellent structures with characteristics such as low density and high energy absorption capacity. In this work, inspired by the microstructures of the Cybister elytra, a novel bio-inspired vertical honeycomb sandwich (BVHS) structure was designed and manufactured by laser powder bed fusion (LPBF) for the application of lightweight BPPs. Compared with the conventional vertical honeycomb sandwich (CVHS) structure formed by LPBF under the same process parameters setting, the introduction of fractal thin walls enabled self-supporting and thus improved LPBF formability. In addition, the BVHS structure exhibited superior energy absorption (EA) capability and bending properties. It is worth noting that, compared with the CVHS structure, the specific energy absorption (SEA) and specific bending strength of the BVHS structure increased by 56.99% and 46.91%, respectively. Finite element analysis (FEA) was employed to study stress distributions in structures during bending and analyze the influence mechanism of the fractal feature on the mechanical properties of BVHS structures. The electrical conductivity of structures were also studied in this work, the BVHS structures were slightly lower than the CVHS structure. FEA was also conducted to analyze the current flow direction and current density distribution of BVHS structures under a constant voltage, illustrating the influence mechanism of fractal angles on electrical conductivity properties. Finally, in order to solve the problem of trapped powder inside the enclosed unit cells, a droplet-shaped powder outlet was designed for LPBF-processed components. The number of powder outlets was optimized based on bending properties. Results of this work could provide guidelines for the design of lightweight BPPs with high mechanical strength and high electrical conductivity.

Dual optimization of LiFePO4 cathode performance using manganese substitution and a hybrid lithiated Nafion-modified PEDOT:PSS coating layer for lithium-ion batteries

The energy storage market necessitates an increase in the specific capacity of battery materials, particularly cathodes, to meet growing demands. Manganese (Mn) substitution of lithium iron phosphate (LFP) cathodes presents a promising avenue, offering high specific capacity and operability at elevated voltages. However, during cycling, the dissolution of Fe/Mn ions into the electrolyte leads to capacity fading. In this study, we enhance the specific capacity of LFP by Mn substitution in the iron position at various ratios (0.1, 0.2, 0.3, and 0.4). LiFe0.6Mn0.4PO4 exhibits the highest capacity of 159.1 mAh g-1 at 0.1C with an initial Coulombic efficiency of 97.9 %. This improvement stems from an enhanced lithium diffusion coefficient, increasing from 1.86 × 10–14 cm2 s-1 for pristine LFP to 2.46 × 10–12 cm2 s-1 for LiFe0.6Mn0.4PO4. However, LiFe0.6Mn0.4PO4 demonstrates the poorest capacity retention among the substituted samples, reaching 78.4 % over 100 cycles due to severe Fe/Mn ion dissolution. To address this issue, we coat Mn-substituted LFP with poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) and lithiated Nafion (LN) polymer, which offer high electronic and lithium-ion conductivity, respectively. This coating layer enhances the capacity retention of LiFe0.6Mn0.4PO4 to 90.1 % at 0.2C after 100 cycles, effectively mitigating active material loss during charge-discharge processes. This study demonstrates that PEDOT:PSS-LN can improve the electronic and ionic conductivity of cathode materials and maintain high capacity retention during cycling.

Turning coal hydrogenation liquefaction residue into high conductivity carbon black with magnesium citrate-assisted steam activation followed by high temperature treatment

The high conductivity carbon black was prepared using coal hydrogenation liquefaction residue as raw material, through a combination methods of solvent extraction purification, magnesium citrate-assisted carbonization, steam activation, and high-temperature treatment. The effects of carbonization and activation process parameters, heat treatment temperatures, and other factors on the microstructure, specific surface area, degree of graphitization, and conductivity of the carbon black were studied. The coal direct liquefaction residue was firstly purified using a xylene and tetrahydrofuran solution with a volume ratio of 1:1 by centrifugal separation method to obtain coal liquefaction asphalt. Then, the coal liquefaction asphalt was mixed with magnesium citrate in a mass ratio of 3:7 and ball-milled for 90 min. After carbonizing at 950 °C for 120 min, magnesium ions were leached out with hydrochloric acid. The obtained sample was activated with steam at 900 °C for 100 min and then underwent high-temperature treatment at 1500 °C under a N2 atmosphere for 120 min. The microstructure of the conductive carbon black exhibited an irregular blocky structure with an average particle size of 2–10 μm. The specific surface area of carbon material was 579.69 m2/g, with the pore distribution predominantly microporous, accounting for 69.81 % of the total pore volume. It featured a higher degree of graphitization (ID/IG=1.06) and fewer surface oxygen-containing functional groups compared with coal direct liquefaction residue. Electrochemical testing showed that the electrical resistance of the carbon material was only 1.55 Ω, and the reversible capacity under a current density of 1 A/g was 96 mAh/g, which are superior to those of the existing commercial conductive carbon black. The microporous structure and higher degree of graphitization facilitate efficient electron transmission, while the lower content of surface oxygen functional groups effectively reduces electron transfer resistance. This work offers new insights into the structural design and performance enhancement of coal liquefaction residue-derived conductive carbon black functional materials. Furthermore, it has significant implications for the future development of conductive carbon black in energy saving and energy storage.

Ion Transport at Polymer-Argyrodite Interfaces.

Solid-state electrolytes, particularly polymer/ceramic composite electrolytes, are emerging as promising candidates for lithium-ion batteries due to their high ionic conductivity and mechanical flexibility. The interfaces that arise between the inorganic and organic materials in these composites play a crucial role in ion transport mechanisms. While lithium ions are proposed to diffuse across or parallel to the interface, few studies have directly examined the quantitative impact of these pathways on ion transport and little is known about how they affect the overall conductivity. Here, we present an atomistic study of lithium-ion (Li+) transport across well-defined polymer-argyrodite interfaces. We present a force field for polymer-argyrodite interfacial systems, and we carry out molecular dynamics and enhanced sampling simulations of several composite systems, including poly(ethylene oxide) (PEO)/Li6PS5Cl, hydrogenated nitrile butadiene rubber (HNBR)/Li6PS5Cl, and poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)/Li6PS5Cl. For the materials considered here, Li-ion exhibits a preference for the ceramic material, as revealed by free energy differences for Li-ion between the inorganic and the organic polymer phase in excess of 13 kBT. The relative free energy profiles of Li-ion for different polymeric materials exhibit similar shapes, but their magnitude depends on the strength of interaction between the polymers and Li-ion: the greater the interaction between the polymer and Li-ions, the smaller the free energy difference between the inorganic and organic materials. The influence of the interface is felt over a range of approximately 1.5 nm, after which the behavior of Li-ion in the polymer is comparable to that in the bulk. Near the interface, Li-ion transport primarily occurs parallel to the interfacial plane, and ion mobility is considerably slower near the interface itself, consistent with the reduced segmental mobility of the polymer in the vicinity of the ceramic material. These findings provide insights into ionic complexation and transport mechanisms in composite systems, and will help improve design of improved solid electrolyte systems.

Hydrotalcite-Enhanced Tough and Strong Hydrogel Endowed by Coordination and Electrostatic Interactions for Both Strain and Pressure Sensors.

Polymer hydrogels have a wide range of applications in the field of flexible wearable devices from the perspective of easy commercialization and environmental compatibility. However, traditional hydrogels often fail to achieve adequate mechanical strength and performance such as toughness, resilience, and ionic conductivity. Herein, a significant enhancement of tensile strength in 2 orders of magnitude (from 36 kPa to 1.5 MPa) is obtained by the introduction of hydrotalcite into polymer network via multiple, multilevel, and strong interactions of strengthened interface interactions, and the enhancement effect is superior to most of known records. Meanwhile, the enhanced conductivity may be rationally attributed to effective channels of hydrotalcite for ion transport. As a result, high toughness (9.5 MJ/m3), stretchability (1520%), excellent resilience (100% rebound of 400% strain), high conductivity (2.6 mS/cm), and low-temperature resistance are successfully achieved. The work shows an efficient approach to design desired ultratough and multifunctional hydrogels.

Preparation of Zirconium-Based MOF-Derived Phosphide on GO/MXene Double Substrates for High-Performance Asymmetric Supercapacitors.

At present, it is very necessary to select and prepare suitable positive and negative electrode materials to fabricate high-performance asymmetric supercapacitors. Metal-organic frameworks (MOFs) have garnered significant attention in the energy storage field due to their high conductivity. As a branch, the zirconium organic framework (UIO-66) is a promising porous material due to its large specific surface area and abundant Zr centers. Graphene oxide (GO) and MXene are very suitable as substrate materials for conducting an MOF due to their abundant active sites and adjustable interlayer distance. The GO/MXene@NiZrP prepared through an in situ composite of GO and Mxene with the hydrothermal method and calcining method showed excellent electrochemical performance. Compared with the precursor UIO-66, the specific capacitance of the final product GO/MXene@NiZrP increases more than ten times, mainly because of its special layered porous structure, and GO/MXene@NiZrP has a larger specific surface area, pore volume, and surface defects caused by unstable Zr4+ than those of UIO-66. Using GO/MXene@NiZrP as the positive electrode and biochar (BC) as the negative electrode, an asymmetric supercapacitor, BC//GO/MXene@NiZrP, is assembled. After 10,000 cycles at a current density of 10 A g-1, the capacitance retention remains at 83.3%, showing excellent cycle stability.

Regulating Strain and Electronic Structure of Indium Tin Oxide Supported IrOx Electrocatalysts for Highly Efficient Oxygen Evolution Reaction in Acid.

The development of proton exchange membrane water electrolysis is a promising technology for hydrogen production, which has always been restricted by the slow kinetics of the oxygen evolution reaction (OER). Although IrOx is one of the benchmark acidic OER electrocatalysts, there are still challenges in designing highly active and stable Ir-based electrocatalysts for commercial application. Herein, a Ru-doped IrOx electrocatalyst with abundant twin boundaries (TB-Ru0.3Ir0.7Ox@ITO) is reported, employing indium tin oxide with high conductivity as the support material. Combing the TB-Ru0.3Ir0.7Ox nanoparticles with ITO support could expose more active sites and accelerate the electron transfer. The TB-Ru0.3Ir0.7Ox@ITO exhibits a low overpotential of 203 mV to achieve 10 mA cm-2 and a high mass activity of 854.45 A g-1noblemetal at 1.53 V vs RHE toward acidic OER, which exceeds most reported Ir-based OER catalysts. Moreover, improved long-term stability could be obtained, maintaining the reaction for over 110 h at 10 mA cm-2 with negligible deactivation. DFT calculations further reveal the activity enhancement mechanism, demonstrating the synergistic effects of Ru doping and strains on the optimization of the d-band center (εd) position and the adsorption free energy of oxygen intermediates. This work provides ideas to realize the trade-off between high catalytic activity and good stability for acidic OER electrocatalysts.

Fluid-Dynamics-Rectified Chemical Vapor Deposition (CVD) Preparing Graphene-Skinned Glass Fiber Fabric and Its Application in Natural Energy Harvest.

Graphene chemical vapor deposition (CVD) growth directly on target using substrates presents a significant route toward graphene applications. However, the substrates are usually catalytic-inert and special-shaped; thus, large-scale, high-uniformity, and high-quality graphene growth is challenging. Herein, graphene-skinned glass fiber fabric (GGFF) was developed through graphene CVD growth on glass fiber fabric, a Widely used engineering material. A fluid dynamics rectification strategy was first proposed to synergistically regulate the distribution of carbon species in 3D space and their collisions with hierarchical-structured substrates, through which highly uniform deposition of high-quality graphene on fibers in large-scale 3D-woven fabric was realized. This strategy is universal and applicable to CVD systems using various carbon precursors. GGFF exhibits high electrical conductivity and photothermal conversion capability, based on which a natural energy harvester was first developed. It can harvest both solar and raindrop energy through solar heating and droplet-based electricity generating, presenting promising potentials to alleviate energy burdens.

Fluorine-Rich Electrolyte Additive for Achieving Dendrite-Free Lithium Anodes at Low Temperatures.

The practical application of lithium metal anodes is significantly impeded by poor interfacial stability and uncontrolled dendrite growth. Herein, we introduce methyl trifluoroacetate (MTFA), a low-melting-point small molecule, as an electrolyte additive in an ether-based electrolyte. This additive facilitates the formation of an in situ composite solid electrolyte interphase (SEI) layer that is rich in LiF and features an ester-based flexible matrix. The resulting composite layer exhibits high ionic conductivity and mechanical stability, effectively regulating the lithium deposition behavior over a broad temperature range and inhibiting dendrite formation. Based on MTFA, the Li||Li symmetrical cell achieves a lifespan exceeding 5000 h at room temperature and 800 h at -20 °C, both with ultralow overpotential and exceptional cycling stability. In Li||LiFePO4 full cells with a high-area loading (10.52 mg cm-2) and an N/P ratio of 1.68, an average capacity decay of merely 0.096% per cycle is observed over 200 cycles. Even at -20 °C, the Li||LiFePO4 cell shows a CE of over 99% and maintains stable cycling performance. This work provides an innovative approach for optimizing lithium metal anode interfaces and enhancing low-temperature operation capabilities through the use of electrolyte additives.