Journal of Solid State Electrochemistry最新文献

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Optimization of stack pressure on interfacial performance of Li6.4La3Zr1.4Ta0.6O12 electrolyte with lithium anode for all-solid-state batteries 全固态电池锂负极Li6.4La3Zr1.4Ta0.6O12电解质堆压对界面性能的影响
IF 2.6 4区 化学
Journal of Solid State Electrochemistry Pub Date : 2026-02-27 DOI: 10.1007/s10008-026-06542-y
Zhijie Zhang, Jian Cao, Xueling Zhang, Huan Li, Xingjiang Liu, Qiang Xu
{"title":"Optimization of stack pressure on interfacial performance of Li6.4La3Zr1.4Ta0.6O12 electrolyte with lithium anode for all-solid-state batteries","authors":"Zhijie Zhang,&nbsp;Jian Cao,&nbsp;Xueling Zhang,&nbsp;Huan Li,&nbsp;Xingjiang Liu,&nbsp;Qiang Xu","doi":"10.1007/s10008-026-06542-y","DOIUrl":"10.1007/s10008-026-06542-y","url":null,"abstract":"<div>\u0000 \u0000 <p>Stack pressure is a key factor for the electrochemical performances of all-solid-state lithium metal batteries (ASSLMBs). Optimizing the stack pressure is important for promoting the interfacial performances of garnet-type ceramic electrolyte (Li<sub>6.4</sub>La<sub>3</sub>Zr<sub>1.4</sub>Ta<sub>0.6</sub>O<sub>12</sub>) with Li metal anode. In this work, ASSLMBs assembled with Li<sub>6.4</sub>La<sub>3</sub>Zr<sub>1.4</sub>Ta<sub>0.6</sub>O<sub>12</sub> electrolytes are investigated under various stack pressures. Experimental results show that 3 MPa stack pressure is the optimal choice. The Li/Li<sub>6.4</sub>La<sub>3</sub>Zr<sub>1.4</sub>Ta<sub>0.6</sub>O<sub>12</sub>/LiFePO<sub>4</sub> battery under 3 MPa achieves a discharge capacity of 129.2 mAh g<sup>− 1</sup> after 100 charge/discharge cycles with a capacity retention rate of 82.1%. The mechanism by which stack pressure affects the interface performance of Li<sub>6.4</sub>La<sub>3</sub>Zr<sub>1.4</sub>Ta<sub>0.6</sub>O<sub>12</sub> electrolyte with Li anode is analyzed. A moderate stack pressure enlarges the contact area between Li<sub>6.4</sub>La<sub>3</sub>Zr<sub>1.4</sub>Ta<sub>0.6</sub>O<sub>12</sub> electrolyte and Li anode through elastic deformation, reducing the interface resistance. Additionally, it facilitates the plastic flow of Li anode via stress yield, minimizing the contact loss of Li anode during charge/discharge process. This work presents the significance of exerting a moderate stack pressure to optimize interfacial performance between Li<sub>6.4</sub>La<sub>3</sub>Zr<sub>1.4</sub>Ta<sub>0.6</sub>O<sub>12</sub> electrolyte and Li anode.</p>\u0000 </div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 5","pages":"1953 - 1963"},"PeriodicalIF":2.6,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147707793","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
Nano-silicon/polythiophene derived high-sulfur hard carbon as lithium-ion battery anode 纳米硅/多噻吩衍生高硫硬碳作为锂离子电池负极
IF 2.6 4区 化学
Journal of Solid State Electrochemistry Pub Date : 2026-02-27 DOI: 10.1007/s10008-026-06541-z
Qingtang Zhang, Zhimin Xie, Xiaomei Wang, Ruijing Cui
{"title":"Nano-silicon/polythiophene derived high-sulfur hard carbon as lithium-ion battery anode","authors":"Qingtang Zhang,&nbsp;Zhimin Xie,&nbsp;Xiaomei Wang,&nbsp;Ruijing Cui","doi":"10.1007/s10008-026-06541-z","DOIUrl":"10.1007/s10008-026-06541-z","url":null,"abstract":"<div>\u0000 \u0000 <p>The silicon-carbon composite is the most prominent high-performance anode material for lithium-ion batteries. Carbon is key to improving the large volume expansion and poor cycling performance of silicon-carbon composites. In this study, the nano-silicon/polythiophene composite (Si@PTh) was synthesized via in-situ polymerization and was then calcined to prepare nano-silicon/polythiophene-derived high-sulfur hard carbon (Si@PSHC). In the Si@PSHC, nano-silicon particles are embedded in the high-sulfur hard carbon, which effectively alleviates the volume changes of nano-silicon particles during the lithiation and delithiation processes and facilitates diffusion of lithium ions. Si@PSHC exhibits superior performance as an anode for lithium-ion batteries. Si@PSHC delivers an initial specific charge capacity of 845.30 mAh g<sup>− 1</sup> at 0.1 A g<sup>− 1</sup>, maintaining a specific charge capacity of 674.40 mAh g<sup>− 1</sup> after 150 cycles at 0.2 A g<sup>− 1</sup>, and exhibiting a specific charge capacity of 372.94 mAh g<sup>− 1</sup> at a high current density of 3.2 A g<sup>− 1</sup>.</p>\u0000 <span>AbstractSection</span>\u0000 Graphical Abstract\u0000 <div><figure><div><div><picture><source><img></source></picture><span>The alternative text for this image may have been generated using AI.</span></div></div></figure></div>\u0000 \u0000 </div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 5","pages":"1941 - 1951"},"PeriodicalIF":2.6,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147707792","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
A three-dimensional cross-linked water-soluble poly(vinyl alcohol)-citric acid binder enables superior-performance graphite anodes for lithium-ion batteries 三维交联水溶性聚乙烯醇-柠檬酸粘合剂使锂离子电池的石墨阳极性能优越
IF 2.6 4区 化学
Journal of Solid State Electrochemistry Pub Date : 2026-02-25 DOI: 10.1007/s10008-026-06529-9
Xiao-Yun Fu, Le-Qing Fan, Fei-Fei Deng, Li-Na Wang, Xin-Yuan Song, Xiao-Tong Zhu, Fu-Da Yu, Yun-Fang Huang, Ji-Huai Wu
{"title":"A three-dimensional cross-linked water-soluble poly(vinyl alcohol)-citric acid binder enables superior-performance graphite anodes for lithium-ion batteries","authors":"Xiao-Yun Fu,&nbsp;Le-Qing Fan,&nbsp;Fei-Fei Deng,&nbsp;Li-Na Wang,&nbsp;Xin-Yuan Song,&nbsp;Xiao-Tong Zhu,&nbsp;Fu-Da Yu,&nbsp;Yun-Fang Huang,&nbsp;Ji-Huai Wu","doi":"10.1007/s10008-026-06529-9","DOIUrl":"10.1007/s10008-026-06529-9","url":null,"abstract":"<div>\u0000 \u0000 <p>Although the amount of the binder in the electrode of lithium-ion batteries (LIBs) is very low, it has a significant impact on the electrochemical performance of LIB devices. Herein, an environment-friendly and low-cost water-soluble binder was developed by the cross-linking of poly(vinyl alcohol) (PVA) and citric acid (CA). The hydrogen bond interactions between the carbonyl groups in CA and hydroxyl groups in PVA construct a three-dimensional cross-linked PVA-CA binder. The as-constructed PVA-CA exhibits satisfactory ionic conductivity of 0.9 µS cm<sup>− 1</sup> together with swelling rate of 6.8%. The application of PVA-CA binder to graphite anode can generate outstanding performance including high peeling strength of 1.63 N, good cycling performance (308.3 mAh g<sup>− 1</sup> at the end of 300 cycles) along with superior rate performance, which exceed polyvinylidene fluoride (PVDF) binder, due to the strong hydrogen bond interactions between binder and graphite/current collector and the abundant carboxyl and hydroxyl groups in PVA-CA binder. In addition, a full cell consisting of a graphite anode with the PVA-CA binder and a lithium iron phosphate (LiFePO<sub>4</sub>) cathode exhibits a high discharge capacity of 44.2 mAh g<sup>− 1</sup> after 300 cycles at 2 C.</p>\u0000 </div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 5","pages":"1931 - 1940"},"PeriodicalIF":2.6,"publicationDate":"2026-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147707767","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
The ionic conductivity of Li-doped high entropy (MgCoNiCuZn)1−x Lix O obtained by hydrothermal method 水热法制备了li掺杂高熵(MgCoNiCuZn)1−x Lix O的离子电导率
IF 2.6 4区 化学
Journal of Solid State Electrochemistry Pub Date : 2026-02-24 DOI: 10.1007/s10008-026-06545-9
He Li, Fengyu Cui, Miao Guo, Jiaxin Zhang, Yanyu Li
{"title":"The ionic conductivity of Li-doped high entropy (MgCoNiCuZn)1−x Lix O obtained by hydrothermal method","authors":"He Li,&nbsp;Fengyu Cui,&nbsp;Miao Guo,&nbsp;Jiaxin Zhang,&nbsp;Yanyu Li","doi":"10.1007/s10008-026-06545-9","DOIUrl":"10.1007/s10008-026-06545-9","url":null,"abstract":"<div>\u0000 \u0000 <p>High-entropy oxides are a new class of functional ceramic materials with applications in thermoelectricity, catalysis, and superionic conductors. The (MgCoNiCuZn)₁₋ₓLiₓO high-entropy oxide, known for its Li superionic conductivity and excellent thermal/electrochemical stability, is a promising electrolyte material that enhances cycling stability and coulombic efficiency. Traditionally, (MgCoNiCuZn)₁₋ₓLiₓO is prepared by the solid-phase method, which requires sintering at 1000 °C for 12 h; however, this prolonged high-temperature process can result in the volatilization of alkali metal ions. To address this limitation, we developed a simple and efficient hydrothermal method that reduces both sintering temperature and time. Using this approach, lithium-doped high-entropy oxide (MgCoNiCuZn)₁₋ₓLiₓO was successfully synthesized. Using polyvinyl butyral (PVB) as a binder, high-density ceramics were obtained through buried powder sintering at 900 °C for 3 h. The resulting ceramics exhibit excellent ionic conductivity (σ = 1.3 × 10⁻³ S cm⁻¹, Eₐ = 0.25 eV), comparable to previously reported values.</p>\u0000 </div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 5","pages":"1923 - 1930"},"PeriodicalIF":2.6,"publicationDate":"2026-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147707768","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
MerR protein functionalized ITO electrode: an electrochemical biosensor for Mercury(II) detection MerR蛋白功能化ITO电极:用于汞(II)检测的电化学生物传感器
IF 2.6 4区 化学
Journal of Solid State Electrochemistry Pub Date : 2026-02-23 DOI: 10.1007/s10008-025-06516-6
Ayushi Tanwar, Debasish Nath,  Mandeep, Saurabh Gupta, Jaydeep Bhattacharya
{"title":"MerR protein functionalized ITO electrode: an electrochemical biosensor for Mercury(II) detection","authors":"Ayushi Tanwar,&nbsp;Debasish Nath,&nbsp; Mandeep,&nbsp;Saurabh Gupta,&nbsp;Jaydeep Bhattacharya","doi":"10.1007/s10008-025-06516-6","DOIUrl":"10.1007/s10008-025-06516-6","url":null,"abstract":"<div>\u0000 \u0000 <p>Mercury (Hg) poses a significant environmental and health threat, necessitating highly sensitive and rapid detection methods beyond costly conventional techniques. This study presents a novel electrochemical biosensor for Hg<sup>2+</sup> ions, leveraging the specific binding properties of the metalloregulatory protein, i.e., mercuric resistance operon regulatory protein (MerR), covalently immobilized on an Indium Tin Oxide (ITO) surface. We used electrochemically inert methoxy Polyethylene Glycol amino (MPA) as a blocking agent, avoiding the specificity issues associated with traditional Bovine Serum Albumin (BSA). Our MerR/ITO biosensor demonstrated exceptional specificity and achieved a limit of detection (LOD) of 0.77 nM. This performance represents a significant advancement for electrochemical mercury biosensors, particularly considering its robust and direct protein based detection mechanism. This approach offers a highly effective solution for precise mercury monitoring.</p>\u0000 </div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 5","pages":"1911 - 1921"},"PeriodicalIF":2.6,"publicationDate":"2026-02-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147707795","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
Simultaneous electrochemical deburring and polishing of digital hydraulic valve spools 数字式液压阀芯同时进行电化学去毛刺和抛光
IF 2.6 4区 化学
Journal of Solid State Electrochemistry Pub Date : 2026-02-20 DOI: 10.1007/s10008-026-06540-0
Shenglong Zhang, Hao Guo, Wei Sun, Xiaozhe Yang, Xu Yang, Zhuangde Jiang
{"title":"Simultaneous electrochemical deburring and polishing of digital hydraulic valve spools","authors":"Shenglong Zhang,&nbsp;Hao Guo,&nbsp;Wei Sun,&nbsp;Xiaozhe Yang,&nbsp;Xu Yang,&nbsp;Zhuangde Jiang","doi":"10.1007/s10008-026-06540-0","DOIUrl":"10.1007/s10008-026-06540-0","url":null,"abstract":"<div>\u0000 \u0000 <p>Digital hydraulic technology is an emerging field in fluid power systems. It requires pilot valve spools with exceptional surface integrity to ensure high response speed and reliability. However, for valve spools with complex geometries, conventional electrochemical polishing struggles to achieve simultaneous burr elimination, superior surface finish, and dimensional accuracy due to non-uniform material removal caused by electric field edge effects and limited electrolyte solution access. To bridge this gap, a novel electrochemical approach that integrates polishing and deburring into a single process is presented. The fundamental mechanisms of burr removal and surface evolution were first elucidated through experiments and electric field simulations on flat samples, establishing an optimal parameter window. Subsequently, a specialized rotary electrochemical machining (RECM) device was developed for valve spools. Crucially, the process was optimized through coupled electric-flow field simulations, guiding the use of rotation to control hydrodynamic conditions, counteract edge effects, and ensure uniform dissolution. The RECM-processed valve spools exhibited remarkable improvement: the low-frequency surface roughness was reduced from Sa 1.258 μm to 0.252 μm, and the high-frequency surface roughness from Sa 0.702 μm to 0.055 μm, while maintaining dimensional uniformity and eliminating burrs. This work provides a practical and efficient solution for the high-performance surface finishing of complex hydraulic components, demonstrating a strategy of multi-physics field coupling for electrochemical manufacturing.</p>\u0000 </div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 5","pages":"1889 - 1909"},"PeriodicalIF":2.6,"publicationDate":"2026-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147707762","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
The influence of exothermic electrode chemical reactions on the temperature of a lead-acid battery 放热电极化学反应对铅酸电池温度的影响
IF 2.6 4区 化学
Journal of Solid State Electrochemistry Pub Date : 2026-02-20 DOI: 10.1007/s10008-026-06543-x
G. V. Kuznetsov, E. V. Kravchenko, N. A. Pribaturin
{"title":"The influence of exothermic electrode chemical reactions on the temperature of a lead-acid battery","authors":"G. V. Kuznetsov,&nbsp;E. V. Kravchenko,&nbsp;N. A. Pribaturin","doi":"10.1007/s10008-026-06543-x","DOIUrl":"10.1007/s10008-026-06543-x","url":null,"abstract":"<div>\u0000 \u0000 <p>Sources of irregular electricity generation (wind generators and solar power plants) cannot guarantee a stable supply of electricity to consumers. The only solution to the problem of involving such non-traditional renewable energy sources in the actual power supply is the accumulation of electricity in energy storage systems (ESS). The battery ESSs are considered promising according to several criteria. The objective lack of statistics on failures of battery energy storage systems and universal mathematical models for predicting the thermal runaway of electrochemical batteries is a limiting factor in the development of such technology for storing large volumes of electricity. This study analyzes the thermal conditions of a large lead-acid energy storage system are analyzed taking into account two mechanisms of heat generation for typical operating modes of battery and varying the heat‑exchange characteristics of the battery system with the external environment: ambient temperature and heat‑exchange intensity. The task of numerical temperature analysis is solved within the framework of a mathematical model with lumped parameters in the form of a system of ordinary differential equations. Numerical analysis made it possible to identify operating modes with a high probability of thermal runaway. It can occur even under conditions of heat exchange between the battery system and the external environment in the typical range of changes in ambient temperatures and heat transfer coefficients. For example, reducing the heat transfer coefficient of the housing surface of the basic cells of the battery assembly to 5 W/(m<sup>2</sup> ·K) leads to thermal runaway of the lead-acid batteries already at an ambient temperature T<sub>surround</sub>=28 °C and other normal parameters.</p>\u0000 </div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 5","pages":"1879 - 1887"},"PeriodicalIF":2.6,"publicationDate":"2026-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147707764","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
Electrical and electrochemical pH sensing technologies: comparative mechanisms, performance, and applications 电和电化学pH传感技术:比较机制、性能和应用
IF 2.6 4区 化学
Journal of Solid State Electrochemistry Pub Date : 2026-02-18 DOI: 10.1007/s10008-026-06534-y
Saroja Rijal, Uda Hashim, M. N. Afnan Uda, M. N. A. Uda, Yuri Pamungkas
{"title":"Electrical and electrochemical pH sensing technologies: comparative mechanisms, performance, and applications","authors":"Saroja Rijal,&nbsp;Uda Hashim,&nbsp;M. N. Afnan Uda,&nbsp;M. N. A. Uda,&nbsp;Yuri Pamungkas","doi":"10.1007/s10008-026-06534-y","DOIUrl":"10.1007/s10008-026-06534-y","url":null,"abstract":"<div>\u0000 \u0000 <p>Reliable pH measurement remains central to chemical, biological, and environmental monitoring, yet conventional electrochemical glass electrodes face persistent challenges of fragility, slow response, and limited integrability. This study presents a comparative analysis between a conventional glass-electrode pH meter and a custom-fabricated aluminum interdigitated electrode (Al-IDE) for full-range pH sensing (pH 1–13). The Al-IDE device, fabricated via standard photolithography on thermally oxidized silicon, was evaluated under identical conditions using pure buffer systems. Electrical measurements revealed a distinct U-shaped current response, decreasing from 3107 nA at pH 1 to 1.03 nA near pH 7, before rising to 781 nA at pH 13. This behaviour reflects the amphoteric nature of the Al₂O₃ surface, governed by protonation–deprotonation equilibria that modulate interfacial charge transport. The proposed nonlinear quadratic model achieved strong segmental correlations (R² &gt; 0.89) for both acidic and alkaline regimes. Comparative assessment against the glass electrode yielded a mean absolute deviation of ≈ 0.19 pH units, confirming excellent agreement between the two modalities. While the glass electrode followed a linear Nernstian slope (–58.6 mV pH⁻¹), the Al-IDE offered rapid, reference-free, and mechanically robust operation with repeatability (RSD) ranging up to 3.5%. These findings establish the Al-IDE as a low-cost, CMOS-compatible alternative for portable or embedded pH monitoring and provide foundational insights for hybrid electro-electrical sensing architectures that integrate the precision of electrochemical systems with the real-time responsiveness of electrical transduction.</p>\u0000 </div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 5","pages":"1869 - 1878"},"PeriodicalIF":2.6,"publicationDate":"2026-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10008-026-06534-y.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147707774","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
Boosting nickel-based electrocatalysts for hydrogen oxidation in alkaline media via low-temperature nitrogen doping 低温氮掺杂增强碱性介质中氢氧化镍基电催化剂
IF 2.6 4区 化学
Journal of Solid State Electrochemistry Pub Date : 2026-02-13 DOI: 10.1007/s10008-026-06527-x
Xin Lu, Xiangwen Ren, Jianlong Huang, Jutao Jin
{"title":"Boosting nickel-based electrocatalysts for hydrogen oxidation in alkaline media via low-temperature nitrogen doping","authors":"Xin Lu,&nbsp;Xiangwen Ren,&nbsp;Jianlong Huang,&nbsp;Jutao Jin","doi":"10.1007/s10008-026-06527-x","DOIUrl":"10.1007/s10008-026-06527-x","url":null,"abstract":"<div><p>Nickel (Ni) is a promising catalyst for the hydrogen oxidation reaction (HOR) in alkaline media; However, its performance is limited by the strong hydrogen adsorption energy on the Ni surface and its susceptibility to oxidation at low operating potentials. Herein, we report a facile low-temperature nitrogen doping method to enhance the HOR performance of nickel-based electrocatalysts in alkaline solution. The resulting nickel particles supported on nitrogen-doped graphene sheets (Ni–N/GS) exhibit a kinetic current density (<i>J</i><sub>k</sub>) of 2.15 mA cm<sup>−2</sup> at an overpotential of 50 mV, significantly higher than that of the non-doped counterpart (Ni/GS, 0.63 mA cm<sup>−2</sup>). Moreover, the Ni–N/GS catalyst demonstrates an electron transfer number of 1.87 and an improved breakdown potential of 0.22 V vs. reversible hydrogen electrode (RHE), outperforming most recently reported Ni-based HOR catalysts. Further studies indicate that nitrogen doping into the graphene lattice can significantly modulate the electronic states of surface atoms on adjacent nickel nanoparticles, leading to strong substrate–catalyst electronic interactions, which in turn enhances both the catalytic activity and stability.</p></div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 5","pages":"1861 - 1867"},"PeriodicalIF":2.6,"publicationDate":"2026-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147707766","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
One-step anodization method for preparing Ce/Co co-doped TiO2 nanotubes as efficient photocathodic protection to Q235 carbon steel 一步阳极氧化法制备Ce/Co共掺杂TiO2纳米管对Q235碳钢的高效光电阴极保护
IF 2.6 4区 化学
Journal of Solid State Electrochemistry Pub Date : 2026-02-11 DOI: 10.1007/s10008-026-06532-0
Jinyi Hu, Jingang Yang, Chonggang Wu, Hongyu Cen
{"title":"One-step anodization method for preparing Ce/Co co-doped TiO2 nanotubes as efficient photocathodic protection to Q235 carbon steel","authors":"Jinyi Hu,&nbsp;Jingang Yang,&nbsp;Chonggang Wu,&nbsp;Hongyu Cen","doi":"10.1007/s10008-026-06532-0","DOIUrl":"10.1007/s10008-026-06532-0","url":null,"abstract":"<div>\u0000 \u0000 <p>Photocatalytic cathodic protection technology involves the generation of photo-generated electrons by photovoltaic materials under illumination, providing cathodic polarization to the protected metal and thereby inhibiting its corrosion. However, issues such as the wide bandgap, rapid recombination of electrons and holes, lacking charge storage capabilities, along with the practical applications results in certain challenges. In this study, TiO<sub>2</sub> nanotube arrays doped with different molar ratios of Ce and Co (Ce<sub>x</sub>-Co<sub>y</sub>/TiO<sub>2</sub>) were synthesized using a one-step anodization method. The results indicate that under illumination conditions, when carbon steel is coupled with Ce<sub>1</sub>-Co<sub>1</sub>/TiO<sub>2</sub>, its open-circuit potential (OCP) shifts negatively by approximately 300 mV and 150 mV relative to the uncoupled carbon steel photoanode materials and the coupled pure TiO<sub>2</sub> conditions, respectively.The photocurrent density shows the 2.4 times higher than that of pure TiO<sub>2</sub>. Additionally, even when the light source was turned off, it could still provide a continuous cathodic protection for carbon steel. The enhanced photocathodic protection can be attributed to the nonlinear distribution of Ce and Co on the Ce<sub>x</sub>-Co<sub>y</sub>/TiO<sub>2</sub> surface with the gradient transition from reduced states to oxidized states at interface, which enhances the system’s light-harvesting capability and forms a heterojunction with TiO<sub>2</sub>, which enhances the separation and migration of photogenerated charge carriers. This study provides a general design and preparation scheme for the application of semiconductor composite materials in the field of photocathode corrosion protection.</p>\u0000 </div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 5","pages":"1845 - 1859"},"PeriodicalIF":2.6,"publicationDate":"2026-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147707761","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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