Ion-selective asymmetric carbon electrodes for enhanced capacitive deionization

With the development of capacitive deionization technology, charge efficiency and electrosorption capacity have become some of the biggest technical bottlenecks. Asymmetric activated carbon electrodes with ion-selective functional groups inspired by membrane capacitive deionization were developed to conquer these issues. The deionization capacity increased from 11.0 mg g⁻¹ to 23.2 mg g⁻¹, and the charge efficiency increased from 0.54 to 0.84, due to ion-selective functional groups minimizing the co-ion effect. The charge efficiency and electrosorption capacity resulting from better wettability of these electrodes are effectively enhanced by grafting ion-selective functional groups, which are propitious to ion movement. In addition, asymmetric deionization capacitors show better cycling stability and higher desalination rates. These experimental results have demonstrated that the modification of the ion-selective (oxygen-containing) functional groups on the surfaces of activated carbon could greatly minimize the co-ion effects and increase the salt removal from the solution. These results have indicated that the ion-selective asymmetric carbon electrodes can promote well the development of deionization capacitors for practical desalination.

Ion-selective asymmetric carbon electrodes are developed for capacitive deionization to minimize the co-ion effects.     

Three-dimensional honeycomb-like porous carbon derived from corncob for the removal of heavy metals from water by capacitive deionization

In this study, porous carbon (3DHPC) with a 3D honeycomb-like structure was synthesized from waste biomass corncob via hydrothermal carbonization coupled with KOH activation and investigated as a capacitive deionization (CDI) electrode material. The obtained 3DHPC possesses a hierarchal macroporous and mesoporous structure, and a large accessible specific surface area (952 m² g⁻¹). Electrochemical tests showed that the 3DHPC electrode exhibited a specific capacitance of 452 F g⁻¹ and good electric conductivity. Moreover, the feasibility of electrosorptive removal of chromium(vi) from an aqueous solution using the 3DHPC electrode was demonstrated. When 1.0 V was applied to a solution containing 30 mg L⁻¹ chromium(vi), the 3DHPC electrode exhibited a higher removal efficiency of 91.58% compared with that in the open circuit condition. This enhanced adsorption results from the improved affinity between chromium(vi) and the electrode under electrochemical assistance involving a non-faradic process. Consequently, the 3DHPC electrode with typical double-layer capacitor behavior is demonstrated to be a favorable electrode material for capacitive deionization.

A porous carbon electrode with a 3D honeycomb-like structure demonstrates a high removal efficiency for the removal of chromium(vi) from water.     

Oxygen functional groups improve the energy storage performances of graphene electrochemical supercapacitors

Graphene is a promising electrode material for supercapacitors due to its superior physical and chemical properties, but the influence of its oxygen functional groups on capacitive performance still remains somewhat uncertain. In this work, graphene sheets with different oxygen content have been prepared through thermal reduction in argon. Furthermore, oxidation and pore-forming treatment of graphene annealed at 800 °C are also performed to explore the important effect of oxygen functional groups. The effects of disorder degree, surface area and oxygen functional groups on the specific capacitance were explored systematically. The content and species of oxygen functional groups are found to be significant factors influencing the electrochemical supercapacitor performance of graphene electrodes. The specific capacitances of graphene annealed at 200, 400 and 800 °C are 201, 153 and 34 F g⁻¹, respectively. However, the specific capacitance of graphene reduced at 800 °C can be increased to 137 F g⁻¹ after nitric acid oxidation treatment, and is only 39 F g⁻¹ after pore forming on graphene surface, demonstrating that the oxygen functional groups can improve the capacitive performances of graphene electrochemical supercapacitors.

The content and species of oxygen functional groups are significant factors influencing the electrochemical supercapacitor performance of graphene electrodes.     

“Water-in-salt” electrolyte enhanced high voltage aqueous supercapacitor with carbon electrodes derived from biomass waste-ground grain hulls

To design high specific surface area and optimize the pore size distribution of materials, we employ a combination of carbonization and KOH activation to prepare activated carbon derived from ground grain hulls. The resulting carbon material at lower temperature (800, BSAC-A-800) exhibits a porous structure with a high specific surface area of 1037.6 m² g⁻¹ and a pore volume of 0.57 m³ g⁻¹. Due to the synergistic structural characteristics, BSAC-A-800 reveals preferable capacitive performance, showing a specific capacitance as high as 313.3 F g⁻¹ at 0.5 A g⁻¹, good rate performance (above 73%), and particularly stable cycling performance (99.1% capacitance retention after 10 000 cycles at a current density of 10 A g⁻¹). More importantly, the assembled symmetric supercapacitor using a water-in-salt electrolyte (17 m NaClO₄) with high discharge specific capacitance (59 F g⁻¹ at 0.5 A g⁻¹), high energy density (47.2 W h kg⁻¹) and high voltage (2.4 V) represents significant progress towards performance comparable to that of commercial salt-in-water electrolyte supercapacitors (with discharge specific capacitance of 50 F g⁻¹, energy densities of ∼28.1 W h kg⁻¹ and voltages of 2.0 V).

To design high specific surface area and optimize the pore size distribution of materials, we employ a combination of carbonization and KOH activation to prepare activated carbon derived from ground grain hulls.     

Properties of amorphous iron phosphate in pseudocapacitive sodium ion removal for water desalination

Capacitive deionization (CDI) is an energy saving and environmentally friendly technology for water desalination. However, classical CDI is challenged by a low salt removal capacity. To improve the desalination capacity, electrode materials utilizing the battery mechanism for salt ion removal have emerged as a new direction more recently. In this work, we report a study of amorphous iron phosphate (FePO₄) as a promising electrode material for pseudocapacitive sodium ion removal. Sodium ions can be effectively, reversibly intercalated and de-intercalated upon its electrochemical reduction and oxidation, with an excellent sodium ion capacity under half-cell testing conditions. By assembling a hybrid CDI (HCDI) system utilizing the FePO₄ electrode for pseudocapacitive sodium ion removal and active carbon electrode for capacitive chloride ion removal, the cell exhibited a high salt removal capacity and good reversibility and durability, which was attributed to the advantageous features of amorphous FePO₄. The HCDI system achieved a high deionization capacity (82 mg g⁻¹) in 10 mM NaCl, a fast deionization rate (0.046 mg g⁻¹ s⁻¹), and good stability and cyclability.

Amorphous iron phosphate (FePO₄) exhibits excellent capacity, reversibility and stability in pseudocapacitive sodium ion removal for water desalination.     

Gamma-radiated biochar carbon for improved supercapacitor performance

Biochar carbon YP-50 exposed to gamma radiation at 50 kGy, 100 kGy, and 150 kGy was used as an electrode for an electric double-layer capacitor. The gamma radiation affected the pore structure and pore volume of the biochar electrodes. The optimized surface morphology, pore structure, and pore volume of the biochar with an irradiation dose of 100 kGy showed outstanding specific capacitance of 246.2 F g⁻¹ compared to the untreated biochar (115.3 F g⁻¹). The irradiation dose of 100 kGy exhibited higher specific power and specific energy of 0.1 kW kg⁻¹ and 34.2 W h kg⁻¹ respectively, with a capacity retention of above 96% after 10 000 cycles at a current density of 2 A g⁻¹. This improvement can be attributed to the decrease in average particle size, an increase in the porosity of biochar carbon. Besides, the charge transfer resistance of supercapacitor is significantly reduced from 21.7 Ω to 7.4 Ω after treating the biochar carbon with 100 kGy gamma radiation, which implies an increase in conductivity. This gamma radiation strategy to pretreat the carbon material for improving the properties of carbon materials can be promising for the development of high-performance supercapacitors for large-scale applications.

(a) Schematic of the biochar carbon YP-50 exposed to gamma radiation. (b) Cyclic Voltammetry of supercapacitor with untreated biochar and biochar treated with 50 kGy, 100 kGy, and 150 kGy gamma-radiation.     

Activated Luffa derived biowaste carbon for enhanced desalination performance in brackish water

Membrane capacitive deionization (MCDI) is an effective process to remove salt ions from brackish water. In this work, a systematic investigation was carried out to study the effects of applied potential and salt concentration on salt adsorption capacity (SAC), charge efficiency (Λ) and energy consumption in an MCDI system using Luffa biowaste derived carbon as electrodes. We studied the comparative MCDI performance of Luffa derived carbon as electrodes before and after activation. Furthermore, the desalination capacities of the electrodes were quantified by batch-mode experiments in a 2500 mg L⁻¹ NaCl solution at 0.8–1.2 V. Activated Luffa carbon showed a high SAC of 38 mg g⁻¹ at 1.2 V in a 2500 mg L⁻¹ NaCl solution with a low energy consumption of 132 kJ mol⁻¹ salt as compared to non-activated samples (22 mg g⁻¹, 143 kJ mol⁻¹). The adsorption mechanisms were investigated using kinetic models and isotherms under various applied potentials. Consequently, the excellent SAC of activated Luffa carbon can be attributed to the presence of micro/mesoporous network structure formed due to the activation process for the propagation of the salt ions.

Membrane capacitive deionization (MCDI) is an effective process to remove salt ions from brackish water.     

Solvothermal synthesis of NiWO4 nanostructure and its application as a cathode material for asymmetric supercapacitors

This study proposes a facile solvothermal synthesis of nickel tungstate (NiWO₄) nanowires for application as a novel cathode material for supercapacitors. The structure, morphology, surface area and pore distribution were characterized and their capacitive performances were investigated. The results showed that the NiWO₄ nanowires synthesized in ethylene glycol solvent could offer a high specific capacitance of 1190 F g⁻¹ at a current density of 0.5 A g⁻¹ and a capacitance retaining ratio of 61.5% within 0.5–10 A g⁻¹. When used as a cathodic electrode of an asymmetric supercapacitor (ASC), the NiWO₄ nanowire based device can be cycled reversibly in a high-voltage region of 0–1.7 V with a high specific capacitance of 160 F g⁻¹ at 0.5 A g⁻¹, which therefore contributed to an energy density of 64.2 W h kg⁻¹ at a power density of 425 W kg⁻¹. Moreover, 92.8% of its initial specific capacitance can be maintained after 5000 consecutive cycles (5 A g⁻¹). These excellent capacitive properties make NiWO₄ a credible electrode material for high-performance supercapacitors.

This study proposes a facile solvothermal synthesis of nickel tungstate (NiWO₄) nanowires for application as a novel cathode material for supercapacitors.     

Facile synthesis of bio-based nitrogen- and oxygen-doped porous carbon derived from cotton for supercapacitors

Biomass-derived O- and N-doped porous carbon has become the most competitive supercapacitor electrode material because of its renewability and sustainability. We herein presented a facile approach to prepare O/N-doped porous carbon with cotton as the starting material. Absorbent cotton immersed in diammonium hydrogen phosphate (DAP) was activated at 800 °C (CDAP800s) and then was oxidized in a temperature range of 300–400 °C. The electrochemical capacitance of the impregnated cotton was significantly improved by doping with O and N, and the yield was improved from 13% to 38%. The sample oxidation at 350 °C (CDAP800-350) demonstrated superior electrical properties. CDAP800-350 showed the highest BET surface area (1022 m² g⁻¹) and a relatively high pore volume (0.53 cm³ g⁻¹). In a three-electrode system, the CDAP800-350 electrodes had high specific capacitances of 292 F g⁻¹ in 6 M KOH electrolyte at a current density of 0.5 A g⁻¹. In the two-electrode system, CDAP800-350 electrode displayed a specific capacitance of 270 F g⁻¹ at 0.5 A g⁻¹ and 212 F g⁻¹ at 10 A in KOH electrolyte. In addition, the CDAP800-350-based symmetric supercapacitor achieved a high stability with 87% of capacitance retained after 5000 cycles at 5 A g⁻¹, as well as a high volumetric energy density (18 W h kg⁻¹ at 250 W kg⁻¹).

Biomass-derived O- and N-doped porous carbon has become one of the most competitive supercapacitor electrode material because of its renewability and sustainability.     

Chitosan-based activated carbon as economic and efficient sustainable material for capacitive deionization of low salinity water

Capacitive deionization (CDI) is a novel low-energy green desalination technology that has attracted much attention in recent years, especially for the desalination of low salinity water. One of the key issues in CDI is the electrode materials, and many efforts have been devoted to developing materials with high specific surface areas, appropriate pore distributions, and good electronic conductivity, in order to obtain a high salt adsorption capacity. In this study, chitosan was selected as a precursor for the preparation of high-performance chitosan-based activated carbon (CTS-AC) for use in CDI electrodes via pyrolysis and KOH activation. The results show that CTS-AC800 (activated at 800 °C) has the largest BET specific surface area (2727 m² g⁻¹), and exhibits an appropriate pore size distribution (<10 nm), nitrogen doping (2.0%) and good electronic conductivity (2.09 S cm⁻¹). The CDI performance results show that the CTS-AC800 electrode has a saturated salt adsorption capacity of 14.12 mg g⁻¹ in a 500 mg L⁻¹ NaCl solution and retains 95% capacity after 150 adsorption–desorption cycles. Thus, chitosan is a promising, sustainable precursor for CDI electrode materials.

Chitosan was selected as a carbonaceous precursor to prepare high-performance chitosan-based activated carbon (CTS-AC) for CDI electrode.     

Biochar derived from corn stalk and polyethylene co-pyrolysis: characterization and Pb(ii) removal potential

Biochar is widely used as adsorbents for gaseous or liquid pollutants due to its special pore structure. Previous studies have shown that the adsorption performance of untreated biomass pyrolysis crude carbon is poor, which can be improved by optimizing physicochemical properties such as pore structure and surface area. The study focused on the co-pyrolysis of skins, pith, and leaves with polyethylene and potassium hydroxide modification to adjust the quality of the biochar, compared with raw materials of corn stalks without separation. The physical and chemical properties of the biochar were analyzed and the adsorption effect, adsorption isotherms, and kinetics of Pb(ii) removal were investigated. Results demonstrated that co-pyrolysis of biomass and polyethylene increase the yield of biochar with an average increase of about 20%. Polyethylene brought high aromaticity, high calorific value and stable material structure to biochar. Potassium hydroxide modification increased its specific surface area and made the pore structure of biochar more uniform, mainly microporous structure. The specific surface areas of the four modified biochar were 521.07 m² g⁻¹, 581.85 m² g⁻¹, 304.99 m² g⁻¹, and 429.97 m² g⁻¹. The adsorption capacity of biochar for Pb(ii) was greatly improved with the increase of the OH functional group of biochar. The stem-pith biochar had the best adsorption effect, with an adsorption amount of 99.95 mg g⁻¹ and a removal efficiency of 50.35%. The Pseudo-second-order model and Langmuir adsorption isotherm model could preferably describe the adsorption process, indicating the adsorption of lead was monolayer accompanied by chemical adsorption. It can be concluded that co-pyrolysis of biomass and polyethylene and modification may be favorable to enhance the properties of biochar. In addition to syngas and bio-oil from co-pyrolysis, biochar may be a valuable by-product for commercial use, which can be used to remove heavy metals in water, especially stem-pith biochar.

Biochar is widely used as adsorbents for gaseous or liquid pollutants due to its special pore structure.     

Novel mesoporous Co3O4–Sb2O3–SnO2 active material in high-performance capacitive deionization

Capacitive deionization (CDI), as an emerging eco-friendly electrochemical brackish water deionization technology, has widely benefited from carbon/metal oxide composite electrodes. However, this technique still requires further development of the electrode materials to tackle the ion removal capacity/rate issues. In the present work, we introduce a novel active carbon (AC)/Co₃O₄–Sb₂O₃–SnO₂ active material for hybrid electrode capacitive deionization (HECDI) systems. The structure and morphology of the developed electrodes were determined using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and Brunauer–Emmett–Teller (BET)/Barrett–Joyner–Halenda (BJH) techniques, as well as Fourier-transform infrared (FT-IR) spectroscopy. The electrochemical properties were also investigated by cyclic voltammetry (CV) and impedance spectroscopy (EIS). The CDI active materials AC/Co₃O₄ and AC/Co₃O₄–Sb₂O₃–SnO₂ showed a high specific capacity of 96 and 124 F g⁻¹ at the scan rate of 10 mV s⁻¹, respectively. In addition, the newly-developed electrode AC/Co₃O₄–Sb₂O₃–SnO₂ showed high capacity retention of 97.2% after 2000 cycles at 100 mV s⁻¹. Moreover, the electrode displayed excellent CDI performance with an ion removal capacity of 52 mg g⁻¹ at the applied voltage of 1.6 V and in a solution of potable water with initial electrical conductivity of 950 μs cm⁻¹. The electrode displayed a high ion removal rate of 7.1 mg g⁻¹ min⁻¹ with an excellent desalination–regeneration capability while retaining about 99.5% of its ion removal capacity even after 100 CDI cycles.

Capacitive deionization (CDI), as an emerging eco-friendly electrochemical brackish water deionization technology, has widely benefited from carbon/metal oxide composite electrodes.     

Enhanced capacitive performance by improving the graphitized structure in carbon aerogel microspheres

Herein, good electrical conductivity and high specific surface area carbon aerogel (CA) microspheres were synthesized by a facile and economical route using a high temperature carbonization and CO₂ activation method. The electroconductive graphitized structure of the CA microspheres could be easily improved by increasing the carbonization temperature. Then the CA microspheres were activated with CO₂ to increase the specific surface area of the electrode material for electric double layer capacitors (EDLC). The sample carbonized at 1500 °C for 0.5 h and CO₂ activated at 950 °C for 8 h showed an acceptable specific surface area and excellent cycle performance and rate capability for EDLC: 98% of the initial value of the capacitance was retained after 10 000 cycles, a specific capacitance of 121 F g⁻¹ at 0.2 A g⁻¹ and 101 F g⁻¹ at 2 A g⁻¹.

Carbon aerogels (CAs) microspheres with good electrical conductivity and high specific surface area were synthesized by high temperature carbonization and CO₂ activation method, which exhibit an enhanced capacitive performance in supercapacitors.     

Structural and adsorption characteristics of potassium carbonate activated biochar

Potassium carbonate activated biochar (450 °C, 600 °C and 750 °C) and nonactivated biochar (600 °C) were prepared by using corn stalk as the raw material. These biochar samples were labeled as KBC450, KBC600, KBC750 and BC600. The physical and chemical properties of the biochar were strongly influenced by the activation of potassium carbonate. After activation with potassium carbonate, the aromatic, hydrophobic and non-polar properties of the biochar were enhanced to form an aromatized non-polar surface, and the aromatic properties were enhanced with the increase of the pyrolysis temperature. The outside surface of the activated biochar was similar to that of porous sponge with a mesoporous–microporous composite structure inside. The specific surface area of KBC600 was 5 times that of BC600, and KBC750 had a maximum surface area of 815 m² g⁻¹. Batch adsorption experiments showed that the adsorption capacity of KBC for naphthalene increased with the increase of pyrolysis temperature. The adsorption capacity of the biochar for naphthalene showed a significant positive correlation with O/C and (O + N)/C. KBC750 with the strongest surface hydrophobicity and the largest specific surface area had the largest adsorption capacity of 130.7 mg g⁻¹. Physical adsorption and π–π EDA were the main adsorption mechanisms.

The structure activation of K₂CO₃ enriches the surface pores of biochar and increases the specific surface area nearly 10 times. The changes of pore structure and surface properties significantly affect the adsorption process of naphthalene.     

Characterization of pruned tea branch biochar and the mechanisms underlying its adsorption for cadmium in aqueous solution

In the present study, discarded pruned tea branch was used to prepare a new biochar, and the physicochemical properties and adsorption characteristics were investigated by characterization and batch experiments. With increasing pyrolysis temperature from 400 to 800 °C, the yield, specific surface area, and acidic functional groups had significant differences. The optimum adsorption conditions were determined as pH = 6 and dosage of 2 g L⁻¹. The pseudo-second-order kinetic and Langmuir isothermal model could fit well to the adsorption data, which showed that the adsorption process was dominated by monolayer chemical adsorption. The highest adsorption property (74.04 mg g⁻¹) was obtained by the pyrolysis of tea branch biochar (TBB) at 700 °C owing to the adsorption mechanisms, including surface complexation, precipitation, metal ion exchange, and Cd²⁺–π interaction. After five cycles of desorption, biochar still showed superior adsorption (80%). Hence, the TBB acted as a regenerable adsorbent for treating Cd²⁺-containing wastewater.

In the present study, discarded pruned tea branch was used to prepare a new biochar, and the physicochemical properties and adsorption characteristics were investigated by characterization and batch experiments.     

N-Enriched carbon nanofibers for high energy density supercapacitors and Li-ion batteries

Nitrogen enriched carbon nanofibers have been obtained by one-step carbonization/activation of PAN-based nanofibers with various concentrations of melamine at 800 °C under a N₂ atmosphere. As synthesised carbon nanofibers were directly used as electrodes for symmetric supercapacitors. The obtained PAN-MEL fibers with 5% melamine stabilised at 280 °C and carbonized at 800 °C under a nitrogen atmosphere showed excellent electrochemical performance with a specific capacitance of up to 166 F g⁻¹ at a current density of 1A g⁻¹ using 6 M KOH electrolyte and a capacity retention of 109.7% after 3000 cycles. It shows a 48% increase as compared to pristine carbon nanofibers. Two electrode systems of the CNFM5 sample showed high energy densities of 23.72 to 12.50 W h kg⁻¹ at power densities from 400 to 30 000 W kg⁻¹. When used as an anode for Li-ion battery application the CNFM5 sample showed a high specific capacity up to 435.47 mA h g⁻¹ at 20 mA g⁻¹, good rate capacity and excellent cycling performance (365 mA h g⁻¹ specific capacity even after 200 cycles at 100 mA g⁻¹). The specific capacity obtained for these nitrogen enriched carbon nanofibers is higher than that for pristine carbon nano-fibers.

Nitrogen enriched carbon nanofibers have been obtained by one-step carbonization/activation of PAN-based nanofibers with various concentrations of melamine at 800 °C under a N₂ atmosphere.     

Lead (Pb2+) sorptive removal using chitosan-modified biochar: batch and fixed-bed studies

Chitosan-Modified fast pyrolysis BioChar (CMBC) was used to remove Pb²⁺ from water. CMBC was made by mixing pine wood biochar with a 2% aqueous acetic acid chitosan (85% deacylated chitin) solution followed by treatment with NaOH. The characterizations of both CMBC and Non-Modified BioChar (NMBC) were done using diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), scanning electron microscopy (SEM), surface area measurements (S_BET), elemental analysis, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and ζ-potential measurements. Elemental analysis indicated that chitosan accounts for about 25% weight of the CMBC. The Langmuir maximum adsorption capacity of CMBC at pH 5 was 134 mg g⁻¹versus 48.2 mg g⁻¹ for NMBC at 318 K. CMBC column adsorption studies resulted in a capacity of 5.8 mg g⁻¹ (Pb²⁺ conc. 150 mg L⁻¹; pH 5; column dia 1.0 cm; column length 20 cm; bed height 5.0 cm; flow rate 2.5 mL min⁻¹). CMBC removed more Pb²⁺ than NMBC suggesting that modification with chitosan generates amine groups on the biochar surface which enhance Pb²⁺ adsorption. The modes of Pb²⁺ adsorption on CMBC were studied by comparing DRIFTS and X-ray photoelectron spectroscopy spectra before and after Pb²⁺ adsorption.

Batch and fixed-bed column studies for the removal of lead (Pb²⁺) from aqueous solution by chitosan-modified pinewood biochar.     

High ion adsorption densities of site-selective nitrogen doped carbon sheets prepared from natural lignin

Carbon fibers and sheets were prepared from jet-milled natural chitin and cellulose samples, and from natural lignin sample using ice-templating technique, respectively. Nitrogen doping treatments using melamine were also performed for the carbon fibers and sheets. Electric double layer capacitor (EDLC) electrode properties of the prepared carbon fibers and sheets including the nitrogen doped samples were investigated with aqueous (sulfuric acid) and organic (tetraethylammonium tetrafluoroborate in propylene carbonate) electrolytes. It was found that the nitrogen doped lignin carbon sheets having very small specific surface area of 66 m² g⁻¹ show very high EDLC capacitances of 227 F g⁻¹ and 80 F g⁻¹ determined by charge–discharge measurements at current density of 50 mA g⁻¹ for aqueous and organic electrolytes, respectively. X-ray photoelectron spectroscopy (XPS) measurements revealed that nitrogen atoms of the nitrogen doped lignin carbon sheets exist dominantly in pyridinic sites unlike other chitin and cellulose carbon fibers. We discussed that this site-selective nitrogen doping gives exceptionally high ion adsorption density per unit surface area of the nitrogen doped lignin carbon sheets.

Carbon fibers and sheets were prepared from jet-milled natural chitin and cellulose samples, and from natural lignin sample using ice-templating technique, respectively.     

Exploring the electrochemical performance of copper-doped cobalt–manganese phosphates for potential supercapattery applications

The significant electrochemical performance in terms of both specific energy and power delivered via hybrid energy storage devices (supercapattery) has raised their versatile worth but electrodes with flashing electrochemical conduct are still craved for better performance. In this work, binary and ternary metal phosphates based on copper, cobalt, and manganese were synthesized by a sonochemical method. Then, the compositions of copper and cobalt were optimized in ternary metal phosphates. The structural studies and morphological aspects of synthesized materials were scrutinized by X-ray diffraction and scanning electron microscopy. Furthermore, the electrochemical characterizations were performed in three- and two-cell configurations. The sample with equal compositions of copper and cobalt (50/50) demonstrates the highest specific capacity of 340 C g⁻¹ at a current density of 0.5 A g⁻¹ among all. This optimized composition was utilized as a positive electrode material in a supercapattery device that reveals a high specific capacity of 247 C g⁻¹. The real device exhibits an excellent energy density of 55 W h kg⁻¹ while delivering a power density of 800 W kg⁻¹. Furthermore, the device was able to provide an outstanding specific power of 6400 W kg⁻¹ while still exhibiting a specific energy of 19 W h kg⁻¹. The stability potential of the device was tested for 2500 continuous charge and discharge cycles at 8 A g⁻¹. Excellent capacitive retention of 90% was obtained, which expresses outstanding cyclic stability of the real device. A theoretical study was performed to investigate the capacitance and diffusion-controlled contribution in the device performance using Dunn''s model. The maximum diffusion-controlled contribution of 85% was found at 3 mV s⁻¹ scan rate. The study demonstrates the utilization of ternary metal phosphates as self-supported electrode materials for potential energy storage applications.

The optimized copper-doped cobalt–manganese phosphate was utilized as a positive electrode in an asymmetric architecture (supercapattery device), which yields enhanced specific energy and power.     

An investigation of Li2TiO3–coke composite anode material for Li-ion batteries

Anode material Li₂TiO₃–coke was prepared and tested for lithium-ion batteries. The as-prepared material exhibits excellent cycling stability and outstanding rate performance. Charge/discharge capacities of 266 mA h g⁻¹ at 0.100 A g⁻¹ and 200 mA h g⁻¹ at 1.000 A g⁻¹ are reached for Li₂TiO₃–coke. A cycling life-time test shows that Li₂TiO₃–coke gives a specific capacity of 264 mA h g⁻¹ at 0.300 A g⁻¹ and a capacity retention of 92% after 1000 cycles of charge/discharge.

Anode material Li₂TiO₃–coke was prepared and tested for lithium-ion batteries. The as-prepared material exhibits excellent cycling stability and outstanding rate performance.