{"title":"Functional Utilization of Aluminum Impurity in Upcycling Li-Ion Battery Cathode Scrap to Ni-Rich LiNiCoMnAlO2","authors":"Sunmin Lee, Gigap Han, Huisu Jeung, Kyungbin Yoo, Byoungki Son, Hyungjoo Noh, Sookyung Kim, Kyungjung Kwon","doi":"10.1002/eom2.70055","DOIUrl":"https://doi.org/10.1002/eom2.70055","url":null,"abstract":"<p>The rapid growth of the lithium-ion battery (LIB) market has led to a surge in cathode-scrap generation, emphasizing the urgent need for resource-efficient and environmentally responsible recycling strategies. While conventional recycling flowsheets effectively recover valuable metals, they typically involve multistep purification to remove Al originating from the cathode current collector. This process often poses technical and environmental challenges, such as managing large volumes of acidic wastewater and the continuous requirement for additional chemical reagents. Herein, a sustainable upcycling route is demonstrated that reutilizes the Al impurity as a functional dopant in Li[Ni<sub>0.9</sub>Co<sub>0.05</sub>Mn<sub>0.05</sub>]<sub>1−x</sub>Al<sub>x</sub>O<sub>2</sub> (NCMA), eliminating the need for dedicated Al-removal and external Al sources. By applying mild-acid leaching to Li[Ni<sub>0.6</sub>Co<sub>0.1</sub>Mn<sub>0.3</sub>]O<sub>2</sub> (NCM613) scrap, the residual Al content in the leachate is tuned and directly utilized during co-precipitation and calcination, completing a closed material loop. This approach not only reduces wastewater discharge and chemical consumption but also simplifies the overall recycling process. The resulting upcycled NCMA cathodes exhibit balanced electrochemical performance, retaining 65% of their initial capacity after 500 cycles while maintaining high-rate capability. These results highlight that impurity-derived Al, when properly managed, can serve as a sustainable dopant, transforming a contaminant into a resource. The developed process exemplifies a circular, low-waste strategy that aligns with next-generation green manufacturing and EU battery regulation frameworks by minimizing secondary waste streams and eliminating the need for virgin Al reagents.</p><p>\u0000 \u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":93174,"journal":{"name":"EcoMat","volume":"8 3","pages":""},"PeriodicalIF":12.6,"publicationDate":"2026-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eom2.70055","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146217212","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EcoMatPub Date : 2026-02-10DOI: 10.1002/eom2.70051
Min Gong, Qiuji Chen, Enhui Zhang, Liang Zhang, Xiang Lin, Fengxian Gao, Zhen Wu, Dongrui Wang
{"title":"Proline-Zwitterion Mediated Competitive Interactions Enabling Robust, Antifreezing, and Dendrite-Suppressing Hydrogel Electrolytes for Aqueous Zinc-Ion Batteries","authors":"Min Gong, Qiuji Chen, Enhui Zhang, Liang Zhang, Xiang Lin, Fengxian Gao, Zhen Wu, Dongrui Wang","doi":"10.1002/eom2.70051","DOIUrl":"https://doi.org/10.1002/eom2.70051","url":null,"abstract":"<p>Aqueous zinc-ion batteries are promising for flexible energy storage; however, water-related issues such as electrolyte decomposition, dendrite growth, and anode corrosion impede practical application. Although hydrogel electrolytes can suppress water activity and guide zinc-ion transport to inhibit dendrites, achieving high strength, high conductivity, and low temperature tolerance together remains challenging. Inspired by natural cryoprotection, a competitive interaction strategy using natural proline is present to enhance the polyvinyl alcohol (PVA)/ZnSO<sub>4</sub> hydrogel electrolyte. The hydrogel is physically crosslinked by PVA crystallites and stabilized by noncovalent interactions among PVA, Zn<sup>2+</sup>, and proline, showing 0.9 MPa tensile strength and 403% elongation. Proline's zwitterionic groups compete with water molecules in zinc-ion solvation, with a higher binding energy of 222.15 kcal/mol compared to 100.42 for water, enabling uniform Zn deposition and dendrite suppression. Zn||MnO<sub>2</sub> cells with this hydrogel retained 61% capacity after 200 cycles at 0.5 C, much better than the 32% with a liquid electrolyte. Proline also breaks the hydrogen bonding network of water, lowering the freezing point of the hydrogel to −27°C and maintaining 1.95 mS/cm conductivity at −20°C. The hydrogel allows flexible pouch cells to operate reliably under deformation and freezing conditions, demonstrating great potential for wearable energy storage.</p><p>\u0000 \u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":93174,"journal":{"name":"EcoMat","volume":"8 2","pages":""},"PeriodicalIF":12.6,"publicationDate":"2026-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eom2.70051","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146256294","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EcoMatPub Date : 2026-02-08DOI: 10.1002/eom2.70048
Dongik Kam, Dayeon Jang, Hee Jae Hwang, Sunmin Jang, Sumin Cho, Donghan Lee, Donghyeon Yoo, Junsang Yoon, Seong Jin Lee, Jongwoo Kim, Kyoung Je Cha, Dongwhi Choi
{"title":"Electrostatically Self-Powered Intelligent Force Sensor With Tunable Performance via Mechanically Guided 3D Morphing","authors":"Dongik Kam, Dayeon Jang, Hee Jae Hwang, Sunmin Jang, Sumin Cho, Donghan Lee, Donghyeon Yoo, Junsang Yoon, Seong Jin Lee, Jongwoo Kim, Kyoung Je Cha, Dongwhi Choi","doi":"10.1002/eom2.70048","DOIUrl":"https://doi.org/10.1002/eom2.70048","url":null,"abstract":"<p>Sensors that capture diverse environmental information are crucial in the elemental technology driving the Fourth Industrial Revolution. However, the trade-off between sensitivity and working range exhibited by conventional sensors results in limitations when the target stimuli deviate from their predesigned specifications. Thus, single sensors with adjustable performance characteristics must be developed to satisfy functionality requirements in diverse environments. In this study, a Tunable Usability-Nourished Electrostatic-based self-powered force sensor (TUNE sensor) is introduced to overcome the limitations of the fixed detection performance of a single sensor. The tunable sensing performance of the TUNE sensor is achieved via mechano-guided geometrical adaptation of its three-dimensional (3D) structure formed via mechanical buckling. Continuous and reversible shape changes in the 3D structure allow modulation of the stiffness of the TUNE sensor, resulting in tunable sensing performance (sensitivity of 0.53~1.08 nC/N and working range of 1.01~0.35 N). The effectiveness of the tunable sensing performance is demonstrated through its implementation in a reconfigurable electronic scale and robotic sensing. This mechano-guided geometrical adaptation strategy offers the potential for extending the use of sensors in multivariate environments and providing new opportunities for intelligent sensing systems in various applications.</p><p>\u0000 \u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":93174,"journal":{"name":"EcoMat","volume":"8 2","pages":""},"PeriodicalIF":12.6,"publicationDate":"2026-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eom2.70048","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146256304","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EcoMatPub Date : 2026-02-01DOI: 10.1002/eom2.70052
Ding Zou, Bin Ai, Yanni Zhang, Xiaoyu Cao, Hongyu Zhen
{"title":"Molecular Cages Based Materials for CO2 Capture, Separation, and Conversion","authors":"Ding Zou, Bin Ai, Yanni Zhang, Xiaoyu Cao, Hongyu Zhen","doi":"10.1002/eom2.70052","DOIUrl":"https://doi.org/10.1002/eom2.70052","url":null,"abstract":"<p>Anthropogenic carbon emissions pose a formidable challenge to contemporary society, driving severe global climate perturbations. In response, direct air capture (DAC) technologies have emerged as crucial tools for removing CO<sub>2</sub> from the atmosphere and curbing global warming. Non-thermal separation methods, particularly adsorption- and membrane-based processes utilizing porous materials, have significant advantages over traditional cryogenic and absorption systems. Porous materials, including zeolites, metal–organic frameworks (MOFs), covalent organic frameworks (COFs), hydrogen-bonded organic frameworks (HOFs), and molecular cages (MCs), are highly promising for advanced CO<sub>2</sub> capture, separation, and conversion due to their ordered and tunable pore architectures. Among these, MCs have emerged as a particularly promising class. MCs are composed of individually designed macromolecules and feature inherent cavities. They are soluble, readily regenerable, and amenable to precise chemical modifications. Over the past several years, MCs have demonstrated substantial potential for CO<sub>2</sub> capture, separation, and conversion, highlighting their value in addressing the global carbon challenge. This review provides a comprehensive examination of advancements in MCs, focusing particularly on their applications in the capture, separation, and conversion of CO<sub>2</sub>. A forward-looking perspective on the future trajectories in this research field is provided. Concurrently, the current challenges requiring more in-depth investigation are discussed.</p><p>\u0000 \u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":93174,"journal":{"name":"EcoMat","volume":"8 2","pages":""},"PeriodicalIF":12.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eom2.70052","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146193384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EcoMatPub Date : 2026-02-01DOI: 10.1002/eom2.70049
Zijian Chen, Jiaheng Liang, Jingjing Fu, Fan Chen, Han Zheng, Jin Chai, Ke Lin, Zhihao Zhou, Peng Li, Zijian Zheng
{"title":"Electronic Bandage With High-Resolution Interdigital Electrode Enhanced Pulsed Electric Field for Accelerated Wound Healing","authors":"Zijian Chen, Jiaheng Liang, Jingjing Fu, Fan Chen, Han Zheng, Jin Chai, Ke Lin, Zhihao Zhou, Peng Li, Zijian Zheng","doi":"10.1002/eom2.70049","DOIUrl":"https://doi.org/10.1002/eom2.70049","url":null,"abstract":"<p>Skin injuries are common and frequently encountered health issues in daily life. Accelerating wound healing is therefore essential for alleviating discomfort and minimizing infection risks. Pulsed electric field (PEF) therapy shows promise for enhancing wound repair by modulating cellular responses and promoting growth factors activity, but conventional PEF systems are limited by their bulkiness, high cost, and poor adaptability to daily care. To address these limitations, we developed a self-powered electronic bandage based on a triboelectric nanogenerator (TENG). This bandage integrates high-resolution flexible interdigital electrodes and a moisture-adaptive layer. The design leverages the millisecond PEF generated by the TENG and the electric field amplification effect provided by the low-cost, high-precision interdigital electrode, thereby compensating for the inadequate electrical stimulation associated with traditional TENG devices in wearable medicine. Thus, this advancement facilitates the miniaturization of PEF devices for wound management. In vitro studies demonstrated its efficacy in enhancing cellular proliferation, while in vivo experiments using diabetic mouse models revealed accelerated wound closure, reduced inflammatory responses, and improved angiogenesis. By combining advanced device manufacturing with therapeutic electrostimulation, this electronic bandage offers a promising solution that combines biological compatibility, mechanical flexibility, and economic feasibility for daily wound care.</p><p>\u0000 \u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":93174,"journal":{"name":"EcoMat","volume":"8 2","pages":""},"PeriodicalIF":12.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eom2.70049","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146176141","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A LiFSI-Based Ultralight Electrolyte for Long-Cycle-Life and High-Energy-Density Lithium-Sulfur Batteries","authors":"Junhua Zhou, Yufeng Luo, Chao Wang, Chuan Xie, Huimin Wang, Yanpeng Guo, Yongqiang Yang, Zhibo Li, Shujing Wen, Jiehua Cai, Qiyao Huang, Zijian Zheng","doi":"10.1002/eom2.70050","DOIUrl":"https://doi.org/10.1002/eom2.70050","url":null,"abstract":"<p>Lithium-sulfur (Li-S) batteries are promising candidates for high-energy storage; however, the high electrolyte uptake of porous S cathodes significantly limits their practical energy density. Although ultralight electrolytes (ULEs) can address this issue, they often suffer from low ionic conductivity, unstable interphases, and sluggish kinetics. This study presents a ULE design based on lithium bis(fluorosulfonyl)imide (LiFSI) salt, which simultaneously achieves a low density (0.89 g cm<sup>−3</sup>) and high Li<sup>+</sup> conductivity (7.05 mS cm<sup>−1</sup>). The LiFSI salt facilitates the formation of a LiF-rich solid electrolyte interphase on the Li metal anode, effectively suppressing polysulfide corrosion and enhancing cycle life. Furthermore, its high donor number improves polysulfide solubility, accelerating conversion kinetics and increasing capacity utilization. As a result, high-loading S cathodes (5 mg cm<sup>−2</sup>) deliver an initial capacity of 1180 mAh g<sup>−1</sup> and retain 70.63% of this capacity after 200 cycles. Pouch cells with the LiFSI-ULE exhibit a 34.5% higher energy density and a 133% longer cycle life compared to those with conventional electrolytes. This study successfully extends the application of LiFSI to Li-S batteries, offering a viable pathway toward long-cycling, high-energy-density energy storage.</p><p>\u0000 \u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":93174,"journal":{"name":"EcoMat","volume":"8 2","pages":""},"PeriodicalIF":12.6,"publicationDate":"2026-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eom2.70050","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146193637","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EcoMatPub Date : 2026-01-28DOI: 10.1002/eom2.70053
Deok Hoon Kim, Yunkyu Kwak, Sang Goo Lee, Ju Hyeon Kim, Hong Suk Kang
{"title":"PVDF-Pyrolyzed Fluorine-Doped TiO2 for Synergistic Adsorption-Enhanced PFOA Photocatalysis","authors":"Deok Hoon Kim, Yunkyu Kwak, Sang Goo Lee, Ju Hyeon Kim, Hong Suk Kang","doi":"10.1002/eom2.70053","DOIUrl":"https://doi.org/10.1002/eom2.70053","url":null,"abstract":"<p>Per- and polyfluoroalkyl substances (PFAS), notably perfluorooctanoic acid (PFOA), are persistent pollutants posing health risks via bioaccumulation and water mobility. While TiO<sub>2</sub> photocatalysis for PFOA degradation is well-reported, efficiency falters in dilute environments due to weak adsorption and rapid charge recombination. This study presents a novel hybrid approach with surface-modified TiO<sub>2</sub> designed to enhance PFOA adsorption while enabling simultaneous degradation. Fluorine-doped TiO<sub>2</sub> (F-TiO<sub>2</sub>) was synthesized through cost-effective, one-step PVDF pyrolysis, promoting nanopores and hydrophobic interactions for PFOA enrichment alongside improved charge separation. UV–vis spectroscopy and UVC tests (254 nm, 1.59 mW/cm<sup>2</sup>) with sodium persulfate showed F-TiO<sub>2</sub> achieving ~92% PFOA removal at 700 mg/L (vs. ~58% for pristine TiO<sub>2</sub>), with nine-fold faster kinetics (rate constant: 0.217 h<sup>−1</sup> vs. 0.024 h<sup>−1</sup>; half-life: ~3.2 h vs. ~28 h). IC analysis confirmed partial PFOA mineralization, with ~25 ppm F<sup>−</sup> detected after 16 h UV irradiation, indicating significant defluorination. Unlike noble-metal or graphene variants, F-TiO<sub>2</sub> exploits fluorine for adsorption-photocatalysis synergy, providing an economical, scalable PFAS remediation in low-concentration waters.</p><p>\u0000 \u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":93174,"journal":{"name":"EcoMat","volume":"8 2","pages":""},"PeriodicalIF":12.6,"publicationDate":"2026-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eom2.70053","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146176532","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EcoMatPub Date : 2026-01-18DOI: 10.1002/eom2.70045
Yuseung Won, Wontae Lee, Munhyeok Choi, Hyeonsu Park, Jaebum Kim, Jeonguk Hwang, Won-Sub Yoon
{"title":"Depth-Dependent Kinetic Limitations and Degradation Mechanisms in High-Loading LiFePO4 Electrodes","authors":"Yuseung Won, Wontae Lee, Munhyeok Choi, Hyeonsu Park, Jaebum Kim, Jeonguk Hwang, Won-Sub Yoon","doi":"10.1002/eom2.70045","DOIUrl":"https://doi.org/10.1002/eom2.70045","url":null,"abstract":"<p>Lithium-ion batteries are integral to the advancement of electric vehicles and energy storage systems. Among cathode materials, lithium iron phosphate (LiFePO<sub>4</sub>, LFP) has gained significant attention due to its low cost and stable lifespan. However, the relatively low energy density of LFP presents a critical challenge. To address this, a thick electrode strategy has been proposed, which reduces the proportion of electrochemically inactive components and increases the loading of active material, thereby enhancing energy density. Despite its potential, thick LFP electrodes suffer from severe capacity degradation during cycling, and the underlying mechanisms remain poorly understood. In this study, we compare reference and thick electrodes with active material loadings of 9 mg/cm<sup>2</sup> and 18 mg/cm<sup>2</sup>, respectively. Through various analysis techniques such as electrochemical tests, scanning electron microscopy, x-ray photoelectron spectroscopy, and synchrotron-based x-ray analyses, we identify that ionic conductivity is the primary kinetic limitation in thick LFP electrodes rather than electronic conductivity, leading to inhomogeneous reactions. Furthermore, side reactions with the electrolyte in the top layer of the thick electrode impose additional kinetic constraints. This work provides critical insights into electrode design strategies and performance optimization for thick LFP electrode systems.</p><p>\u0000 \u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":93174,"journal":{"name":"EcoMat","volume":"8 2","pages":""},"PeriodicalIF":12.6,"publicationDate":"2026-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eom2.70045","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146027533","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EcoMatPub Date : 2025-12-29DOI: 10.1002/eom2.70043
Orhun Oguz, Humza Ashraf, Ozgul Keles, Billur Deniz Karahan
{"title":"Waste to Energy Storage: Fe-Doped ZnO/Carbon Anodes Synthesized From Galvanizing Flue Dust","authors":"Orhun Oguz, Humza Ashraf, Ozgul Keles, Billur Deniz Karahan","doi":"10.1002/eom2.70043","DOIUrl":"https://doi.org/10.1002/eom2.70043","url":null,"abstract":"<p>Zinc, in a complex form, is one of the main components of the flue dust formed during the hot-dip galvanizing (HDG). Its disposal not only causes economic losses but also poses significant environmental challenges. In alignment with circular economy, the utilization of such industrial residues in value-added applications becomes vital. Herein, using HDG flue dust as an input material, a novel approach for synthesizing Fe-doped ZnO/carbon-based composite anode materials for lithium-ion batteries (LIBs) is proposed. In this scope, a three-step process comprising neutral leaching, calcination, and ball milling is employed for the fabrication. Neutral leaching is optimized to enrich the hot-dip galvanizing (HDG) flue dust residue with zinc and iron while simultaneously reducing the concentrations of ammonia and chlorine. The optimal leaching conditions (95.7 wt% Zn retention efficiency) are determined to be 80°C, a solid to liquid ratio of 1:100, and a leaching time of 1 h at 750 rpm. Later, the solid residue is subjected to thermal treatment at 500°C for 4 h, resulting in Fe-doped ZnO powder. Lastly, the synthesized Fe-doped ZnO powder is mechanically ball-milled with activated carbon (AC) at three different weight ratios: Fe-ZnO:C = 1:1, 2:1, and 3:1. Fe-ZnO:C = 3:1 achieves the highest capacity and the best retention: at the 1st and 100th cycles, it delivers 1760.72 and 592.68 mAh g<sup>−1</sup>, respectively. The enhanced performance of the composite is attributed to its unique properties in morphology, structure, and chemistry.</p><p>\u0000 \u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":93174,"journal":{"name":"EcoMat","volume":"8 1","pages":""},"PeriodicalIF":12.6,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eom2.70043","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145887917","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}