首页 > 最新文献

International Journal of Electrochemical Science最新文献

英文 中文
Advances in graphene-assisted flexible substrate sensors for human motion monitoring 用于人体运动监测的石墨烯辅助柔性基底传感器的研究进展
IF 1.3 4区 化学 Q4 ELECTROCHEMISTRY Pub Date : 2024-08-13 DOI: 10.1016/j.ijoes.2024.100760

Graphene, a two-dimensional nanomaterial with exceptional properties, has emerged as a promising candidate for the development of flexible substrate sensors for human motion monitoring. This review comprehensively explores the recent advances in graphene-based sensors, focusing on their fabrication techniques, sensing mechanisms, and applications in detecting various physical and physiological parameters. The unique electrical, mechanical, and chemical properties of graphene, such as high carrier mobility, excellent mechanical strength, and large surface area, are discussed in detail. The review delves into the different synthesis methods of graphene and graphene oxide, as well as the techniques for integrating them onto flexible substrates. Graphene-based strain and pressure sensors, which exploit the piezoresistive and piezoelectric properties of graphene, are extensively examined, along with strategies for enhancing their sensitivity and performance. The application of these sensors in monitoring joint movements, respiration, and cardiovascular parameters is highlighted. Additionally, the review explores the potential of graphene-based electrochemical sensors for detecting electrophysiological signals and biochemical analytes, such as glucose and lactate. Finally, the challenges and future directions in the field of graphene-based flexible substrate sensors are discussed, emphasizing the need for further research to address issues related to scalability, reproducibility, and integration with wireless electronics.

石墨烯是一种具有特殊性能的二维纳米材料,是开发用于人体运动监测的柔性基底传感器的理想候选材料。本综述全面探讨了石墨烯基传感器的最新进展,重点关注其制造技术、传感机制以及在检测各种物理和生理参数方面的应用。文中详细讨论了石墨烯独特的电气、机械和化学特性,如高载流子迁移率、优异的机械强度和大表面积。综述深入探讨了石墨烯和氧化石墨烯的不同合成方法,以及将它们集成到柔性基底上的技术。利用石墨烯的压阻和压电特性,广泛研究了基于石墨烯的应变和压力传感器,以及提高其灵敏度和性能的策略。重点介绍了这些传感器在监测关节运动、呼吸和心血管参数方面的应用。此外,综述还探讨了基于石墨烯的电化学传感器在检测电生理信号和生化分析物(如葡萄糖和乳酸盐)方面的潜力。最后,讨论了基于石墨烯的柔性基底传感器领域所面临的挑战和未来发展方向,强调了进一步研究解决可扩展性、可重复性以及与无线电子设备集成等相关问题的必要性。
{"title":"Advances in graphene-assisted flexible substrate sensors for human motion monitoring","authors":"","doi":"10.1016/j.ijoes.2024.100760","DOIUrl":"10.1016/j.ijoes.2024.100760","url":null,"abstract":"<div><p>Graphene, a two-dimensional nanomaterial with exceptional properties, has emerged as a promising candidate for the development of flexible substrate sensors for human motion monitoring. This review comprehensively explores the recent advances in graphene-based sensors, focusing on their fabrication techniques, sensing mechanisms, and applications in detecting various physical and physiological parameters. The unique electrical, mechanical, and chemical properties of graphene, such as high carrier mobility, excellent mechanical strength, and large surface area, are discussed in detail. The review delves into the different synthesis methods of graphene and graphene oxide, as well as the techniques for integrating them onto flexible substrates. Graphene-based strain and pressure sensors, which exploit the piezoresistive and piezoelectric properties of graphene, are extensively examined, along with strategies for enhancing their sensitivity and performance. The application of these sensors in monitoring joint movements, respiration, and cardiovascular parameters is highlighted. Additionally, the review explores the potential of graphene-based electrochemical sensors for detecting electrophysiological signals and biochemical analytes, such as glucose and lactate. Finally, the challenges and future directions in the field of graphene-based flexible substrate sensors are discussed, emphasizing the need for further research to address issues related to scalability, reproducibility, and integration with wireless electronics.</p></div>","PeriodicalId":13872,"journal":{"name":"International Journal of Electrochemical Science","volume":null,"pages":null},"PeriodicalIF":1.3,"publicationDate":"2024-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1452398124003018/pdfft?md5=3b071a339ca2d410156ebcfb0b567fb9&pid=1-s2.0-S1452398124003018-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141998288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Electrodeposition strategies for synthetic highly dispersed Ru-decorated Co(OH)2 nanoneedles as advanced hydrogen evolution reaction catalysts 作为先进氢进化反应催化剂的高分散 Ru 装饰 Co(OH)2 纳米针的合成电沉积策略
IF 1.3 4区 化学 Q4 ELECTROCHEMISTRY Pub Date : 2024-08-12 DOI: 10.1016/j.ijoes.2024.100758

Ru-based nanomaterials have a lot of potential as electrochemical hydrogen evolution reaction (HER) catalysts; however, achieving a uniform dispersion of Ru nanoparticles on substrate materials remains a key challenge. To achieve this, in the current study, we formed NF/Co(OH)2/Ru by electrodepositing Ru nanoparticles onto Co(OH)2 nanoneedles. The Co and O vacancies in the sample promoted water decomposition and the cleavage of O-H bonds, while the high surface energies at the apexes of the Co(OH)2 nanoneedles supported the even growth and attachment of Ru nanoparticles. In addition, the electron-rich Ru nanoparticles aided in the desorption of hydrogen intermediates. Compared to recently published Ru-based HER materials, the NF/Co(OH)2/Ru material created in this study shown improved electrochemical characteristics, with an overpotential of 20 mV at 10 mA·cm−2 and a Tafel slope of 35.43 mV·dec−1. Therefore, this material and the findings of this study are expected to contribute to HER research.

基于 Ru 的纳米材料作为电化学氢进化反应 (HER) 催化剂具有很大的潜力;然而,如何在基底材料上实现 Ru 纳米颗粒的均匀分散仍然是一个关键挑战。为此,在本研究中,我们将 Ru 纳米粒子电沉积到 Co(OH)2 纳米针上,形成了 NF/Co(OH)2/Ru。样品中的 Co 和 O 空位促进了水的分解和 O-H 键的裂解,而 Co(OH)2 纳米针尖处的高表面能支持了 Ru 纳米粒子的均匀生长和附着。此外,富电子 Ru 纳米粒子还有助于氢中间产物的解吸。与最近发表的 Ru 基 HER 材料相比,本研究创建的 NF/Co(OH)2/Ru 材料显示出更好的电化学特性,在 10 mA-cm-2 条件下过电位为 20 mV,Tafel 斜坡为 35.43 mV-dec-1。因此,这种材料和本研究的结果有望为 HER 研究做出贡献。
{"title":"Electrodeposition strategies for synthetic highly dispersed Ru-decorated Co(OH)2 nanoneedles as advanced hydrogen evolution reaction catalysts","authors":"","doi":"10.1016/j.ijoes.2024.100758","DOIUrl":"10.1016/j.ijoes.2024.100758","url":null,"abstract":"<div><p>Ru-based nanomaterials have a lot of potential as electrochemical hydrogen evolution reaction (HER) catalysts; however, achieving a uniform dispersion of Ru nanoparticles on substrate materials remains a key challenge. To achieve this, in the current study, we formed NF/Co(OH)<sub>2</sub>/Ru by electrodepositing Ru nanoparticles onto Co(OH)<sub>2</sub> nanoneedles. The Co and O vacancies in the sample promoted water decomposition and the cleavage of O-H bonds, while the high surface energies at the apexes of the Co(OH)<sub>2</sub> nanoneedles supported the even growth and attachment of Ru nanoparticles. In addition, the electron-rich Ru nanoparticles aided in the desorption of hydrogen intermediates. Compared to recently published Ru-based HER materials, the NF/Co(OH)<sub>2</sub>/Ru material created in this study shown improved electrochemical characteristics, with an overpotential of 20 mV at 10 mA·cm<sup>−2</sup> and a Tafel slope of 35.43 mV·dec<sup>−1</sup>. Therefore, this material and the findings of this study are expected to contribute to HER research.</p></div>","PeriodicalId":13872,"journal":{"name":"International Journal of Electrochemical Science","volume":null,"pages":null},"PeriodicalIF":1.3,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1452398124002992/pdfft?md5=04f9fe0ebe1ad9f8fa3bbca478b41ccd&pid=1-s2.0-S1452398124002992-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141979400","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Corrosion behavior and mechanism of 921 A high-strength low-alloy steel in harsh marine atmospheric environments 921 A 高强度低合金钢在恶劣海洋大气环境中的腐蚀行为和机理
IF 1.3 4区 化学 Q4 ELECTROCHEMISTRY Pub Date : 2024-08-12 DOI: 10.1016/j.ijoes.2024.100755

High-strength low-alloy 921 A steel faces significant corrosion challenges in harsh marine atmospheric conditions, threatening marine and energy industry safety. This study investigates the corrosion behavior of 921 A steel through accelerated tests in a specially developed multi-factor coupled corrosion chamber. Combining the multi-factor coupling cyclic corrosion test method with finite element numerical simulation, the long-term corrosion behavior can be accurately predicted, and the power function relationship between the corrosion rate and time of the test steel is obtained, which is expressed as C=0.2259 t–0.5182. Analysis identified α-FeOOH, Fe3O4, γ-FeOOH, Cl, and Cr in corrosion layers. First-principles calculations and XPS analysis showed Cr oxidation inhibits Cl adsorption and diffusion, highlighting the steel’s corrosion resistance. Finite element analysis and outdoor corrosion data confirmed the corrosion rate and time correlation, proving simulation reliability. This research provides crucial insights into 921 A steel’s corrosion resistance in marine environments, benefiting marine engineering.

高强度低合金 921 A 钢在恶劣的海洋大气环境条件下面临着巨大的腐蚀挑战,威胁着海洋和能源行业的安全。本研究通过在专门开发的多因素耦合腐蚀室中进行加速试验,研究 921 A 钢的腐蚀行为。将多因素耦合循环腐蚀试验方法与有限元数值模拟相结合,可以准确预测长期腐蚀行为,并得到试验钢腐蚀速率与时间之间的幂函数关系,表示为 C=0.2259 t-0.5182。分析确定了腐蚀层中的α-FeOOH、Fe3O4、γ-FeOOH、Cl-和Cr。第一性原理计算和 XPS 分析表明,铬氧化抑制了 Cl- 的吸附和扩散,突出了钢的耐腐蚀性。有限元分析和室外腐蚀数据证实了腐蚀速率和时间的相关性,证明了模拟的可靠性。这项研究为 921 A 钢在海洋环境中的耐腐蚀性提供了重要见解,对海洋工程大有裨益。
{"title":"Corrosion behavior and mechanism of 921 A high-strength low-alloy steel in harsh marine atmospheric environments","authors":"","doi":"10.1016/j.ijoes.2024.100755","DOIUrl":"10.1016/j.ijoes.2024.100755","url":null,"abstract":"<div><p>High-strength low-alloy 921 A steel faces significant corrosion challenges in harsh marine atmospheric conditions, threatening marine and energy industry safety. This study investigates the corrosion behavior of 921 A steel through accelerated tests in a specially developed multi-factor coupled corrosion chamber. Combining the multi-factor coupling cyclic corrosion test method with finite element numerical simulation, the long-term corrosion behavior can be accurately predicted, and the power function relationship between the corrosion rate and time of the test steel is obtained, which is expressed as C=0.2259 t<sup>–0.5182</sup>. Analysis identified α-FeOOH, Fe<sub>3</sub>O<sub>4</sub>, γ-FeOOH, Cl<sup>—</sup>, and Cr in corrosion layers. First-principles calculations and XPS analysis showed Cr oxidation inhibits Cl<sup>—</sup> adsorption and diffusion, highlighting the steel’s corrosion resistance. Finite element analysis and outdoor corrosion data confirmed the corrosion rate and time correlation, proving simulation reliability. This research provides crucial insights into 921 A steel’s corrosion resistance in marine environments, benefiting marine engineering.</p></div>","PeriodicalId":13872,"journal":{"name":"International Journal of Electrochemical Science","volume":null,"pages":null},"PeriodicalIF":1.3,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1452398124002967/pdfft?md5=bfacdbaf52f09a41dafbc853a8a27815&pid=1-s2.0-S1452398124002967-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141991164","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rapid electrosynthesis of low-loaded platinum nanosheet catalysts for high-performance hydrogen oxidation reactions 快速电合成用于高性能氢氧化反应的低负载铂纳米片催化剂
IF 1.3 4区 化学 Q4 ELECTROCHEMISTRY Pub Date : 2024-08-11 DOI: 10.1016/j.ijoes.2024.100757

The development of fuel cells is urgently needed, leading to increasing demand for electrodes with low catalyst loading, high utilization, and straightforward fabrication. In this work, we successfully designed and synthesized Pt nanosheet electrocatalysts grown in situ on treated carbon cloth (Pt/CC) using a simple and rapid electrodeposition technique. At a pulse peak current density of 300 mA cm−2, the catalyst exhibited impressive Pt surface coverage uniformity, ultralow Pt loading, and an ultrathin nanosheet structure, providing a large number of active sites for electrochemical reactions. With a Pt loading of only 0.02 mg cm−2, Pt/CC-300 provides an 11-fold improvement in hydrogen oxidation reaction (HOR) performance over commercial Pt/C catalysts. The electrode can be directly employed as an anode electrode without any additives or secondary treatment. This not only simplifies the production process but also paves the way for more economical and efficient fuel cell technology.

燃料电池的开发迫在眉睫,因此对催化剂负载量低、利用率高且可直接制造的电极的需求不断增加。在这项工作中,我们采用简单快速的电沉积技术,成功设计并合成了在处理过的碳布(Pt/CC)上原位生长的铂纳米片状电催化剂。在 300 mA cm-2 的脉冲峰值电流密度下,催化剂表现出令人印象深刻的铂表面覆盖均匀性、超低铂负载和超薄纳米片结构,为电化学反应提供了大量活性位点。与商用 Pt/C 催化剂相比,Pt/CC-300 的铂负载量仅为 0.02 mg cm-2,氢氧化反应(HOR)性能提高了 11 倍。该电极可直接用作阳极电极,无需任何添加剂或二次处理。这不仅简化了生产工艺,还为更经济、更高效的燃料电池技术铺平了道路。
{"title":"Rapid electrosynthesis of low-loaded platinum nanosheet catalysts for high-performance hydrogen oxidation reactions","authors":"","doi":"10.1016/j.ijoes.2024.100757","DOIUrl":"10.1016/j.ijoes.2024.100757","url":null,"abstract":"<div><p>The development of fuel cells is urgently needed, leading to increasing demand for electrodes with low catalyst loading, high utilization, and straightforward fabrication. In this work, we successfully designed and synthesized Pt nanosheet electrocatalysts grown in situ on treated carbon cloth (Pt/CC) using a simple and rapid electrodeposition technique. At a pulse peak current density of 300 mA cm<sup>−2</sup>, the catalyst exhibited impressive Pt surface coverage uniformity, ultralow Pt loading, and an ultrathin nanosheet structure, providing a large number of active sites for electrochemical reactions. With a Pt loading of only 0.02 mg cm<sup>−2</sup>, Pt/CC-300 provides an 11-fold improvement in hydrogen oxidation reaction (HOR) performance over commercial Pt/C catalysts. The electrode can be directly employed as an anode electrode without any additives or secondary treatment. This not only simplifies the production process but also paves the way for more economical and efficient fuel cell technology.</p></div>","PeriodicalId":13872,"journal":{"name":"International Journal of Electrochemical Science","volume":null,"pages":null},"PeriodicalIF":1.3,"publicationDate":"2024-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1452398124002980/pdfft?md5=6d63e312b30b96c4f221dd2c1405147d&pid=1-s2.0-S1452398124002980-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142095233","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A highly sensitive and selective electrochemical sensor based on polythiourea modified glassy carbon electrode for detecting fenitrothion in vegetables 一种基于聚硫脲修饰的玻璃碳电极的高灵敏度和选择性电化学传感器,用于检测蔬菜中的杀螟丹
IF 1.3 4区 化学 Q4 ELECTROCHEMISTRY Pub Date : 2024-08-10 DOI: 10.1016/j.ijoes.2024.100754

A sensitive and selective sensor based on a polythiourea-modified glassy carbon electrode (polythiourea/GCE) was fabricated for electrochemical determination of fenitrothion (FT). Cyclic voltammetry and impedance spectroscopy were used to characterize the electrochemical behavior of polythiourea/GCE. The chemical and structural characteristics of the modified electrode were studied with UV-V is and FTIR spectroscopy techniques. The polythiourea (GCE) demonstrated faster electron transfer kinetics, a small charge transfer resistance, and an enhanced electroactive surface area of 0.173 cm2, which was two times greater than that of the bare GCE. The electrochemical behavior of FT at polythiourea/GCE was studied using cyclic voltammetry and square wave voltammetry. The reduction of FT on the surface of the modified electrode followed an adsorption-controlled process, and interestingly, the electrode surface coverage determined from chronocoulometric measurements showed 3.3 times higher accumulation of FT than at the bare GCE. Under optimized experimental parameters, the adsorptive stripping square-wave voltammetric current signal of FT at polythiourea/GCE exhibited an excellent sensitivity of 10.05 μA μM−1, good linearity ranging from 0.05 to 10 µM and 10–50 µM, and low limits of detection and quantification of 2.1 and 7.0 nM, respectively. The selectivity of the sensor was also evaluated in the presence of several common interfering substances, such as nitrophenol, malathion, diazinon, ascorbic acid, K+, Mg2+, and Zn2+ ions, and the percent error was less than ±5 %. The practical application of the suggested electrochemical sensor for FT determination was carried out in tomato, sweet potato, and cabbage samples. The average recoveries of the spiked samples were between 94.3 % and 110 %, indicating that the developed method is accurate for FT determination.

制备了一种基于聚硫脲修饰的玻璃碳电极(聚硫脲/GCE)的灵敏且具有选择性的传感器,用于电化学测定杀螟硫磷(FT)。循环伏安法和阻抗光谱法用于表征聚硫脲/GCE 的电化学行为。利用紫外可见光谱和傅立叶变换红外光谱技术研究了改性电极的化学和结构特征。聚硫脲(GCE)表现出更快的电子转移动力学、更小的电荷转移电阻和更大的电活性表面积(0.173 cm2),是裸 GCE 的两倍。使用循环伏安法和方波伏安法研究了 FT 在聚硫脲/GCE 上的电化学行为。有趣的是,根据计时器测量法确定的电极表面覆盖率显示,FT 在修饰电极表面的还原遵循一个由吸附控制的过程,其积累量是裸 GCE 的 3.3 倍。在优化的实验参数下,聚硫脲/GCE 吸附剥离方波伏安电流信号的灵敏度高达 10.05 μA μM-1,线性范围为 0.05 至 10 µM 和 10 至 50 µM,检出限和定量限分别为 2.1 nM 和 7.0 nM。在几种常见干扰物质(如硝基酚、马拉硫磷、二嗪农、抗坏血酸、K+、Mg2+ 和 Zn2+ 离子)存在的情况下,也对传感器的选择性进行了评估,误差小于 ±5%。将所建议的电化学传感器实际应用于番茄、甘薯和卷心菜样品中的 FT 检测。加标样品的平均回收率在 94.3 % 至 110 % 之间,表明所开发的方法可以准确地测定傅立叶变换素。
{"title":"A highly sensitive and selective electrochemical sensor based on polythiourea modified glassy carbon electrode for detecting fenitrothion in vegetables","authors":"","doi":"10.1016/j.ijoes.2024.100754","DOIUrl":"10.1016/j.ijoes.2024.100754","url":null,"abstract":"<div><p>A sensitive and selective sensor based on a polythiourea-modified glassy carbon electrode (polythiourea/GCE) was fabricated for electrochemical determination of fenitrothion (FT). Cyclic voltammetry and impedance spectroscopy were used to characterize the electrochemical behavior of polythiourea/GCE. The chemical and structural characteristics of the modified electrode were studied with UV-V is and FTIR spectroscopy techniques. The polythiourea (GCE) demonstrated faster electron transfer kinetics, a small charge transfer resistance, and an enhanced electroactive surface area of 0.173 cm<sup>2</sup>, which was two times greater than that of the bare GCE. The electrochemical behavior of FT at polythiourea/GCE was studied using cyclic voltammetry and square wave voltammetry. The reduction of FT on the surface of the modified electrode followed an adsorption-controlled process, and interestingly, the electrode surface coverage determined from chronocoulometric measurements showed 3.3 times higher accumulation of FT than at the bare GCE. Under optimized experimental parameters, the adsorptive stripping square-wave voltammetric current signal of FT at polythiourea/GCE exhibited an excellent sensitivity of 10.05 μA μM<sup>−1</sup>, good linearity ranging from 0.05 to 10 µM and 10–50 µM, and low limits of detection and quantification of 2.1 and 7.0 nM, respectively. The selectivity of the sensor was also evaluated in the presence of several common interfering substances, such as nitrophenol, malathion, diazinon, ascorbic acid, K<sup>+</sup>, Mg<sup>2+,</sup> and Zn<sup>2+</sup> ions, and the percent error was less than ±5 %. The practical application of the suggested electrochemical sensor for FT determination was carried out in tomato, sweet potato, and cabbage samples. The average recoveries of the spiked samples were between 94.3 % and 110 %, indicating that the developed method is accurate for FT determination.</p></div>","PeriodicalId":13872,"journal":{"name":"International Journal of Electrochemical Science","volume":null,"pages":null},"PeriodicalIF":1.3,"publicationDate":"2024-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1452398124002955/pdfft?md5=82879936ef25bba24213d4c077496c18&pid=1-s2.0-S1452398124002955-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142040392","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Study on the synthesis mechanism of new α-FeOOH@3DGF material and its lithium storage performance 新型 α-FeOOH@3DGF 材料的合成机理及其储锂性能研究
IF 1.3 4区 化学 Q4 ELECTROCHEMISTRY Pub Date : 2024-08-10 DOI: 10.1016/j.ijoes.2024.100753

A new self-supporting material contained nanorods α-FeOOH and three-dimensional skeleton graphene foam (3D Graphene Foam, 3DGF) was prepared by hydrothermal method. The growth mechanism and phase change rules of nanorods α-FeOOH@3DGF were studied to obtain the electrochemical lithium storage performance. The results showed that growth mechanism of nanorods α-FeOOH was accompanied by the consumption of nanoparticles β-FeOOH. If the hydrothermal time reached to 12 h, the nanoparticle β-FeOOH phase completely disappeared with only rod-shaped α-FeOOH@3DGF single phase obtained. Rod-shaped α-FeOOH@3DGF was used as anode material of lithium-ion batteries and the reversible specific capacity remained at about 305 mAh·g−1 after charging and discharging 250 times at 500 mA·g−1, with significantly cycling stability compared with that of the monomaterial α-FeOOH.

采用水热法制备了一种含有纳米棒α-FeOOH和三维骨架石墨烯泡沫(3D Graphene Foam,3DGF)的新型自支撑材料。研究了纳米棒 α-FeOOH@3DGF 的生长机理和相变规律,以获得其电化学储锂性能。结果表明,纳米棒 α-FeOOH 的生长机制伴随着纳米颗粒 β-FeOOH 的消耗。水热时间达到 12 h 时,纳米颗粒 β-FeOOH 相完全消失,只得到棒状 α-FeOOH@3DGF 单相。棒状α-FeOOH@3DGF被用作锂离子电池的负极材料,在500 mA-g-1条件下充放电250次后,其可逆比容量仍保持在305 mAh-g-1左右,循环稳定性明显优于单质α-FeOOH。
{"title":"Study on the synthesis mechanism of new α-FeOOH@3DGF material and its lithium storage performance","authors":"","doi":"10.1016/j.ijoes.2024.100753","DOIUrl":"10.1016/j.ijoes.2024.100753","url":null,"abstract":"<div><p>A new self-supporting material contained nanorods α-FeOOH and three-dimensional skeleton graphene foam (3D Graphene Foam, 3DGF) was prepared by hydrothermal method. The growth mechanism and phase change rules of nanorods α-FeOOH@3DGF were studied to obtain the electrochemical lithium storage performance. The results showed that growth mechanism of nanorods α-FeOOH was accompanied by the consumption of nanoparticles β-FeOOH. If the hydrothermal time reached to 12 h, the nanoparticle β-FeOOH phase completely disappeared with only rod-shaped α-FeOOH@3DGF single phase obtained. Rod-shaped α-FeOOH@3DGF was used as anode material of lithium-ion batteries and the reversible specific capacity remained at about 305 mAh·g<sup>−1</sup> after charging and discharging 250 times at 500 mA·g<sup>−1</sup>, with significantly cycling stability compared with that of the monomaterial α-FeOOH.</p></div>","PeriodicalId":13872,"journal":{"name":"International Journal of Electrochemical Science","volume":null,"pages":null},"PeriodicalIF":1.3,"publicationDate":"2024-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1452398124002943/pdfft?md5=b929a8ce729225438a1336c9b55ad38a&pid=1-s2.0-S1452398124002943-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141998289","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Leveling mechanism of plasma electrolytic polishing of titanium alloy with aqueous fluoride-type solution 用氟化物水溶液对钛合金进行等离子电解抛光的平整机理
IF 1.3 4区 化学 Q4 ELECTROCHEMISTRY Pub Date : 2024-08-07 DOI: 10.1016/j.ijoes.2024.100749

It is vital to optimize the processing parameters and reveal the leveling mechanism of various micro-discharges for titanium alloy. In this paper, TC4 titanium alloy was polished within aqueous fluoride-type solution. The polished surface roughness can be reduced from the original Ra 1.13 μm to 0.213 μm with the voltage range of 250–300 V. The process of plasma electrolytic polishing can be divided into three different stages: conventional low voltage electrolysis, vapor gaseous envelope luminescence, and spark micro-discharge. Correspondingly, it appears different colors for the oxidized titanium alloy surface formed with different processing parameters. The mechanism of plasma electrolytic polishing is related with the formation, growth, and loosening of anodic oxides formed on titanium alloy, as well as the final ultrasonic removal of the loosened oxide debris.

优化钛合金的加工参数并揭示各种微放电的平整机理至关重要。本文在氟化水溶液中对 TC4 钛合金进行了抛光。在 250-300 V 的电压范围内,抛光表面粗糙度可从原来的 Ra 1.13 μm 降低到 0.213 μm。等离子体电解抛光过程可分为三个不同阶段:传统低压电解、蒸汽气态包络发光和火花微放电。相应地,不同加工参数下形成的氧化钛合金表面呈现出不同的颜色。等离子电解抛光的机理与钛合金上形成的阳极氧化物的形成、生长和松动以及最后超声波去除松动的氧化物碎片有关。
{"title":"Leveling mechanism of plasma electrolytic polishing of titanium alloy with aqueous fluoride-type solution","authors":"","doi":"10.1016/j.ijoes.2024.100749","DOIUrl":"10.1016/j.ijoes.2024.100749","url":null,"abstract":"<div><p>It is vital to optimize the processing parameters and reveal the leveling mechanism of various micro-discharges for titanium alloy. In this paper, TC4 titanium alloy was polished within aqueous fluoride-type solution. The polished surface roughness can be reduced from the original Ra 1.13 μm to 0.213 μm with the voltage range of 250–300 V. The process of plasma electrolytic polishing can be divided into three different stages: conventional low voltage electrolysis, vapor gaseous envelope luminescence, and spark micro-discharge. Correspondingly, it appears different colors for the oxidized titanium alloy surface formed with different processing parameters. The mechanism of plasma electrolytic polishing is related with the formation, growth, and loosening of anodic oxides formed on titanium alloy, as well as the final ultrasonic removal of the loosened oxide debris.</p></div>","PeriodicalId":13872,"journal":{"name":"International Journal of Electrochemical Science","volume":null,"pages":null},"PeriodicalIF":1.3,"publicationDate":"2024-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1452398124002906/pdfft?md5=bde17f7306cdd2ca7c1b080844617c5e&pid=1-s2.0-S1452398124002906-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141953323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pt-modified NiCo2O4/C as high-performance electrodes for supercapacitors 铂改性 NiCo2O4/C 作为超级电容器的高性能电极
IF 1.3 4区 化学 Q4 ELECTROCHEMISTRY Pub Date : 2024-08-05 DOI: 10.1016/j.ijoes.2024.100752

As a new type of efficient electrochemical energy storage system, the supercapacitor serves as an effective means to support the development of clean energy, with the electrode material being the key determinant of performance. The electrode material Pt-NiCo2O4/C was prepared in this paper by stepwise hydrothermal and calcination methods using ZIF-67 as a template, aiming to improve specific capacitance performance and stability. Pt-NiCo2O4/C achieved a specific capacitance of 1665.3 F/g at a current density of 1.0 A/g, and maintained 94.49 % of the original specific capacity after 3500 cycles at a current density of 4.0 A/g. The excellent specific capacitance performance of the Pt-NiCo2O4/C electrode material makes it a promising potential candidate for energy storage applications.

超级电容器作为一种新型高效电化学储能系统,是支持清洁能源发展的有效手段,而电极材料是决定其性能的关键因素。本文以 ZIF-67 为模板,采用分步水热法和煅烧法制备了电极材料 Pt-NiCo2O4/C,旨在提高比电容性能和稳定性。在电流密度为 1.0 A/g 时,Pt-NiCo2O4/C 的比电容达到 1665.3 F/g,在电流密度为 4.0 A/g 时,经过 3500 次循环后,比电容仍能保持 94.49%。Pt-NiCo2O4/C 电极材料优异的比电容性能使其有望成为储能应用的潜在候选材料。
{"title":"Pt-modified NiCo2O4/C as high-performance electrodes for supercapacitors","authors":"","doi":"10.1016/j.ijoes.2024.100752","DOIUrl":"10.1016/j.ijoes.2024.100752","url":null,"abstract":"<div><p>As a new type of efficient electrochemical energy storage system, the supercapacitor serves as an effective means to support the development of clean energy, with the electrode material being the key determinant of performance. The electrode material Pt-NiCo<sub>2</sub>O<sub>4</sub>/C was prepared in this paper by stepwise hydrothermal and calcination methods using ZIF-67 as a template, aiming to improve specific capacitance performance and stability. Pt-NiCo<sub>2</sub>O<sub>4</sub>/C achieved a specific capacitance of 1665.3 F/g at a current density of 1.0 A/g, and maintained 94.49 % of the original specific capacity after 3500 cycles at a current density of 4.0 A/g. The excellent specific capacitance performance of the Pt-NiCo<sub>2</sub>O<sub>4</sub>/C electrode material makes it a promising potential candidate for energy storage applications.</p></div>","PeriodicalId":13872,"journal":{"name":"International Journal of Electrochemical Science","volume":null,"pages":null},"PeriodicalIF":1.3,"publicationDate":"2024-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1452398124002931/pdfft?md5=447023cef9a64032f9151cf82e16956c&pid=1-s2.0-S1452398124002931-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141984783","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of heat treatment on electrochemical behavior of biocompatible Ti–Ta–Nb–Zr alloys prepared by selective laser melting 热处理对选择性激光熔化制备的生物相容性钛-钽-铌-锆合金电化学行为的影响
IF 1.3 4区 化学 Q4 ELECTROCHEMISTRY Pub Date : 2024-08-03 DOI: 10.1016/j.ijoes.2024.100751

In this paper, cytotoxicity-free Ti-10Ta-2 Nb-2Zr titanium alloy was prepared by selective laser melting additive manufacturing. The effect of solution and annealing heat treatment on the structure and microhardness were investigated. Electrochemical performance in Ringer’s solution at 37℃ was evaluated. This electrochemical evaluation was performed through the open circuit potential variation as the immersed time, potentiodynamic polarization curves, and electrochemical impedance spectroscopy tests. The results show that main phase composition of as-built and heat-treated specimens was the α/α′ phase. The specimen annealed at 500℃ presented a small amount of β phase. The solutionized and annealed specimens had basket-weave microstructure with distributed micro-scaled α/α′ lamellas. The microhardness of as-built specimens was 400.48 ±12.31 HV. After solution and water quenching, the microhardness dramatically increased to 533.85 ±24.67 HV. The microhardness slightly decreased to 495.46 ±4.85 and 488.8 ±13.84 HV after annealing at 300 ℃ and 500 ℃, respectively. Compared with the as-built specimen, the solutionized and annealed specimens had much lower corrosion current density and higher corrosion resistance.

本文采用选择性激光熔融快速成型技术制备了无细胞毒性的 Ti-10Ta-2 Nb-2Zr 钛合金。研究了溶液和退火热处理对其结构和显微硬度的影响。评估了在 37℃的林格氏溶液中的电化学性能。电化学评估是通过开路电位随浸泡时间的变化、电位极化曲线和电化学阻抗谱测试进行的。结果表明,坯料和热处理试样的主要相组成为 α/α′ 相。在 500℃ 下退火的试样含有少量的 β 相。固溶和退火试样的微观结构为篮织结构,分布着微尺度的α/α′层状结构。竣工试样的显微硬度为 400.48 ±12.31 HV。经过水溶液淬火后,显微硬度急剧上升至 533.85 ±24.67 HV。在 300 ℃ 和 500 ℃ 退火后,显微硬度略有下降,分别为 495.46 ±4.85 和 488.8 ±13.84 HV。与竣工试样相比,固溶和退火试样的腐蚀电流密度更低,耐腐蚀性更高。
{"title":"Effect of heat treatment on electrochemical behavior of biocompatible Ti–Ta–Nb–Zr alloys prepared by selective laser melting","authors":"","doi":"10.1016/j.ijoes.2024.100751","DOIUrl":"10.1016/j.ijoes.2024.100751","url":null,"abstract":"<div><p>In this paper, cytotoxicity-free Ti-10Ta-2 Nb-2Zr titanium alloy was prepared by selective laser melting additive manufacturing. The effect of solution and annealing heat treatment on the structure and microhardness were investigated. Electrochemical performance in Ringer’s solution at 37℃ was evaluated. This electrochemical evaluation was performed through the open circuit potential variation as the immersed time, potentiodynamic polarization curves, and electrochemical impedance spectroscopy tests. The results show that main phase composition of as-built and heat-treated specimens was the α/α′ phase. The specimen annealed at 500℃ presented a small amount of β phase. The solutionized and annealed specimens had basket-weave microstructure with distributed micro-scaled α/α′ lamellas. The microhardness of as-built specimens was 400.48 ±12.31 HV. After solution and water quenching, the microhardness dramatically increased to 533.85 ±24.67 HV. The microhardness slightly decreased to 495.46 ±4.85 and 488.8 ±13.84 HV after annealing at 300 ℃ and 500 ℃, respectively. Compared with the as-built specimen, the solutionized and annealed specimens had much lower corrosion current density and higher corrosion resistance.</p></div>","PeriodicalId":13872,"journal":{"name":"International Journal of Electrochemical Science","volume":null,"pages":null},"PeriodicalIF":1.3,"publicationDate":"2024-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S145239812400292X/pdfft?md5=b3c875431baf040a0d72f7f7840c53f1&pid=1-s2.0-S145239812400292X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141951305","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Progress in electrochemical sensing of epinephrine using carbon nanomaterials: A review 利用碳纳米材料对肾上腺素进行电化学传感的研究进展:综述
IF 1.3 4区 化学 Q4 ELECTROCHEMISTRY Pub Date : 2024-08-02 DOI: 10.1016/j.ijoes.2024.100750

This review focuses on the advancements in electrochemical sensing of epinephrine using carbon nanomaterials. Epinephrine, a vital catecholamine, plays a significant role in numerous physiological processes, including the "fight or flight" response, blood pressure regulation, and glucose metabolism. Accurate detection of epinephrine levels is crucial for diagnosing and managing various medical conditions such as anaphylaxis, cardiac arrest, and severe asthma. Carbon nanomaterials have emerged as promising candidates due to their high surface area, excellent conductivity, and biocompatibility, which enhance the sensitivity and selectivity of electrochemical sensors. The review discusses various types of carbon nanomaterials, including graphene, carbon nanotubes, and carbon nanofibers, highlighting their unique properties and applications in epinephrine sensing. It also covers the fabrication techniques of these sensors, their performance metrics, and the challenges faced in their development. This comprehensive overview aims to provide insights into the current state and future prospects of carbon nanomaterial-based electrochemical sensors for epinephrine detection, emphasizing the need for further research to overcome existing limitations and improve clinical applicability.

本综述重点介绍利用碳纳米材料对肾上腺素进行电化学传感的进展。肾上腺素是一种重要的儿茶酚胺,在许多生理过程中发挥着重要作用,包括 "战斗或逃跑 "反应、血压调节和葡萄糖代谢。准确检测肾上腺素水平对于诊断和处理过敏性休克、心脏骤停和严重哮喘等各种病症至关重要。碳纳米材料具有高比表面积、优异的导电性和生物相容性,可提高电化学传感器的灵敏度和选择性,因此已成为前景广阔的候选材料。这篇综述讨论了各种类型的碳纳米材料,包括石墨烯、碳纳米管和碳纳米纤维,重点介绍了它们的独特性能以及在肾上腺素传感中的应用。报告还介绍了这些传感器的制造技术、性能指标以及开发过程中面临的挑战。本综述旨在深入探讨基于碳纳米材料的电化学传感器在肾上腺素检测中的应用现状和未来前景,同时强调了进一步研究的必要性,以克服现有的局限性并提高临床应用性。
{"title":"Progress in electrochemical sensing of epinephrine using carbon nanomaterials: A review","authors":"","doi":"10.1016/j.ijoes.2024.100750","DOIUrl":"10.1016/j.ijoes.2024.100750","url":null,"abstract":"<div><p>This review focuses on the advancements in electrochemical sensing of epinephrine using carbon nanomaterials. Epinephrine, a vital catecholamine, plays a significant role in numerous physiological processes, including the \"fight or flight\" response, blood pressure regulation, and glucose metabolism. Accurate detection of epinephrine levels is crucial for diagnosing and managing various medical conditions such as anaphylaxis, cardiac arrest, and severe asthma. Carbon nanomaterials have emerged as promising candidates due to their high surface area, excellent conductivity, and biocompatibility, which enhance the sensitivity and selectivity of electrochemical sensors. The review discusses various types of carbon nanomaterials, including graphene, carbon nanotubes, and carbon nanofibers, highlighting their unique properties and applications in epinephrine sensing. It also covers the fabrication techniques of these sensors, their performance metrics, and the challenges faced in their development. This comprehensive overview aims to provide insights into the current state and future prospects of carbon nanomaterial-based electrochemical sensors for epinephrine detection, emphasizing the need for further research to overcome existing limitations and improve clinical applicability.</p></div>","PeriodicalId":13872,"journal":{"name":"International Journal of Electrochemical Science","volume":null,"pages":null},"PeriodicalIF":1.3,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1452398124002918/pdfft?md5=a6647a5fdcbc6c4bac223e8a558e86f5&pid=1-s2.0-S1452398124002918-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141951307","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
International Journal of Electrochemical Science
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1