Chemical Synthesis最新文献

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Chiral cage materials with tailored functionalities for enantioselective recognition and separation 具有定制功能的手性笼材料,用于对映选择性识别和分离
Chemical Synthesis Pub Date : 2024-06-14 DOI: 10.20517/cs.2023.54
Tianyu Li, Yuan Pan, Luyao Ding, Yihong Kang, Xin-Qi Hao, Yujing Guo, Linlin Shi
{"title":"Chiral cage materials with tailored functionalities for enantioselective recognition and separation","authors":"Tianyu Li, Yuan Pan, Luyao Ding, Yihong Kang, Xin-Qi Hao, Yujing Guo, Linlin Shi","doi":"10.20517/cs.2023.54","DOIUrl":"https://doi.org/10.20517/cs.2023.54","url":null,"abstract":"Chiral chemistry is often regarded as the science of studying the stereostructure and symmetry of organic molecules. It mainly focuses on the presence of chiral centers in specific structures and their impact on conformation, properties, and functions. In this field, researchers explore the special properties and potential applications of chiral compounds through synthesis, separation, and characterization. Here, we aim to provide a detailed overview of diverse functionalized cages based on chiral skeletons and their applications in enantioselective recognition and separation, and a diversity of chiral caged skeletons bearing customized functionalities conducted on the recognition and separation of chiral guests.","PeriodicalId":381136,"journal":{"name":"Chemical Synthesis","volume":"17 12","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141341367","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A 3D ordered hierarchical crystalline porous organic salt for large-sized enzyme immobilization 用于大尺寸酶固定的三维有序分层结晶多孔有机盐
Chemical Synthesis Pub Date : 2024-06-12 DOI: 10.20517/cs.2024.24
Jinman Wang, Guolong Xing, Yu Zhao, Jinming Zhou, Bo Song, Li‐Hua Chen, Weidong Zhu, Baolian Su, Teng Ben
{"title":"A 3D ordered hierarchical crystalline porous organic salt for large-sized enzyme immobilization","authors":"Jinman Wang, Guolong Xing, Yu Zhao, Jinming Zhou, Bo Song, Li‐Hua Chen, Weidong Zhu, Baolian Su, Teng Ben","doi":"10.20517/cs.2024.24","DOIUrl":"https://doi.org/10.20517/cs.2024.24","url":null,"abstract":"Crystalline porous organic salts (CPOSs) are an emerging class of promising materials with intrinsic highly polar nanoconfined microporosity. However, their single microporous structure greatly hinders their development in the field of catalysis and adsorption. Constructing a hierarchical porous structure can effectively reduce the mass transport resistance, thus expanding the scope of their applications. Herein, we report the synthesis of a three-dimensional (3D) ordered macro-/microporous hierarchical CPOS (HCPOS-1) using a template-assisted approach for the first time. The as-synthesized HCPOS-1 prepared from a polystyrene colloidal crystal template showcases a 3D ordered macroporous structure while also preserving the microporous structure. The 3D ordered macroporous structure in such a hierarchical structure, together with its hydrophilic surface, endows HCPOS-1 with the ability to immobilize large-sized enzymes through physical adsorption under mild conditions. The resulting catalase/HCPOS-1 showcases a high enzyme immobilization capacity and avoids undesired conformational changes of enzymes during the immobilization process, thus exhibiting excellent catalytic activity for the decomposition of hydrogen peroxide.","PeriodicalId":381136,"journal":{"name":"Chemical Synthesis","volume":"127 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141351654","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Facile synthesis of Ag/AgCl/PAF-54 heterojunction photocatalysts for TC degradation 轻松合成用于 TC 降解的 Ag/AgCl/PAF-54 异质结光催化剂
Chemical Synthesis Pub Date : 2024-06-11 DOI: 10.20517/cs.2024.17
Yonghui Lin, Letian Gan, Xiaojun Zhao, Guang Che, Shicheng Wang, Qinhe Pan
{"title":"Facile synthesis of Ag/AgCl/PAF-54 heterojunction photocatalysts for TC degradation","authors":"Yonghui Lin, Letian Gan, Xiaojun Zhao, Guang Che, Shicheng Wang, Qinhe Pan","doi":"10.20517/cs.2024.17","DOIUrl":"https://doi.org/10.20517/cs.2024.17","url":null,"abstract":"Photocatalysis plays an increasingly important role in the field of water treatment. Among the catalysts, Ag nanoparticles (NPs), a type of noble metal NP, show extraordinary potential for photocatalysis. Nevertheless, the aggregation caused by high surface energy limits their applications. The simple synthesis of Ag NPs with uniform size remains a challenge. In this work, a nitrogen-rich porous organic polymer (POP) with reduction ability, porous aromatic framework (PAF)-54, was chosen as the carrier for the in-situ synthesis of Ag NPs. By virtue of the reducing framework of PAF-54 and the formation of the AgCl/PAF-54 heterojunction, the in-situ reduction of Ag(I) was realized, and thus Ag NPs with the particle size of 20-25 nm were uniformly distributed on PAF-54, which exhibit a strong localized surface plasmon resonance (LSPR) effect. Furthermore, the Ag/AgCl/PAF-54 heterojunction effectively suppresses the recombination of photogenerated electrons and holes, leading to the enhanced photocatalytic ability of the composite material. Even with a small catalyst dosage, rapid tetracycline (TC) degradation can be achieved, and the degradation rate of TC reached 94.8% in 30 min. This study offers a facilitated approach for fabricating Ag-based POP composites with superior photocatalytic properties.","PeriodicalId":381136,"journal":{"name":"Chemical Synthesis","volume":"2 3","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141360588","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sustainable synthesis of Fe-MOR zeolite for efficient capture of CO2 可持续合成用于高效捕获二氧化碳的 Fe-MOR 沸石
Chemical Synthesis Pub Date : 2024-06-06 DOI: 10.20517/cs.2023.70
Pei Liu, Qinming Wu, Keping Yan, Liang Wang, Feng-shou Xiao
{"title":"Sustainable synthesis of Fe-MOR zeolite for efficient capture of CO2","authors":"Pei Liu, Qinming Wu, Keping Yan, Liang Wang, Feng-shou Xiao","doi":"10.20517/cs.2023.70","DOIUrl":"https://doi.org/10.20517/cs.2023.70","url":null,"abstract":"Selective adsorption of carbon dioxide (CO2) is significant for carbon neutrality, where searching for efficient CO2 adsorbents is very important. In addition, coal fly ash (CFA) is one of the largest industrial solid wastes with environmental damages, where conversion of the wastes into costly functional materials is attractive. This work showed sustainable synthesis of Fe-containing mordenite (Fe-MOR) zeolite from the CFA waste under solvent-free conditions, and this zeolite is an efficient capturer for CO2 in the mixture of CO2/N2 (15/85, v/v), giving adsorption capacity of 2.07 mmol/g and separation coefficient of 58.9 at 298 K. Very interestingly, the capture of CO2 in the mixture of CO2/N2 (15/85, v/v) is recyclable. This work not only solved the accumulation and pollution of CFA but also prepared a highly efficient adsorbent of Fe-MOR zeolite, which would open a door for utilizing environmentally unfriendly solid wastes as value-added functional materials in the future.","PeriodicalId":381136,"journal":{"name":"Chemical Synthesis","volume":"358 7","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141380936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Graphene oxide membranes using MOF@Chitosan core-shell nanoparticles as dual modulators for dye separation 使用 MOF@ 壳聚糖核壳纳米粒子作为染料分离双重调制剂的氧化石墨烯膜
Chemical Synthesis Pub Date : 2024-05-14 DOI: 10.20517/cs.2023.60
Xingying Wang, Yongmei Guo, Xiaolei Cui, Zhikun Wang, Zhihan Zhang, L. Tosheva, Hailing Guo
{"title":"Graphene oxide membranes using MOF@Chitosan core-shell nanoparticles as dual modulators for dye separation","authors":"Xingying Wang, Yongmei Guo, Xiaolei Cui, Zhikun Wang, Zhihan Zhang, L. Tosheva, Hailing Guo","doi":"10.20517/cs.2023.60","DOIUrl":"https://doi.org/10.20517/cs.2023.60","url":null,"abstract":"Graphene oxide (GO) membranes hold significant promise for the water purification. However, they also face the problem of structural swelling, which limits their use in water treatment applications. In this work, a novel dual-modulated core-shell metal-organic framework@Chitosan (MOF@CS) was successfully synthesized and used as an intercalation cross-linker to optimize the interlayer spacing and stability of GO membranes. Molecular dynamics simulation confirms that MOF@CS, acting as an intercalator, accelerates the water diffusion rate within the channels of the GO layer compared to a pure GO layer. At the same time, Fourier Transform Infrared Spectroscopy analysis reveals that MOF@CS serves as a cross-linker for covalently cross-linking the GO layer. The nanofiltration performance and stability of the improved MOF@CS-GO composite membranes were significantly enhanced. Compared to the pure GO membranes, the MOF@CS-GO composite membranes exhibited enhanced Congo red rejection rates (from 76.5% to 95.6%) while maintaining a high pure water flux (34.5 L·m-2·h-1·bar-1) and good structural stability (stable dye removal performance over 120 h). This dual regulation strategy is expected to effectively solve the swelling problem of GO membranes in aqueous media and open up avenues for advancing their performance.","PeriodicalId":381136,"journal":{"name":"Chemical Synthesis","volume":"19 19","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140982329","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
CoFe2O4 nanoparticles as a bifunctional agent on activated porous carbon for battery-type asymmetrical supercapacitor 将 CoFe2O4 纳米粒子作为活性多孔碳上的双功能剂用于电池型非对称超级电容器
Chemical Synthesis Pub Date : 2024-05-14 DOI: 10.20517/cs.2023.48
Qiang Qu, Zhuo Chen, Guo-Tao Sun, Ling Qiu, Ming-qiang Zhu
{"title":"CoFe2O4 nanoparticles as a bifunctional agent on activated porous carbon for battery-type asymmetrical supercapacitor","authors":"Qiang Qu, Zhuo Chen, Guo-Tao Sun, Ling Qiu, Ming-qiang Zhu","doi":"10.20517/cs.2023.48","DOIUrl":"https://doi.org/10.20517/cs.2023.48","url":null,"abstract":"The low performance of electrode materials is the main obstacle limiting the development of the supercapacitor industry, which can be solved by doping cobalt ferrate nanoparticles (NPs) with carbon materials. Herein, the composites of CoFe2O4 based on activated carbon (AC) were successfully prepared using a one-step solvothermal method and subsequently applied in anodes of battery-type asymmetrical supercapacitors. The effect of solvothermal temperature and heating time on the composite characteristic was systematically evaluated. The electrochemical analysis in the three-electrode system revealed that modified activated carbon heated at 140 °C for 24 h (140MAC24) displayed excellent specific capacitance of 571.36 F/g at the current density of 0.2 A/g due to the synergistic effect of the double-layer and faradic capacitance. Moreover, iron and cobalt elements in CoFe2O4 could change into the oxide form to accelerate charge in potential range window of -1.0 to -0.2 V and discharge from -0.2 to 0.2 V, respectively. Meanwhile, the result of assessing economic feasibility suggested the splendid availability of 140MAC24 electrodes. Additionally, the assembled supercapacitor displayed the outstanding specific capacitance of 171.31 F/g in the potential window of 1.8 V, energy density of 43.5 Wh/kg at the current density of 0.2 A/g, and capacitance retention rate of 82.49% after 10,000 cycles. The excellent electrochemical properties demonstrated that CoFe2O4 could be used as a bifunctional agent for enhancing supercapacitive performance.","PeriodicalId":381136,"journal":{"name":"Chemical Synthesis","volume":"49 9","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140980687","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Highly selective production of renewable methyl acrylate via aldol condensation over Cu modified nitrogen-containing Beta zeolites 在铜修饰的含氮 Beta 沸石上通过醛醇缩合高选择性地生产可再生丙烯酸甲酯
Chemical Synthesis Pub Date : 2024-04-18 DOI: 10.20517/cs.2024.04
Mei Wang, Lulu Xu, Weiping Zhang
{"title":"Highly selective production of renewable methyl acrylate via aldol condensation over Cu modified nitrogen-containing Beta zeolites","authors":"Mei Wang, Lulu Xu, Weiping Zhang","doi":"10.20517/cs.2024.04","DOIUrl":"https://doi.org/10.20517/cs.2024.04","url":null,"abstract":"Highly selective synthesis of renewable methyl acrylate from bio-sourced formaldehyde and methyl acetate through one-step aldol condensation was successfully realized on Cu-modified nitrogen-containing Beta (NBeta) catalysts. Silicon-29 magic angle spinning nuclear magnetic resonance (29Si MAS NMR), Fourier transform infrared spectroscopy (FT-IR), temperature-programmed desorption of ammonia, temperature-programmed desorption of carbon dioxide, and element analysis indicate that nitridation weakens the acid strength, reduces the number of acidic sites and introduces basic sites through the formation of Si−N bond on Beta zeolites, thereby promoting methyl acrylate selectivity and reducing the coke formation. Adding Cu into NBeta further finely tunes the basicity and acidity balance and thus inhibits the by-product acetone. High methyl acrylate selectivity of 95% and formaldehyde conversion of 99% were achieved over Cu/NBeta catalyst under optimized conditions. The coke content decreases remarkably from 28% on H-form Beta (HBeta) zeolites to 17% on NBeta zeolites doped with Cu due to its appropriate basicity/acidity. Cu/NBeta has good regeneration capability, and the weakening of Si-N species may account for the decline of catalytic performance after successive regeneration. The catalytic performance was restored when the regenerated catalyst was nitridated again.","PeriodicalId":381136,"journal":{"name":"Chemical Synthesis","volume":" 30","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140689221","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recycling valuable materials from the spent lithium ion batteries to catalysts: methods, applications, and characterization 从废旧锂离子电池中回收有价值的材料制成催化剂:方法、应用和表征
Chemical Synthesis Pub Date : 2024-04-11 DOI: 10.20517/cs.2023.66
Hao-Long Sun, Yun-Peng Xu, Lian Ding, Yu Gu, Jianfeng Li
{"title":"Recycling valuable materials from the spent lithium ion batteries to catalysts: methods, applications, and characterization","authors":"Hao-Long Sun, Yun-Peng Xu, Lian Ding, Yu Gu, Jianfeng Li","doi":"10.20517/cs.2023.66","DOIUrl":"https://doi.org/10.20517/cs.2023.66","url":null,"abstract":"As the prevailing technology for energy storage, the extensive adoption of lithium-ion batteries (LIBs) inevitably results in the accumulation of numerous spent batteries at the end of their lifecycle. From the standpoints of environmental protection and resource sustainability, recycling emerges as an essential strategy to effectively manage end-of-life LIBs and reclaim valuable elements within them. Hydrometallurgy, closely intertwined with catalysis, stands as a relatively mature strategy for achieving high-value utilization of spent LIBs. In this review, our emphasis is placed on the interconnected themes of catalysis within the realm of hydrometallurgical recycling. Specifically, we delve into the crucial role that catalysis plays in both the recycling process of LIBs and the sustainable utilization of their extracted materials in various catalytic applications. This focused exploration aims to contribute insights into the intricate relationship between catalysis and the broader context of LIB recycling, shedding light on its pivotal role in achieving both environmental sustainability and functional material repurposing. Moreover, we highlight advanced characterization techniques, represented by surface-sensitive enhanced Raman spectroscopy, to fundamentally understand the reaction mechanism of catalysts, which, in turn, would inform more rational catalyst designs.","PeriodicalId":381136,"journal":{"name":"Chemical Synthesis","volume":"21 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140715734","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biological metal–organic frameworks for natural gas purification and MTO product separation 用于天然气净化和 MTO 产品分离的生物金属有机框架
Chemical Synthesis Pub Date : 2024-04-08 DOI: 10.20517/cs.2023.69
Wen Li, Dan Wang, Yi Wang, Zhaohui Shi, Junxue Liu, Lirong Zhang, Dongxu Xue, Yunlin Liu
{"title":"Biological metal–organic frameworks for natural gas purification and MTO product separation","authors":"Wen Li, Dan Wang, Yi Wang, Zhaohui Shi, Junxue Liu, Lirong Zhang, Dongxu Xue, Yunlin Liu","doi":"10.20517/cs.2023.69","DOIUrl":"https://doi.org/10.20517/cs.2023.69","url":null,"abstract":"The use of porous solid adsorbents is an effective and excellent approach for the separation and purification of methanol-to-olefins product and methane (CH4). In this particular study, a series of adenine (AD)-based biological metal–organic frameworks (Bio-MOFs) {Their general formula is Cu 2 (AD) 2 (X) 2 [X = formic acid, acetic acid (AA), and propionic acid]} were proposed, which exhibited remarkable efficiency in the purification of CH4 and the separation of C3H6 from methanol-to-olefins product, ultimately yielding purified C2H4. The experimental findings demonstrate that different terminal ligands induce alterations in the pore microenvironment, consequently leading to variations in adsorption capacities and stability. Specifically, Cu-AD-AA exhibits the highest adsorption capacity and selectivity among the three MOFs, as confirmed by static adsorption isotherm testing and theoretical evaluation using ideal adsorbed solution theory (IAST) simulation. At 298 K and 1 bar, Cu-AD-AA exhibits 786 and 10.9 selectivity for C3H8/CH4 and C3H6/C2H4, respectively, surpassing the majority of MOFs materials. Furthermore, breakthrough experiments conducted in ambient conditions reveal that Cu-AD-AA possesses commendable separation capabilities, enabling one-step purification of C2H4 at varying proportions (C2H4/C3H6 = 50:50, 50:20, and 90:10), along with satisfactory recycling performance. Importantly, the synthesis of Cu-AD-AA utilizes simple and easily obtainable raw materials, thereby offering advantages such as cost-effectiveness, low toxicity, and facile synthesis that enhance its potential for industrial applications.","PeriodicalId":381136,"journal":{"name":"Chemical Synthesis","volume":"262 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140730471","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Macrocycle-based covalent-organic-polymer as efficient oxygen electrocatalysts for zinc-air flow batteries 基于大环的共价有机聚合物作为锌-空气液流电池的高效氧气电催化剂
Chemical Synthesis Pub Date : 2024-04-03 DOI: 10.20517/cs.2023.64
Yiming Leng, Tengge Chen, Yuanyuan Yin, Jizhen Li, Xueli Li, Zhonghua Xiang
{"title":"Macrocycle-based covalent-organic-polymer as efficient oxygen electrocatalysts for zinc-air flow batteries","authors":"Yiming Leng, Tengge Chen, Yuanyuan Yin, Jizhen Li, Xueli Li, Zhonghua Xiang","doi":"10.20517/cs.2023.64","DOIUrl":"https://doi.org/10.20517/cs.2023.64","url":null,"abstract":"Covalent organic polymers (COPs), as emerging porous materials with well-defined architectures and high hydrothermal stability, have attracted extensive attention in the field of electrocatalysis. Herein, we report a rational design method for preparing oxygen reduction reaction electrocatalysts with the assistance of a predesigned macrocyclic COP model molecular. With the predesigned nitrogen position and structural features in macrocyclic chain-like COP-based materials, the obtained COPMCT-Co-900 catalyst provided excellent oxygen reduction performance, where the half-wave potential (E1/2) reaches 0.85 V (vs . RHE), comparable to commercial Pt/C. We also extended the strategy to similar macrocycle COPs and Fe-based and Ni-based metal sources and studied the oxygen reduction reaction performance of corresponding catalysts, proving the universality of the method. Interestingly, we assemble COPMCT-Co-900 catalyst as air electrode catalyst of the self-made rechargeable zinc-air flow batteries, which exhibit outstanding power density (155.6 mW·cm-2) and long cycle life (90 h, 270 cycles at 10 mA·cm-2). Our studies provide a new method for the development of high-performance oxygen electrodes applied in zinc-air flow battery devices.","PeriodicalId":381136,"journal":{"name":"Chemical Synthesis","volume":"8 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140748252","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","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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