Ya KONG , Shi-peng ZHANG , Yu-ling YIN , Zi-xuan ZHANG , Xue-ting FENG , Feng DING , Jin ZHANG , Lian-ming TONG , Xin GAO
{"title":"Microwave-enabled rapid, continuous, and substrate-free synthesis of few-layer graphdiyne nanosheets for enhanced potassium metal battery performance","authors":"Ya KONG , Shi-peng ZHANG , Yu-ling YIN , Zi-xuan ZHANG , Xue-ting FENG , Feng DING , Jin ZHANG , Lian-ming TONG , Xin GAO","doi":"10.1016/S1872-5805(25)60987-5","DOIUrl":"10.1016/S1872-5805(25)60987-5","url":null,"abstract":"<div><div>Graphdiyne (GDY) is a two-dimensional carbon allotrope with exceptional physical and chemical properties that is gaining increasing attention. However, its efficient and scalable synthesis remains a significant challenge. We present a microwave-assisted approach for its continuous, large-scale production which enables synthesis at a rate of 0.6 g/h, with a yield of up to 90%. The synthesized GDY nanosheets have an average diameter of 246 nm and a thickness of 4 nm. We used GDY as a stable coating for potassium (K) metal anodes (K@GDY), taking advantage of its unique molecular structure to provide favorable paths for K-ion transport. This modification significantly inhibited dendrite formation and improved the cycling stability of K metal batteries. Full-cells with perylene-3,4,9,10-tetracarboxylic dianhydride (PTCDA) cathodes showed the clear superiority of the K@GDY anodes over bare K anodes in terms of performance, stability, and cycle life. The K@GDY maintained a stable voltage plateau and gave an excellent capacity retention after 600 cycles with nearly 100% Coulombic efficiency. This work not only provides a scalable and efficient way for GDY synthesis but also opens new possibilities for its use in energy storage and other advanced technologies.\u0000\t\t\t\t<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (156KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":"40 3","pages":"Pages 642-650"},"PeriodicalIF":5.7,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144501880","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yong-fang ZHU , Xiao-dong JI , Wen-kai PAN , Geng WU , Peng LI , Bo LIU , Da-ping HE
{"title":"A review of graphene assembled films as platforms for electrochemical reactions","authors":"Yong-fang ZHU , Xiao-dong JI , Wen-kai PAN , Geng WU , Peng LI , Bo LIU , Da-ping HE","doi":"10.1016/S1872-5805(25)60992-9","DOIUrl":"10.1016/S1872-5805(25)60992-9","url":null,"abstract":"<div><div>Because of their low electrical conductivity, sluggish ion diffusion, and poor stability, conventional electrode materials are not able to meet the growing demands of energy storage and portable devices. Graphene assembled films (GAFs) formed from graphene nanosheets have an ultrahigh conductivity, a unique 2D network structure, and exceptional mechanical strength, which give them the potential to solve these problems. However, a systematic understanding of GAFs as an advanced electrode material is lacking. This review focuses on the use of GAFs in electrochemistry, providing a comprehensive analysis of their synthesis methods, surface/structural characteristics, and physical properties, and thus understand their structure-property relationships. Their advantages in batteries, supercapacitors, and electrochemical sensors are systematically evaluated, with an emphasis on their excellent electrical conductivity, ion transport kinetics, and interfacial stability. The existing problems in these devices, such as chemical inertness and mechanical brittleness, are discussed and potential solutions are proposed, including defect engineering and hybrid structures. This review should deepen our mechanistic understanding of the use of GAFs in electrochemical systems and provide actionable strategies for developing stable, high-performance electrode materials.\u0000\t\t\t\t<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (117KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":"40 3","pages":"Pages 519-538"},"PeriodicalIF":5.7,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144502029","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Chang-lin HE , Zhi-chao SHANG , Wei-guang WANG , Xiang-ming LI , Kun WANG , Yue-xing CHEN , Xin-tan BAI , Pei-pei WANG , Xiang JI , Xuan-ru REN , A Levashov Evgeny , Kiryukhantsev-Korneev Ph V , Pei-zhong FENG
{"title":"Improving the oxidation resistance of HfB2-SiC coatings on carbon/carbon composites by CeO2 doping","authors":"Chang-lin HE , Zhi-chao SHANG , Wei-guang WANG , Xiang-ming LI , Kun WANG , Yue-xing CHEN , Xin-tan BAI , Pei-pei WANG , Xiang JI , Xuan-ru REN , A Levashov Evgeny , Kiryukhantsev-Korneev Ph V , Pei-zhong FENG","doi":"10.1016/S1872-5805(25)60994-2","DOIUrl":"10.1016/S1872-5805(25)60994-2","url":null,"abstract":"<div><div>To improve the oxidation resistance of HfB<sub>2</sub>-SiC coatings on carbon/carbon composites at 1700 °C in air, CeO<sub>2</sub> was introduced to improve oxygen blocking and its mechanism was investigated. During the rapid oxidation stage, CeO<sub>2</sub> accelerated the formation of a multiphase glass layer on the coating surface. The maximum oxidation rates of CeO<sub>2</sub>-HfB<sub>2</sub>-SiC coatings with 1%, 3%, and 5% CeO<sub>2</sub> were 24.1%, 20.3%, and 53.2% higher than that of the unmodified HfB<sub>2</sub>-SiC coating, respectively. In the stable oxidation stage, the maximum oxidation rates of coatings with 1% and 3% CeO<sub>2</sub> decreased by 31.4% and 21.9%, respectively, demonstrating adequate inert protection. CeO<sub>2</sub> is a “coagulant” and “stabilizer” in the composite glass layer. However, increasing the CeO<sub>2</sub> content accelerates the reaction between the SiO<sub>2</sub> glass phase and SiC, leading to a higher SiO<sub>2</sub> consumption and reduced self-healing ability of the glass layer. The 1% CeO<sub>2</sub>-60% HfB<sub>2</sub>-39%SiC coating showed improved glass layer viscosity and stability, moderate SiO<sub>2</sub> consumption, and better self-healing ability, significantly boosting the oxidation protection of the coating.\u0000\t\t\t\t<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (106KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":"40 3","pages":"Pages 688-701"},"PeriodicalIF":5.7,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144501884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hui-jun LI , Qing ZHANG , Kun HUANG , Song-feng PEI , Wen-cai REN
{"title":"A review of thermally conductive graphene-based films","authors":"Hui-jun LI , Qing ZHANG , Kun HUANG , Song-feng PEI , Wen-cai REN","doi":"10.1016/S1872-5805(25)60990-5","DOIUrl":"10.1016/S1872-5805(25)60990-5","url":null,"abstract":"<div><div>With the miniaturization and high integration of electronic devices, problems such as heat accumulation and non-uniform temperature distribution during operation have significantly compromised the reliability and stability of electronic systems, thereby hindering the advance of electronic technology. Because of the exceptionally high in-plane thermal conductivity of graphene, its films can effectively spread heat from localized hotspots to a larger heat dissipation area, thereby increasing the heat dissipation and reducing the operating temperatures of the device. As a result, such films are critical materials for thermal management in electronic equipment. This review systematically examines the relationship between their structure and thermal conductivity, outlines their main fabrication methods, explores the mechanisms for controlling defects in them using different precursors, formation processes, and heat treatments, and summarizes existing research aimed at improving their thermal conductivity. Finally, the problems associated with these films and their future development are discussed.\u0000\t\t\t\t<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (96KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":"40 3","pages":"Pages 540-552"},"PeriodicalIF":5.7,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144502030","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Research progress on the preparation of bamboo-based activated carbon for CO2 adsorption","authors":"Bing-jie Wang, Qiang Xie, Yu-tong Sha, Jin-chang Liu, Ding-cheng Liang","doi":"10.1016/S1872-5805(25)60956-5","DOIUrl":"10.1016/S1872-5805(25)60956-5","url":null,"abstract":"<div><div>The ecological and environmental issues caused by CO<sub>2</sub> emissions are becoming increasingly severe. Adsorption separation is recognized as one of the effective approaches for CO<sub>2</sub> capture, with activated carbon serving as a widely used adsorbent. As high-quality coal resources for activated carbon production are gradually being depleted, the use of bamboo, anabundant resource in China, as a raw material for activated carbon has become a rational alternative. This paper reviews the mechanisms influencing the CO<sub>2</sub> adsorption performance of activated carbon, such as pore structure and surface chemistry, and thoroughly explores the relationship between its composition, structure, and CO<sub>2</sub> adsorption performance. It focuses on the important process aspects of pore regulation, surface modification strategies, and molding techniques for bamboo-based activated carbon, summarizing research progress in the preparation and modification methods of bamboo-based activated carbon for CO<sub>2</sub> adsorption. Technical challenges in its current production are evaluated and future development directions are proposed, aim-ing to provide technical insights for promoting the use of bamboo-based activated carbon for CO<sub>2</sub> capture.\u0000\t\t\t\t<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (92KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":"40 2","pages":"Pages 317-332"},"PeriodicalIF":5.7,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143887618","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A review of the use of electrospinning in the preparation of flexible lithium-ion batteries","authors":"Jia-yi XING , Yu-zhuo ZHANG , Shu-xin FENG , Ke-meng JI","doi":"10.1016/S1872-5805(25)60962-0","DOIUrl":"10.1016/S1872-5805(25)60962-0","url":null,"abstract":"<div><div>Electrospinning technology has emerged as a promising method for fabricating flexible lithium-ion batteries (FLIBs) due to its ability to create materials with desirable properties for energy storage applications. FLIBs, which are foldable and have high energy densities, are becoming increasingly important as power sources for wearable devices, flexible electronics, and mobile energy applications. Carbon materials, especially carbon nanofibers, are pivotal in improving the performance of FLIBs by increasing electrical conductivity, chemical stability, and surface area, as well as reducing costs. These materials also play a significant role in establishing conducting networks and improving structural integrity, which are essential for extending the cycle life and enhancing the safety of the batteries. This review considers the role of electrospinning in the fabrication of critical FLIB components, with a particular emphasis on the integration of carbon materials. It explores strategies to optimize FLIB performance by fine-tuning the electrospinning parameters, such as electric field strength, spinning rate, solution concentration, and carbonization process. Precise control over fiber properties is crucial for enhancing battery reliability and stability during folding and bending. It also highlights the latest research findings in carbon-based electrode materials, high-performance electrolytes, and separator structures, discussing the practical challenges and opportunities these materials present. It underscores the significant impact of carbon materials on the evolution of FLIBs and their potential to shape future energy storage technologies.\u0000\t\t\t\t<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (127KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":"40 2","pages":"Pages 270-291"},"PeriodicalIF":5.7,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143887621","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ning-Jing SONG , Can-liang MA , Nan-nan GUO , Yun ZHAO , Wan-xi LI , Bo-qiong LI
{"title":"Tailoring the pore structure of hard carbon for enhanced sodium-ion battery anodes","authors":"Ning-Jing SONG , Can-liang MA , Nan-nan GUO , Yun ZHAO , Wan-xi LI , Bo-qiong LI","doi":"10.1016/S1872-5805(25)60967-X","DOIUrl":"10.1016/S1872-5805(25)60967-X","url":null,"abstract":"<div><div>Biomass-derived hard carbons, usually prepared by pyrolysis, are widely considered the most promising anode materials for sodium-ion batteries (SIBs) due to their high capacity, low potential, sustainability, cost-effectiveness, and environmental friendliness. The pyrolysis method affects the microstructure of the material, and ultimately its sodium storage performance. Our previous work has shown that pyrolysis in a sealed graphite vessel improved the sodium storage performance of the carbon, however the changes in its microstructure and the way this influences the sodium storage are still unclear. A series of hard carbon materials derived from corncobs (CCG-<em>T</em>, where <em>T</em> is the pyrolysis temperature) were pyrolyzed in a sealed graphite vessel at different temperatures. As the pyrolysis temperature increased from 1000 to 1400 °C small carbon domains gradually transformed into long and curved domains. At the same time, a greater number of large open pores with uniform apertures, as well as more closed pores, were formed. With the further increase of pyrolysis temperature to 1600 °C, the long and curved domains became longer and straighter, and some closed pores gradually became open. CCG-1400, with abundant closed pores, had a superior SIB performance, with an initial reversible capacity of 320.73 mAh g<sup>−1</sup> at a current density of 30 mA g<sup>−1</sup>, an initial Coulomb efficiency (ICE) of 84.34%, and a capacity retention of 96.70% after 100 cycles. This study provides a method for the precise regulation of the microcrystalline and pore structures of hard carbon materials.\u0000\t\t\t\t<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (100KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":"40 2","pages":"Pages 367-380"},"PeriodicalIF":5.7,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143887575","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Bei CHENG , Xing-yan XIE , Liu WAN , Jian CHEN , Yan ZHANG , Cheng DU , Xue-feng GUO , Ming-jiang XIE
{"title":"Controlling the conductivity and microporosity of biocarbon to produce supercapacitors with battery-level energies at an ultrahigh power","authors":"Bei CHENG , Xing-yan XIE , Liu WAN , Jian CHEN , Yan ZHANG , Cheng DU , Xue-feng GUO , Ming-jiang XIE","doi":"10.1016/S1872-5805(25)60960-7","DOIUrl":"10.1016/S1872-5805(25)60960-7","url":null,"abstract":"<div><div>In order to meet the demands of new-generation electric vehicles that require high power output (over 15 kW/kg), it is crucial to increase the energy density of carbon-based supercapacitors to a level comparable to that of batteries, while maintaining a high power density. We report a porous carbon material produced by immersing poplar wood (PW) sawdust in a solution of KOH and graphene oxide (GO), followed by carbonization. The resulting material has exceptional properties as an electrode for high-energy supercapacitors. Compared to the material prepared by the direct carbonization of PW, its electrical conductivity was increased from 0.36 to 26.3 S/cm. Because of this and a high microporosity of over 80%, which provides fast electron channels and a large ion storage surface, when used as the electrodes for a symmetric supercapacitor, it gave a high energy density of 27.9 Wh/[email protected] kW/kg in an aqueous electrolyte of 1.0 mol/L Na<sub>2</sub>SO<sub>4</sub>. The device also had battery-level energy storage with maximum energy densities of 73.9 Wh/[email protected] kW/kg and 67.6 Wh/kg@40 kW/kg, an ultrahigh power density, in an organic electrolyte of 1.0 mol/L TEABF<sub>4</sub>/AN. These values are comparable to those of 30−45 Wh/kg for Pb-acid batteries and 30−55 Wh/kg for aqueous lithium batteries. This work indicates a way to prepare carbon materials that can be used in supercapacitors with ultrahigh energy and power densities.\u0000\t\t\t\t<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (106KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":"40 2","pages":"Pages 397-407"},"PeriodicalIF":5.7,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143887577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Low-value biomass-derived carbon composites for electromagnetic wave absorption and shielding: A review","authors":"Sahoo Sumanta , Kumar Rajesh , Soo Han Sung","doi":"10.1016/S1872-5805(25)60965-6","DOIUrl":"10.1016/S1872-5805(25)60965-6","url":null,"abstract":"<div><div>The rising concern over electromagnetic (EM) pollution is responsible for the rapid progress in EM interference (EMI) shielding and EM wave absorption in the last few years, and carbon materials with a large surface area and high porosity have been investigated. Compared to other carbon materials, biomass-derived carbon (BC) are considered efficient and eco-friendly materials for this purpose. We summarize the recent advances in BC materials for both EMI shielding and EM wave absorption. After a brief overview of the synthesis strategies of BC materials and a precise outline of EM wave interference, strategies for improving their EMI shielding and EM wave absorption are discussed. Finally, the existing challenges and the future prospects for such materials are briefly summarized.\u0000\t\t\t\t<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (141KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":"40 2","pages":"Pages 293-316"},"PeriodicalIF":5.7,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143887622","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Su-xia QI , Tao YANG , Yan SONG , Ning ZHAO , Jun-qing LIU , Xiao-dong TIAN , Jin-ru WU , Hui LI , Zhan-jun LIU
{"title":"Impact of pitch fraction oxidation on the structure and sodium storage properties of derived carbon materials","authors":"Su-xia QI , Tao YANG , Yan SONG , Ning ZHAO , Jun-qing LIU , Xiao-dong TIAN , Jin-ru WU , Hui LI , Zhan-jun LIU","doi":"10.1016/S1872-5805(25)60961-9","DOIUrl":"10.1016/S1872-5805(25)60961-9","url":null,"abstract":"<div><div>Pitch produced by the liquefaction of coal was divided into two fractions: soluble in toluene (TS) and insoluble in toluene but soluble in pyridine (TI-PS), and their differences in molecular structure and oxidation activity were studied. Several different carbon materials were produced from them by oxidation in air (350 °C, 300 mL/min) followed by carbonization (1000 °C in Ar), and the effect of the cross-linked structure on their structure and sodium storage properties was investigated. The results showed that the two pitch fractions were obviously different after the air oxidation. The TS fraction with a low degree of condensation and abundant side chains had a stronger oxidation activity and thus introduced more cross-linked oxygen-containing functional groups C(O)―O which prevented carbon layer rearrangement during the carbonization. As a result, a disordered hard carbon with more defects was formed, which improved the electrochemical performance. Therefore, the carbon materials derived from TS (O-TS-1000) had an obvious disordered structure and a larger layer spacing, giving them better sodium storage performance than those derived from the TI-PS fraction (O-TI-PS-1000). The specific capacity of O-TS-1000 was about 250 mAh/g at 20 mA/g, which was 1.67 times higher than that of O-TI-PS-1000 (150 mAh/g).\u0000\t\t\t\t<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (107KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":"40 2","pages":"Pages 409-421"},"PeriodicalIF":5.7,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143887652","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}