Qinglu Li , Sufeng Zhang , Xiaokai Jing , Nan Li , Ning Wei , Lei Li , Yao Feng , Jinrui Li , Yali Liu
{"title":"纸卷铅笔启发自组装多层交织纳米纤维素超级电容器电极实现跨尺度应力阻抗与电化学稳定性耦合","authors":"Qinglu Li , Sufeng Zhang , Xiaokai Jing , Nan Li , Ning Wei , Lei Li , Yao Feng , Jinrui Li , Yali Liu","doi":"10.1016/j.carbpol.2025.124165","DOIUrl":null,"url":null,"abstract":"<div><div>The practical application of flexible supercapacitors is often constrained by the critical contradiction between structural disintegration of electrode materials under mechanical deformation and deterioration of electrochemical performance. Inspired by the multilayer wrapping structure of paper-roll-pencils, we propose a self-assembled multilayer interwoven electrode architecture. In this design, bacterial cellulose (BC) forms a multilayered outer scaffold via alternating winding, while polydopamine (PDA) enhances interfacial adhesion and electronic coupling between nitrogen-doped graphene (N-rGO). A continuous polypyrrole (PPy) pseudocapacitive layer further encapsulates the structure to form a conductive network, collaboratively forming a continuous cross-interface transport channel from nanoscale to microscale. This unique electrode architecture simultaneously enables stress-gradient buffering and electrochemical stability regulation under mechanical load. As a result, the electrode retains 96.3 % of its capacitance after 10,000 charge-discharge cycles and ultrasonic agitation (40 kHz/200 W). This work offers a novel strategy for constructing flexible energy storage electrodes with integrated cross-scale stress impedance and high electrochemical durability.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"368 ","pages":"Article 124165"},"PeriodicalIF":12.5000,"publicationDate":"2025-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Paper-roll-pencils inspired self-assembled multilayer interwoven nanocellulose supercapacitor electrode enables cross-scale stress impedance coupled with electrochemical stability\",\"authors\":\"Qinglu Li , Sufeng Zhang , Xiaokai Jing , Nan Li , Ning Wei , Lei Li , Yao Feng , Jinrui Li , Yali Liu\",\"doi\":\"10.1016/j.carbpol.2025.124165\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The practical application of flexible supercapacitors is often constrained by the critical contradiction between structural disintegration of electrode materials under mechanical deformation and deterioration of electrochemical performance. Inspired by the multilayer wrapping structure of paper-roll-pencils, we propose a self-assembled multilayer interwoven electrode architecture. In this design, bacterial cellulose (BC) forms a multilayered outer scaffold via alternating winding, while polydopamine (PDA) enhances interfacial adhesion and electronic coupling between nitrogen-doped graphene (N-rGO). A continuous polypyrrole (PPy) pseudocapacitive layer further encapsulates the structure to form a conductive network, collaboratively forming a continuous cross-interface transport channel from nanoscale to microscale. This unique electrode architecture simultaneously enables stress-gradient buffering and electrochemical stability regulation under mechanical load. As a result, the electrode retains 96.3 % of its capacitance after 10,000 charge-discharge cycles and ultrasonic agitation (40 kHz/200 W). This work offers a novel strategy for constructing flexible energy storage electrodes with integrated cross-scale stress impedance and high electrochemical durability.</div></div>\",\"PeriodicalId\":261,\"journal\":{\"name\":\"Carbohydrate Polymers\",\"volume\":\"368 \",\"pages\":\"Article 124165\"},\"PeriodicalIF\":12.5000,\"publicationDate\":\"2025-08-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Carbohydrate Polymers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0144861725009506\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbohydrate Polymers","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0144861725009506","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
The practical application of flexible supercapacitors is often constrained by the critical contradiction between structural disintegration of electrode materials under mechanical deformation and deterioration of electrochemical performance. Inspired by the multilayer wrapping structure of paper-roll-pencils, we propose a self-assembled multilayer interwoven electrode architecture. In this design, bacterial cellulose (BC) forms a multilayered outer scaffold via alternating winding, while polydopamine (PDA) enhances interfacial adhesion and electronic coupling between nitrogen-doped graphene (N-rGO). A continuous polypyrrole (PPy) pseudocapacitive layer further encapsulates the structure to form a conductive network, collaboratively forming a continuous cross-interface transport channel from nanoscale to microscale. This unique electrode architecture simultaneously enables stress-gradient buffering and electrochemical stability regulation under mechanical load. As a result, the electrode retains 96.3 % of its capacitance after 10,000 charge-discharge cycles and ultrasonic agitation (40 kHz/200 W). This work offers a novel strategy for constructing flexible energy storage electrodes with integrated cross-scale stress impedance and high electrochemical durability.
期刊介绍:
Carbohydrate Polymers stands as a prominent journal in the glycoscience field, dedicated to exploring and harnessing the potential of polysaccharides with applications spanning bioenergy, bioplastics, biomaterials, biorefining, chemistry, drug delivery, food, health, nanotechnology, packaging, paper, pharmaceuticals, medicine, oil recovery, textiles, tissue engineering, wood, and various aspects of glycoscience.
The journal emphasizes the central role of well-characterized carbohydrate polymers, highlighting their significance as the primary focus rather than a peripheral topic. Each paper must prominently feature at least one named carbohydrate polymer, evident in both citation and title, with a commitment to innovative research that advances scientific knowledge.