Search

The development of supercapacitors with ultrahigh power density, high energy density, and compatible integration for wearable microelectronic devices is significant but challenging. Herein, a bimetallic metal–organic framework (Ni/Co-MOF) with oriented nanosheets was obtained via triethylamine (TEA) guiding using a hydrothermal treatment, in which the TEA guides the vertically oriented array structures of the Ni/Co-MOF and ensures a fast ion/electron transmission path. Subsequently, an asymmetric supercapacitor was rationally designed by applying the bimetallic MOF cathode and an activated carbon (AC) anode. The obtained Ni/Co-MOF sample offers a high storage capacity of 2034 F g−1 at 0.5 A g−1 by harnessing the optimized Ni/Co-MOF with uniformly oriented nanosheet arrays. The constructed asymmetric supercapacitors exhibited a large voltage window of 1.4 V in 3.0 M KOH and an outstanding energy density of 29.5 Wh kg−1 at a power density of 199.1 W kg−1 was obtained, with a remarkable capacitance retention of 89% after 2000 cycles. [ABSTRACT FROM AUTHOR]

The scalable fabrication of cost-efficient bifunctional catalysts with enhanced hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) performance plays a significant role in overall water splitting in hydrogen production fields. MoSe2 is considered to be one of the most promising candidates because of its low cost and high catalytic activity. Herein, hierarchical nitrogen-doped carbon networks were constructed to enhance the catalytic activity of the MoSe2-based materials by scalable free-drying combined with an in situ selenization strategy. The rationally designed carbonaceous network-encapsulated MoSe2 composite (MoSe2/NC) endows a continuous honeycomb-like structure. When utilized as a bifunctional electrocatalyst for both HER and OER, the MoSe2/NC electrode exhibits excellent electrochemical performance. Significantly, the MoSe2/NC‖MoSe2/NC cells require a mere 1.5 V to reach a current density of 10 mA cm−2 for overall water splitting in 1 M KOH. Ex situ characterizations and electrochemical kinetic analysis reveal that the superior catalytic performance of the MoSe2/NC composite is mainly attributed to fast electron and ion transportation and good structural stability, which is derived from the abundant active sites and excellent structural flexibility of the honeycomb-like carbon network. This work offers a promising pathway to the scalable fabrication of advanced non-noble bifunctional electrodes for highly efficient hydrogen evolution. [ABSTRACT FROM AUTHOR]

Zinc-ion capacitors (ZICs), combining the merits of both high-energy zinc-ion batteries and high-power supercapacitors, are known as high-potential electrochemical energy storage (EES) devices. However, the research on ZICs still faces many challenges because of the lack of appropriate cathode materials with robust crystal structures and rich channels for stable and fast Zn2+ ion transport. In this study, we synthesized a robust, conductive, two-dimensional metal–organic framework (MOF) material, zinc-benzenehexathiolate (Zn-BHT), and investigated its electrochemical performance for zinc storage. Zn2+ ions could insert into/extricate from the host structure with a high diffusion rate, enabling the Zn-BHT cathode to exhibit a surface-controlled charge storage mechanism. Due to its unique structure, Zn-BHT exhibited a good reversible discharge capacity approaching 90.4 mAh g−1 at 0.1 A g−1, as well as a desirable rate capability and good cycling performance. In addition, a ZIC device was fabricated using the Zn-BHT cathode and a polyaniline-derived porous carbon (PC) anode, which depicted a high working voltage of up to 1.8 V and a high energy density of ~37.2 Wh kg−1. This work shows that conductive MOFs are high-potential electrode materials for ZICs and provide new enlightenment for the development of electrode materials for EES devices. [ABSTRACT FROM AUTHOR]

This work reviews the progression of chemical analysis via Cherenkov emissions, i.e., Cherenkov Photometry and Cherenkov Emission Spectroscopy, from its introduction in the literature up to modern developments. In presenting the history of this field, we aim to consolidate the literature, both for reference and contextualization. We present an argument aiming to untangle why this corner of research has seen little progress while so many other directly related aspects of Cherenkov research have flourished, as well as speak to the progress of the field in recent years and prospective direction in years to come. [ABSTRACT FROM AUTHOR]

Designing innovative anode materials that exhibit excellent ion diffusion kinetics, enhanced structural stability, and superior electrical conductivity is imperative for advancing the rapid charge–discharge performance and widespread application of sodium-ion batteries. Hollow-structured materials have received significant attention in electrode design due to their rapid ion diffusion kinetics. Building upon this, we present a high-performance, free-standing MoO2@hollow carbon nanofiber (MoO2@HCNF) electrode, fabricated through facile coaxial electrospinning and subsequent heat treatment. In comparison to MoO2@carbon nanofibers (MoO2@CNFs), the MoO2@HCNF electrode demonstrates superior rate capability, attributed to its larger specific surface area, its higher pseudocapacitance contribution, and the enhanced diffusion kinetics of sodium ions. The discharge capacities of the MoO2@HCNF (MoO2@CNF) electrode at current densities of 0.1, 0.2, 0.5, 1.0, 2.0 and 5.0 A g−1 are 195.55 (155.49), 180.98 (135.20), 163.81 (109.71), 144.05 (90.46), 121.16 (71.21) and 88.90 (44.68) mAh g−1, respectively. Additionally, the diffusion coefficients of sodium ions in the MoO2@HCNFs are 8.74 × 10−12 to 1.37 × 10−12 cm2 s−1, which surpass those of the MoO2@CNFs (6.49 × 10−12 to 9.30 × 10−13 cm2 s−1) during the discharging process. In addition, these prepared electrode materials exhibit outstanding flexibility, which is crucial to the power storage industry and smart wearable devices. [ABSTRACT FROM AUTHOR]

Rechargeable aqueous zinc-ion batteries have attracted a lot of attention owing to their cost effectiveness and plentiful resources, but less research has been conducted on the aspect of high volumetric energy density, which is crucial to the space available for the batteries in practical applications. In this work, highly crystalline V2O5 microspheres were self-assembled from one-dimensional V2O5 nanorod structures by a template-free solvothermal method, which were used as cathode materials for zinc-ion batteries with high performance, enabling fast ion transport, outstanding cycle stability and excellent rate capability, as well as a significant increase in tap density. Specifically, the V2O5 microspheres achieve a reversible specific capacity of 414.7 mAh g−1 at 0.1 A g−1, and show a long-term cycling stability retaining 76.5% after 3000 cycles at 2 A g−1. This work provides an efficient route for the synthesis of three-dimensional materials with stable structures, excellent electrochemical performance and high tap density. [ABSTRACT FROM AUTHOR]

Numerous endeavors have been dedicated to the development of composite polymer electrolyte (CPE) membranes for all-solid-state batteries (SSBs). However, insufficient ionic conductivity and mechanical properties still pose great challenges in practical applications. In this study, a flexible composite electrolyte membrane (FCPE) with fast ion transport channels was prepared using a phase conversion process combined with in situ polymerization. The polyvinylidene fluoride-hexafluoro propylene (PVDF-HFP) polymer matrix incorporated with lithium lanthanum zirconate (LLZTO) formed a 3D net-like structure, and the in situ polymerized polyvinyl ethylene carbonate (PVEC) enhanced the interface connection. This 3D network, with multiple rapid pathways for Li+ that effectively control Li+ flux, led to uniform lithium deposition. Moreover, the symmetrical lithium cells that used FCPE exhibited high stability after 1200 h of cycling at 0.1 mA cm−2. Specifically, all-solid-state lithium batteries coupled with LiFePO4 cathodes can stably cycle for over 100 cycles at room temperature with high Coulombic efficiencies. Furthermore, after 100 cycles, the infrared spectrum shows that the structure of FCPE remains stable. This work demonstrates a novel insight for designing a flexible composite electrolyte for highly safe SSBs. [ABSTRACT FROM AUTHOR]

Hard carbon, which features recyclability, low costs, and environmental friendliness, is an attractive anode material for K+ storage. Nevertheless, the state-of-the-art hard carbon is still unsatisfactory due to its poor multiplication performance and unclear energy storage mechanism. In this study, a one-pot carbonisation method using coconut solid waste biomass is applied to obtain high-performance hard-carbon (CHC) anode materials. The microstructure and electrochemical properties of the CHC are investigated at different carbonisation temperatures (1100–1500 °C). The CHC materials prepared at 1300 °C (CHC1300) have a high capacity of 265.8 mAh g−1 at a current density of 25 mA g−1 and a superior cyclability of 1000 cycles at 1.0 A g−1 with a capacity retention of 96.6%. This approach, referred to as the "biomass-to-application" strategy, holds promise for advancing the development of cost-effective and sustainable KIBs. [ABSTRACT FROM AUTHOR]

Herein, the effects of the precursor solution's acidity level on the crystal structure, morphology, nucleation, and growth of WO3·nH2O and WO3 nanostructures are reported. Structural investigations on WO3·nH2O using X-ray diffraction and Fourier–transform infrared spectroscopy confirm that the quantity of hydrate groups increases due to the interaction between H+ and water molecules with increasing HCl volume. Surface analysis results support our claim that the evolution of grain size, surface roughness, and growth direction on WO3·nH2O and WO3 nanostructures rely on the precursor solution's pH value. Consequently, the photocurrent density of a WO3 photoanode using a HCl-5 mL sample achieves the best results with 0.9 mA/cm2 at 1.23 V vs. a reversible hydrogen electrode (RHE). We suggest that the improved photocurrent density of the HCl-5 mL sample is due to the efficient light absorption from the densely grown WO3 nanoplates on a substrate and that its excellent charge transport kinetics originate from the large surface area, low charge transfer resistance, and fast ion diffusion through the photoanode/electrolyte interface. [ABSTRACT FROM AUTHOR]

Aqueous zinc-ion batteries (ZIBs) have significant potential for large energy storage systems because of their high energy density, cost-effectiveness and environmental friendliness. However, the limited voltage window, poor reaction kinetics and structural instability of cathode materials are current bottlenecks which contain the further development of ZIBs. In this work, we rationally design a Ni-doped V2O5@3D Ni core/shell composite on a carbon cloth electrode (Ni-V2O5@3D Ni@CC) by growing Ni-V2O5 on free-standing 3D Ni metal nanonets for high-voltage and high-capacity ZIBs. Impressively, embedded Ni doping increases the interlayer spacing of V2O5, extending the working voltage and improving the zinc-ion (Zn302+) reaction kinetics of the cathode materials; at the same time, the 3D structure, with its high specific surface area and superior electronic conductivity, aids in fast Zn302+ transport. Consequently, the as-designed Ni-V2O5@3D Ni@CC cathodes can operate within a wide voltage window from 0.3 to 1.8 V vs. Zn30/Zn302+ and deliver a high capacity of 270 mAh g−1 (~1050 mAh cm−3) at a high current density of 0.8 A g−1. In addition, reversible Zn2+ (de)incorporation reaction mechanisms in the Ni-V2O5@3D Ni@CC cathodes are investigated through multiple characterization methods (SEM, TEM, XRD, XPS, etc.). As a result, we achieved significant progress toward practical applications of ZIBs. [ABSTRACT FROM AUTHOR]

(1) Background: Radioprotective agents have garnered considerable interest due to their prospective applications in radiotherapy, public health medicine, and situations of large-scale accidental radiation exposure or impending radiological emergencies. Cystamine, an organic diamino–disulfide compound, is recognized for its radiation-protective and antioxidant properties. This study aims to utilize the aqueous ferrous sulfate (Fricke) dosimeter to measure the free-radical scavenging capabilities of cystamine during irradiation by fast carbon ions. This analysis spans an energy range from 6 to 500 MeV per nucleon, which correlates with "linear energy transfer" (LET) values ranging from approximately 248 keV/μm down to 9.3 keV/μm. (2) Methods: Monte Carlo track chemistry calculations were used to simulate the radiation-induced chemistry of aerated Fricke–cystamine solutions across a broad spectrum of cystamine concentrations, ranging from 10−6 to 1 M. (3) Results: In irradiated Fricke solutions containing cystamine, cystamine is observed to hinder the oxidation of Fe2+ ions, an effect triggered by oxidizing agents from the radiolysis of acidic water, resulting in reduced Fe3+ ion production. Our simulations, conducted both with and without accounting for the multiple ionization of water, confirm cystamine's ability to capture free radicals, highlighting its strong antioxidant properties. Aligning with prior research, our simulations also indicate that the protective and antioxidant efficiency of cystamine diminishes with increasing LET of the radiation. This result can be attributed to the changes in the geometry of the track structures when transitioning from lower to higher LETs. (4) Conclusions: If we can apply these fundamental research findings to biological systems at a physiological pH, the use of cystamine alongside carbon-ion hadrontherapy could present a promising approach to further improve the therapeutic ratio in cancer treatments. [ABSTRACT FROM AUTHOR]

In this work, using photoluminescence (PL), optical absorption (OA), Raman spectroscopy (RS), and atomic force microscopy (AFM), the radiation damage of BaFBr crystals irradiated with 147 MeV 84Kr ions to fluences (1010–1014) cm2 was investigated. The manifestations of the oxygen impurity contained in the studied crystals on the effects associated with ion irradiation are also considered. In unirradiated crystals, the PL spectra exhibited bands related to the oxygen impurity. Moreover, it was found that quenching and a shift of the PL maximum occur, which is due to the fact that, with increasing dose, aggregation of defects occurs. Electronic and hole aggregate color centers appear mainly in the bromide sublattice. A detailed study of the Raman spectra and comparison with the corresponding data for KBr single crystals made it possible to reveal the corresponding manifestations of the Raman modes of complex Br 3 − -type hole centers. [ABSTRACT FROM AUTHOR]

Due to their reliability, affordability and high safety, rechargeable aqueous zinc ion batteries (ZIBs) have garnered a lot of attention. Nevertheless, undesirable long-term cycle performance and the inadequate energy density of cathode materials impede the development of ZIBs. Herein, we report a layered CaV4O9-MXene (Ti3C2Tx) composite assembled using CaV4O9 nanosheets on Ti3C2Tx and investigate its electrochemical performance as a new cathode for ZIBs, where CaV4O9 nanosheets attached on the surface of MXene and interlamination create a layered 2D structure, efficiently improving the electrical conductivity of CaV4O9 and avoiding the stacking of MXene nanosheets. The structure also enables fast ion and electron transport. Further discussion is conducted on the effects of adding MXene in various amounts on the morphology and electrochemical properties. The composite shows an improved reversible capacity of 274.3 mA h g−1 at 0.1 A g−1, superior rate capabilities at 7 A g−1, and a high specific capacity of 107.6 mA h g−1 can be delivered after 2000 cycles at a current density of 1 A g−1. The improvement of the electrochemical performance is due to its unique layered structure, high electrical conductivity, and pseudo capacitance behavior. [ABSTRACT FROM AUTHOR]

Owing to the unique virtues of specific energy/power densities, lithium-ion capacitors (LICs) have been increasingly attracting research attention. However, the LICs are greatly restrained by the slow Li+-reaction kinetics of battery-type anodes, which is still a challenging task. In this work, we construct a superior LIC using ultrafine MnO/dual N-doped carbon (MnO/DNC) anode and activated N-doped porous carbon (ANC) derived from a homologous polypyrrole precursor. The uniform MnO ultrafine particles (~10 nm size) are well encapsulated into a dual-carbon framework, which provides fast ion/electron transportation and structural cushion for high-rate and long-durable energy storage. Accordingly, the anodic MnO/DNC achieves an impressive rate performance (179 mAh g−1 @10 A g−1) and a stable 500-cycling lifespan. The as-constructed LICs could deliver a large specific energy of 172 Wh kg−1 at 200 W kg−1 and retain at 37 Wh kg−1 even at a high specific power of 15 kW kg−1. It is believed that the design strategy of confining ultrafine conversion-type anode materials into a dual-carbon structure will expedite the development of advanced LICs. [ABSTRACT FROM AUTHOR]

Carbon materials, such as graphite and activated carbon, have been widely used as electrodes in batteries and electric double-layer capacitors (EDLCs). Graphene, which has an extremely thin sheet-like structure, is considered as a fundamental carbon material. However, it was less investigated as an electrode material than graphite and activated carbons. This is because graphene is a relatively new material and is difficult to handle. However, using graphene electrodes can enhance the performance of nanodevices. Here, the performance of EDLCs based on single-layer and bilayer graphene electrodes in LiCl, NaCl, and KCl aqueous electrolyte solutions was evaluated using cyclic voltammetry, and the charging mechanism was evaluated using molecular dynamics simulations. KCl aqueous solution provided the highest capacitance compared to LiCl and NaCl aqueous solutions in the case of single-layer graphene electrodes. In contrast, the dependence of the capacitance on the ion species was hardly observed in the case of bilayer graphene. This indicates that Li and Na ions also contributed to the capacitances. The high EDLC performance can be attributed to the fast ion transfer promoted by the dehydration and modification of the second hydration shell on the bilayer graphene because of the relatively strong interaction of ions with the bilayer graphene. [ABSTRACT FROM AUTHOR]

Lithium-ion batteries are gaining more attention due to the rapid growth of electrical vehicles (EVs). Additionally, the industry is putting a lot of effort into reusing EV batteries in energy storage systems (ESS). The optimal performance of the repurposed battery system is highly dependent on the individual batteries used in it. These batteries need to be similar in terms of battery capacity, state of health (SOH), and remaining useful life (RUL). Therefore, battery grading techniques are expected to play a vital role in this newly emerging industry. There are various methods suggested to evaluate the aging of a battery in terms of capacity, SOH, and RUL. The use of ohmic resistance is one approach, as it varies with the aging of the battery. In order to measure the ohmic resistance, electrochemical impedance spectroscopy (EIS) is used, followed by the curve fitting procedures. In this research a novel method is suggested to measure the ohmic resistance without performing the broadband conventional EIS test and the curve fitting. Since the battery is perturbed for a specified frequency band (1 kHz to 100 Hz) using the linearly distributed phased multi-sine signal, only 1 sec perturbation is required, and the ohmic resistance can be directly calculated by using two impedance values. Thus, the measurement speed is several times faster than that of the conventional EIS methods. Hence, it is a suitable and convenient technique for the mass testing of the batteries. The accuracy and validity of the proposed technique are verified by testing three types of batteries. The percentage difference in the measured ohmic resistance value between the conventional and the proposed technique is less than 0.15% for all the batteries tested. [ABSTRACT FROM AUTHOR]

Mathematical modelling of heating and current drive as well as yields and distributions of fusion products in a magnetically confined plasma subject to neutral beam injection requires, in turn, modelling of distributions of fast ions, which is a complex task including calculations of the source of suprathermal particles, i.e., the number of fast ions occurring in unit volume during unit time owing to the injection of fast atoms. The knowledge of the magnetohydrodynamic equilibrium, beam injection geometry and spatial distribution of the magnetic field are the necessary prerequisites. Explicit general analytical formulae for the source of fast ions have been obtained by two different methods. In addition, a method of statistical modelling is presented. Calculations of spatial and angular distributions of the fast ion source for a tokamak and verifications of the obtained results have been performed by a number of methods. [ABSTRACT FROM AUTHOR]

Featured Application: Numerical modelling of yields and distributions of nuclear fusion products in magnetically confined plasma. Velocity distributions of fuel nuclei enter the formulae for distributions of products of fusion reactions in plasma. The formulae contain multiple integration, which is a computationally heavy task. Therefore, simplifications of the integrand are advantageous. One of possible simplifications is the use of closed-form analytical distributions of fast deuterons and tritons, accounting for slowing down and pitch-angle scattering and neglecting the speed diffusion. The plausibility of such a model has been studied from the viewpoint of its influence on the calculated spectra of fusion neutrons. Calculations have shown that the speed diffusion effect on suprathermal ion distribution tails does not significantly alter the qualitative behaviour of energy and angle distributions of fusion products in a beam-heated plasma. [ABSTRACT FROM AUTHOR]

Semiconductor-based composites are potential anodes for Li-ion batteries, owing to their high theoretical capacity and low cost. However, low stability induced by large volumetric change in cycling restricts the applications of such composites. Here, a hierarchical SnO2@Ni6MnO8 composite comprising Ni6MnO8 nanoflakes growing on the surface of a three-dimensional (3D) SnO2 is developed by a hydrothermal synthesis method, achieving good electrochemical performance as a Li-ion battery anode. The composite provides spaces to buffer volume expansion, its hierarchical profile benefits the fast transport of Li+ ions and electrons, and the Ni6MnO8 coating on SnO2 improves conductivity. Compared to SnO2, the Ni6MnO8 coating significantly enhances the discharge capacity and stability. The SnO2@Ni6MnO8 anode displays 1030 mAh g−1 at 0.1 A g−1 and exhibits 800 mAh g−1 under 0.5 A g−1, along with high Coulombic efficiency of 95%. Furthermore, stable rate performance can be achieved, indicating promising applications. [ABSTRACT FROM AUTHOR]

The search for hydrogen storage materials is a challenging task. In this work, we tried to test metallic glass-based pseudocapacitive material for electrochemical hydrogen storage potential. An alloy ingot with an atomic composition of Ni60Pd20P16B4 was prepared via arc melting of extremely pure elements in an Ar environment. A ribbon sample with a width of 2 mm and a thickness of 20 mm was produced via melt spinning of the prepared ingot. Electrochemical dealloying of the ribbon sample was conducted in 1 M H2SO4 to prepare a nanoporous glassy alloy. The Brunauer–Emmett–Teller (BET) and Langmuir methods were implemented to obtain the total surface area of the nanoporous glassy alloy ribbon. The obtained values were 6.486 m2/g and 15.082 m2/g, respectively. The Dubinin–Astakhov (DA) method was used to calculate pore radius and pore volume; those values were 1.07 nm and 0.09 cm3/g, respectively. Cyclic voltammetry of the dealloyed samples revealed the pseudocapacitive nature of this alloy. Impedance of the dealloying sample was measured at different frequencies through use of electrochemical impedance spectroscopy (EIS). A Cole–Cole plot established a semicircle with a radius of ~6 Ω at higher frequency, indicating low interfacial charge-transfer resistance, and an almost vertical Warburg slope at lower frequency, indicating fast diffusion of ions to the electrode surface. Charge–discharge experiments were performed at different constant currents (75, 100, 125, 150, and 200 mA/g) under a cutoff potential of 2.25 V vs. Ag/AgCl electrode in a 1 M KOH solution. The calculated maximum storage capacity was 950 mAh/g. High-rate dischargeability (HRD) and capacity retention ( S n ) for the dealloyed glassy alloy ribbon sample were evaluated. The calculated capacity retention rate at the 40th cycle was 97%, which reveals high stability. [ABSTRACT FROM AUTHOR]

Neutral beam injection is supposed to be the main source of high-energy particles, driving non-inductive current and generating primary neutrons in fusion neutron sources design based on tokamaks. Numerical simulation of high-energy particles' thermalization in plasma and fusion neutron emission is calculated by novel dedicated software (NESTOR code). The neutral beam is reproduced statistically by up to 109 injected particles. The beam efficiency and contribution to primary neutron generation is shown to be dependent on the injection energy, input current, and plasma temperature profile. A beam-driven plasma operation scenario, specific for FNS design, enables the fusion rate and neutron generation in plasma volume to be controlled by the beam parameters; the resultant primary neutron yield can be efficiently boosted in plasma maintained at a relatively low temperature when compared to 'pure' fusion reactors. NESTOR results are applicable to high-precision nuclear and power balance estimations, neutron power loads distribution among tokamak components, tritium generation in hybrid reactors, and for many other tasks critical for FNS design. [ABSTRACT FROM AUTHOR]

In most present-day tokamaks, the majority of the heating power comes from sources such as neutral-beam injection (NBI) and other types of auxiliary heating which allow for the transfer of energy to the plasma by a small population of externally introduced fast particles. The behavior of the fast ions is important for the overall plasma dynamics, and understanding their influence is vital for the success of any future magnetic confinement devices. In the TUMAN-3M tokamak, it has been noted that the loss of fast particles during NBI can lead to dramatic changes in the rotation velocity profiles, as they are responsible for the negative radial electric field on the periphery. [ABSTRACT FROM AUTHOR]

Controlled ion release and mineralization of bioactive glasses are essential to their applications in bone regeneration. Tuning the chemical composition and surface structure of glasses are the primary means of achieving this goal. However, most bioactive glasses exhibit a non-linear ion release behavior. Therefore, modifying the immersion environment of glasses through external stimuli becomes an approach. In this study, the ion release and mineralization properties of a borosilicate bioactive glass were investigated in the Tris buffer and K2HPO4 solutions with different pH. The glass had a faster ion release rate at a lower pH, but the overly acidic environment was detrimental to hydroxyapatite production. Using a direct current (DC) electric field as an external stimulus, the pH of the immersion solution could be modulated within a narrow range, thereby modulating ion release from the glass. As a result, significant increases in ion release were observed after three days, and the development of porous mineralization products on the glass surface after six days. This study demonstrates the effectiveness of the DC electric field in modulating the ion release of the bioactive glass in vitro and provides a potential way to regulate the degradation of the glass in vivo. [ABSTRACT FROM AUTHOR]

To maximize the performance of energy storage systems more effectively, modern batteries/supercapacitors not only require high energy density but also need to be fully recharged within a short time or capable of high-power discharge for electric vehicles and power applications. Thus, how to improve the rate capability of batteries or supercapacitors is a very important direction of research and engineering. Making low-tortuous structures is an efficient means to boost power density without replacing materials or sacrificing energy density. In recent years, numerous manufacturing methods have been developed to prepare low-tortuous configurations for fast ion transportation, leading to impressive high-rate electrochemical performance. This review paper summarizes several smart manufacturing processes for making well-aligned 3D microstructures for batteries and supercapacitors. These techniques can also be adopted in other advanced fields that require sophisticated structural control to achieve superior properties. [ABSTRACT FROM AUTHOR]

In advancing battery technologies, primary attention is paid to developing and optimizing low-cost electrode materials capable of fast reversible ion insertion and extraction with good cycling ability. Sodium-ion batteries stand out due to their inexpensive price and comparable operating principle to lithium-ion batteries. To achieve this target, various graphene-based nanocomposites fabricate strategies have been proposed to help realize the nanostructured electrode for high electrochemical performance sodium-ion batteries. In this review, the graphene-based nanocomposites were introduced according to the following main categories: graphene surface modification and doping, three-dimensional structured graphene, graphene coated on the surface of active materials, and the intercalation layer stacked graphene. Through one or more of the above strategies, graphene is compounded with active substances to prepare the nanocomposite electrode, which is applied as the anode or cathode to sodium-ion batteries. The recent research progress of graphene-based nanocomposites for SIBs is also summarized in this study based on the above categories, especially for nanocomposite fabricate methods, the structural characteristics of electrodes as well as the influence of graphene on the performance of the SIBs. In addition, the relevant mechanism is also within the scope of this discussion, such as synergistic effect of graphene with active substances, the insertion/deintercalation process of sodium ions in different kinds of nanocomposites, and electrochemical reaction mechanism in the energy storage. At the end of this study, a series of strategies are summarized to address the challenges of graphene-based nanocomposites and several critical research prospects of SIBs that provide insights for future investigations. [ABSTRACT FROM AUTHOR]

Novel two-dimensional materials (2DMs) with balanced electrical conductivity and lithium (Li) storage capacity are desirable for next-generation rechargeable batteries as they may serve as high-performance anodes, improving output battery characteristics. Gaining an advanced understanding of the electrochemical behavior of lithium at the electrode surface and the changes in interior structure of 2DM-based electrodes caused by lithiation is a key component in the long-term process of the implementation of new electrodes into to a realistic device. Here, we showcase the advantages of bilayer-patched epitaxial graphene on 4H-SiC (0001) as a possible anode material in lithium-ion batteries. The presence of bilayer graphene patches is beneficial for the overall lithiation process because it results in enhanced quantum capacitance of the electrode and provides extra intercalation paths. By performing cyclic voltammetry and chronoamperometry measurements, we shed light on the redox behavior of lithium at the bilayer-patched epitaxial graphene electrode and find that the early-stage growth of lithium is governed by the instantaneous nucleation mechanism. The results also demonstrate the fast lithium-ion transport (~4.7–5.6 × 10−7 cm2∙s−1) to the bilayer-patched epitaxial graphene electrode. Raman measurements complemented by in-depth statistical analysis and density functional theory calculations enable us to comprehend the lithiation effect on the properties of bilayer-patched epitaxial graphene and ascribe the lithium intercalation-induced Raman G peak splitting to the disparity between graphene layers. The current results are helpful for further advancement of the design of graphene-based electrodes with targeted performance. [ABSTRACT FROM AUTHOR]

This study compared the apatite-forming ability (AFA) levels of flowable and putty formulations of Nishika Canal Sealer BG Multi (F-NBG and P-NBG, respectively) and attempted to clarify the cause of differences in the AFA levels of F-NBG and P-NBG. NBG samples were aged in simulated body fluid (SBF) or 1-, 5-, or 10-g/L bovine serum albumin-containing SBF (BSA-SBF) and analyzed in terms of their ultrastructures, elemental compositions, and Raman spectra to identify apatite formation. The phosphate ion consumption rates of NBG samples in the media were evaluated as an indicator of apatite growth. The original elemental composition, calcium ion release, and alkalizing ability levels of F-NBG and P-NBG were also evaluated. Apparent apatite formation was detected on all NBG samples except F-NBG aged in 10-g/L BSA-SBF. P-NBG consumed phosphate ions faster than F-NBG. As-prepared P-NBG showed more silicon elements on its surface than as-prepared F-NBG. P-NBG released more calcium ions than F-NBG, although their alkalizing ability levels did not differ statistically. In conclusion, the AFA of P-NBG was greater than that of F-NBG, probably because of the greater ability of P-NBG to expose silanol groups on the surface and release calcium ions. [ABSTRACT FROM AUTHOR]

Lithium ion cells that can be quickly charged are of critical importance for the continued and accelerated penetration of electric vehicles (EV) into the consumer market. Considering this, the U.S. Department of Energy (DOE) has set a cell recharge time goal of 10-15 min. The following study provides an investigation into the effect of cell design, specifically negative to positive matching ratio (1.2:1 vs. 1.7:1) on fast charging performance. By using specific charging procedures based on negative electrode performance, as opposed to the industrial standard constant current constant voltage procedures, we show that the cells with a higher N:P ratio can be charged to ~16% higher capacity in the ten-minute time frame. Cells with a higher N:P ratio also show similar cycle life performance to those with a conventional N:P ratio, despite the fact that these cells experience a much higher irreversible capacity loss, leading to a lower reversible specific capacity. [ABSTRACT FROM AUTHOR]

Three-dimensional vertically aligned graphene (3DVAG) was prepared by a unidirectional freezing method, and its electrochemical performances were evaluated as electrode materials for zinc−ion hybrid supercapacitors (ZHSCs). The prepared 3DVAG has a vertically ordered channel structure with a diameter of about 20−30 μm and a length stretching about hundreds of microns. Compared with the random structure of reduced graphene oxide (3DrGO), the vertical structure of 3DVAG in a three−electrode system showed higher specific capacitance, faster ion diffusion, and better rate performance. The specific capacitance of 3DVAG reached 66.6 F·g−1 and the rate performance reached 92.2%. The constructed 3DVAG zinc−ion hybrid supercapacitor also showed excellent electrochemical performance. It showed good capacitance retention up to 94.6% after 3000 cycles at the current density of 2 A·g−1. [ABSTRACT FROM AUTHOR]

Copper-coated nanofibrous materials are desirable for catalysis, electrochemistry, sensing, and biomedical use. The preparation of copper or copper-coated nanofibers can be pretty challenging, requiring many chemical steps that we eliminated in our robust approach, where for the first time, Cu was deposited by magnetron sputtering onto temperature-sensitive polymer nanofibers. For the first time, the large-scale modeling of PCL films irradiation by molecular dynamics simulation was performed and allowed to predict the ions penetration depth and tune the deposition conditions. The Cu-coated polycaprolactone (PCL) nanofibers were thoroughly characterized and tested as antibacterial agents for various Gram-positive and Gram-negative bacteria. Fast release of Cu2+ ions (concentration up to 3.4 µg/mL) led to significant suppression of E. coli and S. aureus colonies but was insufficient against S. typhimurium and Ps. aeruginosa. The effect of Cu layer oxidation upon contact with liquid media was investigated by X-ray photoelectron spectroscopy revealing that, after two hours, 55% of Cu atoms are in form of CuO or Cu(OH)2. The Cu-coated nanofibers will be great candidates for wound dressings thanks to an interesting synergistic effect: on the one hand, the rapid release of copper ions kills bacteria, while on the other hand, it stimulates the regeneration with the activation of immune cells. Indeed, copper ions are necessary for the bacteriostatic action of cells of the immune system. The reactive CO2/C2H4 plasma polymers deposited onto PCL-Cu nanofibers can be applied to grafting of viable proteins, peptides, or drugs, and it further explores the versatility of developed nanofibers for biomedical applications use. [ABSTRACT FROM AUTHOR]

Spinel-structured solids were studied to understand if fast Li+ ion conduction can be achieved with Li occupying multiple crystallographic sites of the structure to form a "Li-stuffed" spinel, and if the concept is applicable to prepare a high mixed electronic-ionic conductive, electrochemically active solid solution of the Li+ stuffed spinel with spinel-structured Li-ion battery electrodes. This could enable a single-phase fully solid electrode eliminating multi-phase interface incompatibility and impedance commonly observed in multi-phase solid electrolyte–cathode composites. Materials of composition Li1.25M(III)0.25TiO4, M(III) = Cr or Al were prepared through solid-state methods. The room-temperature bulk Li+-ion conductivity is 1.63 × 10−4 S cm−1 for the composition Li1.25Cr0.25Ti1.5O4. Addition of Li3BO3 (LBO) increases ionic and electronic conductivity reaching a bulk Li+ ion conductivity averaging 6.8 × 10−4 S cm−1, a total Li-ion conductivity averaging 4.2 × 10−4 S cm−1, and electronic conductivity averaging 3.8 × 10−4 S cm−1 for the composition Li1.25Cr0.25Ti1.5O4 with 1 wt. % LBO. An electrochemically active solid solution of Li1.25Cr0.25Mn1.5O4 and LiNi0.5Mn1.5O4 was prepared. This work proves that Li-stuffed spinels can achieve fast Li-ion conduction and that the concept is potentially useful to enable a single-phase fully solid electrode without interphase impedance. [ABSTRACT FROM AUTHOR]

Hybrid scaffolds based on bioactive glass (BAG) particles (<38 µm), covalently linked to gelatin (G*) using 3-glycidoxypropyltrimethoxysilane (GPTMS), have been studied for bone bioengineering. In this study, two glass compositions (13-93 and 13-93B20 (where 20% of the SiO2 was replaced with B2O3)) were introduced in the gelatin matrix. The Cfactor (gelatin/GPTMS molar ratio) was kept constant at 500. The hybrids obtained were found to be stable at 37 °C in solution, the condition in which pure gelatin is liquid. All hybrids were characterized by in vitro dissolution in Tris(hydroxymethyl)aminomethane (TRIS) solution (for up to 4 weeks) and Simulated Body Fluid (SBF) (for up to 2 weeks). Samples processed with 13-93B20 exhibited faster initial dissolution and significantly faster precipitation of a hydroxyapatite (HA) layer. The faster ion release and HA precipitation recorded from the G*/13-93B20 samples are attributable to the higher reactivity of borosilicate compared to silicate glass. The MC3T3-E1 cell behavior in direct contact with the hybrids was investigated, showing that the cells were able to proliferate and spread on the developed biomaterials. Tailoring the glass composition allows us to better control the material's dissolution, biodegradability, and bioactivity. Bioactive (especially with 13-93B20 BAG) and biocompatible, the hybrids are promising for bone application. [ABSTRACT FROM AUTHOR]

The influence of the charge state q on surface modifications induced by the impact of individual fast, heavy ions on muscovite mica was investigated. Beams of 593 MeV 197 Au q + with well-defined initial charge states over a relatively broad range of values (30 to 51) and at different irradiation geometries were used. At normal incidence, the impact features are rounded protrusions (hillocks) with ≳20 nm in diameter. At grazing angles, besides the hillocks, craters and elongated tails (up to 350 nm-long) extending along the direction of ion penetration are produced. It is shown that the impact features at normal incidence depend strongly on the initial charge state of the projectiles. This dependence is very weak at grazing angles as the ion reaches the equilibrium charge state closer to the surface. At normal ion incidence, the hillock volume scales with q 3.3   ±   0.6 . This dependence stems largely from the increase in the hillock height, as a weak dependence of the diameter was observed. [ABSTRACT FROM AUTHOR]

Fuel cells using biomaterials have the potential for environmentally friendly clean energy and have attracted a lot of interest. Moreover, biomaterials are expected to develop into in vivo electrical devices such as pacemakers with no side effects. Ion channels, which are membrane proteins, are known to have a fast ion transport capacity. Therefore, by using ion channels, the realization of fuel cell electrolytes with high-proton conductivity can be expected. In this study, we have fabricated a fuel cell using an ion channel electrolyte for the first time and investigated the electrical properties of the ion channel electrolyte. It was found that the fuel cell using the ion channel membrane shows a power density of 0.78 W/cm2 in the humidified condition. On the other hand, the power density of the fuel cell blocking the ion channel with the channel blocker drastically decreased. These results indicate that the fuel cell using the ion channel electrolyte operates through the existence of the ion channel and that the ion channel membrane can be used as the electrolyte of the fuel cell in humidified conditions. Furthermore, the proton conductivity of the ion channel electrolyte drastically increases above 85% relative humidity (RH) and becomes 2 × 10−2 S/m at 96% RH. This result indicates that the ion channel becomes active above 96%RH. In addition, it was deduced from the impedance analysis that the high proton conductivity of the ion channel electrolyte above 96% RH is caused by the activation of ion channels, which are closely related to the fractionalization of water molecule clusters. From these results, it was found that a fuel cell using the squid axon becomes a new fuel cell using the function of the ion channel above 96% RH. [ABSTRACT FROM AUTHOR]

Due to their cost effectiveness, high safety, and eco-friendliness, zinc-ion batteries (ZIBs) are receiving much attention nowadays. In the production of rechargeable ZIBs, the cathode plays an important role. Manganese oxide (MnO2) is considered the most promising and widely investigated intercalation cathode material. Nonetheless, MnO2 cathodes are subjected to challenging issues viz. limited capacity, low rate capability and poor cycling stability. It is seen that the MnO2 heterostructure can enable long-term cycling stability in different types of energy devices. Herein, a versatile chemical method for the preparation of MnO2 heterostructure on multi-walled carbon nanotubes (MNH-CNT) is reported. Besides, the synthesized MNH-CNT is composed of δ-MnO2 and γ-MnO2. A ZIB using the MNH-CNT cathode delivers a high initial discharge capacity of 236 mAh g−1 at 400 mA g−1, 108 mAh g−1 at 1600 mA g−1 and excellent cycling stability. A pseudocapacitive behavior investigation demonstrates fast zinc ion diffusion via a diffusion-controlled process with low capacitive contribution. Overall, the MNH-CNT cathode is seen to exhibit superior electrochemical performance. This work presents new opportunities for improving the discharge capacity and cycling stability of aqueous ZIBs. [ABSTRACT FROM AUTHOR]

Polymerized ionic liquids (PILs) show potential to be used as new water-free polyelectrolyte-based electrorheological (ER) material. To direct ER material design at the molecular level, unveiling structure-property relationships is essential. While a few studies compare the mobile ions in PILs there is still a limited understanding of how the structure of tethered counterions on backbone influences ER property. In this study, three PILs with same mobile anions but different tethered countercations (e.g., poly(dimethyldiallylammonium) P[DADMA]+, poly(benzylethyl) trimethylammonium P[VBTMA]+, and poly(1-ethyl-4-vinylimidazolium hexafluorophosphate) P[C2VIm]+) are prepared and the influence of tethered countercations on the ER property of PILs is investigated. It shows that among these PILs, P[DADMA]+ PILs have the strongest ER property and P[C2VIm]+ PILs have the weakest one. By combining dielectric spectra analysis with DFT calculation and activation energy measurement, it can clarify that the influence of tethered counterions on ER property is mainly associated with ion-pair interaction energy that is affecting ionic conductivity and interfacial polarization induced by ion motion. P[DADMA]+ has the smallest ion-pair interaction energy with mobile ions, which can result in the highest ionic conductivity and the fastest interfacial polarization rate for its strongest ER property. [ABSTRACT FROM AUTHOR]

Radiolysis of biomolecules by fast ions has interest in medical applications and astrobiology. The radiolysis of solid D-valine (0.2–2 μm thick) was performed at room temperature by 1.5 MeV H+, He+, N+, and 230 MeV S15+ ion beams. The samples were prepared by spraying/dropping valine-water-ethanol solution on ZnSe substrate. Radiolysis was monitored by infrared spectroscopy (FTIR) through the evolution of the intensity of the valine infrared 2900, 1329, 1271, 948, and 716 cm−1 bands as a function of projectile fluence. At the end of sample irradiation, residues (tholins) presenting a brownish color are observed. The dependence of the apparent (sputtering + radiolysis) destruction cross section, σd, on the beam stopping power in valine is found to follow the power law σd = aSen, with n close to 1. Thus, σd is approximately proportional to the absorbed dose. Destruction rates due to the main galactic cosmic ray species are calculated, yielding a million year half-life for solid valine in space. Data obtained in this work aim a better understanding on the radioresistance of complex organic molecules and formation of radioproducts. [ABSTRACT FROM AUTHOR]

Motional Stark effect (MSE) spectroscopy represents a unique diagnostic tool capable of determining the magnitude of the magnetic field and its direction in the core of fusion plasmas. The primary excitation channel for fast hydrogen atoms in injected neutral beams, with energy in the range of 25–1000 keV, is due to collisions with protons and impurity ions (e.g., He 2 + and heavier impurities). As a result of such excitation, at the particle density of 10 13 –10 14 cm − 3 , the line intensities of the Stark multiplets do not follow statistical expectations (i.e., the populations of fine-structure levels within the same principal quantum number n are not proportional to their statistical weights). Hence, any realistic modeling of MSE spectra has to include the relevant collisional atomic data. In this paper we provide a general expression for the excitation cross sections in parabolic states within n = 3 for an arbitrary orientation between the direction of the motion-induced electric field and the proton-atom collisional axis. The calculations make use of the density matrix obtained with the atomic orbital close coupling method and the method can be applied to other collisional systems (e.g., He 2 + , Be 4 + , C 6 + , etc.). The resulting cross sections are given as simple fits that can be directly applied to spectral modeling. For illustration we note that the asymmetry detected in the first classical cathode ray experiments between the red- and blue-shifted spectral components can be quantitatively studied using the proposed approach. [ABSTRACT FROM AUTHOR]

A new member of sodium metal diphosphate-diarsenate, Na2CuP1.5As0.5O7, was synthesized as polycrystalline powder by a solid-state route. X-ray diffraction followed by Rietveld refinement show that the studied material, isostructural with β-Na2CuP2O7, crystallizes in the monoclinic system of the C2/c space group with the unit cell parameters a = 14.798(2) Å; b = 5.729(3) Å; c = 8.075(2) Å; β = 115.00(3)°. The structure of the studied material is formed by Cu2P4O15 groups connected via oxygen atoms that results in infinite chains, wavy saw-toothed along the [001] direction, with Na+ ions located in the inter-chain space. Thermal study using DSC analysis shows that the studied material is stable up to the melting point at 688 °C. The electrical investigation, using impedance spectroscopy in the 260–380 °C temperature range, shows that the Na2CuP1.5As0.5O7 compound is a fast-ion conductor with σ350 °C = 2.28 10−5 Scm−1 and Ea = 0.6 eV. Na+ ions pathways simulation using bond-valence site energy (BVSE) supports the fast three-dimensional mobility of the sodium cations in the inter-chain space. [ABSTRACT FROM AUTHOR]

The iron titanium oxide ilmenite (FeTiO3) is a technologically and economically important mineral in the industrial preparation of titanium-based pigments and spintronic devices. In this study, atomistic simulation techniques based on classical pair potentials are used to examine the energetics of the intrinsic and extrinsic defects and diffusion of Fe2+ ions in FeTiO3. It is calculated that the cation anti-site (Fe‒Ti) cluster is the most dominant defect, suggesting that a small amount of cations exchange their positions, forming a disordered structure. The formation of Fe Frenkel is highly endoergic and calculated to be the second most stable defect process. The Fe2+ ions migrate in the ab plane with the activation energy of 0.52 eV, inferring fast ion diffusion. Mn2+ and Ge4+ ions are found to be the prominent isovalent dopants at the Fe and Ti site, respectively. The formation of additional Fe2+ ions and O vacancies was considered by substituting trivalent dopants (Al3+, Mn3+, Ga3+, Sc3+, In3+, Yb3+, Y3+, Ga3+, and La3+) at the Ti site. Though Ga3+ is found to be the candidate dopant, its solution enthalpy is >3 eV, suggesting that the formation is not significant at operating temperatures. [ABSTRACT FROM AUTHOR]

About 71% of the Earth's surface is covered with water. Human beings, animals, and plants need water in order to survive. Therefore, it is one of the most important substances that exist on Earth. However, most of the water resources nowadays are insufficiently clean, since they are contaminated with toxic metal ions due to the improper disposal of pollutants into water through industrial and agricultural activities. These toxic metal ions need to be detected as fast as possible so that the situation will not become more critical and cause more harm in the future. Since then, numerous sensing methods have been proposed, including chemical and optical sensors that aim to detect these toxic metal ions. All of the researchers compete with each other to build sensors with the lowest limit of detection and high sensitivity and selectivity. Graphene quantum dots (GQDs) have emerged as a highly potential sensing material to incorporate with the developed sensors due to the advantages of GQDs. Several recent studies showed that GQDs, functionalized GQDs, and their composites were able to enhance the optical detection of metal ions. The aim of this paper is to review the existing, latest, and updated studies on optical sensing applications of GQDs-based materials toward toxic metal ions and future developments of an excellent GQDs-based SPR sensor as an alternative toxic metal ion sensor. [ABSTRACT FROM AUTHOR]

The objective of this work is to investigate the magnetite-accelerated corrosion phenomenon of SA508 used as tubesheet material in simulated secondary side environments of pressurized water reactors through immersion and electrochemical tests. The presence of sulfate ions induced the fast growth of a corrosion product layer on SA508, and this phenomenon was accelerated when the SA508 was coupled to magnetite. From the perspective of electrochemical behavior, it was found that SA508 behaves as an anodic member in the coupling system with magnetite, resulting in an increased corrosion rate. [ABSTRACT FROM AUTHOR]

Redox-active polymer networks based on stable nitroxide radicals are a very promising class of materials to be used in the so-called organic radical batteries. In order to obtain fast-charging and high power electrodes, however, excellent ionic conductivity inside the electrode material is required to allow easy diffusion of ions and fast redox reactions. In this contribution, we investigated redox-active poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methacrylate) chains cross-linked through ionic liquid-like 1,2,3-triazolium groups. Different networks were prepared in which the amount of cross-linker and the counter-anion associated to the 1,2,3-triazolium group were varied. The ionic conductivities of the different polymer networks were first measured in the solid state by electrochemical impedance spectroscopy at different temperatures, and an increased ionic conductivity was measured when 1,2,3-triazolium groups were present in the network. The effects of the chemical nature of the counterions associated to the 1,2,3-triazolium groups and of the crosslinking density were then studied. The best ionic conductivities were obtained when bis (trifluoromethane)sulfonamide (TFSI) counter-anions were used, and when the crosslinking density of the TFSI-containing gel was higher. Finally, those ion-conducting gels were loaded with free LiTFSI and the transference number of lithium ions was accordingly measured. The good ionic conductivities and lithium ions transference numbers measured for the investigated redox-active gels make them ideal candidates for application as electrode materials for either organic radical batteries or pseudo-capacitors energy storage devices. [ABSTRACT FROM AUTHOR]

The concept and structure of the Simulation of Spectra (SOS) code is described starting with an introduction to the physics background of the project and the development of a simulation tool enabling the modeling of charge-exchange recombination spectroscopy (CXRS) and associated passive background spectra observed in hot fusion plasmas. The generic structure of the code implies its general applicability to any fusion device, the development is indeed based on over two decades of spectroscopic observations and validation of derived plasma data. Four main types of active spectra are addressed in SOS. The first type represents thermal low-Z impurity ions and the associated spectral background. The second type of spectra represent slowing-down high energy ions created from either thermo-nuclear fusion reactions or ions from injected high energy neutral beams. Two other modules are dedicated to CXRS spectra representing bulk plasma ions (H+, D+, or T+) and beam emission spectroscopy (BES) or Motional Stark Effect (MSE) spectrum appearing in the same spectral range. The main part of the paper describes the physics background for the underlying emission processes: active and passive CXRS emission, continuum radiation, edge line emission, halo and plume effect, or finally the charge exchange (CX) cross-section effects on line shapes. The description is summarized by modeling the fast ions emissions, e.g., either of the α particles of the fusion reaction or of the beam ions itself. [ABSTRACT FROM AUTHOR]

Nickel–manganese–cobalt oxides, with LiNi0.33Mn0.33Co0.33O2 (NMC) as the most prominent compound, are state-of-the-art cathode materials for lithium-ion batteries in electric vehicles. The growing market for electro mobility has led to a growing global demand for Li, Co, Ni, and Mn, making spent lithium-ion batteries a valuable secondary resource. Going forward, energy- and resource-inefficient pyrometallurgical and hydrometallurgical recycling strategies must be avoided. We presented an approach to recover NMC particles from spent lithium-ion battery cathodes while preserving their chemical and morphological properties, with a minimal use of chemicals. The key task was the separation of the cathode coating layer consisting of NMC, an organic binder, and carbon black, from the Al substrate foil. This can be performed in water under strong agitation to support the slow detachment process. However, the contact of the NMC cathode with water leads to a release of Li+ ions and a fast increase in the pH. Unwanted side reactions may occur as the Al substrate foil starts to dissolve and Al(OH)3 precipitates on the NMC. These side reactions are avoided using pH-adjusted solutions with sufficiently high buffer capacities to separate the coating layer from the Al substrate, without precipitations and without degradation of the NMC particles. [ABSTRACT FROM AUTHOR]