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Enhancing Sodium Ion Battery Performance through Biphasic Layered Oxide Cathodes
IF 3.5 4区 化学
ChemElectroChem Pub Date : 2025-02-18 DOI: 10.1002/celc.202400657
Seung-Jun Kang, Sung-Joon Park, Kwan Woo Nam, Seung-Ho Yu
{"title":"Enhancing Sodium Ion Battery Performance through Biphasic Layered Oxide Cathodes","authors":"Seung-Jun Kang,&nbsp;Sung-Joon Park,&nbsp;Kwan Woo Nam,&nbsp;Seung-Ho Yu","doi":"10.1002/celc.202400657","DOIUrl":"https://doi.org/10.1002/celc.202400657","url":null,"abstract":"<p>Biphasic layered cathodes represent a strategic advancement in overcoming the inherent limitations of single-phase materials by synergistically integrating distinct phase characteristics. Among these, the P2/O3 biphasic cathode stands out due to its integration of the rapid diffusion kinetics of the P2 phase with the high capacity of the O3 phase, resulting in superior battery performance. Given the critical role of phase ratio in determining the performance of biphasic cathodes, this work systematically examines the influence of synthesis methods, sintering temperatures, and sodium and dopant compositions on phase modulation. A comprehensive analysis of the kinetic and thermodynamic properties of the P2/O3 cathode is conducted, with findings correlated to electrochemical data to elucidate how thermodynamic stability and efficient diffusion kinetics contribute to enhanced functionality. Finally, a brief overview of other biphasic cathodes is provided, comparing their distinctive properties relative to those of the P2/O3 system.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 7","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400657","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143770507","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
Front Cover: Perovskite Oxides for Electrocatalytic Hydrogen/Oxygen Evolution Reaction (ChemElectroChem 4/2025)
IF 3.5 4区 化学
ChemElectroChem Pub Date : 2025-02-17 DOI: 10.1002/celc.202580401
Lu Lu, Mingzi Sun, Tong Wu, Qiuyang Lu, Baian Chen, Cheuk Hei Chan, Hon Ho Wong, Zikang Li, Bolong Huang
{"title":"Front Cover: Perovskite Oxides for Electrocatalytic Hydrogen/Oxygen Evolution Reaction (ChemElectroChem 4/2025)","authors":"Lu Lu,&nbsp;Mingzi Sun,&nbsp;Tong Wu,&nbsp;Qiuyang Lu,&nbsp;Baian Chen,&nbsp;Cheuk Hei Chan,&nbsp;Hon Ho Wong,&nbsp;Zikang Li,&nbsp;Bolong Huang","doi":"10.1002/celc.202580401","DOIUrl":"https://doi.org/10.1002/celc.202580401","url":null,"abstract":"<p><b>To provide a solid reference</b> for the design of novel perovskite-oxide electrocatalysts for efficient water splitting, the fundamental HER and OER mechanisms, synthetic methods, tuning strategies, and material properties have been demonstrated in this review. In addition, the main challenges in further improving the material stability and electrocatalytic water splitting efficiency of current perovskite-oxide electrocatalysts for practical applications have also been discussed in detail. More details can be found in the Review by Bolong Huang and co-workers (DOI: 10.1002/celc.202400648).\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 4","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202580401","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143431281","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
Advancing Bipolar Electrochemistry for Targeted Deposition of Biocompatible Polymers in Electrolyte-Free Solutions via Finite Element Modeling
IF 3.5 4区 化学
ChemElectroChem Pub Date : 2025-02-17 DOI: 10.1002/celc.202400506
Dr. Michal Wagner, Dr. Áine Brady, Oisín F. Doyle, Prof. Robert J. Forster
{"title":"Advancing Bipolar Electrochemistry for Targeted Deposition of Biocompatible Polymers in Electrolyte-Free Solutions via Finite Element Modeling","authors":"Dr. Michal Wagner,&nbsp;Dr. Áine Brady,&nbsp;Oisín F. Doyle,&nbsp;Prof. Robert J. Forster","doi":"10.1002/celc.202400506","DOIUrl":"https://doi.org/10.1002/celc.202400506","url":null,"abstract":"<p>The spatially controlled, template-free, deposition of electroactive and biocompatible materials on 3D objects is of great interest for wireless cell stimulation intended for diverse applications ranging from electroceuticals to advanced sensor development. Bipolar electrochemistry provides the possibility of depositing electrically conducting polymers controlled through the (shaped) electric field distribution. A second advantage is that electrochemistry can be performed in electrolyte-free media potentially removing the “interfering” effect of added electrolyte. Here, poly(3,4-ethylenedioxythiophene) (PEDOT) films have been deposited on bipolar electrodes directly in ultrapure water. Significantly, the deposition patterns cannot be fully explained using a linear change in the solution-phase potential, which is a common assumption for bipolar electrochemical systems. 3D finite element modeling and diffusive mass transport considerations have been combined to map the electric field distribution in this very low conductivity medium and demonstrate that homogenous rather than heterogeneous electron transfer is likely to play an important role in polymer deposition. Moreover, modeling predictions were compared to electrochemical impedance and cyclic voltammetry results and non-linear behaviours qualitatively matched, through film capacitances, and deposition patterns. The proposed framework opens up significant opportunities for the template-free deposition of various electroactive materials on bipolar electrodes in low-conductivity solutions.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 6","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400506","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143639045","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
Inorganic Solid-State Electrolytes in Potassium Batteries: Advances, Challenges, and Future Prospects
IF 3.5 4区 化学
ChemElectroChem Pub Date : 2025-02-14 DOI: 10.1002/celc.202400598
Titus Masese, Godwill Mbiti Kanyolo
{"title":"Inorganic Solid-State Electrolytes in Potassium Batteries: Advances, Challenges, and Future Prospects","authors":"Titus Masese,&nbsp;Godwill Mbiti Kanyolo","doi":"10.1002/celc.202400598","DOIUrl":"https://doi.org/10.1002/celc.202400598","url":null,"abstract":"<p>Potassium-ion batteries (KIBs) are increasingly attractive owing to their high voltage and projected low cost. However, the advancement of KIBs has been constrained by challenges related to electrolyte stability and interface compatibility. Traditional liquid electrolytes pose significant risks, including leakage and flammability, prompting a shift towards solid-state electrolytes, which offer improved energy density, safety and thermal stability. This <i>Perspective</i> explores the current state of inorganic solid-state electrolytes entailing oxides, chalcogenides, halides and hydrides. We delve into their recent advancements, identifying key challenges and future research opportunities, with the aim of advancing the development of high-performance all-solid-state potassium batteries.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 5","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400598","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143530438","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
Enhanced Protection of Carbon Steel Against Acid Corrosion: Synergistic Effect of s-Triazine-Anilino-Morpholino-Pyrazolyl Hybrids Through Electrochemical and Computational Insights
IF 3.5 4区 化学
ChemElectroChem Pub Date : 2025-02-11 DOI: 10.1002/celc.202400515
Ihab Shawish, Hassan H. Hammud, Waleed A. Aljamhi, Hany M. Abd El-Lateef, Nur Hazimah B. Z. Arfan, Malai Haniti S. A. Hamid, Nadeem S. Sheikh, Samha Alayoubi, Mohamed Bououdina, Assem Barakat, Ayman El-Faham
{"title":"Enhanced Protection of Carbon Steel Against Acid Corrosion: Synergistic Effect of s-Triazine-Anilino-Morpholino-Pyrazolyl Hybrids Through Electrochemical and Computational Insights","authors":"Ihab Shawish,&nbsp;Hassan H. Hammud,&nbsp;Waleed A. Aljamhi,&nbsp;Hany M. Abd El-Lateef,&nbsp;Nur Hazimah B. Z. Arfan,&nbsp;Malai Haniti S. A. Hamid,&nbsp;Nadeem S. Sheikh,&nbsp;Samha Alayoubi,&nbsp;Mohamed Bououdina,&nbsp;Assem Barakat,&nbsp;Ayman El-Faham","doi":"10.1002/celc.202400515","DOIUrl":"https://doi.org/10.1002/celc.202400515","url":null,"abstract":"<p>Corrosion inhibitors extend material lifespan and reduce maintenance costs by forming protective layers on metallic surfaces. Herein, two molecular hybrids: <i>N</i>-(4-chlorophenyl)-4-(3,5-dimethyl-1<i>H</i>-pyrazol-1-yl)-6-morpholino-1,3,5-triazin-2-amine (1) and 4-(3,5-dimethyl-1<i>H</i>-pyrazol-1-yl)-<i>N</i>-(4-methoxyphenyl)-6-morpholino-1,3,5-triazin-2-amine (2) were prepared and characterized. Corrosion inhibition efficiencies of C-steel in acid were evaluated using weight loss, impedimetric, and potentiometric techniques, complemented by computational calculations. The inhibition efficiency (%IE) was 96.5 % for inhibitor (1) and 99.2 % for (2) at 100 ppm (0.26 mM). The inhibitors functioned as mixed-type corrosion inhibitors, effectively protecting the steel surface, as demonstrated by scanning electron microscopy (SEM). Inhibitors (1) and (2) followed Temkin and Langmuir adsorption model respectively. Moreover, density functional theory (DFT) for the neutral and protonated forms in both gaseous and aqueous phases, revealed that derivative (2), incorporating methoxy group, exhibited greater inhibition efficiency on a metal surface compared to derivative (1) incorporating Cl-(electron-withdrawing group). This is attributed to the electron-donating effect of the methoxy group in (2), in consistence with the experimental results. Additionally, MC simulations indicated a higher value of ΔEads/ΔNi associated with the metal adsorbate interaction for derivative (2), and thus more favorable and stable adsorption on the metal surface. This stronger interaction contributed significantly to its superior corrosion inhibition performance compared to derivative (1).</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 7","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400515","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143770119","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
Enhanced Performance of Photocatalytic CO2 Reduction Using Cu@Graphene Nanoparticle-Decorated Co3O4 Nanoneedles
IF 3.5 4区 化学
ChemElectroChem Pub Date : 2025-02-11 DOI: 10.1002/celc.202400689
Yi-Xuan Lin, Dung-Sheng Tsai, Zi-Yu Chen, Chuan-Pei Lee
{"title":"Enhanced Performance of Photocatalytic CO2 Reduction Using Cu@Graphene Nanoparticle-Decorated Co3O4 Nanoneedles","authors":"Yi-Xuan Lin,&nbsp;Dung-Sheng Tsai,&nbsp;Zi-Yu Chen,&nbsp;Chuan-Pei Lee","doi":"10.1002/celc.202400689","DOIUrl":"https://doi.org/10.1002/celc.202400689","url":null,"abstract":"<p>A composite photocatalyst comprising cobalt oxide nanoneedles (Co₃O₄-NDs) modified with multilayer graphene-wrapped copper nanoparticles (MLG-CuNPs) was synthesized for efficient photocatalytic CO₂ reduction. The Co₃O₄-NDs and MLG-CuNPs were prepared via hydrothermal method and low-pressure chemical vapor deposition (LPCVD) technique, respectively. The related material characterizations of MLG-Cu/Co₃O₄-NDs are well investigated by scanning electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction, Raman spectroscopy, and UV–vis spectroscopy. Photocatalytic carbon dioxide (CO<sub>2</sub>) reduction tests revealed that the carbon monoxide (CO) was identified as the primary product, accompanied by a small amount of methane (CH₄). The photocatalysis performance of MLG-Cu/Co₃O₄-NDs exhibited a total yield that was 2.59 and 3.52 times higher than those of MLG-CuNPs and Co₃O₄-NDs, respectively. The superior performance of MLG-Cu/Co₃O₄-NDs is attributed to the synergistic effects of Co₃O₄-NDs and MLG-CuNPs, as well as the LSPR effect of CuNPs. Additionally, the hierarchical heterostructure facilitates efficient electron-hole pair separation, thereby enhancing overall photocatalytic efficiency. This study highlights the potential of combining metal oxides with conductive materials (i. e., graphene and copper) to develop highly active and stable photocatalysts for sustainable CO₂ conversion.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 7","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400689","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143770522","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
Unraveling Influential Factors of Stainless-Steel Dissolution in High-Energy Lithium Ion Batteries with LiFSI-Based Electrolytes 揭示使用 LiFSI 型电解质的高能量锂离子电池中不锈钢溶解的影响因素
IF 3.5 4区 化学
ChemElectroChem Pub Date : 2025-02-09 DOI: 10.1002/celc.202400632
Marian Cristian Stan, Peng Yan, Gerrit Michael Overhoff, Nick Fehlings, Hyung-Tae Kim, Robert Tobias Hinz, Tjark Thorben Klaus Ingber, Rayan Guerdelli, Christian Wölke, Martin Winter, Gunther Brunklaus, Isidora Cekic-Laskovic
{"title":"Unraveling Influential Factors of Stainless-Steel Dissolution in High-Energy Lithium Ion Batteries with LiFSI-Based Electrolytes","authors":"Marian Cristian Stan,&nbsp;Peng Yan,&nbsp;Gerrit Michael Overhoff,&nbsp;Nick Fehlings,&nbsp;Hyung-Tae Kim,&nbsp;Robert Tobias Hinz,&nbsp;Tjark Thorben Klaus Ingber,&nbsp;Rayan Guerdelli,&nbsp;Christian Wölke,&nbsp;Martin Winter,&nbsp;Gunther Brunklaus,&nbsp;Isidora Cekic-Laskovic","doi":"10.1002/celc.202400632","DOIUrl":"https://doi.org/10.1002/celc.202400632","url":null,"abstract":"<p>Leveraging physicochemical advantages over lithium hexafluorophosphate (LiPF<sub>6</sub>), lithium bis(fluorosulfonyl)imide (LiFSI) is being investigated as a conducting salt for lithium manganese-rich cathodes (LMR) and micro-crystalline silicon anodes (μ-Si). Nevertheless, its behavior towards the aluminum (Al) current collector and stainless-steel (SUS) coin cell parts limits its application under operating conditions requiring potentials higher than 3.9 V <i>vs</i>. Li|Li<sup>+</sup>. Using a mixture of organic carbonate-based solvents, various functional additives, and LiPF<sub>6</sub> lithium salt concentrations up to 1.0 M, the instability issue of the Al current collector in the presence of LiFSI is avoided. However, stainless-steel dissolution remains, being confirmed by both potentiodynamic measurements and SEM morphology investigations of the coin cell components after linear sweep voltammetry measurements carried out to 5.0 V. The results also indicate that the amount of stainless-steel dissolution is influenced by both the LiFSI amount in the electrolyte and the quality (grade) of stainless-steel used. Using Al-coated SUS 316L coin cell parts and/or high concentration electrolytes (HCE) with LiFSI (≈4 M LiFSI), the observed stainless-steel dissolution process can be fully avoided, allowing the evaluation of the electrochemical performance of LMR cathodes with μ-Si anodes in LiFSI-based electrolytes.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 6","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400632","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143638845","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
Design Strategies to Enhance Copper Electrocatalytic Performance for Nitrate-to-Ammonia Electroreduction
IF 3.5 4区 化学
ChemElectroChem Pub Date : 2025-02-09 DOI: 10.1002/celc.202400482
Simone Lombardi, Silvia Mostoni, Lorenzo Mirizzi, Roberto Scotti, Rosanna Viscardi, Mohsin Muhyuddin, Prof. Massimiliano D'Arienzo, Prof. Carlo Santoro
{"title":"Design Strategies to Enhance Copper Electrocatalytic Performance for Nitrate-to-Ammonia Electroreduction","authors":"Simone Lombardi,&nbsp;Silvia Mostoni,&nbsp;Lorenzo Mirizzi,&nbsp;Roberto Scotti,&nbsp;Rosanna Viscardi,&nbsp;Mohsin Muhyuddin,&nbsp;Prof. Massimiliano D'Arienzo,&nbsp;Prof. Carlo Santoro","doi":"10.1002/celc.202400482","DOIUrl":"https://doi.org/10.1002/celc.202400482","url":null,"abstract":"<p>Electrochemical nitrate reduction (NO<sub>3</sub><sup>−</sup>RR) is being recognized as a sustainable approach to synthesizing ammonia which is essential for the chemical industry and a key agricultural input conventionally produced through the hard-to-abate Haber Bosch process. Among various transition metals, copper-based electrocatalysts stand out in efficaciously carrying out this reaction owing to their superior electrocatalytic activity and selectivity. In this context, here, current state of research and advanced scientific understandings of employing Copper for NO₃<sup>−</sup>RR are succinctly, but comprehensively, presented while focusing on its design strategies to enhance the electrocatalytic performance. First, the NO<sub>3</sub><sup>−</sup>RR reaction mechanisms taking place at the surface of copper are described, followed by a discussion of its unique attributes in facilitating ammonia electrosynthesis. Then, various electrocatalyst fabrication routes and designing strategies are reviewed, emphasizing the role of the evolved structure, morphology, textural properties and surface chemistries in improving the reaction kinetics. Nanostructuring, facet and defect engineering, support, doping, alloying, heterojunction and the role of single active catalysts (SACs) centers as the key parameters for enhanced electrocatalytic behavior are highlighted.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 7","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400482","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143770217","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
Aptamer-Driven Biosensor Technology for the Quantitative Analysis of C-Reactive Protein
IF 3.5 4区 化学
ChemElectroChem Pub Date : 2025-02-09 DOI: 10.1002/celc.202400667
Marlon Oranzie, Jaymi L. January, Nelia A. Sanga, Zandile D. Leve, Sixolile Mini, Candice Cupido, Samantha F. Douman, Emmanuel I. Iwuoha
{"title":"Aptamer-Driven Biosensor Technology for the Quantitative Analysis of C-Reactive Protein","authors":"Marlon Oranzie,&nbsp;Jaymi L. January,&nbsp;Nelia A. Sanga,&nbsp;Zandile D. Leve,&nbsp;Sixolile Mini,&nbsp;Candice Cupido,&nbsp;Samantha F. Douman,&nbsp;Emmanuel I. Iwuoha","doi":"10.1002/celc.202400667","DOIUrl":"https://doi.org/10.1002/celc.202400667","url":null,"abstract":"<p>C-reactive protein (CRP) is a widely recognized biomarker for early myocardial infarction (MI) detection, released into the bloodstream during heart inflammation. Traditional assays for CRP detection, like ELISA and immunoradiometric assays, are costly, time-consuming, and require large sample volumes. Aptasensors are becoming increasingly popular for MI diagnosis due to their affordability, simplicity, and potential for point-of-care use. In this study, an electrochemical aptasensor incorporating mercaptosuccinic acid-capped nickel selenide quantum dots (MSA-NiSe<sub>2</sub> QD) were developed for CRP detection. The amine-modified aptamer was immobilized on the MSA-NiSe<sub>2</sub> QD using EDC/NHS coupling chemistry. Chronocoulometric measurements showed high selectivity towards CRP in phosphate buffer, with a linear range of 10–110 pg/mL and a detection limit of 2.80 pg/mL. Cross-reactivity experiments confirmed the aptasensor's high selectivity for CRP. Testing in human serum samples demonstrated recovery rates of 94–100.5 %, indicating its suitability for clinical diagnostics. Validation studies with a commercial CRP ELISA kit showed the aptasensor's superior sensitivity in both physiological buffer and human serum.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 7","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400667","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143770060","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
Influence of Hard/Soft Carbon Ratio in Composite Anodes for Enhanced Performance in Sodium-Ion Battery
IF 3.5 4区 化学
ChemElectroChem Pub Date : 2025-02-09 DOI: 10.1002/celc.202400586
Israr Ahmed, Lucas Rosson, Maria Forsyth, Nolene Byrne
{"title":"Influence of Hard/Soft Carbon Ratio in Composite Anodes for Enhanced Performance in Sodium-Ion Battery","authors":"Israr Ahmed,&nbsp;Lucas Rosson,&nbsp;Maria Forsyth,&nbsp;Nolene Byrne","doi":"10.1002/celc.202400586","DOIUrl":"https://doi.org/10.1002/celc.202400586","url":null,"abstract":"<p>Sodium-ion batteries (SIBs) are an emerging next-generation technology for sustainable energy storage. In this study, the synthesis and performance of carbon anode materials for SIBs, produced via direct co-carbonisation of textile waste-derived hard carbon (HC) and pitch-derived soft carbon (SC) at various ratios, were investigated. It was found that, as the ratio of HC increased, the rate capacity of the composite carbon anode improved, with the best performing composite anode exhibiting a specific capacity of 334 mAh g<sup>−1</sup> at a current density of 50 mA g<sup>−1</sup> which exceeded the specific capacity of 100 %HC and 100 %SC. The co carbonisation of the HC with the SC is critical to ensure the stabilisation of the pitch composite with in the new composite anode. A detailed examination of morphology, microstructure and electrochemical properties is reported here.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 6","pages":""},"PeriodicalIF":3.5,"publicationDate":"2025-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400586","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143638988","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
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