Active Material Research Articles

Investigation of the Single-Particle Scale Structure-Activity Relationship Providing New Insights for the Development of High-Performance Batteries.

As electric vehicles, portable electronic devices and tools have increasingly high requirements for battery energy density and power density, constantly improving battery performance has become a research focus. Accurate measurement of the structure-activity relationship of active materials is the key to advancing the research of high-performance batteries. However, the conventional performance tests of active materials are based on the electrochemical measurement of porous composite electrodes containing active materials, polymer binders, and conductive carbon additives, which cannot establish an accurate structure-activity relationship with the physical characterization of microregions. In this review, in order to promote the accurate measurement and understanding of the structure-activity relationship of materials, the electrochemical measurement and physical characterization of energy storage materials at single-particle scale are reviewed. The potential problems and possible improvement schemes of the single particle electrochemical measurement and physical characterization are proposed. Their potential applications in single particle electrochemical simulation and machine learning are prospected. This review aims to promote the further application of single particle electrochemical measurement and physical characterization in energy storage materials, hoping to achieve three-dimensional unified evaluation of physical characterization, electrochemical measurement, and theoretical simulation at the single particle scale to provide new inspiration for the development of high-performance batteries. This article is protected by copyright. All rights reserved.

Radical Polymer-based Positive Electrodes for Dual-Ion Batteries: Enhancing Performance with γ-Butyrolactone-based Electrolytes.

Dual-ion batteries (DIBs) represent a promising alternative for lithium ion batteries (LIBs) for various niche applications. DIBs with polymer-based active materials, here poly(2,2,6,6-tetramethylpiperidinyl-N-oxyl methacrylate) (PTMA), are of particular interest for high power applications, though they require appropriate electrolyte formulations. As the anion mobility plays a crucial role in transport kinetics, Li salts are varied using the well-dissociating solvent γ-butyrolactone (GBL). Lithium difluoro(oxalate)borate (LiDFOB) and lithium bis(oxalate)borate (LiBOB) improve cycle life in PTMA||Li metal cells compared to other Li salts and a LiPF6- and carbonate-based reference electrolyte, even at specific currents of 1.0Ag-1 (≈10C). Further, the use of LiDFOB reveals a superior rate performance, i.e., ≈90% capacity at 5.0Ag-1 (≈50C). This is attributed to faster charge-transfer/mass transport, enhanced pseudo-capacitive contributions during the de-/insertion of the anions into the PTMA electrode and to lower overpotentials at the Li metal electrode.

Experimental and Theoretical Predictors for Redox Potentials of Bispyridinylidene Electron Donors.

Bispyridinylidenes are neutral organic molecules capable of two-electron oxidation at a range of redox potentials that are widely tunable by choice of substituent, making them attractive as homogeneous organic reductants and active materials in redox flow batteries. In an effort to readily predict the redox potentials of this important class of compounds, we have developed correlations between the experimental redox potentials and both experimental and theoretical predictors. On the experimental side, we show that multinuclear NMR chemical shifts of related pyridinium ions correlate well with the redox potentials of bispyridinylidenes, with R2 and standard errors (S) reaching 0.9810 and 0.048 V, respectively, when the 13C (N-CH3) and 1H (ortho) chemical shifts are used together. Theoretical studies of the bispyridinylidenes and their doubly oxidized bipyridinium ions gave a range of predictively valuable equations at various levels of computational cost. This ranged from a simple model using only the EHOMO of the bispyridinylidenes (R2 = 0.9689; S = 0.060 V), to a more computationally intensive model which include solvation effects for both redox states which gave the highest predictive value for all methods (R2 = 0.9958; S = 0.022 V). This work will guide further studies of this important class of molecules.

Variation in survival, growth and stem straightness in Eucalyptus urophylla provenances in the Southern Highlands region, Tanzania

Lack of quality planting materials has significantly limited productivity and quality of commercial forestry plantations in Tanzania. A provenance/progeny trial of Eucalyptus urophylla was established to test performance in order to select the best planting materials for future plantation activities. A complete randomised block design was used whereby 30 families from 8 provenances within 6 replications were tested. At 13 years tree survival, growth (diameter at breast height and height) and stem straightness were assessed. The results indicate that there were highly significant differences (p < 0.05) among provenances and families in survival, height, breast height diameter (DBH) and stem straightness. The overall survival ranged from 79.0% to 96.2%; height ranged between 24.9 and 32.5 m; and DBH ranged from 18.7 to 24.5 cm. Overall, results from this study show that provenances Alassannaru, Elun kirpas, Nesunhuhun and Nakana ulam have better growth performance and stem form than others. These results provide valuable information on the growth performance of different provenances and families of E. urophylla. The provenances and families selected with best performance can be used in developing improved seeds for plantation establishment and/or selection of plus trees for vegetative propagation as candidate clones for a clonal testing programme in Tanzania.

Self-Heating of Planar Perovskite Solar Cells Depending on Active Material Properties

Self-Heating of Planar Perovskite Solar Cells Depending on Active Material Properties

The antimicrobial synergy of polymer based nanofiber mats reinforced with antioxidants intercalated layered double hydroxides as a potential active packaging material

Abstract Perishable food post-harvest loss is a major global concern, and research is currently concentrated on creating active packaging materials. This research is focused in multiple antioxidants intercalated Layered Double Hydroxides (LDH) that are combined in one matrix, and their overall effect that defines as synergism, which successfully preserves perishable food by releasing antioxidants slowly. For this purpose, a hybrid LDH material of ascorbic-LDH, salicylic-LDH, and citric-LDH was synthesized, characterized and incorporate into electrospun nanofiber mat to be used as a potential active packaging material. Antioxidants intercalated Mg/Al LDH was synthesized and successfully characterized by PXRD, FTIR, XPS, Raman, SEM and EDS. The shifts in the LDHs' peaks in PXRD indicated the successful incorporation of antioxidants into LDH. FTIR, Raman and XPS data clearly indicated the establishment of metal-oxygen bonds by observing the characteristic peaks. Morphological features and layered structure were clearly observed by SEM images. Antioxidants were slowly released from LDHs, and it was evaluated for time intervals up to 24 hrs. The hybrid LDH material exhibited the highest antioxidant activity with an IC50 value of 132.5µg/mL, where 234.1, 354.5, and 402.2µg/mL were reported for ascorbic-LDH, salicylic-LDH, and citric-LDH respectively. The hybrid LDH material incorporated electrospun mats showed the best antibacterial activity against the tested bacteria and clearly evidenced the synergistic activity of the combination of the nanohybrids. It has showed a minimal bacterial growth compared to other control samples (∼2.41 log CFU/mL). The shelf life of cherry tomatoes was studied at different physiochemical parameters with and without hybrid LDH material incorporated electrospun mats. The mat showed an extended shelf life of 42 days for cherry tomatoes, whereas the control sample showed a shelf life of 17 days. It is concluded that hybrid LDH material exhibited synergistic performance and the best antioxidant activity when comparing with mono LDH materials.

Stabilized Nickel‐Rich‐Layered Oxide Electrodes for High‐Performance Lithium‐Ion Batteries

Next‐generation Li‐ion batteries are expected to exhibit superior energy and power density, along with extended cycle life. Ni‐rich high‐capacity layered nickel manganese cobalt oxide electrode materials (NMC) hold promise in achieving these objectives, despite facing challenges such as capacity fade due to various degradation modes. Crack formation within NMC‐based cathode secondary particles, leading to parasitic reactions and the formation of inactive crystal structures, is a critical degradation mechanism. Mechanical and chemical degradation further deteriorate capacity and lifetime. To mitigate these issues, an artificial cathode electrolyte interphase can be applied to the active material before battery cycling. While atomic layer deposition (ALD) has been extensively explored for active material coatings, molecular layer deposition (MLD) offers a complementary approach. When combined with ALD, MLD enables the deposition of flexible hybrid coatings that can accommodate electrode material volume changes during battery operation. This study focuses on depositing ‐titanium terephthalate thin films on a electrode via ALD‐MLD. The electrochemical evaluation demonstrates favorable lithium‐ion kinetics and reduced electrolyte decomposition. Overall, the films deposited through ALD‐MLD exhibit promising features as flexible and protective coatings for high‐energy lithium‐ion battery electrodes, offering potential contributions to the enhancement of advanced battery technologies and supporting the growth of the EV and stationary battery industries.

Boost the Circularly Polarized Phosphorescence of Chiral Organometallic Platinum Complexes by Hierarchical Assembly into Fibrillar Networks.

Circularly polarized luminescence (CPL)-active molecular materials have drawn increasing attention due to their promising applications for next-generation display and optoelectronic technologies. Currently, it is challenging to obtain CPL materials with both large luminescence dissymmetry factor (glum) and high quantum yield (Φ). A pair of enantiomeric N N C-type Pt(II) complexes (L/D)-1 modified with chiral Leucine methyl ester are presented herein. Though the solutions of these complexes are CPL-inactive, the spin-coated thin films of (L/D)-1 exhibit giantly-amplified circularly polarized phosphorescences with |glum| of 0.53 at 560 nm and Φair of ~50 %, as well as appealing circular dichroism (CD) signals with the maximum absorption dissymmetry factor |gabs| of 0.37-0.43 at 480 nm. This superior CPL performance benefits from the hierarchical formation of crystalline fibrillar networks upon spin coating. Comparative studies of another pair of chiral Pt(II) complexes (L/D)-2 with a symmetric N C N coordination mode suggest that the asymmetric N N C coordination of (L/D)-1 are favorable for the efficient exciton delocalization to amplify the CPL performance. Optical applications of the thin films of (L/D)-1 in CPL-contrast imaging and inducing CP light generation from achiral emitters and common light-emitting diode lamps have been successfully realized.

Boost the Circularly Polarized Phosphorescence of Chiral Organometallic Platinum Complexes by Hierarchical Assembly into Fibrillar Networks

AbstractCircularly polarized luminescence (CPL)‐active molecular materials have drawn increasing attention due to their promising applications for next‐generation display and optoelectronic technologies. Currently, it is challenging to obtain CPL materials with both large luminescence dissymmetry factor (glum) and high quantum yield (Φ). A pair of enantiomeric N N C‐type Pt(II) complexes (L/D)‐1 modified with chiral Leucine methyl ester are presented herein. Though the solutions of these complexes are CPL‐inactive, the spin‐coated thin films of (L/D)‐1 exhibit giantly‐amplified circularly polarized phosphorescences with |glum| of 0.53 at 560 nm and Φair of ~50 %, as well as appealing circular dichroism (CD) signals with the maximum absorption dissymmetry factor |gabs| of 0.37–0.43 at 480 nm. This superior CPL performance benefits from the hierarchical formation of crystalline fibrillar networks upon spin coating. Comparative studies of another pair of chiral Pt(II) complexes (L/D)‐2 with a symmetric N C N coordination mode suggest that the asymmetric N N C coordination of (L/D)‐1 are favorable for the efficient exciton delocalization to amplify the CPL performance. Optical applications of the thin films of (L/D)‐1 in CPL‐contrast imaging and inducing CP light generation from achiral emitters and common light‐emitting diode lamps have been successfully realized.

Flame Spray Pyrolysis Synthesis of Ultra-Small High-Entropy Alloy-Supported Oxide Nanoparticles for CO2 Hydrogenation Catalysts.

The synthesis of high-entropy alloys (HEAs) with ultra-small particle sizes has long been a challenging task. The complex and time-consuming synthesis process hinders their practical application and widespread adoption. This study presents the novel synthesis of TiO2 nanoparticles loaded with a quinary high-entropy alloy through flame spray pyrolysis (FSP) for the first time. The extremely fast heating rate of flame combustion makes the precursor fast pyrolysis gasification, high temperature in the flame field promotes the metal vapor mixing uniformly, and the fast quenching process can reduce the particle aggregation sintering, the ultra-small particle size of HEA firmly attached to the TiO2 surface. The catalysts prepared via this gas-to-particle pathway exhibit excellent performance in CO2 hydrogenation, achieving a conversion rate of 62% at 450°C, and maintaining their activity for over 220h without significant particle agglomeration. This finding provides valuable insights for the future design of catalytically active materials with enhanced activity and long-term stability.

Unveiling the Degradation Mechanism of Sodium Ion Batteries based on Na4Fe3(PO4)2P2O7 Cathode and Hard carbon Anode suggests Anode Particle Size Reduction for Cycling Stability

To improve the cycle life of sodium‐ion batteries, it is essential to understand the microscopic processes that lead to cell degradation. The mismatched response time of anode and cathode has profound but poorly understood impact on cycle life. In this research, we combine electrochemical and materials characterization combined with electrochemical modeling to investigate the root cause of degradation in sodium‐ion full cells made from Na4Fe3(PO4)2P2O7 (NFPP) cathodes and hard carbon (HC) anode. Our results pinpoint to the slow diffusion of Na in HC as the main cause of diffusional polarization that leads to cathode experiencing high local potentials and ultimately to active material loss over cycling. We demonstrate that by reducing the anode particle size, the diffusional timescales in anode can be matched with that of cathode to improve both extractable capacity as well as cycle life. These observations shed light on non‐intuitive and intricate ways in which cathode and anode can interact with each other to cause degradation in Na‐ion batteries and how microscopic understanding of these cause and effects can help design long lasting batteries.

Stable and improved voltage plate of Li/SOCl2 battery using carbon electrodes with active carbon

Abstract Active carbon (AC) is synthesized using pitch coke as a precursor with a KOH activation approach followed. AC with different specific surface areas can be obtained by controlling the activation time of KOH. The activation time of AC1, AC2 and AC3 is 1 hour, 1.5 hours and 2 hours, with the surface areas of 1233, 1484 and 1639 m2 g-1, respectively. The phase, surface chemical structure, morphology as well as the microstructure of the AC are investigated by XRD, Raman, IR, XPS, BET, SEM and TEM. The obtained ACs displayed a size around 300 μm with lots of nanoholes and functional group involving -OH, -COOH. When employed as the catalytic active materials in the carbon cathodes for Li/SOCl2 batteries, the discharged voltage was improved to around 0.15 V with an enhanced stable platform. Whereas the energy of the batteries containing the ACs is similar as that the conventional batteries, as well as the morphology of the carbon cathode with ACs exhibited a dense LiCl on the surface, suggesting that the ACs can enhance the reduction reaction of SOCl2, but could not act as the nucleation sites for the synthesis of nanoscale LiCl to form a loose film for a long discharge life

Formulating Interfacial Impedances for Designing High-Energy and High-Power All-Solid-State Battery Cathodes.

All-solid-state batteries (ASSBs) are safe, high-energy-storage systems. However, despite the progress achieved in the development of high-ionic-conductivity solid electrolytes (SEs), the power performance of ASSBs remains low because of the high interfacial impedances in composite cathodes. Therefore, understanding the interfacial factors is crucial for obtaining high power ASSBs. This study provides a quantitative analysis of the influence of these factors using impedance spectroscopy measurements, which enables the elucidation of the interfacial impedance values of two key parameters, the grain-boundary resistance (ri,gb) and charge-transfer resistance (ri/e). Systematic investigation revealed an unexpected increase in the cathodic resistance with the decrease in the size of the cathode active material (CAM) particles, indicating that even high-reaction-surface-area CAMs yield low ri/e but high ri,gb values owing to their high porosity, resulting in a trade-off relationship. In contrast, this phenomenon is unlikely to occur in liquid-electrolyte-based batteries. Notably, we discuss how composite cathode design impacts performances of stable, high-power, and high-energy ASSBs.

Mechanical behavior and microstructure evolution of slag-fly ash based geopolymer stabilized sand

Geopolymers made from ground granulated blast-furnace slag and fly ash could effectively address the issues of high energy consumption and emissions associated with Portland cement, which is commonly used as a soil curing agent. In this study, the unconfined compressive strength and microstructure of geopolymer-solidified sand were presented and analyzed. The study focused on effect of the type and ratio of activator, the ratio of slag to fly ash, and the ratio of water to (activator and cementitious materials) (W/(A + C)) on the behavior of geopolymer stabilized sand. The results of computed tomography (CT), and scanning electron microscope (SEM) indicate that the variation in initial water content significantly affects the porosity of the specimen, which increased as initial water content increased. The cracks were mainly found at the joints between the individual aggregates and at the edges of the individual aggregates. The pore size distribution of the specimens was concentrated in the range 0.0761–5 μm, while the polymer particle distribution was concentrated in the range 0.0761–10 μm, with a concentration of over 90 %. A significant amount of cementing material was densely distributed around both the aggregates and the pores. CT and SEM testing techniques enable a thorough analysis and mutual verification of the self-compacting process, pore distribution, and size, as well as the distribution of cementing material within the specimens. The optimum ratio for B-S19 has been determined.

Dynamic Near‐Infrared Circularly Polarized Luminescence Encoded by Transient Supramolecular Chiral Assemblies

Circularly polarized luminescence (CPL) is promising for applications in many fields. However, most systems involving CPL are within the visible range; near‒infrared (NIR) CPL‒active materials, especially those that exhibit high glum values and can be controlled spatially and temporally, are rare. Herein, dynamic NIR‒CPL with a glum value of 2.5[[EQUATION]]10‒2 was achieved through supramolecular coassembly and energy transfer strategies. The chiral assemblies formed by the coassembly between adenosine triphosphate (ATP) and a pyrene derivative exhibit a red CPL signal (glum of 10‒3). The further introduction of sulfo‒cyanine5 resulted in a cooperative energy transfer process, which not only aroused the NIR CPL but also increased the glum value to 10‒2. Temporal control of these chiral assemblies was realized by introducing alkaline phosphatase to fabricate a biomimetic enzyme‒catalyzed network, allowing the dynamic NIR CPL signal to be turned on. Based on these enzyme‐regulated temporally controllable dynamic CPL‐active chiral assemblies, a multilevel information encryption system was further developed. Our work provides a pioneering example for constructing dynamic NIR CPL materials holding the ability to perform temporal control via the supramolecular assembly strategy, which is expected to aid in the design of supramolecular complex systems that more closely resemble natural biological systems.

Dynamic Near-Infrared Circularly Polarized Luminescence Encoded by Transient Supramolecular Chiral Assemblies.

Circularly polarized luminescence (CPL) is promising for applications in many fields. However, most systems involving CPL are within the visible range; near‒infrared (NIR) CPL‒active materials, especially those that exhibit high glum values and can be controlled spatially and temporally, are rare. Herein, dynamic NIR‒CPL with a glum value of 2.5[[EQUATION]]10‒2 was achieved through supramolecular coassembly and energy transfer strategies. The chiral assemblies formed by the coassembly between adenosine triphosphate (ATP) and a pyrene derivative exhibit a red CPL signal (glum of 10‒3). The further introduction of sulfo‒cyanine5 resulted in a cooperative energy transfer process, which not only aroused the NIR CPL but also increased the glum value to 10‒2. Temporal control of these chiral assemblies was realized by introducing alkaline phosphatase to fabricate a biomimetic enzyme‒catalyzed network, allowing the dynamic NIR CPL signal to be turned on. Based on these enzyme-regulated temporally controllable dynamic CPL-active chiral assemblies, a multilevel information encryption system was further developed. Our work provides a pioneering example for constructing dynamic NIR CPL materials holding the ability to perform temporal control via the supramolecular assembly strategy, which is expected to aid in the design of supramolecular complex systems that more closely resemble natural biological systems.

High-Area-Capacity Cathode by Ultralong Carbon Nanotubes for Secondary Binder-Assisted Dry Coating Technology.

Thick electrodes with high mass loading and increased content of active materials are critical for achieving higher energy density in contemporary lithium-ion batteries (LIBs). Nonetheless, producing thick electrodes through the commonly used slurry coating technology remains a formidable challenge. In this study, we have addressed this challenge by developing a dry electrode technology by using ultralong multiwalled carbon nanotubes (MWCNT) as a conductive additive and secondary binder. The mixing process of electrode compositions and the fibrillation process of the polytetrafluoroethylene (PTFE) binder were optimized. The resulting LiCoO2 (LCO) electrode exhibited a remarkable mass loading of 48 mg cm-2 and an active material content of 95 wt %. Notably, the thick LCO electrode demonstrated a superior mechanical strength and electrochemical performance. After 100 cycles at a current density of 1/3 C, the electrode still exhibited a capacity retention of 91% of its initial capacity. This dry electrode technology provides a practicable and scalable approach to the powder-to-film LIB electrode manufacturing process.

PENDAMPINGAN KOMUNITAS BELAJAR SEKOLAH PENGGERAK MELALUI LOKAKARYA REFLEKSI UNTUK MENINGKATKAN KUALITAS PROSES PEMBELAJARAN DI SEKOLAH DASAR

Driving schools, especially elementary schools in Wajo Regency, have several learning communities with different teacher competencies. Most teachers have not fully mastered the differentiation learning process in the Merdeka Belajar curriculum. The aim of this mentoring activity is to assist learning community teachers in planning, organizing and implementing an effective and creative Merdeka curriculum learning process. The method used in this service is a workshop form which includes stages starting from self, collaboration space, contextual demonstration and real action. Meanwhile, the material in this service activity uses teaching materials that have been determined by the Directorate General of Teachers and Education Personnel, Ministry of Education and Culture, Research and Technology. The results of the service show that the learning community that was accompanied has been able to create a plan for real action for a quality learning process that will be implemented in their respective educational units. Apart from that, the participants increasingly understand the function and role of the Learning Community in improving student performance and solving every problem in the Education Unit

Multiphysics simulations of a cylindrical waveguide optical switch using phase change materials on silicon

This work presents the design and multiphysics simulation of a cylindrical waveguide-based optical switch using germanium-antimony-tellurium (GST) as an active phase change material. The innovative cylindrical architecture is theoretically analyzed and evaluated at 1550 nm wavelength for telecommunication applications. The dispersion relation is derived analytically for the first time to model the optical switch, while finite element method (FEM) and finite difference time domain (FDTD) techniques are utilized to simulate the optical modes, light propagation, and phase change dynamics. The fundamental TE01 and HE11 modes are studied in detail, enabling switching between low-loss amorphous and high-loss crystalline GST phases. Increasing the GST thickness is found to increase absorption loss in the crystalline state but also slows down phase transition kinetics, reducing switching speeds. A 10 nm GST layer results in competitive performance metrics of 0.79 dB insertion loss, 13.47 dB extinction ratio, 30 nJ average power consumption, and 3.5 Mb/s bit rate. The combined optical, thermal, and electrical simulation provides comprehensive insights towards developing integrated non-volatile photonic switches and modulators utilizing phase change materials.

Magnetic Force Dilatometry for Operando Coin Cell Electrochemical Dilation Measurements

Abstract Operando characterization of the physical and chemical changes occurring within batteries during electrochemical cycling has become a powerful tool for next generation technology development. In particular, a better understanding of the expansion (dilation) behavior of active materials during charge/discharge is critical for mitigating performance degradation, particularly for high expansion materials like Li or Si. However, current dilatometry devices rely on direct mechanical coupling or line-of-sight measurements with pouch- or custom-cells, which prohibits their use in the most common and accessible research battery format: coin cells. To this end, we propose a novel magnetic force dilatometry (MFD) technique for operando electrochemical dilation measurements. Our custom low-cost dilatometer utilizes magnetic force sensing for contactless expansion measurements via facile replacement of the austenitic spacer with a ferritic spacer within a coin cell. To validate this setup, we demonstrate operando electrochemical dilatometry of a LiNi0.6Mn0.2Co0.2O2 (NMC622) || Li metal full cell in a CR2032 format. Our MFD accurately captures cell expansion/contraction with sensitivities of less than 0.1 μm, and reliability for over hundreds of hours and cycles. This new MFD method is expected to increase the accessibility of electrochemical dilatometry by eliminating the need for pouch cells or other specialized cell expansion measurement configurations.