Journal of Electroanalytical Chemistry最新文献

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Preparation of mesoporous hard carbon anode materials by nitrogen doping of biomass to enhance the specific capacity of sodium ion adsorption 生物质氮掺杂制备中孔硬碳负极材料,提高钠离子吸附比容量
IF 4.1 3区 化学
Journal of Electroanalytical Chemistry Pub Date : 2025-05-15 DOI: 10.1016/j.jelechem.2025.119190
Wei Meng, Yinyi Gao, Kai Zhu, Dianxue Cao
{"title":"Preparation of mesoporous hard carbon anode materials by nitrogen doping of biomass to enhance the specific capacity of sodium ion adsorption","authors":"Wei Meng,&nbsp;Yinyi Gao,&nbsp;Kai Zhu,&nbsp;Dianxue Cao","doi":"10.1016/j.jelechem.2025.119190","DOIUrl":"10.1016/j.jelechem.2025.119190","url":null,"abstract":"<div><div>This study synthesized a hard carbon anode material (HC-N1300) with hierarchical micro/mesoporous structure through biomass-derived nitrogen doping, aiming to explore its application in sodium-ion batteries (SIB). Structural characterization reveals that HC-N1300 possesses well-developed micro/mesopores, which significantly shorten the diffusion pathways for sodium ions (Na<sup>+</sup>). Compositional analysis further demonstrates an increased ratio of pyridinic-N to pyrrolic-N configurations, providing abundant electrochemically active sites. These synergistic structural and compositional advantages collectively enhance the adsorption capability in the slope region. In half-cell evaluations, the HC-N1300 delivered an initial discharge capacity of 486 mAh g<sup>−1</sup> at 0.1 A g<sup>−1</sup> with a reversible capacity of 330 mAh g<sup>−1</sup>. Remarkably, it maintained 88.5 % capacity retention after 1000 cycles at 0.5 A g<sup>−1</sup>. Mechanistic analysis revealed that nitrogen doping plays a crucial role in pore formation during carbonization. The hierarchical porous architecture not only increases active sites but also facilitates rapid Na<sup>+</sup> diffusion, thereby effectively improving both plateau capacity and rate capability. This work provides valuable insights for designing high-performance anode materials for SIB.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"991 ","pages":"Article 119190"},"PeriodicalIF":4.1,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144083815","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Amorphous-adjustable fluorinated Ni-based MOFs for enhanced alkaline oxygen evolution 用于增强碱性析氧的非晶可调氟化镍基mof
IF 4.1 3区 化学
Journal of Electroanalytical Chemistry Pub Date : 2025-05-15 DOI: 10.1016/j.jelechem.2025.119202
Honghao Zhong, Mohan Luo, Luping Wu, Ke Yang, Ruishi Xie, Yuanli Li
{"title":"Amorphous-adjustable fluorinated Ni-based MOFs for enhanced alkaline oxygen evolution","authors":"Honghao Zhong,&nbsp;Mohan Luo,&nbsp;Luping Wu,&nbsp;Ke Yang,&nbsp;Ruishi Xie,&nbsp;Yuanli Li","doi":"10.1016/j.jelechem.2025.119202","DOIUrl":"10.1016/j.jelechem.2025.119202","url":null,"abstract":"<div><div>Crystalline-amorphous hybrid materials possess the benefits of both crystalline and amorphous phases. Nevertheless, the successful incorporation of amorphous structural units into ordered crystalline materials and the exact regulation of interface electrical effects continue to pose a considerable challenge. Herein, we successfully incorporate disordered amorphous structural units onto ordered Ni-based MOFs to enhance the performance of alkaline oxygen evolution reaction by simply adjusting the proportion of organic ligands. The obtained series of fluorinated Ni-based MOFs (<em>x</em>F-N-MOFs, <em>x</em> = 0, 1/8, 1/2, and 1/4) exhibits adjustable amorphous units from 65.89 % to 82.1 %. XPS fine analysis reveals that its electrons are enriched on the crystalline-amorphous interface of Ni-based MOFs, resulting in regulating the kinetics of reaction intermediates and achieving higher electron storage. Accordingly, the optimized 1/8F-Ni-MOF exhibited a remarkably low overpotential of 291 mV at 100 mA·cm<sup>−2</sup>, which was 115 mV lower than that of Ni-MOF nanosheets. This work provides valuable insights into comprehending the influence of interactions between crystalline and amorphous states on electrocatalyst performance.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"991 ","pages":"Article 119202"},"PeriodicalIF":4.1,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144072241","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Electrochemical detection of lead, cadmium, and mercury with selective preconcentration on ligand-modified electrodes 在配体修饰电极上选择性富集铅、镉和汞的电化学检测
IF 4.1 3区 化学
Journal of Electroanalytical Chemistry Pub Date : 2025-05-15 DOI: 10.1016/j.jelechem.2025.119189
Gaël Levanen , Florence Razan , Sara Bretin , Stéphanie Betelu , Karine Michel , Florence Geneste
{"title":"Electrochemical detection of lead, cadmium, and mercury with selective preconcentration on ligand-modified electrodes","authors":"Gaël Levanen ,&nbsp;Florence Razan ,&nbsp;Sara Bretin ,&nbsp;Stéphanie Betelu ,&nbsp;Karine Michel ,&nbsp;Florence Geneste","doi":"10.1016/j.jelechem.2025.119189","DOIUrl":"10.1016/j.jelechem.2025.119189","url":null,"abstract":"<div><div>Detecting Metallic Trace Elements (MTEs), especially toxic ones like cadmium, lead, and mercury, remains a key research focus. While methods using aptamers, molecularly imprinted polymers (MIPs), and metal-organic frameworks (MOFs) are gaining attention, electrochemical sensors with organic ligands remain widely studied due to their simple preparation, durability, and reusability. Metal-selective ligands are also increasingly integrated with MOFs and MIPs for enhanced performance. This review examines recent advancements in electrochemical sensors based on metal-ligand complexation over the past seven years, with a focus on ligand design role in sensor efficiency. The first part addresses generic ligands and strategies for achieving sensor selectivity and sensitivity. The subsequent sections review the literature on specific sensors designed for cadmium, lead, and mercury detection. Special consideration is given to sensor stability and repeatability, key parameters for practical applications. The discussion also covers sensor performance in real samples and interference studies, highlighting their relevance for environmental monitoring.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"991 ","pages":"Article 119189"},"PeriodicalIF":4.1,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144123184","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An insight into synergistic effects of In2O3 and ZnO nanoparticles co-deposited on TiO2 nanotubes for a photoanode with enhanced photoelectrochemical performance 在TiO2纳米管上共沉积In2O3和ZnO纳米粒子的协同效应,以增强光电电化学性能
IF 4.1 3区 化学
Journal of Electroanalytical Chemistry Pub Date : 2025-05-14 DOI: 10.1016/j.jelechem.2025.119186
Mina Ebrahimi , Abbas Bahrami , Masoud Atapour , Mohamad Mohsen Momeni , Mahsa Ebrahimi
{"title":"An insight into synergistic effects of In2O3 and ZnO nanoparticles co-deposited on TiO2 nanotubes for a photoanode with enhanced photoelectrochemical performance","authors":"Mina Ebrahimi ,&nbsp;Abbas Bahrami ,&nbsp;Masoud Atapour ,&nbsp;Mohamad Mohsen Momeni ,&nbsp;Mahsa Ebrahimi","doi":"10.1016/j.jelechem.2025.119186","DOIUrl":"10.1016/j.jelechem.2025.119186","url":null,"abstract":"<div><div>In this work, titanium dioxide nanotubes (TNTs) were successfully synthesized through a simple one-step electrochemical anodization process. To enhance their functionality, zinc oxide and indium oxide nanoparticles were subsequently deposited onto the TNTs using a chemical bath deposition (CBD) method. This approach aimed to develop advanced TNT-based photoanodes and evaluate their potential in providing photoelectrochemical cathodic protection (PEC) for AISI 304 stainless steel (304SS). A combination of analytical techniques—including FE-SEM, EDS, TEM, XRD, XPS, and UV–vis DRS—was employed to examine the structural and optical properties of the prepared photoanodes. Their PEC performance was tested in a 3.5 wt% NaCl solution under both light and dark conditions. The results showed that heterojunction formation among ZnO, In<sub>2</sub>O<sub>3</sub>, and TiO<sub>2</sub> greatly enhanced light absorption and facilitated efficient charge separation. When exposed to light, the potential of 304SS coupled with the optimized photoanode shifted to values more negative than its corrosion potential (approximately −780 mV), indicating effective cathodic protection. The cathodic protection effect persisted even after the light source was turned off, demonstrating durable photoinduced charge storage behavior. The findings demonstrate the significant potential of the modified TNT photoanodes for effective corrosion prevention and highlight the essential influence of CBD conditions on enhancing their electrochemical performance.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"989 ","pages":"Article 119186"},"PeriodicalIF":4.1,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144105520","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Wood-derived cobalt nickel phosphide electrocatalyst as self-supporting electrodes for efficient overall water splitting 木材衍生的磷化钴镍电催化剂作为高效整体水分解的自支撑电极
IF 4.1 3区 化学
Journal of Electroanalytical Chemistry Pub Date : 2025-05-13 DOI: 10.1016/j.jelechem.2025.119198
Zhihui Peng , Tingzhen Li , Yuling Luo, Jiaojiao Ma, Zehong Chen, Wu Yang, Chuanfu Liu, Xinwen Peng
{"title":"Wood-derived cobalt nickel phosphide electrocatalyst as self-supporting electrodes for efficient overall water splitting","authors":"Zhihui Peng ,&nbsp;Tingzhen Li ,&nbsp;Yuling Luo,&nbsp;Jiaojiao Ma,&nbsp;Zehong Chen,&nbsp;Wu Yang,&nbsp;Chuanfu Liu,&nbsp;Xinwen Peng","doi":"10.1016/j.jelechem.2025.119198","DOIUrl":"10.1016/j.jelechem.2025.119198","url":null,"abstract":"<div><div>Biomass-based transition metal carbon catalysts have gained significant attention in water splitting due to their ability to enhance the electrocatalytic activity and chemical stability of the hydrogen evolution reaction (HER). However, designing and optimizing these catalysts as self-supporting electrodes remains a significant challenge. Herein, we developed a wood-derived cobalt‑nickel phosphide electrocatalyst as a self-supporting electrode by pretreating wood chips with gluconic acid-based proton ionic liquids (GILs), followed by carbonization, electrodeposition, and phosphating. The self-supporting electrodes with a stable three-dimensional nanosheet structure exhibited superior HER performance, achieving a low overpotential of 107.62 mV at 10 mA cm<sup>−2</sup> and small Tafel slope of 79.52 mV dec<sup>−1</sup> in alkaline solution. Furthermore, the assembled two-electrode electrolyzer exhibited a water splitting voltage of only 1.66 V at the current density of 10 mA cm<sup>−2</sup>. More importantly, the synergistic effect of phosphating bimetals significantly boosted electrocatalytic activity, leading to remarkable water splitting performance. This work introduces a novel approach for developing GILs, as well as providing a potential avenue for wood in the direction of self-supporting catalytic electrode.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"991 ","pages":"Article 119198"},"PeriodicalIF":4.1,"publicationDate":"2025-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143947407","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Investigating enhanced OER activity through novel MnMoSe2/ppy composite material in alkaline medium
IF 4.1 3区 化学
Journal of Electroanalytical Chemistry Pub Date : 2025-05-12 DOI: 10.1016/j.jelechem.2025.119173
Amisha Soni, Sarvatej Kumar Maurya, Manisha Malviya, Dhanesh Tiwary
{"title":"Investigating enhanced OER activity through novel MnMoSe2/ppy composite material in alkaline medium","authors":"Amisha Soni,&nbsp;Sarvatej Kumar Maurya,&nbsp;Manisha Malviya,&nbsp;Dhanesh Tiwary","doi":"10.1016/j.jelechem.2025.119173","DOIUrl":"10.1016/j.jelechem.2025.119173","url":null,"abstract":"<div><div>The development of reliable and economically viable functional catalysts for alkaline water oxidation is crucial for progressing electrocatalytic water splitting technologies. This article outlines a novel strategy utilizing a distinctive heterostructure catalyst, carefully crafted to improve efficiency in OER. Through a sophisticated hydrothermal synthesis method followed by solid state grinding, we have synthesized a novel MnMoSe<sub>2</sub>/ppy material showcasing enhanced electrocatalytic properties and numerous active sites, which effectively reduces overpotential. The morphological and crystal structure of the MnMoSe<sub>2</sub>/ppy catalyst was determined utilizing HR-TEM, FE-SEM, and PXRD. The outcomes indicate that the MnMoSe<sub>2</sub>/ppy composite demonstrates exceptional catalytic performance, starting OER at a notably lesser overpotential (η<sub>10</sub>) of 205 mV (vs. RHE), accompanied by a lower Tafel slope which is found to be 70 mV dec<sup>−1</sup>. The <em>operando</em> UV–Vis spectro-electrochemical analysis sheds light on the active intermediate species that participate in the OER, offering important insights into the catalytic mechanism. This study presents a novel high-performance catalyst and marks a considerable progression in renewable energy technology development, providing a viable solution for sustainable energy applications.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"991 ","pages":"Article 119173"},"PeriodicalIF":4.1,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143941598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Electrochemical hydrogen evolution reaction enhanced by dynamic bubble-template synthesized CoP/NiCu/Cu catalysts 动态气泡模板合成CoP/NiCu/Cu催化剂促进电化学析氢反应
IF 4.1 3区 化学
Journal of Electroanalytical Chemistry Pub Date : 2025-05-10 DOI: 10.1016/j.jelechem.2025.119188
Sina Mohammadi , Ali Ghaffarinejad , Mohammad Ali Ghaffarirad
{"title":"Electrochemical hydrogen evolution reaction enhanced by dynamic bubble-template synthesized CoP/NiCu/Cu catalysts","authors":"Sina Mohammadi ,&nbsp;Ali Ghaffarinejad ,&nbsp;Mohammad Ali Ghaffarirad","doi":"10.1016/j.jelechem.2025.119188","DOIUrl":"10.1016/j.jelechem.2025.119188","url":null,"abstract":"<div><div>In this research, a new CoP/NiCu composite was synthesized using an efficient and fast two-step electrodeposition method and employed as an advanced electrocatalyst for the hydrogen evolution reaction (HER). Initially, a cedar-leaf-like NiCu structure was fabricated on a copper sheet substrate, followed by the electrodeposition of CoP nanosheets onto the NiCu layer, forming a hierarchical heterostructure. Optimization of deposition potential (−1.2 V) and duration (1800 s) led to an electrode with significant catalytic properties, porosity, and enhanced wettability. The optimized CoP/NiCu/Cu electrode demonstrated excellent performance for HER in 1 M of NaOH with the overpotential of −228 mV and − 64 mV at current densities of −100 and − 10 mA. cm<sup>−2</sup>, respectively. Stability tests under industrial-scale conditions confirmed the electrode's robustness over 12 h of operation. The synergistic integration of NiCu and CoP layers enhanced electron transfer, increased active site exposure, and improved catalytic efficiency, positioning the CoP/NiCu/Cu electrode as a promising candidate for practical hydrogen production applications.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"991 ","pages":"Article 119188"},"PeriodicalIF":4.1,"publicationDate":"2025-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143947405","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Phase-engineered molybdenum carbide embedded in nitrogen-doped carbon nanofiber composites for enhanced hydrogen evolution 相工程碳化钼嵌入氮掺杂碳纳米纤维复合材料中以增强析氢
IF 4.1 3区 化学
Journal of Electroanalytical Chemistry Pub Date : 2025-05-09 DOI: 10.1016/j.jelechem.2025.119187
Sejin Park , Jae Young Kim , Duck Hyun Youn
{"title":"Phase-engineered molybdenum carbide embedded in nitrogen-doped carbon nanofiber composites for enhanced hydrogen evolution","authors":"Sejin Park ,&nbsp;Jae Young Kim ,&nbsp;Duck Hyun Youn","doi":"10.1016/j.jelechem.2025.119187","DOIUrl":"10.1016/j.jelechem.2025.119187","url":null,"abstract":"<div><div>Herein, heterostructured Mo<sub>2</sub>C-MoC nanoparticles embedded in nitrogen-doped carbon nanofibers (Mo<sub>2</sub>C-MoC/NCNF) were synthesized via a facile electrospinning and annealing process. This method enables the straightforward fabrication of one-dimensional catalysts while allowing phase control of molybdenum carbide by simply adjusting the annealing temperature. The resulting Mo<sub>2</sub>C-MoC/NCNF exhibits excellent HER performance in 1 M KOH, with low overpotentials of 106.8 and 169.1 mV at current densities of 10 and 50 mA cm<sup>−2</sup>, respectively, along with outstanding stability over 24 h. The enhanced HER activity is attributed to the synergistic effect between the heterostructured Mo<sub>2</sub>C-MoC, which serves as an active site by modulating hydrogen binding energy, and the NCNF, which provides a large surface area and high electrical conductivity.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"990 ","pages":"Article 119187"},"PeriodicalIF":4.1,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143937485","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Research progress on metallic Ni-based catalysts for electrolytic oxygen evolution reaction 金属镍基电解析氧催化剂的研究进展
IF 4.1 3区 化学
Journal of Electroanalytical Chemistry Pub Date : 2025-05-08 DOI: 10.1016/j.jelechem.2025.119174
Qi Yu , Zhexiu Liu , Jiefei Li , Yaoyao Zhang
{"title":"Research progress on metallic Ni-based catalysts for electrolytic oxygen evolution reaction","authors":"Qi Yu ,&nbsp;Zhexiu Liu ,&nbsp;Jiefei Li ,&nbsp;Yaoyao Zhang","doi":"10.1016/j.jelechem.2025.119174","DOIUrl":"10.1016/j.jelechem.2025.119174","url":null,"abstract":"<div><div>As a pivotal renewable energy carrier, hydrogen has emerged as a clean and sustainable alternative to fossil fuels, offering significant potential for industrial development, agricultural modernization, and daily life applications. Among various hydrogen production technologies, proton exchange membrane (PEM) water electrolysis stands out as one of the most promising approaches for green hydrogen generation. However, the practical implementation of this technology faces substantial challenges due to the inherently sluggish kinetics of the anodic oxygen evolution reaction (OER), resulting in compromised hydrogen production efficiency and accelerated catalyst degradation. These limitations highlight the urgent need to develop cost-effective OER electrocatalysts with enhanced activity and long-term durability. This review first introduces the two reaction pathways of OER mechanisms: the conventional adsorbate evolution mechanism (AEM) and the lattice oxygen-mediated mechanism (LOM). It then summarizes and discusses recent advances in non-precious metal Ni-based electrocatalysts for the OER, which have demonstrated remarkable potential for practical applications. We comprehensively analyze various strategies for catalyst optimization, including morphological control, heterostructure, alloying, heteroatom doping, composite strategies, single-atom catalyst engineering, and other strategies. Finally, we present a forward-looking perspective on the challenges and opportunities in developing next-generation Ni-based OER electrocatalysts.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"991 ","pages":"Article 119174"},"PeriodicalIF":4.1,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143947406","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Oxalic acid enhanced nano zero-valent iron for Electrocatalytic nitrate reduction to Ammonia 草酸增强纳米零价铁电催化硝酸还原制氨研究
IF 4.1 3区 化学
Journal of Electroanalytical Chemistry Pub Date : 2025-05-08 DOI: 10.1016/j.jelechem.2025.119185
Pengfei Xu , Sisi Han , Fengjiao Quan , Xiufan Liu , Wenjuan Shen , Yuhao Li , Jianfen Li , Yun He , Kebing Song
{"title":"Oxalic acid enhanced nano zero-valent iron for Electrocatalytic nitrate reduction to Ammonia","authors":"Pengfei Xu ,&nbsp;Sisi Han ,&nbsp;Fengjiao Quan ,&nbsp;Xiufan Liu ,&nbsp;Wenjuan Shen ,&nbsp;Yuhao Li ,&nbsp;Jianfen Li ,&nbsp;Yun He ,&nbsp;Kebing Song","doi":"10.1016/j.jelechem.2025.119185","DOIUrl":"10.1016/j.jelechem.2025.119185","url":null,"abstract":"<div><div>Ammonia (NH<sub>3</sub>), a widely used chemical product, has various applications in numerous fields. However, the high energy consumption of the traditional ammonia synthesis process is inconsistent with the pursuit of “zero carbon,” and there is an urgent need for a new method to synthesize NH<sub>3</sub>. The electrocatalytic NO<sub>3</sub><sup>−</sup>-to-NH<sub>3</sub> (NITRR) offers an ideal route to synthesizing NH<sub>3</sub> under ambient conditions. Nano zero-valent iron (nZVI) has been widely used in nitrate wastewater treatment due to its environmental friendliness, low cost, and high activity. However, nZVI is difficult to recover and prone to deactivation because of its tendency to corrode and agglomerate. Here, we report a method to enhance the activity and stability of nZVI through oxalic acid modification. In this study, oxalic acid and citric acid modified nZVI on foam nickel substrates (OA-nZVI/NF) was examined as examples. Experiments confirmed that the Faraday efficiency of NH<sub>3</sub> (FE<sub>NH3</sub>) from OA-nZVI/NF was 84.9 %, respectively, at −0.4 V vs. RHE, which was significantly higher than that of nZVI/NF (64.5 %). More importantly, the FE<sub>NH3</sub> of OA-nZVI/NF electrod did not decrease significantly after continuous electrolysis for 100 h. Subsequently, electrochemical characterization and control experiments revealed that oxalic acid modification reduced the corrosion potential of nZVI/NF and promoted the generation of hydrogen-free radicals (H*) from nZVI/NF. This work provides an economical and feasible approach to improving the stability and activity of corrosion-prone and deactivated materials.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"990 ","pages":"Article 119185"},"PeriodicalIF":4.1,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143937486","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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