고체전해질은 높은 에너지 밀도와 안전성을 갖춘 차세대 리튬이온전지에 꼭 필요한 핵심 요소다. 이러한 고체전 해질의 제작을 위해서 기존 고체전해질의 낮은 이온전도도와 높은 계면저항 문제를 해결해야 한다. 본 연구에서는 강화된 이 온 전도성과 계면 안정성을 지닌 PVDF-HFP 고분자에 분산된 Li7La3Zr2O12 (LLZO) 나노와이어 복합체를 기반으로 하는 새 로운 전해질(PVDF-HFP/LLZO/SN, PHLS membrane)을 제안한다. PHLS에 용매 열압착(Sovlent heat press, SHP)을 통해 계 면 저항과 내부 공극이 감소된 PHLS-(SHP)는 30°C에서 2.06 × 10-4 S/cm의 높은 이온 전도도, 4.5 V (vs. Li/Li+)의 넓은 전 기화학적 전위 창, 리튬 금속과 전해질 사이의 안정된 계면 안정성을 나타냈다. 0.2 mA/cm2에서 수행된 Li 대칭 셀을 사용한 전기화학적 테스트에서 150 시간 이상 안정성을 유지하는 것으로 확인되었으며, 이는 당사의 복합 기반 고체 전해질을 활용 하여 전기화학적 성능이 향상되었음을 시사한다.

Activated carbon is generally recognized as an applicable material for gas or liquid adsorption and electrochemical devices, such as electric double-layer capacitors (EDLCs). Owing to the continuous increase in its price, research aimed at discovering alternative materials and improving its fabrication yield is important. Herein, organic pigments were ingeniously employed to enhance the fabrication of high-surface-area activated carbon with remarkable efficiency. Moreover, the focus was centered on the assessment of activated carbon derived from 2,9-dimethylquinacridone, also known as CI Pigment Red 122 for its capacity to adsorb tetracycline (TC) and its applicability as an electrode material for EDLCs. Activating these organic pigments with varying potassium hydroxide ratios allowed the fabrication of activated carbon with a higher yield than that for conventional activated carbon. Furthermore, it was confirmed that activated carbon with a very high specific surface area can be efficiently fabricated, demonstrating a remarkable potential in various application fields. Notably, this activated carbon exhibited an impressive maximum specific surface area and a total pore volume of 3,935 m2/ g and 2.324 cm3/ g, respectively, showcasing its substantial surface area and distinctive porous characteristics. Additionally, the Langmuir and Freundlich isotherm models were employed to examine the TC adsorption on the activated carbon, with the Langmuir model demonstrating superior suitability than the Freundlich model. Furthermore, the electrochemical performance of an activated carbon-based electrode for EDLCs was rigorously evaluated through cyclic voltammetry. The specific capacitance exhibited a considerable increase in proportion to the expanding specific surface area of the activated carbon.

Gold nanoparticles (Au NPs) decorated carbon nanofibers (CNFs) have been prepared by an electrospinning approach and then carbonized. The prepared Au-CNFs were employed to modifying a screen printed electrode (SPE) for simultaneous determination of ascorbic acid (AA), dopamine (DA) and uric acid (UA). Au NPs are uniformly dispersed on carbon nanofibers were confirmed by the structure and morphological studies. The modified electrodes were tested in cyclic voltammetry (CV), differential pulse voltammetry (DPV) and chronoamperometry (CA) to characterize their electrochemical responses. Compared to bare SPE, the Au-CNFs/SPE had a better sensing response to AA, DA, and UA. The electrochemical oxidation signal of AA, DA and UA are well separated into three distinct peaks with peak potential separation of 280 mV, 159 mV and 439 mV between AA-DA, DA-UA and AA-UA respectively in CV studies and the corresponding peak potential separation in DPV studies are 290 mV, 166 mV and 456 mV. The Au-CNFs/SPE has a wide linear response of AA, DA and UA in DPV analysis over the range of 5–40 μM ( R2 = 0.9984), 2–16 μM ( R2 = 0.9962) and 2–16 μM ( R2 = 0.9983) with corresponding detection limits of 0.9 μM, 0.4 μM and 0.3 μM at S/N = 3, respectively. The developed modified SPE based sensor exhibits excellent reproducibility, stability, and repeatability. The excellent sensing response of Au-CNFs could reveal to a promising approach in electrochemical sensor.

In recent years, the search on fabrication of highly efficient, stable, and cost-effective alternative to Pt for the hydrogen evolution reaction (HER) has led to the development of new catalysts. In this study, we investigated the electrocatalytic HER activity of the Toray carbon substrate by creating defect sites in its graphitic layer through ultrasonication and anodization process. A series of Toray carbon substrates with active sites are prepared by modifying its surface through ultrasonication, anodization, and ultrasonication followed by anodization procedures at different time periods. The anodization process significantly enhances the surface wettability, consequently resulting in a substantial increase in proton flux at the reaction sites. As an implication, the overpotential for HER is notably reduced for the Toray carbon (TC-3U-10A), subjected to 3 min of ultrasonification followed by 10 min of anodization, which exhibits a significantly lower Tafel slope value of 60 mV/dec. Furthermore, the reactivity of the anodized surface for HER is significantly elevated, especially at higher concentrations of sulfuric acid, owing to the enhanced wettability of the substrate. The lowest Tafel slope value recorded in this study stands at 60 mV/dec underscoring the substantial improvements achieved in catalytic efficiency of the defect-rich carbon materials. These findings hold promise for the advancement of electrocatalytic applications of carbon materials and may have significant implications for various technological and industrial processes.

In this study, carbon coating was carried out by physical vapor deposition (PVD) on SiOx surfaces to investigate the effect of the deposited carbon layer on the performance of lithium-ion batteries as a function of the asphaltene content of petroleum residues. The petroleum residue was separated into asphaltene-free petroleum residue (ASF) and asphaltene-based petroleum residue (AS) containing 12.54% asphaltene by a solvent extraction method, and the components were analyzed. The deposited carbon coating layer became thinner, with the thickness decreasing from 15.4 to 8.1 nm, as the asphaltene content of the petroleum residue increased, and a highly crystalline layer was obtained. In particular, the SiOx electrode carbon-coated with AS exhibited excellent cycling performance with an initial efficiency of 85.5% and a capacity retention rate of 94.1% after 100 cycles at a current density of 1.0 C. This is because the carbon layer with enhanced crystallinity had sufficient thickness to alleviate the volume expansion of SiOx, resulting in stable SEI layer formation and enhanced structural stability. In addition, the SiOx electrode exhibited the lowest resistance with a low impedance of 23.35 Ω, attributed to the crystalline carbon layer that enhanced electrical conductivity and the mobility of Li ions. This study demonstrated that increasing the asphaltene content of petroleum residues is the simplest strategy for preparing SiOx@C anode materials with thin, crystalline carbon layers and excellent electrochemical performance with high efficiency and high rate performance.

Herein, facile room-temperature self-assembly and high-temperature pyrolysis strategy was successively conducted for in situ synthesizing novel TiO2/ TiN@N-C heterostructure by using typical sandwich-like precursors (MXene/ZIF-8). Zerodimensional (0D) TiO2, TiN and N-doped carbon nanoparticles were in situ formed and randomly anchored on the twodimensional (2D) N-doped carbon substrate surface, making TiO2/ TiN@N-C exhibit unique 0D/2D heterostructure. Relative to the extensively studied ZIF-8-derived N-doped carbon nanoparticles, TiO2/ TiN@N-C heterostructure displayed greatly boosted electrochemical active specific surface. Benefiting from the enhanced electrochemical property of TiO2/ TiN@N-C heterostructure, remarkable signal enhancement effect was achieved in terms of the oxidation of multiple hazardous substances, including clozapine, sunset yellow and benomyl. As a result, a novel electrochemical platform was constructed, the linear detection range were 10–1000 nM, 2.5–1250 nM, 10–1000 nM while the detection limits were evaluated to be 3.5 nM, 1.2 nM, 4.5 nM for clozapine, sunset yellow and benomyl, respectively. Besides, the practicability of the newly developed electrochemical method was verified by assessing the content of clozapine, sunset yellow and benomyl in real food samples.

Among the products of the electrocatalytic reduction of carbon dioxide (CO2RR), CO is currently the most valuable product for industrial applications. However, poor stability is a significant obstacle to CO2RR. Therefore, we synthesized a series of bimetallic organic framework materials containing different ratios of tungsten to copper using a hydrothermal method and used them as precursors. The precursors were then subjected to pyrolysis at 800 °C under argon gas, and the M-N bimetallic sites were formed after 2 h. Loose porous structures favorable for electrocatalytic reactions were finally obtained. The material could operate at lower reduction potentials than existing catalysts and obtained higher Faraday efficiencies than comparable catalysts. Of these, the current density of WCu-C/N (W:Cu = 3:1) could be stabilized at 7.9 mA ‧ cm-2 and the FE of CO reached 94 % at a hydrogen electrode potential of -0.6 V (V vs. RHE). The novel materials made with a two-step process helped to improve the stability and selectivity of the electrocatalytic reduction of CO2 to CO, which will help to promote the commercial application of this technology.

Pyrochemical processing and molten-salt reactors have recently garnered significant attention as they are promising options for future nuclear technologies, such as those for recycling spent nuclear fuels and the next generation of nuclear reactors. Both of these technologies require the use of high-temperature molten salt. To implement these technologies, one must understand the electrochemical behavior of fission products in molten salts, lanthanides, and actinides. In this study, a rotating-disk-electrode (RDE) measurement system for high-temperature molten salts is constructed and tested by investigating the electrochemical reactions of Sm3+ in LiCl–KCl melts. The results show that the reduction of Sm3+ presents the Levich behavior in LiCl–KCl melts. Using the RDE system, not only is the diffusion-layer thickness of Sm3+ measured in high-temperature molten salts but also various electrochemical parameters for Sm3+ in LiCl–KCl melts, including the diffusion coefficient, Tafel slope, and exchange current density, are determined.

Transition metal oxide-based materials have mainly been studied as electrodes for energy storage devices designed to meet essential energy demands. Among transition metal oxide-based materials, hydrated vanadium pentoxide (V2O5 ‧ nH2O), a vanadium oxide material, has demonstrated great electrochemical performance in the electrodes of energy storage devices. Graphene oxide (GO), a carbon-based material with high surface area and high electrical conductivity, has been added to V2O5 ‧ nH2O to compensate for its low electrical conductivity and structural instability. Here, V2O5 ‧ nH2O/GO nanobelts are manufactured with water without adding acid to ensure that the GO is uniformly dispersed, using a microwave-assisted hydrothermal synthesis. The resulting V2O5 ‧ nH2O/GO nanobelts exhibited a high specific capacitance of 206 F/g and more stable cycling performance than V2O5 ‧ nH2O without GO. The drying conditions of the carbon paper electrodes also resulted in more stable cycling performance when conducted at high vacuum and high temperature, compared with low vacuum and room temperature conditions. The improvement in electrochemical performance due to the addition of GO and the drying conditions of carbon paper electrodes indicate their great potential value as electrodes in energy storage devices.

The electrochemical properties of a CFX cathode were improved by defluorination of the surface with a N2 plasma and using a silica wafer. Compared to the N2 plasma treatment alone, when the CFX and silica were reacted together, the C-F bonds were modified and the surface was etched efficiently, so defluorination was enhanced. An electrochemical analysis confirmed that Half-cells prepared by treating CFx and silica with nitrogen plasma exhibited a capacity of about 400 mAh/g at 5C. In addition, it was confirmed that the loss of charge transfer was reduced by up to 71% compared to that for pristine CFX. As shown by a GITT analysis, when the CFx and silica were treated with N2 plasma together, the ion conductivity gradually increased due to a decrease in the ion diffusion barriers and the formation of a carbon layer. Therefore, this is a simple and effective way to improve the conductivities of CFX cathode materials with the energy of a N2 plasma and the silica-fluorine reaction.

pH plays a pivotal role in influencing various aspects of proton-coupled electron transfer (PCET) reactions in electrochemical systems. These reactions are affected by pH in terms of mass transport, electrochemical double layer (EDL) structure, and surface adsorption energy, all of which impact the overall electrochemical processes. This review article aims to provide a comprehensive understanding of the research progress made in elucidating the effects of pH on different electrochemical reactions, the hydrogen evolution reaction/hydrogen oxidation reaction (HER/HOR), oxygen reduction reaction/oxygen evolution reaction (ORR/OER), and carbon dioxide reduction reaction ( CO2RR). To embark on this endeavor, we have conducted a bibliometric analysis to clearly outline of the research trends and advancements in the field concerning the pH effects. Subsequently, we present a systematic overview of the mechanisms governing these reactions, with a special focus on pH’s influence on both the proton and electron aspects. We conclude by discussing the current challenges in this area and suggesting future research avenues that could further our understanding of pH's role in electrochemical reactions.

Flexible self-supported laser-induced graphene (LIG) electrode devices were facilely fabricated through laser ablation technique by employing commercial polyimide film as the precursor material. Compared with the widely used traditional glassy carbon electrodes, the resulted LIG electrodes displayed abundant porous structure and surface defects. Notably, the onestep yielded LIG electrode devices were endowed with large electrochemically active surface area and accelerated electron transfer ability. Benefiting from its superior electrochemical property, these unmodified LIG electrodes exhibited remarkable enhanced electrochemical oxidation reactivity toward the food additive molecule Allura Red. Based on the augmented oxidation signal of Allura Red molecules on the LIG electrodes, a novel electrochemical sensor with high sensitivity for the detection of Allura Red was successfully developed. The sensor demonstrated a linear detection range spanning from 5 nM to 1 μM and exhibited a detection limit as low as 2.5 nM. Besides, the sensitivity was calculated to be 240.62 μA μM−1 cm− 2. More importantly, the sensor manifested outstanding stability, reproducibility, and practicality, further emphasizing its potential for real-world application.

Bortezomib (BTZ) and dasatinib (DA) are two substantial anti-cancer agents with side effects on the human body. In this research, we fabricated a novel electrochemical sensor modified by CuFe2O4/ SmVO4 nanocomposite and 1-ethyl-3-methylimidazolium chloride (1E3MC) as an ionic liquid (IL) ( CuFe2O4/SmVO4/IL/CPE) for coinciding investigation of BTZ and DA for the first time. The CuFe2O4/ SmVO4 synthesized were determined and certified through field-emission scanning electron microscopy (FE-SEM), energy diffraction X-ray (EDX), and X-ray diffraction (XRD). The capability of the sensor was investigated by different electrochemical techniques such as cyclic voltammetry (CV), chronoamperometry (CHA), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS). The attained data showed that the oxidation signal of bortezomib and dasatinib promoted as an innovative electrochemical sensor. After optimization of the conditions using this sensor at pH 7.0, the oxidation signal of bortezomib and dasatinib showed to be linear with drug concentrations in the range of 0.09–90 μM and 100–500 μM with a detection limit of 5.4 nM and 7.0 μM, respectively, using differential pulse voltammetry method. The values of D and electro-transfer coefficient (α) achieved 2.5 × 10− 5 cm2 s− 1 and 0.99, respectively. The proposed electrochemical sensor exhibited acceptable selectivity and sensitivity for simultaneous detection of bortezomib and dasatinib in pharmaceutical and biological samples.