High-Performance Li-Ion and Na-Ion Capacitors Based on a Spinel Li4Ti5O12 Anode and Carbonaceous Cathodes.

Lithium-ion hybrid capacitors (LICs) have become promising electrochemical energy storage systems that overcome the limitations of lithium-ion batteries and electrical double-layer capacitors. The asymmetric combination of these devices enhances the overall electrochemical performance by delivering simultaneous energy and power capabilities. Lithium titanate (Li4Ti5O12, LTO), a spinel zero-strain material, has been studied extensively as an anode material for LIC applications because of its high-rate capability, negligible volume change, and enhanced cycling performance. Here, the different synthetic methods and modifications of the intercalation-type LTO to enhance the overall electrochemical performance of LICs are mainly focused. Moreover, the cathodic part (i.e., the activated carbon derived from various sources, including natural products, polymers, and inorganic materials) is also dealt with as it contributes substantially to the overall performance of the LIC. Not only do the anode and cathode, but also the electrolytes have a substantial influence on LIC performance. The electrolytes used in LTO-based LICs as well as in flexible and bendable configurations are also mentioned. Overall, the previous work along with other available reports on LTO-based LICs in a simplified way is analyzed.

Mechanically Exfoliated Graphite for Highly Reversible Na-Storage with Carbon Coated Na3V2(PO4)3 Cathode with Low-Temperature Conditions.

Tremendous efforts are put forward to develop novel high-performance electrodes for Na-ion batteries (SIBs) in order to replace commercial Li-ion batteries (LIBs). Graphite, the most versatile anode for LIBs, fails to accommodate Na+ions owing to the poor thermodynamic stability of the binary graphite intercalation compound. This study aims to exfoliate the layers of graphite through a simple mechanical process at different time intervals (1, 5, 10, 20, 40, and 80 h) and examine the potential candidate for Na-storage in the presence of carbonate-based electrolytes. This study reports that ball milling plays a vital role in the performance of the graphite in Na-storage. The graphite exfoliated for 80 h (EG-80h) rendered an excellent reversible capacity of 209 mAh g-1 with coulombic efficiency of >99% after 100 cycles in EC-based electrolyte. In situ impedance analysis is performed to validate the charge storage mechanism and Na-ion kinetics. The performance of EG-80h in a full-cell assembly is evaluated with a carbon-coated Na3V2(PO4)3 cathode, which exhibited an initial capacity of ≈75 mAh g-1 and energy density of 201 Wh kg-1. In addition, the adaptability of the NVPC/EG-80h cell at different temperatures is examined from -10 to 50 °C, displaying excellent performance in both high and low-temperature conditions.

Controlled Synthesis of SnO2 Nanostructures as Alloy Anode via Restricted Potential Toward Building High-Performance Dual-Ion Batteries with Graphite Cathode.

Dual-ion batteries (DIBs) are considered one of the promising energy storage devices in which graphite serves as a bi-functional electrode, i.e., anode and cathode in the aprotic organic solvents. Unlike conventional lithium-ion batteries (LIBs), DIBs reversibly store the cations and anions in the anode and cathodes during redox reactions, respectively. The electrolyte is a source for both cations and anions, so the choice of electrolyte plays a vital role. In the present work, the synthesis of SnO2 nanostructures is reported as a possible alternative for graphite anode, and the Li-storage performance is optimized in half-cell (Li/SnO2 ) assembly with varying amounts of conductive additive (acetylene black) and limited working potential (1 V vs Li). Finally, a DIB using recovered graphite (RG) fabricated from spent LIB as a cathode and SnO2 nanostructures as an anode under balanced loading conditions. Prior to the fabrication, both electrodes are pre-cycled to eliminate irreversibility. An in-situ impedance study has been employed to validate the passivation layer formation during the charge-discharge process. The high-performance SnO2 /RG-based DIB delivered a maximum discharge capacity of 380 mAh g-1 . The electrochemical performance of DIB has been assessed by varying temperature conditions to evaluate their suitability in different climatic conditions.

Microwave-assisted green synthesis of fluorescent carbon quantum dots from Mexican Mint extract for Fe3+ detection and bio-imaging applications.

Biomass-derived carbon quantum dots have drawn special interest owing to their admirable photostability, biocompatibility, fluorescence, high solubility, sensitivity and environmentally friendly properties. In the present work, the Carbon Quantum Dots (CQDs) was synthesized from the Plectranthus amboinicus (Mexican Mint) leaves via the microwave-assisted reflux method. The strong absorption peaks observed from UV-vis spectra at 291 and 330 nm corresponds to the π-π* and n-π* transitions, respectively, reveal the formation of CQDs. The synthesized CQDs showed bright blue fluorescence under UV irradiation with a fluorescence quantum yield of 17% and a maximum emission of 436 nm in the blue region at an excitation wavelength of 340 nm. The HRTEM analysis elucidates that the synthesized CQDs were crystalline and spherical in shape with a particle size of 2.43 ± 0.02 nm. The FT-IR spectroscopy confirms the presence of the different functional groups such as -OH, -CH, CO and C-O. The chemical composition of CQD was revealed through XPS analysis. The synthesized CQDs were used as a fluorescent probe to detect different metal ions, where high selectivity was obtained for Fe3+ ions through quenching phenomenon. The emission intensity of CQD showed a good linear relationship with R2 = 0.9111 with the concentration of Fe3+ ions in the range of 0-15 µM. The fluorescence emission of CQD was turned OFF upon the binding of Fe3+ ions and turned - ON with the addition of ascorbic acid. With this fluorescent turn ON-OFF behaviour of CQD, the NOT and IMPLICATION logic gates were constructed and studied for different input conditions. The biocompatibility of CQD was tested via MTT assay using MCF7 breast cancer cell line, which revealed that CQD synthesized from the Mexican Mint leaves possess less cytotoxicity. Further, the prepared CQD was applied effectively as fluorescent probes in a cell imaging application.

A sustainable green synthesis of functionalized biocompatible carbon quantum dots from Aloe barbadensis Miller and its multifunctional applications.

Herein, we demonstrated a sustainable green approach for the preparation of fluorescent biocompatible carbon quantum dots by microwave-assisted reflux synthesis from Aloe barbadensis Miller (Aloe vera) extract. The Transmission Electron Microscopic images reveal that the as-prepared CQDs are spherical with less than 5 nm in size. The CQDs are amorphous, showed an excitation-independent behaviour, emitted blue fluorescence and have a fluorescence quantum yield of 31%. The presence of -OH groups contributed to the blue emission and helped CQDs to disperse uniformly in an aqueous solution. The prepared CQDs were employed as a photocatalyst for the environmental remediation to degrade the anionic dye, eosin yellow under visible light irradiation. The results showed that the CQDs exhibited excellent photocatalytic efficiency of 98.55% within 80 min and a 100% efficiency within 100 min. Further, the cytotoxic properties of as-prepared CQDs are investigated in the MCF-7 breast cancer cell line using MTT assay. The results demonstrated a notable reduction in cell viability in a dose-subjected manner, and the cell viability decreased to 50% (IC50) at a concentration of 52.2 ± 1.35 µg/mL. Furthermore, cellular internalization of CQDs in breast cancer cells is studied. As expected, CQDs are found to internalize by the cancer cells with blue emission as revealed by fluorescence microscope. In the end, CQDs in human breast cancer cells demonstrate the anti-proliferative effect and are found to be an impressive fluorescent probe for live-cell imaging, paving a path for its potential biomedical applications.

Highly Perforated V2 O5 Cathode with Restricted Lithiation toward Building "Rocking-Chair" Type Cell with Graphite Anode Recovered from Spent Li-Ion Batteries.

Current research motivation on fabricating next-generation lithium-ion batteries by averting the growing demand for battery raw materials brings enormous interest on the V2 O5 cathode again as a result of its abundance, ease synthesis, and tunable Li-intercalation properties. So far, the research activities are mainly focused on V2 O5 to attain a maximum capacity (>300 mAh g-1 ) for more than 1 mol. Li-intercalation which results in poor structural stability. Keeping this issue in mind, here, the full-cell assembly by limiting 1 mol is proposed and constructed. Li-insertion in V2 O5 as a cathode and LiC6 as an anode for the first time. Prior to the full-cell assembly, hydrothermally prepared rod-like V2 O5 reveals the specific capacity of 143 mAh g-1 in half-cell configuration with good cycling stability. The full-cell, V2 O5 /LiC6, offers a specific capacity of ≈236 mAh g-1 with a maximum energy density of ≈197.1 Wh kg-1 . Furthermore, the practical feasibility of the cell has been examined at different temperatures that divulged a maximum energy density of 136 Wh kg-1 at 50 °C. Also, the obtained results encourage V2 O5 as a strong contender for the commercial LiFePO4 /C system andpave the new directions for advanced battery technology.

Nanoengineered Organic Electrodes for Highly Durable and Ultrafast Cycling of Organic Sodium-Ion Batteries.

Sodium-ion batteries (SIBs) have become increasingly important as next-generation energy storage systems for application in large-scale energy storage. It is very crucial to develop an eco-friendly and green SIB technique with superior performance for sustainable future use. Replacing the conventional inorganic electrode materials with green and safe organic electrodes will be a promising approach. However, the poor electrochemical kinetics, unstable electrode-electrolyte interface, high solubility of the electrodes in the electrolyte, and large amount of conductive carbon present great challenges for organic SIBs. In this study, the issues of organic electrodes are addressed through atomic-level manipulation of these organic molecules using a series of ultrathin (Å-level) metal oxide coatings (Al2 O3 , ZnO, and TiO2 ). Uniform and precise coatings on the perylene-3,4,9,10-tetracarboxylicacid dianhydride by gas-phase atomic layer deposition technique shows a stable interphase, enhanced electrochemical kinetics (71C, 10 A g-1 ), and excellent stability (89%-500 cycles) compared to conventional organic electrode (70%-200 cycles). Further studies reveal that the chemical stability of the metal oxide coating layer plays a critical role in influencing the redox behavior, and improving kinetics of organic electrodes. This study opens a new avenue for developing high-energy organic SIBs with performance equivalent to inorganic counterparts.

Robust Construction Safety System (RCSS) for Collision Accidents Prevention on Construction Sites.

A proximity warning system to detect the presence of a worker/workers and to warn heavy equipment operators is highly needed to prevent collision accidents at construction sites. In this paper, we developed a robust construction safety system (RCSS), which can activate warning devices and automatically halt heavy equipment, simultaneously, to prevent possible collision accidents. The proximity detection of this proposed system mainly relies on ultra-wideband (UWB) sensing technologies, which enable instantaneous and simultaneous alarms on (a) a worker's personal safety (personal protection unit (PPU)) device and (b) hazard area device (zone alert unit (ZAU)). This system also communicates with electronic control sensors (ECSs) installed on the heavy equipment to stop its maneuvering. Moreover, the RCSS has been interfaced with a global positioning system communication unit (GCU) to acquire real-time information of construction site resources and warning events. This enables effective management of construction site resources using an online user interface. The performance and effectiveness of the RCSS have been validated at laboratory scale as well as at real field (construction site and steel factory). Conclusively, the RCSS can significantly enhance construction site safety by pro-actively preventing collision of a worker/workers with heavy equipment.

Hybrid Blockchain and Internet-of-Things Network for Underground Structure Health Monitoring.

The Internet-of-things (IoT) and blockchain are growing realities of modern society, and both are rapidly transforming civilization, either separately or in combination. However, the leverage of both technologies for structural health monitoring (SHM) to enable transparent information sharing among involved parties and autonomous decision making has not yet been achieved. Therefore, this study combines IoT with blockchain-based smart contracts for SHM of underground structures to define a novel, efficient, scalable, and secure distributed network for enhancing operational safety. In this blockchain-IoT network, the characteristics of locally centralized and globally decentralized distribution have been activated by dividing them into core and edge networks. This division enhances the efficiency and scalability of the system. The proposed system was effective in simulation for autonomous monitoring and control of structures. After proper design, the decentralized blockchain networks may effectively be deployed for transparent and efficient information sharing, smart contracts-based autonomous decision making, and data security in SHM.

Development of a Cloud Computing-Based Pier Type Port Structure Stability Evaluation Platform Using Fiber Bragg Grating Sensors.

Structure Health Monitoring is a topic of great interest in port structures due to the ageing of structures and the limitations of evaluating structures. This paper presents a cloud computing-based stability evaluation platform for a pier type port structure using Fiber Bragg Grating (FBG) sensors in a system consisting of a FBG strain sensor, FBG displacement gauge, FBG angle meter, gateway, and cloud computing-based web server. The sensors were installed on core components of the structure and measurements were taken to evaluate the structures. The measurement values were transmitted to the web server via the gateway to analyze and visualize them. All data were analyzed and visualized in the web server to evaluate the structure based on the safety evaluation index (SEI). The stability evaluation platform for pier type port structures involves the efficient monitoring of the structures which can be carried out easily anytime and anywhere by converging new technologies such as cloud computing and FBG sensors. In addition, the platform has been successfully implemented at “Maryang Harbor” situated in Maryang-Meyon of Korea to test its durability.

Graphene supercapacitor with both high power and energy density.

Supercapacitors, based on fast ion transportation, are specialized to provide high power, long stability, and efficient energy storage using highly porous electrode materials. However, their low energy density excludes them from many potential applications that require both high energy density and high power density performances. Using a scalable nanoporous graphene synthesis method involving an annealing process in hydrogen, here we show supercapacitors with highly porous graphene electrodes capable of achieving not only a high power density of 41 kW kg-1 and a Coulombic efficiency of 97.5%, but also a high energy density of 148.75 Wh kg-1. A high specific gravimetric and volumetric capacitance (306.03 F g-1 and 64.27 F cm-3) are demonstrated. The devices can retain almost 100% capacitance after 7000 charging/discharging cycles at a current density of 8 A g-1. The superior performance of supercapacitors is attributed to their ideal pore size, pore uniformity, and good ion accessibility of the synthesized graphene.

All-in-All: Dead Lithium-Ion Battery to Active Lithium-Ion Capacitor.

Here, we have developed lithium-ion capacitors (LICs) with all the components, except the electrolyte solution, effectively recycled from the spent Lithium-ion batteries (LIBs). Hybrid capacitors, such as LICs, are potential breakthroughs in electrochemical energy storage devices, where most research is focused. These devices can simultaneously guarantee high energy and power by hybridizing battery-type and capacitive-type electrodes with two different reaction mechanisms. We have successfully upcycled the graphite, current collector, separator, etc., from the spent LIBs to fabricate a high-performance LIC. Our LIC consists of recovered graphite (RG) coated over recovered copper foil as an anode, recycled polypropylene as the separator, and reduced graphene oxide (rGO) synthesized from RG as the cathode. The RG half-cell exhibited an excellent specific capacity of 302 mAh g-1 even after 75 charge-discharge cycles with a coulombic efficiency of >99 %. The Li/rGO displayed remarkable cycling performance for over 1000 cycles with high stability and reversibility. Subsequently, the pre-lithiated RG (p-RG) electrode is paired with the rGO electrode under the balanced loading conditions to construct LIC, rGO/p-RG, delivering a maximum energy density of 185 Wh kg-1 with ultra-long durability of more than 10,000 cycles. The possibility of LIC under different climatic conditions is also explored, and its remarkable performance under various temperature conditions is worth mentioning.

Synthesis and Characterization of the New Li1+xAl1+xSi1-xO4 (x = 0-0.25) Solid Electrolyte for Lithium-Ion Batteries.

A systematic study was performed to investigate the effect of the sintering temperature, sintering duration, and aluminum doping on the crystalline structure and ionic conductivity of the Li1+xAl1+xSi1-xO4 (LASO; x = 0-0.25) solid electrolyte. There was a strong indication that an increase in the sintering temperature and sintering time increased the ionic conductivity of the electrolyte. In particular, the doping concentration and composition ratio (Li1+xAl1+xSi1-xO4; x = 0-0.25) were found to be crucial factors for achieving high ionic conductivity. The sintering time of 18 h and lithium concentration influenced the lattice parameters of the LASO electrolyte, resulting in a significant improvement in ionic conductivity from 2.11 × 10-6 (for pristine LASO) to 1.07 × 10-5 S cm-1. An increase in the lithium concentration affected the stoichiometry, and it facilitated a smoother Li-ion transfer process since lithium served as an ion-conducting bridge between LASO grains.

Investigating neuromodulatory effect of transauricular vagus nerve stimulation on resting-state electroencephalography.

Purpose: The purpose of this study was to investigate the neuromodulatory effects of transauricular vagus nerve stimulation (taVNS) and determine optimal taVNS duration to induce the meaningful neuromodulatroty effects using resting-state electroencephalography (EEG). Method: Fifteen participants participated in this study and taVNS was applied to the cymba conchae for a duration of 40 min. Resting-state EEG was measured before and during taVNS application. EEG power spectral density (PSD) and brain network indices (clustering coefficient and path length) were calculated across five frequency bands (delta, theta, alpha, beta and gamma), respectively, to assess the neuromodulatory effect of taVNS. Moreover, we divided the whole brain region into the five regions of interest (frontal, central, left temporal, right temporal, and occipital) to confirm the neuromodulation effect on each specific brain region. Result: Our results demonstrated a significant increase in EEG frequency powers across all five frequency bands during taVNS. Furthermore, significant changes in network indices were observed in the theta and gamma bands compared to the pre-taVNS measurements. These effects were particularly pronounced after approximately 10 min of stimulation, with a more dominant impact observed after approximately 20-30 min of taVNS application. Conclusion: The findings of this study indicate that taVNS can effectively modulate the brain activity, thereby exerting significant effects on brain characteristics. Moreover, taVNS duration of approximately 20-30 min was considered appropriate for inducing a stable and efficient neuromodulatory effects. Consequently, these findings have the potential to contribute to research aimed at enhancing cognitive and motor functions through the modulation of EEG using taVNS. Supplementary Information: The online version contains supplementary material available at 10.1007/s13534-024-00361-8.

The Relationship between Depression Severity and Prefrontal Hemodynamic Changes in Adolescents with Major Depression Disorder: A Functional Near-infrared Spectroscopy Study.

Objective: : Numerous studies have identified hemodynamic changes in adults with major depressive disorder (MDD) by using functional near-infrared spectroscopy (fNIRS). However, studies on adolescents with MDD are limited. As adolescence is a stage of rapid brain development, differences may occur depending on age. This study used fNIRS as an objective tool to investigate hemodynamic changes in the frontal lobe according to depression severity and age in adolescents with MDD. Methods: : Thirty adolescents (12 aged 12-15 years and 18 aged 16-18 years) were retrospectively investigated. The Children's Depression Inventory was used as a psychiatric evaluation scale, fNIRS was used as an objective brain function evaluation tool, and the Verbal Fluency Test was performed. Results: : During the Verbal Fluency Test, in the younger MDD group, oxygenated-hemoglobin concentration increased in the right dorsolateral prefrontal cortex region as the severity of depression increased. In the older MDD group, the oxygenated-hemoglobin concentration decreased in the right dorsolateral prefrontal cortex region as the severity of depression increased. Conclusion: : These results suggest that fNIRS may be an objective tool for identifying age differences among adolescents with MDD. To generalize the results and verify fNIRS as a potential biomarker tool, follow-up studies with a larger sample group should be conducted.

Highly promoted solvent-co-intercalation process in pencil graphite anode and Na3V2(PO4)3 cathode in full-cell Na-ion battery.

The electrochemical performance of graphite recovered from 6H-pencil with the highest content of SiO2 is evaluated in both Na-ion half and full-cell assemblies. The concept of sodium co-intercalation into graphite is exploited by fabricating cells with electrolytes based on tetraethylene glycol dimethyl ether (G4) and diethylene glycol dimethyl ether (G2). The capacity at high current rates is maximum when the G2-based electrolyte is used, both in half and full cells, while the capacity retention after high current rates is better in a G4-based system. Upon calculating the capacity contribution, the G2-based system shows prominent capacitance-based charge storage, whereas the G4-based system has a higher contribution from the Faradaic mechanism. The former also shows a faster diffusion mechanism. While G2 based system has higher capacity retention in half-cell, G4 based system has higher capacity retention in full-cell. When G2 is used as the electrolyte solvent, the irreversibility during cycling is high, affecting cell performance. The full cells with G4 and G2 electrolytes show maximum energy/power densities of 33 Wh kg-1/2.7 kW kg-1 and 23 Wh kg-1/1.4 kW kg-1, respectively. Our study shows that the charge storage mechanism can be varied by tuning the electrolyte solvent. This study is the first to explore pencil graphite for sodium-ion storage.

Interphase stabilized electrospun SnO2 fibers as alloy anode via restricted cycling for Li-ion capacitors with high energy and wide temperature operation.

The second-generation supercapacitor comprises the hybridized energy storage mechanism of Lithium-ion batteries and electrical double-layer capacitors, i.e, Lithium-ion capacitors (LICs). The electrospun SnO2 nanofibers are synthesized by a simple electrospinning technique and are directly used as anode material for LICs with activated carbon (AC) as a cathode. However, before the assembly, the battery-type electrode SnO2 is electrochemically pre-lithiated (LixSn + Li2O), and AC loading is balanced with respect to its half-cell performance. First, the SnO2 is tested in the half-cell assembly with a limited potential window of 0.005 to 1 V vs. Li to avoid the conversion reaction of Sn0 to SnOx. Also, the limited potential window allows only the reversible alloy/de-alloying process. Finally, the assembled LIC, AC/(LixSn + Li2O), displayed a maximum energy density of 185.88 Wh kg-1 with ultra-long cyclic durability of over 20,000 cycles. Further, the LIC is also exposed to various temperature conditions (-10, 0, 25, & 50 °C) to study the feasibility of using them in different environmental conditions.

Effect of Sodium Phosphate Coating on Cu and Mg-Substituted P2-Na0.67Ni0.33Mn0.67O2 for Improving the Cycling Performance of Sodium-Ion Capacitors.

Sodium-ion capacitors (SICs) bridge the performance gaps between batteries and supercapacitors by providing a high energy and power density in a single configuration. As battery-type active materials, sodium preintercalated layered metal oxides are desirable owing to their unique crystal structure, simple synthesis process, and high working voltage. However, their poor cyclic stability and low kinetics limit their application. Herein, we report increased rate capability and cycle stability achieved by introducing transition metal substitution and surface coating strategies. By substituting a portion of Ni and Mn with Cu and Mg (the sample name was denoted as NMCM), the P2-O2 transition which occurs at high voltages was alleviated. Additionally, a thin and uniform sodium phosphate coating layer suppressed surface side reactions occurring during charge-discharge processes, as observed through ex-situ X-ray photoelectron spectroscopy and ex-situ transmission electron microscopy. Compared to the pristine sample, the capacity improved by 48% at a high current density of 4 A g-1. After 100 cycles, the sodium-phosphate-coated sample (NMCM@P) retained about 90% of its capacity, whereas NMCM had a capacity retention of 63%. When evaluating the longer stability of SIC full cells, NMCM@P exhibited an outstanding stability of 71% after 5000 cycles. This was higher than that of NMCM, which retained only 17% of its initial capacity.

Neuromodulatory feasibility of a current limiter-based tDCS device: a resting-state electroencephalography study.

Recently, we introduced a current limiter-based novel transcranial direct-current stimulation (tDCS) device that does not generate significant tDCS-induced electrical artifacts, thereby facilitating simultaneous electroencephalography (EEG) measurement during tDCS application. In this study, we investigated the neuromodulatory effect of the tDCS device using resting-state EEG data measured during tDCS application in terms of EEG power spectral densities (PSD) and brain network indices (clustering coefficient and path length). Resting-state EEG data were recorded from 10 healthy subjects during both eyes-open (EO) and eyes-closed (EC) states for each of five different conditions (baseline, sham, post-sham, tDCS, and post-tDCS). In the tDCS condition, tDCS was applied for 12 min with a current intensity of 1.5 mA, whereas tDCS was applied only for the first 30 s in the sham condition. EEG PSD and brain network indices were computed for the alpha frequency band most closely associated with resting-state EEG. Both alpha PSD and network indices were found to significantly increase during and after tDCS application compared to those of the baseline condition in the EO state, but not in the EC state owing to the ceiling effect. Our results demonstrate the neuromodulatory effect of the tDCS device that does not generate significant tDCS-induced electrical artifacts, thereby allowing simultaneous measurement of electrical brain activity. We expect our novel tDCS device to be practically useful in exploring the impact of tDCS on neuromodulation more precisely using ongoing EEG data simultaneously measured during tDCS application.

Fabrication of Na-Ion Full-Cells using Carbon-Coated Na3 V2 (PO4 )2 O2 F Cathode with Conversion Type CuO Nanoparticles from Spent Li-Ion Batteries.

Spent lithium-ion batteries (LIBs) offer immense potential in the form of resources such as Li, transition metals (Co, Ni, and Mn), graphite, and Cu, which can be recovered through suitable recycling procedures. The Cu-current collector is recovered from spent LIBs and converted as a copper oxide (CuO) anode for Na-ion batteries. The performance of CuO is evaluated with carboxymethyl cellulose (CMC) (CuO-C), and polyvinylidene fluoride (PVdF) (CuO-P) binders in CuO half-cell and CuO/carbon-coated Na3 V2 (PO4 )2 O2 F (CuO/NVPOF) full-cell assemblies. The CuO-C half-cell displays superior electrochemical performance than CuO-P in terms of cycling and rate performance showing 88% more capacity. To study the stabilization and solid electrolyte interphase growth in CuO-C, an in situ impedance study is conducted. However, the full-cell, CuO-P/NVPOF displays better capacity retention during cycling with Coulombic efficiency >95% from the second cycle, whereas CuO-C/NVPOF could hardly maintain only >90%. For conversion type CuO, it is apparent that, though the CMC binder supports half-cell performance, the PVdF binder is suitable for the practical cell/full-cell configuration.