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Dielectric and electrochemical behavior of hydrothermally synthesized Zn-doped titanate nanotubes
(2026-11-01)
Masakul, Pristanuch
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Krongkitsiri, Pacharee
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Thongbai, Prasit
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Kidkhunthod, Pinit
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Maensiri, Santi
A bstract Zn-doped titanate nanotubes (Zn-doped TNTs) with the composition of Zn<inf>x</inf>Ti<inf>3-x</inf>O<inf>7</inf>, (Na<inf>0.96</inf>H<inf>1.04</inf>∙3.42H<inf>2</inf>O) (where x = 0, 0.05, 0.1, and 0.2) were synthesized via a hydrothermal method at 130 °C for 24 h. Structural and morphological characterization using X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), UV-Vis (Ultraviolet-Visible), X-ray Absorption Near Edge Structure (XANES), and Brunauer-Emmett-Teller (BET) techniques confirmed the formation of well-defined nanotubes with controlled dimensions. Transmission electron microscopy (TEM) images of undoped and Zn-doped titanate nanotubes reveal uniform hollow nanotubular structures with diameters of ∼7–15 nm and multilayered walls. The dielectric properties of the Zn-doped TNTs were examined using an LCR meter across a frequency range of 102–106 Hz. The results revealed a remarkably high dielectric constant (ε′) (∼104-105 at 30 °C and 1 kHz), which was attributed to Debye-like relaxation governed by Maxwell-Wagner polarization. The dielectric response exhibited a strong dependence on Zn doping levels, with higher Zn content leading to enhanced permittivity. Electrochemical properties were evaluated through cyclic voltammetry (CV), galvanostatic charge-discharge (GCD), and electrochemical impedance spectroscopy (EIS). The Zn-doped TNTs demonstrated a specific capacitance ( C ) of 23 F g−1 at a scan rate of 1 mV s−1, indicating their potential for energy storage applications. This systematic investigation of Zn incorporation provides critical insights into its impact on the structural, dielectric, and electrochemical properties of titanate nanotubes (TNTs). These findings provide useful insight for further optimization of doped titanate nanostructures toward advanced multifunctional dielectric and electrochemical energy-storage applications.
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Multi-phase structure electrospun CNF@Ag/Mn/Bi/Fe composite nanofiber enhanced supercapacitor behavior
(2025-02-15)
Sinprachim, Tanayt
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Klompong, Narit
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Chanlek, Narong
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Kidkhunthod, Pinit
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Maensiri, Santi
This study presents the development of carbon-based multiphase metal oxide nanocomposites (CNF@MO<inf>x</inf>; M = Ag, Mn, Bi, and Fe) incorporating silver, manganese, bismuth, and iron nanoparticles within polyacrylonitrile (PAN)-derived carbon nanofibers. These nanocomposites were fabricated via the electrospinning technique with metal oxide concentrations of 10, 20, and 40 %w. This was followed by annealing in an argon atmosphere. The resulting nanofibers exhibited diameters ranging from 559 to 830 nm, with embedded nanoparticles measuring from 9 to 21 nm. Comprehensive characterization revealed that the nanofibers possessed uniform morphology, high porosity, and robust thermal stability. X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS) confirmed the valence states of the metal oxides (Ag⁰, Bi³⁺, Mn²⁺, Mn³⁺, Fe²⁺, and Fe³⁺), which are integral to redox reactions and charge storage mechanisms. Among the fabricated composites, CNF@Ag/Mn/Bi/Fe-20 demonstrated the best electrochemical performance, achieving a specific capacitance of 156 F g−1 at a scan rate of 2 mV s−1 and outstanding cycling stability with a capacity retention of over 96 % after 1400 charge-discharge cycles. The synergistic combination of double-layer capacitance and pseudocapacitance mechanisms in these nanofibers represents a significant improvement over conventional electrode material. This study highlights CNF@Ag/Mn/Bi/Fe nanocomposites as highly promising candidates for advanced energy storage applications, particularly in supercapacitor technologies.
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Enhancing activated carbon supercapacitor electrodes using sputtered Cu-doped BiFeO3 thin films
(2024-12-01)
Tanapongpisit, Nantawat
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Wongprasod, Suchunya
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Laohana, Peerawat
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Sonsupap, Somchai
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Khajonrit, Jessada
This work describes the fabrication of a composite supercapacitor electrode made of Cu-doped BiFeO3 (Cu-BFO) films on an activated carbon (AC) electrode using radio-frequency (RF) magnetron sputtering. To prevent exfoliation of Cu-BFO and AC upon immersion in an electrolyte, the nickel foam sandwiching electrode technique was introduced. The Cu-BFO films significantly enhanced electrochemical properties, increasing specific capacitance by up to 151% compared to that of an AC electrode. This was attributed to Faradaic reactions and specific surface area in the Cu-BFO/AC electrode. The highest specific capacitance achieved was 169 F g-1 at 0.5 A g-1, and cycling stability retention was 93.12% after 500 cycles. However, the remaining percentage of the specific capacitance decreased differently with increasing thickness, which is also discussed. Furthermore, an asymmetric supercapacitor using Cu-BFO/AC and AC electrodes demonstrated a high energy density of 4.71 Wh kg-1, power density of 2.66 kW kg-1, and over 90% retention after 1000 cycles, highlighting its durability. The uniform RF magnetron sputtering deposition is vital for mass production. Combined with impressive retention in asymmetric supercapacitors, this scalability suggests a promising pathway for large-scale manufacturing. Consequently, this work could pave the way for the large-scale production of supercapacitors.
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Glass-sulfur composite cathodes: A new strategy for improving the performance of lithium-sulfur batteries
(2024-10-01)
Siriroj, Sumeth
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Padchasri, Jintara
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Montreeuppathum, Amorntep
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Sonsupap, Somchai
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Maensiri, Santi
In this study, we investigated the potential of glass-sulfur composites to improve lithium–sulfur battery (LSB) performance. Glass-sulfur composites were prepared by the precipitation method, and the effect of varying carbon black content was studied. The results showed that glass addition improved the battery performance due to the high ion-conductivity of its structural motif. The 75 % glass variant demonstrated the best results, in both the low carbon and high carbon cases. The cyclic voltammetry (CV) and electrical impedance spectroscopy (EIS) measurements showed that glass-sulfur composites had lower resistivity than pure sulfur, which was beneficial for battery performance. The XANES analysis revealed that the incorporated glass interacted with and modified the properties of sulfur, leading to a higher proportion of sulfur in the -1 oxidation state (S−1). This suggests that the high proportion of S−1 phase benefitted battery capacity. Overall, glass-sulfur composites prepared using the precipitation method and incorporating a high content of carbon show promise as a novel and improved cathode material for LSBs.
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Customized electrospun multilayer composite polymer electrolytes: PEO-PAN-NbO2 nanofiber membrane for enhancing the performance of lithium-ion batteries
(2024-06-01)
Yonchai, Chutarat
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Kidkhunthod, Pinit
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Siriroj, Sumeth
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Padchasri, Jintara
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Sonsupap, Somchai
Ground-breaking research into the development of a multilayer composite polymer electrolyte aims to enhance the safety associated with liquid electrolytes utilized in lithium batteries. The electrolyte consists of two outer layers made of electrospun poly(vinylidene fluoride) (PVDF) and a middle layer comprised of a fibrous membrane containing PEO, PAN-PEO, PEO-NbO<inf>2</inf>, and PAN-PEO-NbO<inf>2</inf>. The investigated PEO-PAN-NbO<inf>2</inf> system demonstrates a higher room temperature ionic conductivity of 2.451 × 10−1 mS cm−1 than that of single-phase electrolyte systems. Incorporating inorganic fillers such as NbO<inf>2</inf> into PEO polymer electrolytes, in conjunction with PAN copolymerization, significantly enhances ionic conductivity and amplifies surface area. Consequently, the utilization of these techniques that demonstrate increased polymer membranes leads to improved efficiency and security of solid-state electrochemical devices. The multilayer composite polymer electrolyte is created by continuous electrospinning, which allows for precise control and improves safety features.
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Porous Electrospun Carbon Nanofibers Bearing TiO2 Hollow Nanospheres for Supercapacitor Electrodes
(2024-03-22)
Wongprasod, Suchunya
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Tanapongpisit, Nantawat
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Laohana, Peerawat
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Huyen Nguyen, Thi My
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Van, Hoang Quy
A facile fabrication method was introduced to enhance the specific surface area and porosity of the carbon nanofibers. The carbon nanofibers bearing TiO<inf>2</inf> hollow nanosphere electrodes were synthesized using an electrospinning technique followed by heat treatment. Varying amounts of as-prepared TiO<inf>2</inf> hollow nanospheres were incorporated into the polymer precursor to examine their impact on the electrode enhancement. The electrochemical performance of supercapacitor electrodes composed of carbon nanofibers bearing TiO<inf>2</inf> hollow nanospheres was investigated. Results revealed that the specific capacitance of the bare carbon nanofibers electrode (170 F g-1 at a current density of 0.5 A g-1) was significantly improved upon when embedded with 5 wt % TiO<inf>2</inf> hollow nanospheres of 191 F g-1. Additionally, the carbon nanofibers bearing 5 wt % TiO<inf>2</inf> hollow nanosphere electrodes demonstrated excellent cycling stability, retaining 97% of its initial specific capacitance even after 10000 cycles. Additionally, the electrochemical performance of asymmetric supercapacitors from these electrodes was also demonstrated. These findings highlight the ability of as-prepared TiO<inf>2</inf> hollow nanospheres to improve the efficiency of the carbon nanofibers electrode due to the optimum porosity to the amount of TiO<inf>2</inf> hollow nanospheres in the carbon nanofibers, opening up possibilities for the development of high-performance supercapacitors.
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Fabrication and thermoelectric conversion of thermoelectric concrete brick with buried unileg N-type CaMnO3 thermoelectric module inside
(2023-12-01)
Maneesai, Keerati
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Khammahong, Sunisar
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Siripoom, Pongsakorn
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Phrompet, Chaiwat
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Sriwong, Chaval
To investigate the effect of heat loss reduction due to thermal insulator and thermal interface resistance due to multi-layer structure in order to improve the efficiency of a thermoelectric device, a thermoelectric concrete brick was fabricated using a unileg n-type CaMnO<inf>3</inf> thermoelectric module inside. CaMnO<inf>3</inf> thermoelectric materials were synthesized by starting materials CaCO<inf>3</inf> and MnO<inf>2</inf> to produce a unileg n-type CaMnO<inf>3</inf> module. Thermoelectric concrete brick consisted of two types: I-layer brick (one layer of concrete thermal insulator) and III-layer brick (three layers of different concrete insulators). The occurring temperature difference, electric current and voltage on the CaMnO<inf>3</inf> module and thermoelectric concrete brick were measured in closed and open circuits. The temperature difference, thermal distribution, and output voltage when applying constant temperatures of 100, 200 and 400 °C were measured. Computer simulations of the Finite Element Method (FEM) were performed to compare with the experimental results. The trends of the temperature difference and the output voltage from the experimental and computer simulations were in good agreement. The results of the temperature difference during the hotter side temperature of 200 °C exhibited the temperature difference along the vertical direction of the thermoelectric concrete bricks for both types of the III-layer brick of 172 °C and the I-layer brick of 132 °C are larger than that of the CaMnO<inf>3</inf> TEG module without using a thermal concrete insulator of 108 °C. The thermoelectric concrete bricks of the III-layer brick type of 27.70 mV displayed output voltage results being higher than those of the I-layer brick of 26.57 mV and the CaMnO<inf>3</inf> TEG module without using a thermal concrete insulator of 24.35 mV. Thermoelectric concrete brick of the III-layer brick type displayed higher electric generation power than the I-layer brick and the CaMnO<inf>3</inf> TEG module. Additionally, the results exhibited the capability of thermoelectric concrete brick in the III-layer brick model for electric generation power based on the temperature difference. The TEG concrete brick of I-layer concrete covering the series–parallel combination circuit of 120 modules of the unileg n-type CaMnO<inf>3</inf> was constructed and then embedded on the outer surface of the furnace. During the maximum hotter side temperature of 580 °C of the concrete brick, the temperature difference between the hotter side and the cooler side of the brick occurred at 365 °C and the maximum output voltage was obtained at 581.7 mV.
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Preface
(2021-09-20)
Thammavintorn, Preecha
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Limkaisang, Viroj
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Charoenprakdee, Anek
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Seetawan, Tosawat
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Kimura, Kaoru
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Effect of free oxygen radical anions and free electrons in a Ca12Al14O33 cement structure on its optical, electronic and antibacterial properties
(2019-05-01)
Phrompet, Chaiwat
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Sriwong, Chaval
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Srepusharawoot, Pornjuk
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Maensiri, Santi
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Chindaprasirt, Prinya
The aim of this work was to investigate the effect of free oxygen radicals and free electrons in a Ca<inf>12</inf>Al<inf>14</inf>O<inf>33</inf> (C12A7) cement structure on the optical, electronic and antibacterial activity of this material. Ca<inf>12</inf>Al<inf>14</inf>O<inf>33</inf> was successfully fabricated via rapid heating to high temperatures by high frequency electromagnetic induction. Ca<inf>12</inf>Al<inf>14</inf>O<inf>33</inf> cement samples were characterized using XRD and UV-Vis-DRS spectroscopy. The morphology and chemical composition of the samples were also investigated using SEM and EDS techniques. The presence of free oxygen radicals (O<inf>2</inf> −ions) in the insulating structure of Ca<inf>12</inf>Al<inf>14</inf>O<inf>33</inf> was confirmed using Raman spectroscopy showing a spectrum peak at 1067 cm−1. The excitation of free electrons in the Ca<inf>12</inf>Al<inf>14</inf>O<inf>33</inf> cement was indicated by UV-Vis absorption spectra at 2.8 eV and an optical energy gap of 3.5 eV, which is consistent with the first-principles calculations for the band energy level. The effects of free oxygen radicals and free electrons in the Ca<inf>12</inf>Al<inf>14</inf>O<inf>33</inf> structure as antibacterial agents against Escherichia Coli (E. coli) and Staphylococcus Aureus (S. aureus) were investigated using an agar disk-diffusion method. The presence of O<inf>2</inf> − anions as a reactive oxygen species (ROS) at the surface of Ca<inf>12</inf>Al<inf>14</inf>O<inf>33</inf> caused inhibition of E. coli and S. aureus cells. The free electrons in the conducting C12A7 reacted with O<inf>2</inf> gas to produce ROS, specifically super oxides (O<inf>2</inf> −), superoxide radicals (O<inf>2</inf> •-), hydroxyl radicals (OH•) and hydrogen peroxide (H<inf>2</inf>O<inf>2</inf>), which exhibited antibacterial properties. Both mechanisms were active against bacteria without effects from nano-particle sized materials and photocatalytic activity. The experimental results showed that the production of ROS from free electrons was greater than that of the free O<inf>2</inf> − anions in the structure of Ca<inf>12</inf>Al<inf>14</inf>O<inf>33</inf>. The antibacterial actions for insulating and conducting Ca<inf>12</inf>Al<inf>14</inf>O<inf>33</inf> were different for E. coli and S. aureus. Thus, Ca<inf>12</inf>Al<inf>14</inf>O<inf>33</inf> cement has antibacterial properties that do not require the presence of nano-particle sizes materials or photocatalysis.
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Disentangling small-polaron and Anderson-localization effects in ceria: Combined experimental and first-principles study
(2019-01-23)
Kolodiazhnyi, Taras
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Tipsawat, Pannawit
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Charoonsuk, Thitirat
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Kongnok, Thanundon
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Jungthawan, Sirichok
By comparison of the electrical conductivity of ceria doped with penta- and hexavalent ions, we separate the total electron localization energy into the two contributions originating from the small polaron effects and the Coulomb interaction with the donor ions. The upper bound of the itinerant small polaron hopping energy is estimated at 66±20 meV. The binding energy of the Ce3+-M5+/6+ defect complex increases from 121 meV for M=Nb5+/Ta5+ to 243 meV for M=W6+/U6+. The first-principles simulations are in qualitative agreement with the experimental findings. At low temperatures the f electrons bound to the donor defects show dielectric relaxation with the lowest activation energy of 2.7 and 17 meV for Nb(Ta)- and W-doped ceria, respectively. Remarkably, these energies are significantly smaller than the hopping energy of the itinerant small polarons. While both the electron-lattice and the electron-defect interactions cause the f electron localization in real-case ceria, the latter effects seem to be the dominant.

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