Power Density Research Articles

Thermal damage to the skin from 8.2 and 95 GHz microwave exposures in swine

A study of burn thresholds from superficially penetrating radio-frequency (RF) energy at 8.2 and 95 GHz for swine skin was conducted. The study determined the thresholds for superficial, partial-thickness, and full-thickness burn severities after 5 seconds of exposure at power densities of 4–30 W/cm2 and 2–15 W/cm2 at 8.2 and 95 GHz, respectively. There were significant differences in he burn thresholds at the different severities between the two frequencies due to the large difference in energy penetration depths. Biopsies were collected from each burn site at 1, 24, 72, and 168 hr post exposure. Each sample was assessed by a burn pathologist against 20 histological factors to characterize the damage resulting from these RF overexposures. A one-dimensional, layered digital phantom that utilized realistic values for dielectric and thermal properties was used to explain some observed thresholds. The results of the heating and cooling response of the animal model and histology scores of each exposure are provided to enhance future efforts at simulation of RF overexposures and to establish damage thresholds.

Tm3+ mediated multicolor luminescence of NaYbF4:Er,Tm@NaYF4 for advanced anti-counterfeiting.

Lanthanide doped multicolor luminescent materials have attracted extensive attention due to their advanced anti-counterfeiting properties. However, designing a simple, hard-to-copy and multicolor anti-counterfeiting strategy based on upconversion nanoparticles (UCNPs) remains a huge challenge. Herein, a strategy to modulate luminescence color by altering the mediating action of Tm3+ was proposed. As a proof of concept, the mediating action of Tm3+ was explored in NaYbF4:30%Er,1%Tm@NaYF4 by changing the doping ratio of Yb3+/Er3+/Tm3+, and red, yellow and blue luminescence was successfully obtained. Then, NaYbF4:x%Er,1%Tm@NaYF4 (x = 2, 10, 30, 50, 99), NaYbF4:x%Er@NaYF4 (x = 2, 10, 30, 50, 100) and NaYbF4:1%Tm@NaYF4:x%Er@NaYF4 (x = 2, 10, 30, 50, 100) were synthesized to further identify that the mediating action of Tm3+ was related to the doping ratio and distance between dopant ions. In addition, the luminescence color of NaYbF4:30%Er,1%Tm@NaYF4 changed from red to yellow with the increase of excitation power density. Based on the above, NaYbF4:Er,Tm@NaYF4 UCNPs show excellent performance in anti-counterfeiting of paintings, thus revealing their great potential in advanced anti-counterfeiting applications.

Feasibility of Wind Energy Utilization for Sustainable Power Generation in Ilorin, Kwara State, Nigeria's North-Central Region

The escalating energy demands across Nigeria, especially in remote rural areas, have outpaced the capacity of the national electricity grid, necessitating the development of independent and sustainable energy sources. Among the renewable options, wind energy stands out as a promising solution. This study focuses on assessing the potential of wind energy in Ilorin, located in Kwara State, within Nigeria's north-central region. Utilizing data collected from 2007 to 2021 by the Nigerian Meteorological Agency, the research examines monthly average wind speeds at two specific coordinates in Ilorin, considering variations in air density. The study utilizes a 15-year set of monthly average wind velocities obtained from the Nigerian Meteorological Agency (NiMet) Headquarters in Abuja, measured at a height of 10 meters above ground level. By employing the 2-coefficient Weibull statistical model and extrapolation principles across different altitudes ranging from 150 to 900 meters above ground level, the study reveals distinct seasonal patterns of wind speeds ranging from 1.1 to 5.1 m/s in Ilorin. Furthermore, wind power density values ranging from 6.7 to 39.20 W/m2 are identified, with optimal wind attributes observed at altitudes exceeding 900 meters. These findings provide valuable insights for assessing the feasibility of wind energy utilization and designing efficient systems in Nigeria's north-central regions, aiding in the sustainable energy transition.

Simultaneously realizing high energy density and high efficiency in NaNbO3–BaTiO3‐based ceramic capacitors

AbstractDielectric capacitors, which can achieve tremendous power density and ultrafast charge/discharge speed, are crucial components for high power equipment. Yet, the synchronous achievement in high recoverable energy density (Wrec) and high efficiency (η) is a long‐term difficulty for dielectric ceramics. Herein, the (0.85 − x)NaNbO3–0.15BaTiO3–xBi(Mg1/3Ta2/3)O3 (NN–BT–xBMT) relaxor ferroelectric ceramics were proposed and studied. The doping of BMT was conducive to promoting the microstructure and bandgap and improving the dielectric relaxation properties of NN–BT ceramics. Finally, the sample of x = 0.10 presented a high Wrec of 5.9 J/cm3 and a high η of 90% simultaneously. In addition, the sample also exhibited superb charge/discharge performances with large power density (PD = 137 MW/cm3) and fast charge/discharge speed (t0.9 = 39 ns). The above results reveal that the NaNbO3‐based ceramics could serve as potential alternatives for advanced dielectric capacitors.

Photodynamic therapy of leukoplakia of the oral mucosa: experience of using method in 223 patients

The aim of this study was to analyze the immediate and long-term results of using photodynamic therapy (PDT) in patients with leukoplakia of the oral mucosa. The retrospective study included 223 patients with morphologically verified leukoplakia of the oral mucosa. Patients received treatment at the hyperthermia and photodynamic therapy department from 2013 to 2023. The average age was 51.9±8.9 years. Clinically, 211 patients (94.6%) had a flat form of the disease, 12 patients (5.4%) had a verrucous form. The photosensitizer (PS), based on chlorin e6, was administered intravenously once in doses of 1.7 to 2.5 mg/kg body weight. Irradiation of pathologically changed lesions was carried out 2-2.5 hours after the end of its infusion, using a semiconductor laser device “UPL PDT”, with a wavelength λ=665±5 nm. The laser radiation dose density varied from 25 to 100 J/cm², the power density from 0.07 to 0.32 W/cm², the duration of one irradiation field - from 2 to 13.5 minutes, depending on its linear dimensions. The severity of adverse reactions was assessed on days 1-30 after treatment using the CTCAE 4.03 scale. The immediate results of treatment were assessed up to 3 months after PDT, with morphological confirmation of the response to treatment. No serious adverse reactions were observed during PS infusion and irradiation. No symptoms of dermal phototoxicity were reported. During control examinations, up to 3 months after irradiation in patients with flat and verrucous forms, the frequency of complete regressions was 97.1% (n=205) and 58.3% (n=6) cases, partial regressions - 2,9% (n=7) and 25% (n=3) of cases, respectively. Objective response rates were observed at 100% and 83.3%, respectively. The period of observation of patients varies from 3 to 120 months. (average 66 months). The frequency of disease relapses during this period was 9%. Patients with partial regression and identified relapse were treated with repeated PDT sessions. PDT is a well-tolerated and effective treatment method for patients with leukoplakia of the oral mucosa, which has significant advantages over traditional methods of treating this precancerous pathology. These include minimal toxicity to the normal tissues surrounding the pathological foci due to the selective accumulation of PS in leukoplakia tissues, a slight risk of serious adverse reactions, the possibility of an outpatient session, the possibility of repeated treatment over a large area of damage and good cosmetic results).

Synthesis of low cost cathode electrocatalyst Pt‐Ni/CAB using DMSO as a solvent for low temperature proton exchange membrane fuel cell application

AbstractIn the present study, low cost platinum based bimetallic electrocatalyst Pt‐Ni/CAB with varying Pt to Ni atomic ratios 3:1, 1:1, and 1:3 were successfully synthesized for oxygen reduction reaction (ORR) of the developed proton exchange membrane fuel cell (PEMFC). The solvothermal process was adopted for the synthesis of Pt‐Ni(3:1)/CAB, Pt‐Ni(1:1)/CAB, and Pt‐Ni(1:3)/CAB using dimethyl sulfoxide (DMSO) as solvent at a temperature of 190°C which is very close to the boiling point. The Pt‐Ni/CAB exhibited the highest activity for the ORR in half‐cell and single cell PEMFC performance. The electrocatalysts Pt‐Ni(1:3)/CAB appeared with smallest crystalline FCC structures having crystallite size of 8.33 nm. The transmission electron microscopy (TEM) analysis also show that the Pt‐Ni(1:3)/CAB has smallest particle size of 1.67 ± 0.45 nm. The cyclic voltammetry (CV) analysis shows Pt‐Ni(1:3)/CAB electrocatalyst offers less activation loss at ORR peak at a potential of 0.16 V as compared to Pt‐Ni(3:1)/CAB (ORR peak – 0.12) and Pt‐Ni(1:1)/CAB (ORR peak – 0.11). The synthesized Pt‐Ni(1:3)/CAB produced a maximum power density of 18.86 mW/cm2 at a maximum current density of 44.8 mA/cm2 with an open‐circuit voltage of 0.914 V at a room temperature of 33°C. The power density improved around 1.34 times when the cell temperature was raised from 33 to 70°C. The Pt‐Ni(1:3)/CAB cathode electrocatalyst could be used as economical to substitute costly commercial pure platinum based electrocatalyst.

Advances in Contact Mechanics

Advancements in contact mechanics play an important role in the design of modern mechanical and bio-medical systems, enhancing their efficiency, power density, and reliability [...]

Planar Chlorination Engineering: A Strategy of Completely Breaking the Geometric Symmetry of Fe-N4 Site for Boosting Oxygen Electroreduction.

Introducing asymmetric elements and breaking the geometric symmetry of traditional metal-N4 site for boosting oxygen reduction reaction (ORR) are meaningful and challenging. Herein, the planar chlorination engineering of Fe-N4 site was firstly proposed for remarkably improving the ORR activity. The Fe-N4/CNCl catalyst with broken symmetry exhibited a half-wave potential (E1/2) of 0.917V versus RHE, 49mV and 72mV higher than those of traditional Fe-N4/CN and commercial 20 wt% Pt/C catalysts. The Fe-N4/CNCl catalyst also had excellent stability for 25,000 cycles and good methanol tolerance ability. For Zn-air battery test, the Fe-N4/CNCl catalyst had the maximum power density of 228mW/cm2 and outstanding stability during 150h charge-discharge test, as the promising substitute of Pt-based catalysts in energy storage and conversion devices. The density functional theory calculation demonstrated the adjacent C-Cl bond effectively broke the symmetry of Fe-N4 site, downward shifted the d-band center of Fe, facilitated the reduction and release of OH*, and remarkably lower the energy barrier of rate-determining step. This work revealed the enormous potentials of planar chlorination engineering for boosting the ORR activity of traditional metal-N4 site by thoroughly breaking their geometric symmetry. This article is protected by copyright. All rights reserved.

Spontaneously established reverse electric field to enhance the performance of triboelectric nanogenerators via improving Coulombic efficiency

Mechanical energy harvesting using triboelectric nanogenerators is a highly desirable and sustainable method for the reliable power supply of widely distributed electronics in the new era; however, its practical viability is seriously challenged by the limited performance because of the inevitable side-discharge and low Coulombic-efficiency issues arising from electrostatic breakdown. Here, we report an important progress on these fundamental problems that the spontaneously established reverse electric field between the electrode and triboelectric layer can restrict the side-discharge problem in triboelectric nanogenerators. The demonstration employed by direct-current triboelectric nanogenerators leads to a high Coulombic efficiency (increased from 28.2% to 94.8%) and substantial enhancement of output power. More importantly, we demonstrate this strategy is universal for other mode triboelectric nanogenerators, and a record-high average power density of 6.15 W m−2 Hz−1 is realized. Furthermore, Coulombic efficiency is verified as a new figure-of-merit to quantitatively evaluate the practical performance of triboelectric nanogenerators.

High-performance piezoelectric energy harvesting in amorphous perovskite thin films deposited directly on a plastic substrate

Most reported thin-film piezoelectric energy harvesters have been based on cantilever-type crystalline ferroelectric oxide thin films deposited on rigid substrates, which utilize vibrational input sources. Herein, we introduce flexible amorphous thin-film energy harvesters based on perovskite CaCu3Ti4O12 (CCTO) thin films on a plastic substrate for highly competitive electromechanical energy harvesting. The room-temperature sputtering of CCTO thin films enable the use of plastic substrates to secure reliable flexibility, which has not been available thus far. Surprisingly, the resultant amorphous nature of the films results in an output voltage and power density of ~38.7 V and ~2.8 × 106 μW cm−3, respectively, which break the previously reported record for typical polycrystalline ferroelectric oxide thin-film cantilevers. The origin of this excellent electromechanical energy conversion is systematically explored as being related to the localized permanent dipoles of TiO6 octahedra and lowered dielectric constant in the amorphous state, depending on the stoichiometry and defect states. This is the leading example of a high-performance flexible piezoelectric energy harvester based on perovskite oxides not requiring a complex process for transferring films onto a plastic substrate.

Eggshell-Like Carbon Microspheres with Curvature Scheme: Distorted Energy Band and Atomic Charge Waves-Driven High Performance for Zinc-Air Battery.

A metal-free nanocarbon with an eggshell structure is synthesized from chitosan (CS) and natural spherical graphite (NSG) as a cathode electrocatalyst for clean zinc-air batteries and fuel cells. It is developed using CS-derived carbons as an eggshell, covering NSG cores. The synthesis involves the in situ growth of CS on NSG, followed by ammonia-assisted pyrolysis for carbonization. The resulting catalyst displays a curved structure and completely coated NSG, showing superior oxygen reduction reaction (ORR) performance. In 1 M NaOH, the ORR half-wave potential reached 0.93 V, surpassing the commercial Pt/C catalyst by 50 mV. Furthermore, a zinc-air battery featuring the catalyst achieves a peak power density of 167 mW cm-2 with excellent stability, outperforming the Pt/C. The improved performance of the eggshell carbons can be attributed to the distorted energy band of the active sites in the form of N-C moieties. More importantly, the curved thin eggshells induce built-in electric fields that can promote electron redistribution to generate atomic charge waves around the N-C moieties on the carbon shells. As a result, the high positively charged and stable C+ sites adjacent to N atoms optimize the adsorption strength of oxygen molecules, thereby facilitating performance.

Oxygen Vacancy-Rich NiCo2O4 on Carbon Framework with Controlled Pore Architectures as Efficient Bifunctional Electrocatalysts for Zn-Air Batteries

Transition metal oxides are considered alternative electrocatalysts for ZAB owing to their multiple oxidation states. However, they have limitations such as low electrical conductivity and the deficiency of reactive sites. In this study, to overcome these shortcomings and improve electrocatalytic activity, oxygen vacancies and porous architectures were introduced through a partial reduction process and a porous carbon framework. Open porous carbon microspheres with uniformly loaded NiCo2O4 nanosheets and oxygen vacancies (V-NCO/OPC) displayed enhanced electrocatalytic performance with a low Tafel slope (68 mV dec-1) in the oxygen reduction reaction (ORR) and a low overpotential (402 mV) at 10 mA cm–2 in the oxygen evolution reaction (OER). The combined effect of the oxygen vacancies and porous architecture can offer sufficient active sites, modify the electronic structure of the metal oxide surface, and facilitate mass transport, enhancing the electrocatalytic properties of V-NCO/OPC. Furthermore, when applied for ZAB, V-NCO/OPC demonstrated better electrochemical performance including discharge power density (154.9 mW cm-2) at the current density of 175.9 mA cm-2, low voltage gap (0.85 V) at the initial cycle, and long-term (250 h) cycle stability at the current density of 10 mA cm−2 than those of noble-metal electrocatalysts.

Ni Single Atom Decorated Porous Hollow Carbon Nanosphere-Based Electrodes for High Performance Symmetric Solid-State Supercapacitors.

Ni single atom containing hollow carbon nanospheres with nitrogen doping has been synthesized by carbonization of Ni(NO3)2/phloroglucinol-formaldehyde polymer/silica composite. The samples have been characterized by powder X-ray diffraction, nitrogen adsorption/desorption, electron microscopic, Raman and X-ray photoelectron spectroscopic studies. The microstructure and surface area vary with the amount of Ni(NO3)2 employed in the syntheses and the carbonization environment. An optimized amount of nickel and argon as the carbonization gas afford Ni-1.0@N@HCN-Ar which possesses overall superior features. The uniformly dispersed Ni single atoms within the hollow porous carbon framework fully utilize all the electroactive sites thereby improving the supercapacitive performance. The specific capacitance of Ni-1.0@N@HCN-Ar reaches 777 F∙g-1 at 1 A∙g-1 with a Coulombic efficiency of 98.4% and excellent recyclability. The energy and power density of Ni-1.0@N@HCN-Ar are found to be high; at 1 A∙g-1 its energy density is 155.4 Wh∙kg-1 with a power density of 600.3 W∙kg-1. At a high current density of 10 A∙g-1 the material shows a high energy density of 118.4 Wh∙kg-1 with excellent power density of 6003.4 W∙kg-1. A symmetric solid-state supercapacitor assembled with this material, Ni-1.0@N@HCN-Ar//Ni-1.0@N@HCN-Ar using H2SO4/PVA gel electrolyte shows a superior energy density value of 30 Wh∙kg-1 at a power density of 1200 W∙kg-1.

Optimizing Transport Carrier Free All-Polymer Solar Cells for Indoor Applications: TCAD Simulation under White LED Illumination.

This work inspects the utilization of all-polymer solar cells (APSCs) in indoor applications under LED illumination, with a focus on boosting efficiency through simulation-based design. The study employs a SCAPS TCAD device simulator to investigate the performance of APSCs under white LED illumination at 1000 lux, with a power density of 0.305 mW/cm2. Initially, the simulator is validated against experimental results obtained from a fabricated cell utilizing CD1:PBN-21 as an absorber blend and PEDOT:PSS as a hole transportation layer (HTL), where the initial measured efficiency is 16.75%. The simulation study includes an examination of both inverted and conventional cell structures. In the conventional structure, where no electron transportation layer (ETL) is present, various materials are evaluated for their suitability as the HTL. NiO emerges as the most promising HTL material, demonstrating the potential to achieve an efficiency exceeding 27%. Conversely, in the inverted configuration without an HTL, the study explores different ETL materials to engineer the band alignment at the interface. Among the materials investigated, ZnS emerges as the optimal choice, recording an efficiency of approximately 33%. In order to reveal the efficiency limitations of these devices, the interface and bulk defects are concurrently investigated. The findings of this study underscore the significance of careful material selection and structural design in optimizing the performance of APSCs for indoor applications.

Co nanoparticle-loaded porous carbon for high-performance supercapacitors

Porous carbon materials doped with transition metals have emerged as promising electrode materials in the field of energy storage due to their higher theoretical capacitance and cost-effectiveness. In this study, metallic cobalt nanoparticles (Co NPs) were successfully loaded into porous carbon via one-step carbonization method for electrochemical research applications as electrode materials (Co/CM). A comparative investigation was conducted by varying the content of polystyrene microspheres (PS) to optimize the porous morphology. Scanning electron microscopy (SEM) analysis revealed that the Co/CM-3 composite displayed a plate-like porous structure, while transmission electron microscopy (TEM) confirmed the uniform loading of Co NPs within the porous carbon skeleton. The composite with the optimal PS content (Co/CM-3) exhibited a specific capacitance of up to 810 F g−1 (at 1 A g−1) in the three-electrode system. Furthermore, asymmetric supercapacitors assembled with the prepared electrode as the positive electrode and activated carbon as the negative electrode demonstrated an impressive energy density of up to 40 Wh kg−1 (at a power density of 746 W kg−1). Remarkably, the capacitance retention rate remained at 88.24 % even after 5000 consecutive charge and discharge cycles, highlighting the promising potential of this electrode material for practical applications in energy storage.

Basic and acidic electrolyte mediums impact on MnO2-Mn2O3/Poly-2-methylaniline hexagonal nanocomposite pseudo-supercapacitor

A highly efficient MnO2-Mn2O3/Poly-2-methylaniline (MnO2-Mn2O3/P2MA) hexagonal nanocomposite is synthesized using a one-pot technique involving oxidation polymerization. The hexagonal morphology and crystalline nature of this nanocomposite, as evidenced by the XRD pattern, affirm its exceptional characteristics. The electrical properties are assessed through charge/discharge behavior and cyclic voltammetry curves, elucidating the storage capabilities of this pseudo supercapacitor using different electrolytes NaOH and HCl. The fabricated supercapacitor exhibits impressive efficiency values of 22 F g−1 in a basic medium and a notably higher 72 F g−1 in an acidic medium at a current density of 0.2 A/g. Similarly, the power density values are calculated at 480 and 478 W.kg−1 for the basic and acidic electrolyte, correspondingly. In the basic medium, the series resistance (RS) and charge transfer resistance (RCT) are 5.2 and 0.7 Ω, respectively. In the acidic medium, these values are notably lower, with RS at 2.82 Ω and RCT at 0.2 Ω. Remarkably, even after 500 cycles, the supercapacitor stability remains high at 95% in both media, underscoring the enduring stability attributed to the oxides and polymer materials within the supercapacitor. The combination of cost-effectiveness, ease of fabrication, and potential for mass production positions this supercapacitor as a promising candidate for industrial applications of polymer-based supercapacitors.

Coconut Husk Waste‐Derived Nitrogen‐Doped Mesoporous Carbon Nanomaterial as an Efficient and Sustainable Supercapacitor

Sustainability and waste management are equally important in the era of growing energy demands. This study focuses on integrating strategies that balance energy efficiency, reduce waste generation, and promote sustainable practices. The coconut husk is processed and converted into mesoporous carbon nanomaterial through hydrothermal‐assisted thermal annealing. Nitrogen is doped through melamine to increase reactive sites and hence the catalytic activity. The sphere‐like morphology was confirmed by field emission scanning electron microscope and high‐resolution transmission electron microscope images indicate a carbon dot‐like structure. The high Brunauer‐Emmett‐Teller surface area achieved for this nanostructure is 1383.40 m2 g−1, with pore width and volume at 2.2660 nm and 0.2995 cm3 g−1, respectively. The as‐synthesized nanostructure is explored for its electrochemical performance as electrodes for the supercapacitor application, where materials achieve a wide potential window (−1.4 to 1.4 V) in the minimum time of 50 s at the current density of 0.6 A g−1. Moreover, the highest specific capacitance obtained from the nanomaterial is 115.39 F g−1 in the potential window and current density of 2 V and 0.6 A g−1, respectively. The energy density, power density, and coulombic efficiency at the set parameter are 62.31 Wh Kg−1, 1166.4 W Kg−1, and 79.61%, respectively. Finally, the practical device is assembled with the nanomaterial, where a red LED bulb glows after 1 min of charging.

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

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

A Remarkable Pt Doped CNT Catalyst as a Double Functional Material: Its Application for Hydrogen Production and Supercapacitor

In this study, by producing bifunctional material, hydrolysis, and supercapacitor applications were investigated. The carbon nanotube-supported Pt catalyst was prepared using the sodium borohydride (NaBH<sub>4</sub>) reduction. Surface characterization of the synthesized Pt/CNT catalyst was performed using scanning electron microscopy-energy dıstrıbutıon X-ray spectrometer (SEM-EDX), X-ray diffraction (XRD), and transmission electron microscopy (TEM). Hydrolysis experiments were performed after deciding on the appropriate atomic ratio from the Pt/CNT catalysts synthesized in different nuclear ratios. The parameters affecting the hydrogen production from NaBH<sub>4</sub> were examined. As a result of the kinetic calculations, the initial rates of reaction for 30°C and 60°C were calculated as 21949,69 mlH<sub>2</sub>g<sub>cat</sub>min<sup>-1</sup> and 70018,18 mlH<sub>2</sub>g<sub>cat</sub>min<sup>-1</sup>. Galvastonic charge-discharge (GCD), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) were used as characterization techniques for the use of Pt/CNT catalysts as electrodes in supercapacitor applications. The specific capacitance value of 7% Pt/CNT catalyst at 1 A/g current density was calculated as 57,78 F/g. Energy and power density were calculated as 8,025 Wh/kg and 963 W/kg, respectively. Therefore, this catalyst is called a “cap-cat” with capacitor properties. The catalyst used in this study is promising for this recently studied topic.

Supercapacitor performance enhancement with the BaS3:Cu2S:Mn2S trichalcogenide semiconductor synthesized via dithiocarbamate precursors

AbstractDue to its potential uses, including e‐vehicles, electrochemical energy storage has attracted a lot of interest from the scientific community and energy stakeholders. With the usage of the novel semiconductor chalcogenide BaS3:Cu2S:Mn2S, which is synthesized by chelating with diethyldithiocarbamate ligand, the current work seeks to enhance the performance of charge‐storage devices. An energy band gap of 2.57 eV was found for this semiconductor, which showed remarkable photoactivity. The chalcogenide that was produced had favorable crystallinity, with an average crystallite size of 26.92 nm and mixed crystalline phases. Additionally, metallic sulfide linkages were identified using infrared spectroscopy, and they were reported to range from 400 to 845 cm−1. Thermal breakdown in two steps was verified using thermogravimetric analysis. Particles with different forms and a rod‐like fusion suggested a higher volume–surface area ratio and many locations. The electrochemical performance of the BaS3:Cu2S:Mn2S was evaluated using a traditional three‐electrode setup with a background electrolyte of 1‐M KOH. BaS3:Cu2S:Mn2S is a great electrode material for energy storage applications, with a specific power density of 10 618 W kg−1 and a specific capacitance of up to 694 F g−1. The same series resistance (Rs) = 0.46 Ω further supported this remarkable electrochemical performance.