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Recent advances in TiO2 nanotube arrays-based electrocatalysts for electrochemical water splitting and CO2 reduction 二氧化钛纳米管阵列电催化剂在电化学水分解和CO2还原中的研究进展
IF 2.6 4区 化学
Ionics Pub Date : 2025-05-28 DOI: 10.1007/s11581-025-06408-9
Khaled M. AlAqad
{"title":"Recent advances in TiO2 nanotube arrays-based electrocatalysts for electrochemical water splitting and CO2 reduction","authors":"Khaled M. AlAqad","doi":"10.1007/s11581-025-06408-9","DOIUrl":"10.1007/s11581-025-06408-9","url":null,"abstract":"<div><p>Self-organized titanium oxide nanotube arrays (TNTs) have attracted considerable attention as a promising semiconductor substrate for water splitting due to their unique properties, including high electron mobility, large surface area, and strong mechanical stability. This has prompted extensive research efforts focused on the fabrication structure and enhancement of the electronic characteristics, structure modification, and applications of these one-dimensional substrates as TNT-based electrocatalysts. This review comprehensively addresses all these topics, which were not previously covered. It begins with the preparation techniques, modification strategies of TNTs, and the formation of TNT factors, elaborating on each in depth. The review also discusses the chemical and physical properties of TNTs, the fundamental principles of the electrocatalytic process using TNTs, and their application in water electrolysis and CO<sub>2</sub> reduction. The main electrocatalytic potential of TNTs, including hydrogen and oxygen gas generation, is discussed extensively, considering the reported experiments conducted in the last decade. For example, 1D TNTs supported PtOx nanoclusters were studied as a more effective electrocatalyst for the hydrogen evolution reaction, achieving an overpotential of -30 mV to produce -10 mA cm<sup>−2</sup>. Thus, the PtOx/TNTs electrocatalyst was superior to that of PtOx loaded on TiO<sub>2</sub> nanoparticles and the benchmark electrode (Pt/C). This outstanding activity can be attributed to the strong interaction between the TNTs and the Pt nanoclusters. This review aims to enhance understanding of TNT-based nanostructured materials and their potential applications as effective substrates in electrocatalytic processes. The challenges of using conductive or semiconductor support for loading the co-catalyst in the future include the need for it to be low-cost, robust, scalable, and sustainable; however, titanium oxide nanotubes (TNTs) can address all of these challenges and pave the way for long-term sustainable energy applications.</p><h3>Graphical abstract</h3>\u0000<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"6601 - 6633"},"PeriodicalIF":2.6,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145170350","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Cold start simulation study at the key material level of fuel cell 燃料电池关键材料水平冷启动仿真研究
IF 2.6 4区 化学
Ionics Pub Date : 2025-05-27 DOI: 10.1007/s11581-025-06376-0
Shaofang Lin, Jianbin Su, Lei Shi
{"title":"Cold start simulation study at the key material level of fuel cell","authors":"Shaofang Lin,&nbsp;Jianbin Su,&nbsp;Lei Shi","doi":"10.1007/s11581-025-06376-0","DOIUrl":"10.1007/s11581-025-06376-0","url":null,"abstract":"<div><p>Cold start simulation analysis is widely recognized in the industry as an efficient approach for rapidly developing cold start strategies and improving start-up performance. Currently, one-dimensional models are commonly employed to quickly investigate the thermo-hydraulic behavior of fuel cells under various start-up strategies, while three-dimensional models offer more intuitive insights into internal mass transport and phase change phenomena. However, the influence of key material properties on cold start performance remains insufficiently explored and warrants further investigation. Accordingly, this study develops a one-dimensional multiphase model to investigate how key material parameters affect fuel cell cold start performance. Results show that optimizing parameters such as the thickness and contact angle of the catalyst layer, gas diffusion layer thickness, and membrane thickness can significantly reduce ice formation and improve cold start success. Specifically, thicker gas diffusion layers enhance moisture management, while an 8-μm catalyst layer balances ice accommodation and voltage output. Higher contact angles lower freezing points, and increased membrane thickness delays freezing and boosts internal heat. These optimizations notably improve cold start performance at − 10 °C and − 15 °C.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"7105 - 7123"},"PeriodicalIF":2.6,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145170658","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Synergistic design of In2O3/g-C3N4 hybrid photocatalyst for enhanced visible light degradation of emerging pollutants 协同设计In2O3/g-C3N4杂化光催化剂增强可见光降解新兴污染物
IF 2.6 4区 化学
Ionics Pub Date : 2025-05-27 DOI: 10.1007/s11581-025-06396-w
V. Subha, T. Kamatchi, R. Venkatesh, S. Jagan Raj
{"title":"Synergistic design of In2O3/g-C3N4 hybrid photocatalyst for enhanced visible light degradation of emerging pollutants","authors":"V. Subha,&nbsp;T. Kamatchi,&nbsp;R. Venkatesh,&nbsp;S. Jagan Raj","doi":"10.1007/s11581-025-06396-w","DOIUrl":"10.1007/s11581-025-06396-w","url":null,"abstract":"<div><p>In this study, a novel In₂O₃/g-C₃N₄ hybrid photocatalyst was developed via an ultrasonic-assisted hydrothermal route to address the challenge of removing organic dyes and heavy metals from water. The hybrid displayed a reduced band gap energy (2.47 eV) and significantly enhanced BET surface area (114 m<sup>2</sup>/g), facilitating superior light absorption and catalytic activity. Under natural sunlight, the hybrid achieved 92% degradation of Rhodamine B (RhB) and 72% reduction of Cr (VI) within 90 min, substantially outperforming pristine In₂O₃. Kinetic studies confirmed the improved reaction rate with a pseudo-first-order rate constant of 0.0943 min⁻<sup>1</sup> for RhB degradation. The enhanced performance is attributed to efficient charge separation and suppressed recombination, as supported by photoluminescence and photocurrent measurements. Notably, the hybrid retained over 90% of its activity after five cycles, demonstrating excellent reusability and stability. These findings underscore the potential of the In₂O₃/g-C₃N₄ hybrid as a visible-light-responsive photocatalyst for practical environmental remediation.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"7217 - 7231"},"PeriodicalIF":2.6,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145170656","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Expeditious photocatalytic degradation of methylene blue using ZnO decorated Ti3C2Tx matrix ZnO修饰Ti3C2Tx基质快速光催化降解亚甲基蓝
IF 2.6 4区 化学
Ionics Pub Date : 2025-05-27 DOI: 10.1007/s11581-025-06389-9
Helen Treasa Mathew, K. Greeshma, Kumar Abhisek, Shashikant Shivaji Vhatkar, K. M. Nissamudeen, Ramesh Oraon
{"title":"Expeditious photocatalytic degradation of methylene blue using ZnO decorated Ti3C2Tx matrix","authors":"Helen Treasa Mathew,&nbsp;K. Greeshma,&nbsp;Kumar Abhisek,&nbsp;Shashikant Shivaji Vhatkar,&nbsp;K. M. Nissamudeen,&nbsp;Ramesh Oraon","doi":"10.1007/s11581-025-06389-9","DOIUrl":"10.1007/s11581-025-06389-9","url":null,"abstract":"<div><p>Recognizing the imperative need to eliminate synthetic dyes from industrial effluents and water sources using sustainable solar energy, extensive research has explored diverse 2D nanomaterials and their hybrid combinations. Among these, MXenes have emerged as a focal point due to their exceptional physio-chemical properties, holding great promise in catalysis and adsorption studies. This investigation primarily centres on the hydrothermal synthesis of ZnO/Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> composites, poised for application in the photocatalytic breakdown of dyes. The FESEM analysis reveals the transformation of particulate ZnO to fleet-like decoration assisted by the MXene flakes and however some of the ZnO particles got embedded onto the surface and growing in the interlayers. Through XRD the size of the particles were found to be 38 nm with an interplanar spacing justifying the higher absorption surface. Remarkably, the composite demonstrated exceptional degradation capabilities as MB solution was degraded by 97% of its initial concentration within 45 min with good recyclability over 2 cycles. The exceptional photocatalytic efficacy of the catalyst can be attributed to various factors, including precise band alignment, Schottky barrier creation, and an extensive surface area. The rate of each cycle is found to be varying from 0.0658 to 0.06171 min<sup>−1</sup> and 0.01599 min<sup>−1</sup> in every cycle. This study lays a solid foundation for future explorations involving diverse MXene-Metal Oxide composites, promising significant strides to effectively harness renewable energy for environmental remediation. The findings herein shift towards cleaner industrial processes and safeguarding precious water resources from the detrimental impact of synthetic dyes.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"7191 - 7204"},"PeriodicalIF":2.6,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145169466","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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 pure SnSb nanocrystals for reversible sodium storage in sodium-ion batteries 用于钠离子电池可逆钠存储的纯SnSb纳米晶体
IF 2.6 4区 化学
Ionics Pub Date : 2025-05-26 DOI: 10.1007/s11581-025-06375-1
Kiran B. Kore, Sandeep C. Kanade, Rahul Mahadeo Mendhe, Shivkumar R. Newaskar, Sandesh R. Jadkar, Musthafa Ottakam Thotiyl, Adinath M. Funde
{"title":"Phase pure SnSb nanocrystals for reversible sodium storage in sodium-ion batteries","authors":"Kiran B. Kore,&nbsp;Sandeep C. Kanade,&nbsp;Rahul Mahadeo Mendhe,&nbsp;Shivkumar R. Newaskar,&nbsp;Sandesh R. Jadkar,&nbsp;Musthafa Ottakam Thotiyl,&nbsp;Adinath M. Funde","doi":"10.1007/s11581-025-06375-1","DOIUrl":"10.1007/s11581-025-06375-1","url":null,"abstract":"<div><p>The pursuit of increased energy densities in lithium-ion and sodium-ion batteries is gaining significant traction. The effectiveness of sodium-ion batteries heavily relies on electrode materials, prompting considerable research focused on creating innovative materials that enhance stability and boost energy storage capacity. We present the synthesis of high-quality, phase-pure SnSb alloy nanocrystals measuring approximately 20 nm developed through a straightforward, rapid, and cost-effective reductive co-precipitation technique. The SnSb alloy serves as an anode material for reversible sodium-ion storage in rechargeable sodium-ion batteries. We investigated its electrochemical performance through cyclic voltammetry, rate capability tests, cyclic stability evaluations, and electrochemical impedance spectroscopy. The SnSb alloy nanocrystals demonstrate impressive Na-ion storage traits, showcasing a notable energy density (initial capacity: roughly 300 mAh/g), excellent cyclability (around 110 mAh/g after 100 cycles), and outstanding rate capability (2000 mA/g).</p><h3>Graphical Abstract</h3>\u0000<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"6975 - 6984"},"PeriodicalIF":2.6,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s11581-025-06375-1.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145169531","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
Experimental and DFT calculations for C/ZnO@S cathode and prelithiation Si anode for advanced sulfur-based batteries 先进硫基电池C/ZnO@S阴极和预锂化硅阳极的实验和DFT计算
IF 2.6 4区 化学
Ionics Pub Date : 2025-05-26 DOI: 10.1007/s11581-025-06416-9
Maryam Sadat Kiai, Navid Aslfattahi, Mubashir Mansoor, Deniz Karatas, Nilgun Baydogan, Lingenthiran Samylingam, Kumaran Kadirgama, Chee Kuang Kok
{"title":"Experimental and DFT calculations for C/ZnO@S cathode and prelithiation Si anode for advanced sulfur-based batteries","authors":"Maryam Sadat Kiai,&nbsp;Navid Aslfattahi,&nbsp;Mubashir Mansoor,&nbsp;Deniz Karatas,&nbsp;Nilgun Baydogan,&nbsp;Lingenthiran Samylingam,&nbsp;Kumaran Kadirgama,&nbsp;Chee Kuang Kok","doi":"10.1007/s11581-025-06416-9","DOIUrl":"10.1007/s11581-025-06416-9","url":null,"abstract":"<div><p>The advancement of modified electrodes for the next generation of sulfur-based batteries has become a prominent focus of research. This study introduces a detailed DFT calculations for the cell with carbon-doped ZnO/S as a potential cathode material through urea-assisted thermal decomposition of zinc acetate. Ultralong cycling stability is achieved after 500 cycles at 2 C for C-doped ZnO, resulting in an impressive reversibility of 981 mAh g<sup>−1</sup>, with a capacity retention of 86.2% and minimal capacity degradation of just 0.023% per cycle. The carbon-doped ZnO/LiS<sub>2</sub> model has a higher electrical conductivity compared to the Li<sub>2</sub>S/ZnO model. The DFT result proved the strong interaction of silicon with both carbon and oxygen; subsequently, the interaction in ZnO models containing SiS₂ was much higher, especially in the model containing carbon, which is in good agreement with our experiments.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"6819 - 6828"},"PeriodicalIF":2.6,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s11581-025-06416-9.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145169291","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
Preparation of Sn/Zn/Co-NPC composite anode materials via impregnation method for sodium-ion batteries with enhanced cycling stability 浸渍法制备提高循环稳定性的Sn/Zn/Co-NPC复合钠离子电池负极材料
IF 2.6 4区 化学
Ionics Pub Date : 2025-05-24 DOI: 10.1007/s11581-025-06352-8
Mingzhao Li, Xinyu Liu, Chonghua Shi, Jing Wang, Shaowei Yao
{"title":"Preparation of Sn/Zn/Co-NPC composite anode materials via impregnation method for sodium-ion batteries with enhanced cycling stability","authors":"Mingzhao Li,&nbsp;Xinyu Liu,&nbsp;Chonghua Shi,&nbsp;Jing Wang,&nbsp;Shaowei Yao","doi":"10.1007/s11581-025-06352-8","DOIUrl":"10.1007/s11581-025-06352-8","url":null,"abstract":"<div><p>Bimetallic zeolitic imidazolate framework materials (Zn/Co-ZIFs) represent a notable class within the field of metal–organic frameworks (MOFs). These materials are characterized by their advantageous properties typical of MOFs, including a high specific surface area and tunable pore sizes, in addition to exhibiting the structural stability that is characteristic of zeolites. In contrast, although tin-based materials demonstrate a high theoretical specific capacity, they experience significant volume changes during the charge and discharge cycles of batteries, leading to materal degradation and reduced cycling stability. In this study, Sn doping was successfully achieved in Zn/Co-NPC (N-doped porous carbon) by thermally treating Zn/Co-ZIFs at 700℃ through an impregnation method. This doping enhanced the sodium storage capacity of Zn/Co-NPC and improved its electrochemical performance. Experimental data indicate that the Sn/Zn/Co-NPC composite has a specific surface area of 332.80 m<sup>2</sup> g<sup>−1</sup> and an average pore diameter of 7.30 nm. When this composite is used as the anode material in sodium-ion batteries, it demonstrates outstanding performance: after 100 cycles, its reversible specific capacity reaches 344.20 mAh g<sup>−1</sup> (at a current density of 100 mA g<sup>−1</sup>) and exhibits excellent rate capability. Consequently, this study provides substantial insight into the prospective advancement of structurally stable and high-capacity anode materials for sodium-ion batteries.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"6963 - 6974"},"PeriodicalIF":2.6,"publicationDate":"2025-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145169023","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Interface-engineered amorphous-crystalline Mo/NixS heterojunctions for efficient urea electrooxidation 界面工程非晶Mo/NixS异质结用于高效尿素电氧化
IF 2.6 4区 化学
Ionics Pub Date : 2025-05-23 DOI: 10.1007/s11581-025-06405-y
Liu Zhou, Chenmeng Jiang, Lang Gan
{"title":"Interface-engineered amorphous-crystalline Mo/NixS heterojunctions for efficient urea electrooxidation","authors":"Liu Zhou,&nbsp;Chenmeng Jiang,&nbsp;Lang Gan","doi":"10.1007/s11581-025-06405-y","DOIUrl":"10.1007/s11581-025-06405-y","url":null,"abstract":"<div><p>Developing nickel-based urea oxidation reaction (UOR) catalysts with low-cost, high activity is still in challenges. In this work, we report an amorphous Mo/crystalline Ni<sub><i>x</i></sub>S heterojunction (A/C-Mo/Ni<sub><i>x</i></sub>S) through a dual-phase engineering strategy involving sulfurization of nickel foam followed by magnetron-sputtered Mo deposition. Remarkably, the optimized A/C-Mo/Ni<sub><i>x</i></sub>S achieves an ultralow potential of 1.42 V (vs. RHE) at 50 mA cm⁻<sup>2</sup>, while maintaining stable operation over 60 h with negligible activity decay. Characterization results reveal that the crystalline Ni<sub><i>x</i></sub>S substrate provides excellent electrical conductivity through its ordered atomic arrangement, whereas the amorphous Mo overlayer creates abundant unsaturated coordination sites that synergistically optimize urea adsorption and intermediate stabilization. Particularly, the unique amorphous-crystalline interface induces strong electronic coupling between Mo and Ni<sub><i>x</i></sub>S, which not only accelerates the dehydrogenation kinetics of *CONH₂ intermediates but also effectively suppresses Ni leaching through enhanced charge transfer.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"7169 - 7175"},"PeriodicalIF":2.6,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145168831","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Carbazole-based porous polymers for utilization in supercapacitors and adsorption of bromothymol blue dye 卡唑基多孔聚合物在超级电容器中的应用及对溴百里酚蓝染料的吸附
IF 2.6 4区 化学
Ionics Pub Date : 2025-05-23 DOI: 10.1007/s11581-025-06349-3
C. Raju, Reddi Mohan Naidu Kalla, Sunkara Srinivasa Rao, Sreedhar Doraswamy, Sarah A. Alshehri, Jaewoong Lee
{"title":"Carbazole-based porous polymers for utilization in supercapacitors and adsorption of bromothymol blue dye","authors":"C. Raju,&nbsp;Reddi Mohan Naidu Kalla,&nbsp;Sunkara Srinivasa Rao,&nbsp;Sreedhar Doraswamy,&nbsp;Sarah A. Alshehri,&nbsp;Jaewoong Lee","doi":"10.1007/s11581-025-06349-3","DOIUrl":"10.1007/s11581-025-06349-3","url":null,"abstract":"<div><p>Hyper-crosslinked microporous polycarbazole was synthesized by polymerizing carbazole with dimethoxymethane as a bridging agent, without using templates. Furthermore, it was directly carbonized by chemical activation using potassium carbonate to enhance the surface area of the porous polymer. The product was then characterized by Fourier-transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy, and Brunauer–Emmett–Teller analysis, proving the formation of porous polymers with good surface areas of 230 and 1210 m<sup>2</sup> g<sup>–1</sup>. Applied as an electrode material in a supercapacitor and a dye adsorption study, the carbonized polymer showed good specific capacitance of 215 (F/g) at 0.5 (A/g) and maximum adsorption capacity of 30.58 mg/g.\u0000</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"7273 - 7282"},"PeriodicalIF":2.6,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145168828","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
OER Catalytic performances of self-supporting NiFe-LDH/Ti3C2Tx/NF composite modified by plasma discharge treatment 等离子体放电改性自支撑NiFe-LDH/Ti3C2Tx/NF复合材料的催化性能
IF 2.6 4区 化学
Ionics Pub Date : 2025-05-22 DOI: 10.1007/s11581-025-06397-9
Sikai Peng, Huimin Yu, Ya Wen, Weiliang Peng
{"title":"OER Catalytic performances of self-supporting NiFe-LDH/Ti3C2Tx/NF composite modified by plasma discharge treatment","authors":"Sikai Peng,&nbsp;Huimin Yu,&nbsp;Ya Wen,&nbsp;Weiliang Peng","doi":"10.1007/s11581-025-06397-9","DOIUrl":"10.1007/s11581-025-06397-9","url":null,"abstract":"<div><p>Hydrogen production via water electrolysis is gaining attention as a method of renewable energy storage for its efficiency and eco-friendliness. However, efficient catalysts are still lacking to overcome the slow kinetics of the oxygen evolution reaction (OER). In this study, we synthesized a composite catalyst consisting of NiFe-layered double hydroxide (NiFe-LDH) and titanium carbide MXene (Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub>) for catalyzing the oxygen evolution reaction in electrochemical water splitting. The composite catalyst was optimized through a plasma discharge treatment for introducing oxygen vacancy and integrating it with nickel foam (NF) as support. This optimized catalyst O<sub>v</sub>-NiFe-LDH/Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub>/NF exhibits remarkable catalytic activity and stability. At a current density of 100 mA/cm<sup>2</sup>, the required overpotential is a mere 229 mV, and it sustains high catalytic performance even after 20 h of operation at a substantial current density of 1000 mA/cm<sup>2</sup>. Our findings offer valuable insights into the development of efficient OER catalysts for water splitting applications.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"7155 - 7168"},"PeriodicalIF":2.6,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145168441","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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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