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23rd International Conference on Composite Materials, ICCM 2023

作者： Zeng, Songshan Shen, Kuangyu Li, Rui Smith, Andrew Zhang, Dianyun Sun, Luyi Polymer Program Institute of Materials Science Department of Chemical & Biomolecular Engineering University of Connecticut United States

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A Review on Interface engineering of MXenes for Perovskite Solar Cells

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Nano-Micro Letters 2023年第8期15卷 270-308页

作者： Srikanta Palei G.Murali Choong‑Hee Kim Insik In Seul‑Yi Lee Soo‑Jin Park Department of Chemistry Inha University100 InharoIncheon 22212South Korea Department of Polymer Science and Engineering Department of IT‑Energy Convergence(BK21 Four)Chemical Industry InstituteKorea National University of TransportationChungju 27469South Korea

With an excellent power conversion efficiency of 25.7%,closer to the Shockley–Queisser limit,perovskite solar cells(PSCs)have become a strong candidate for a next-generation energy ***,the lack of stability and reliability in PSCs remained challenging for ***,such as interfacial and structural engineering,have a more critical influence on enhanced ***,two-dimensional materials,have emerged as promising materials in solar cell applications due to their metallic electrical conductivity,high carrier mobility,excellent optical transparency,wide tunable work function,and superior mechanical *** to different choices of transition elements and surface-terminating functional groups,MXenes possess the feature of tuning the work function,which is an essential metric for band energy alignment between the absorber layer and the charge transport layers for charge carrier extraction and collection in ***,adopting MXenes to their respective components helps reduce the interfacial recombination resistance and provides smooth charge transfer paths,leading to enhanced conductivity and operational stability of *** review paper aims to provide an overview of the applications of MXenes as components,classified according to their roles as additives(into the perovskite absorber layer,charge transport layers,and electrodes)and themselves alone or as interfacial layers,and their significant importance in PSCs in terms of device performance and ***,we discuss the present research status and future directions toward its use in PSCs.

关键词： MXenes Perovskite solar cells Additives Interfacial layer Electrodes

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Edge atomic Fe sites decorated porous graphitic carbon as an efficient bifunctional oxygen catalyst for Zinc-air batteries

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Journal of Energy chemistry 2023年第8期83卷 602-611,I0014页

作者： Ruihui Gan Yali Wang Xiangwu Zhang Yan Song Jingli Shi Chang Ma Tianjin Municipal Key Lab of Advanced Fiber and Energy Storage Technology Tiangong UniversityTianjin 300387China Fiber and Polymer Science Program Department of Textile EngineeringChemistry and ScienceWilson College of TextilesNorth Carolina State UniversityRaleighNC 27695-8301uNITED sTATES CAS Key Laboratory of Carbon Materials Institute of Coal ChemistryChinese Academy of SciencesTaiyuan 030001ShanxiChina

The development of advanced bifunctional oxygen electrocatalysts for oxygen reduction and evolution reactions(ORR and OER) is critical to the practical application of zinc-air batteries(ZABs). Herein, a silica-assisted method is reported to integrate numerous accessible edge Fe-Nx sites into porous graphitic carbon(named Fe-N-G) for achieving highly active and robust oxygen electrocatalysis. Silica facilitates the formation of edge Fe-Nx sites and dense graphitic domains in carbon by inhibiting iron *** purification process creates a well-developed mass transfer channel for Fe-N-G. Consequently,Fe-N-G delivers a half-wave potential of 0.859 V in ORR and an overpotential of 344 m V at10 m A cm^(-2)in OER. During long-term operation, the graphitic layers protect edge Fe-Nx sites from demetallation in ORR and synergize with Fe OOH species endowing Fe-N-G with enhanced OER *** functional theory calculations reveal that the edge Fe-Nx site is superior to the in-plane Fe-Nx site in terms of OH* dissociation in ORR and OOH* formation in OER. The constructed ZAB based on Fe-N-G cathode shows a higher peak power density of 133 m W cm^(-2)and more stable cycling performance than Pt/C + RuO2counterparts. This work provides a novel strategy to obtain high-efficiency bifunctional oxygen electrocatalysts through space mediation.

关键词： Bifunctionality EdgeFe-Nxsites Oxygen catalysis Graphitic domains Zinc-air batteries

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Histidine N-Thiocarboxyanhydride:Direct Synthesis and polymerization without Protection towards Well-defined Polyhistidine

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Chinese Journal of polymer science 2025年

作者： Song-Yi Xu Tian-Wen Bai Bo-Tuo Zheng Ze-Hua Li Jun Ling MOE Key Laboratory of Macromolecular Synthesis and Functionalization Department of Polymer Science and EngineeringZhejiang University College of Biological Chemical Sciences and EngineeringJiaxing University College of Chemistry and Materials Science Fujian Key Laboratory of Polymer MaterialsFujian Normal University

Consisting of natural histidine residues,polyhistidine （PHis） simulates functional *** approaches towards PHis require the protection of imidazole groups before monomer synthesis and polymerization to prevent degradation and side *** the contribution,histidine N-thiocarboxyanhydride （His-NTA） is directly synthesized in aqueous solution without *** the self-catalysis of the imidazole side group,the ring-closing reaction to form His-NTA does not require any activating reagent （e.g.,phosphorus tribromide）,which is elucidated by density functional theory （DFT） ***-NTA directly polymerizes into PHis bearing unprotected imidazole groups with designable molecular weights （4.2-7.7 kg/mol） and low dispersities （1.10-1.19）.Kinetic experiments and Monte Carlo simulations reveal the elementary reactions and the relationship between the conversion of His-NTA and time during *** copolymerization of His-NTA with sarcosine N-thiocarboxyanhydride （Sar-NTA） demonstrate versatile construction of functional polypept（o）*** triblock copoly（amino acid） PHis-b-PSar-b-PHis is capable to reversibly coordinate with transition metal ions (Fe2+,Co2+,Ni2+,Cu2+and Zn2+) to form pH-sensitive hydrogels.

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Effect of poly(4-tert-butylstyrene)block length on the microphase structure of poly(ethylene oxide)-b-poly(4-vinylbenzyl chloride)-b-poly(4-tert-butylstyrene)triblock terpolymers

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Chinese Chemical Letters 2023年第6期34卷 551-555页

作者： Kun An Jia Gao Yihang Chen Jingjing Nie Yongjin Li Junting Xu Binyang Du State Key Laboratory of Motor Vehicle Biofuel Technology Department of Polymer Science&EngineeringZhejiang UniversityHangzhou 310027China College of Material Chemistry and Chemical EngineeringHangzhou Normal UniversityHangzhou 310036China Department of Chemistry Zhejiang UniversityHangzhou 310027China

A series of linear poly(ethylene oxide)-b-poly(4-vinylbenzyl chloride)-b-poly(4-tert-butylstyrene)(PEO_(113)-b-PVBC_(130)-b-Pt BS_(x)or E_(113)V_(130)T_(x))triblock terpolymers with various lengths x(=20,33,66,104,215)of Pt BS block were synthesized via a two-step reversible addition-fragmentation chain transfer(RAFT)*** E_(113)V_(130)T_(x)triblock terpolymers were non-crystalline because the PVBC and Pt BS blocks strongly hindered the crystallization of PEO *** effects of Pt BS block length x on the phase structures of E_(113)V_(130)T_(x)triblock terpolymers were investigated by combined techniques of small-angle X-ray scattering(SAXS)and transmission electron microscopy(TEM).It was found that with increasing x from20 to 215,the phase structure of E_(113)V_(130)T_(x)triblock terpolymers became more ordered and changed from disordered structure,hexagonally-packed cylinder(HEX),hexagonally perforated layer(HPL),to lamellar(LAM)phase ***-variable SAXS measurements showed that the HEX,HPL and LAM phase structures obtained for E_(113)V_(130)T_(66),E_(113)V_(130)T_(104)and E_(113)V_(130)T_(215)by thermal annealing,respectively,were thermodynamically stable in the temperature range of 30-170℃.

关键词： ABC triblock terpolymer Phase structure SAXS HPL Thermodynamically stable

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Unraveling the Fundamental Mechanism of Interface Conductive Network Influence on the Fast‑Charging Performance of SiO‑Based Anode for Lithium‑Ion Batteries

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Nano-Micro Letters 2024年第3期16卷 53-68页

作者： Ruirui Zhang Zhexi Xiao Zhenkang Lin Xinghao Yan Ziying He Hairong Jiang Zhou Yang Xilai Jia Fei Wei Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology Department of Chemical EngineeringTsinghua UniversityBeijing 100084People’s Republic of China School of Materials Science and Engineering University of Science and Technology BeijingBeijing 100083People’s Republic of China Beijing Key Laboratory of Chemical Power Source and Green Catalysis School of Chemistry and Chemical EngineeringBeijing Institute of TechnologyBeijing 100081People’s Republic of China Institute of Polymer Science and Engineering Department of Chemical EngineeringTsinghua UniversityBeijing 100084People’s Republic of China

Progress in the fast charging of high-capacity silicon monoxide(SiO)-based anode is currently hindered by insufficient conductivity and notable volume *** construction of an interface conductive network effectively addresses the aforementioned problems;however,the impact of its quality on lithium-ion transfer and structure durability is yet to be ***,the influence of an interface conductive network on ionic transport and mechanical stability under fast charging is explored for the first time.2D modeling simulation and Cryo-transmission electron microscopy precisely reveal the mitigation of interface polarization owing to a higher fraction of conductive inorganic species formation in bilayer solid electrolyte interphase is mainly responsible for a linear decrease in ionic diffusion energy ***,atomic force microscopy and Raman shift exhibit substantial stress dissipation generated by a complete conductive network,which is critical to the linear reduction of electrode residual *** study provides insights into the rational design of optimized interface SiO-based anodes with reinforced fast-charging performance.

关键词： Fast charging SiO anode Interface conductive network Ionic transport Mechanical stability

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Gradient layered MXene/Fe_(3)O_(4)@CNTs/TOCNF ultrathin nanocomposite paper exhibiting effective electromagnetic shielding and multifunctionality

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Nano Research 2024年第9期17卷 8233-8242页

作者： Zhengkun Ma Jingzong He Shilin Liu Xiaoxuan Qie Meiheng Gan Ruonan Cheng Qilin Wu Malcolm Xing State Key Laboratory for Modification of Chemical Fibers and Polymer Materials College of Materials Science and EngineeringDonghua UniversityShanghai 201620China College of Chemistry and Chemical Engineering Donghua UniversityShanghai 201620China Department of Mechanical Engineering University of ManitobaWinnipegMB R3T 2N2Canada

As wearable electronic devices are rapidly developing,there is an urgent need for lightweight,flexible,and ultrathin multifunctional electromagnetic interference(EMI)shielding ***,the flexible ultrathin paper that combines efficient shielding and multifunctional integration remains a considerable ***,a novel MXene/Fe_(3)O_(4)@CNTs/TOCNF(MCT,MXene=transition metal carbide/carbonitride,CNTs=carbon nanotubes,TOCNF=TEMPO-oxidized cellulose nanofiber,TEMPO=2,2,6,6-tetramethylpiperidine-1-oxyl radical)nanocomposite paper with a multilayer electromagnetic gradient structure and electromagnetic dual losses was successfully prepared by a simple filtration *** from effective gradient design and adjusting the proportion of TOCNF,the composite paper(only 18μm)exhibits outstanding shielding effectiveness(SE)of 66 dB in the X-band,ultrahigh thickness-specific SE and surface-specific SE values of 3300 dB·mm-1 and 31,428 dB·cm^(2)·g^(-1)***,dehydroxylation treatment improves MCT paper's hydrophobicity,environmental stability,and mechanical strength,expanding its range of ***,the highly efficient Joule heating properties and hydrophobicity provide MCT additional de-icing *** also simulated the electromagnetic shielding effects of MCT composite paper,which was applied in *** study documents an innovative and intriguing material combination,providing a simple and effective manufacturing strategy for developing EMI shielding *** paper is highly suitable for outdoor portable or wearable electronic devices and has significant application potential in humid/severe cold environments.

关键词： cellulose fiber thin papers nanocomposites electromagnetic interference(EMI)shielding

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Recent progress on the use of lignin-based porous carbon in supercapacitors

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新型炭材料(中英文) 2025年第1期40卷 50-80页

作者： ZHA Ding-chen WANG Jia-heng Hao Rui-xiang Wu Yun-feng LI Xiu-he ZHAO Jia-wen LI Wen PIAO Wen-xiang JIANG Nan-zhe Department of Polymer Materials and Engineering College of EngineeringYanbian UniversityYanji 133002China Department of Materials and Chemical Engineering College of EngineeringYanbian UniversityYanji 133002China Department of Chemistry College of ScienceYanbian UniversityYanji 133002China

With the development of electronics and portable devices,there is a significant drive to develop electrode materials for supercapacitors that are lightweight,economical,and provide high energy and power ***-based porous carbons have recently been extensively studied for en-ergy storage applications because of their characteristics of large specific surface area,easy doping,and high *** progress in the synthesis of porous carbons derived from lignin,using different strategies for their preparation and modification with heteroatoms,metal oxides,met-al sulfides,and conductive polymers is considered and their electrochemical performances and ion storage mechanisms are *** fo-cus is directed towards the challenges encountered in using lignin-based por-ous carbons and the ways to optimize specific capacity and energy density for supercapacitor ***,the limitations of existing technolo-gies and research directions for improving the performance of lignin-based carbons are discussed.

关键词： Lignin Porous carbon Supercapacitor Carbonization

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Highly elastic and degradable vitrimeric elastomers using polycondensation

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Chinese Chemical Letters 2024年第3期35卷 434-438页

作者： Yue Liu Yongshuang Huang Chao Li Guifu Si Min Chen Institutes of Physical Science and Information Technology Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of EducationAnhui UniversityHefei 230601China CAS Key Laboratory of Soft Matter Chemistry Department of Polymer Science and EngineeringUniversity of Science and Technology of ChinaHefei 230026China

Introducing covalently crosslinked network to polymer matrix can merge the advantages in reprocessing and durability of *** this contribution,a series of high-performance vitrimeric elastomers were achieved via *** topological structures of polymers were tuned by varying the feeding ratios of bisacetoacetate,hex–substituted bisacetoacetate,bisamine and tris(2-aminoethyl)*** these structural manipulations,the vitrimeric elastomers presented great elastic recovery properties(strain recovery value up to 80%)benefiting from the introduction of long chain ***,the elastomers exhibited excellent reprocessing property,water vapor/oxygen barrier and adhesive ***,the elastomers could be degraded into monomer under acid conditions which enabled the elastomer synthesis again in closed loop recycling *** ease of the polycondensation in this work to prepare highly elastic and recyclable vitrimeric elastomers demonstrated exciting opportunities for the synthesis of sustainable polymers.

关键词： Polycondensation Vitrimeric elastomers Highly elastic Degradable polymers

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Ion-Anchoring Dipole-Integrated Composite Elastomer Electrolyte and Cathode for High-Performance Lithium Metal Batteries via Multiple-Bridge engineering

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Advanced Energy Materials 2025年

作者： Cho, A Hyeon Je, Ji Hyang Choi, U Hyeok Department of Polymer Science and Engineering and Program in Environmental and Polymer Engineering Inha University Incheon22212 Korea Republic of

Solid-state electrolytes (SSEs) hold significant potential for advancing lithium metal batteries (LMBs) by enhancing safety through the replacement of liquid electrolytes. However, challenges such as low ionic conductivity, limited electrochemical stability, and poor electrolyte/electrode interface compatibility hinder the development of high-energy-density LMBs. Herein, a strategy for designing SSEs is proposed using multiple-bridge engineered composite elastomer electrolytes (CEEs) that incorporate ion-rotating dipole interactions, ion-anchoring dipole interactions, and hydrogen bonding, along with a CEE-based composite elastomer cathode (CEC). This design combines a volume-adaptive elastomer matrix, a high-Li+ conducting deep eutectic electrolyte, and robust nanowires. The resultant CEE exhibits high ionic conductivity (1.7 × 10−3 S cm−1), a lithium transference number of 0.72, and a wide electrochemical stability window (up to 4.9 V) at 298 K. The engineered uniform Li+ flux also promotes stable Li plating/stripping for over 900 h at 0.1 mA cm−2. Furthermore, the LFP-based CEC|CEE|Li full cells deliver a reversible capacity of 133 mAh g−1 with 95% retention after 300 cycles in coin cells, and 129 mAh g−1 with 96% retention after 250 cycles in pouch cells at 1 C. This strategy presents a promising approach for designing solid-state polymer electrolytes to extend the lifespan of high-energy-density LMBs. © 2025 Wiley-VCH GmbH.

关键词： Elastomers

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