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Nanofiber Materials for Lithium‑Ion Batteries

Advanced Fiber Materials 2023年第4期5卷 1141-1197页

作者： Xinwang Cao Chang Ma Lei Luo Lei Chen Hui Cheng Raphael Simha Orenstein Xiangwu Zhang National Engineering Laboratory for Advanced Yarn and Fabric Formation and Clean Production College of Textiles Science and EngineeringWuhan Textile UniversityWuhan 430200China 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 27695USA

The lithium-ion(Li-ion)battery has received considerable attention in the field of energy conversion and storage due to its high energy density and *** academic and commercial progress has been made in Li-ion battery *** area of advancement has been the addition of nanofiber materials to Li-ion batteries due to their unique and desirable structural features including large aspect ratios,high surface areas,controllable chemical compositions,and abundant composite *** the past few decades,considerable research efforts have been devoted to constructing advanced nanofiber materials possessing conductive networks to facilitate efficient electron transport and large specific surface areas to support catalytically active sites,both for the purpose of boosting electrochemical ***,we focus on recent advancements of nanofiber materials with carefully designed structures and enhanced electrochemical properties for use in Li-ion *** synthesis,structure,and properties of nanofiber cathodes,anodes,separators,and electrolytes,and their applications in Li-ion batteries are *** research challenges and prospects of nanofiber materials in Li-ion battery applications are delineated.

关键词： Nanofiber Lithium-ion battery Cathode Anode Separator Electrolyte

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Ethanol steam reforming over Ni/ZSM-5 nanosheet for hydrogen production

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Chinese Journal of Chemical Engineering 2024年第3期67卷 247-256页

作者： Porapak Suriya Shanshan Xu Shengzhe Ding Sarayute Chansai Yilai Jiao Joseph Hurd Daniel Lee Yuxin Zhang Christopher Hardacre Prasert Reubroycharoen Xiaolei Fan Department of Chemical Engineering School of EngineeringThe University of ManchesterManchester M139PLUnited Kingdom Program of Petrochemistry and Polymer Science Faculty of ScienceChulalongkorn UniversityBangkok10330Thailand Shenyang National Laboratory for Materials Science Institute of Metal ResearchChinese Academy of SciencesShenyang 110016China Liaoning Academy of Materials Shenyang 110167China Center of Excellence in Catalysis for Bioenergy and Renewable Chemicals(CBRC) andDepartment of Chemical TechnologyFaculty of ScienceChulalongkorn UniversityBangkok 10330Thailand Nottingham Ningbo China Beacons of Excellence Research and Innovation Institute University of Nottingham Ningbo ChinaNingbo315100China

Compared to reforming reactions using hydrocarbons,ethanol steam reforming(ESR)is a sustainable alternative for hydrogen(H_(2))production since ethanol can be produced sustainably using *** work explores the catalyst design strategies for preparing the Ni supported on ZSM-5 zeolite catalysts to promote ***,two-dimensional ZSM-5 nanosheet and conventional ZSM-5 crystal were used as the catalyst carriers and two synthesis strategies,i.e.,in situ encapsulation and wet impregnation method,were employed to prepare the *** on the comparative characterization of the catalysts and comparative catalytic assessments,it was found that the combination of the in situ encapsulation synthesis and the ZSM-5 nanosheet carrier was the effective strategy to develop catalysts for promoting H_(2) production via ESR due to the improved mass transfer(through the 2-D structure of ZSM-5 nanosheet)and formation of confined small Ni nanoparticles(resulted via the in situ encapsulation synthesis).In addition,the resulting ZSM-5 nanosheet supported Ni catalyst also showed high Ni dispersion and high accessibility to Ni sites by the reactants,being able to improve the activity and stability of catalysts and suppress metal sintering and coking during ESR at high reaction ***,the Ni supported on ZSM-5 nanosheet catalyst prepared by encapsulation showed the stable performance with~88% ethanol conversion and~65% H_(2) yield achieved during a 48-h longevity test at 550-C.

关键词： ZSM-5 nanosheet In situ encapsulation Ni catalyst Ethanol steam reforming Hydrogen production

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Smart Soft Materials with Multiscale Architecture and Dynamic Surface Topographies

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Accounts of Materials Research 2022年第11期3卷 1115-1126页

作者： Songshan Zeng Andrew T.Smith Kuangyu Shen Luyi Sun Polymer Program Institute of Materials Science and Department of Chemical&Biomolecular EngineeringUniversity of ConnecticutStorrsConnecticut 06269United StatesPresent Address:Macao Institute of Materials Science and Engineering(MIMSE)Zhuhai MUST Science and Technology Research InstituteFaculty of Innovation EngineeringMacao University of Science and TechnologyTaipa999078MacaoChina Polymer Program Institute of Materials Science and Department of Chemical&Biomolecular EngineeringUniversity of ConnecticutStorrsConnecticut 06269United States

CONSPECTUS:Smart soft materials have one or more characteristics that can be significantly altered in convertible fashions by external stimuli,such as light,moisture,mechanical force,temperature,electric/magnetic fields,pH,and so *** materials can lead to widespread application in multifunctional smart ***,various smart soft materials have been developed under the inspiration of the intriguing multiscale structures,adaptive mechanisms,and dynamic responses of natural life,with an aim to further design advanced material systems with novel,intriguing,and unprecedented properties.

关键词： Smart properties. Dynamic

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Nanoconfinement effect of nanoporous carbon electrodes for ionic liquid-based aluminum metal anode

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Journal of Energy Chemistry 2022年第11期31卷 121-127,I0005页

作者： Juhee Yoon Seongbak Moon Son Ha Hyung-Kyu Lim Hyoung-Joon Jin Young Soo Yun Program in Environmental and Polymer Engineering Inha UniversityIncheon 22212South Korea Department of Polymer Science and Engineering Inha UniversityIncheon 22212South Korea KU-KIST Graduate School of Converging Science and Technology Korea UniversitySeoul 02841South Korea Division of Chemical Engineering and Bioengineering Kangwon National UniversityGangwon-do 24341South Korea Department of Integrative Energy Engineering Korea UniversitySeoul 02841South Korea

Rechargeable aluminum batteries(RABs),which use earth-abundant and high-volumetric-capacity metal anodes(8040 m Ah cm-3),have great potential as next-generation power sources because they use cheaper resources to deliver higher energies,compared to current lithium ion ***,the mechanism of charge delivery in the newly developed,ionic liquid-based electrolytic system for RABs differs from that in conventional organic ***,targeted research efforts are required to address the large overpotentials and cycling decay encountered in the ionic liquid-based electrolytic *** this study,a nanoporous carbon(NPC)electrode with well-developed nanopores is used to develop a high-performance aluminum *** negatively charged nanopores can provide quenched dynamics of electrolyte molecules in the aluminum deposition process,resulting in an increased collision *** fast chemical equilibrium of anionic species induced by the facilitated anionic collisions leads to more favorable reduction reactions that form aluminum *** nanoconfinement effect causes separated nucleation and growth of aluminum nanoparticles in the multiple confined nanopores,leading to higher coulombic efficiencies and more stable cycling performance compared with macroporous carbon black and 2D stainless steel electrodes.

关键词： Nanoconfinement effect Nanoporous carbon Ionic liquid electrolyte Metal anode Aluminum batteries Multivalent batteries

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Fabrication of versatile poly(xylitol sebacate)-co-poly(ethylene glycol) hydrogels through multifunctional crosslinkers and dynamic bonds for wound healing

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Acta Biomaterialia 2023年 170卷 344-359页

作者： Yeh, Ying-Yu Lin, Yi-Yun Wang, Ting-Teng Yeh, Yu-Jia Chiu, Ting-Hsiang Wang, Reuben Bai, Meng-Yi Yeh, Yi-Cheun Institute of Polymer Science and Engineering National Taiwan University Taipei Taiwan Institute of Biomedical Engineering National Taiwan University Taipei Taiwan Biomedical Engineering Program Graduate Institute of Applied Science and Technology National Taiwan University of Science and Technology Taipei Taiwan Institute of Food Safety and Health National Taiwan University Taipei Taiwan Graduate Institute of Biomedical Engineering National Taiwan University of Science and Technology Taipei Taiwan Adjunct Appointment to the Department of Biomedical Engineering National Defense Medical Center Taipei Taiwan Program National Taiwan University Taipei Taiwan GIP-TRIAD Master's Degree in Agro-Biomedical Science National Taiwan University Taipei Taiwan

Poly(polyol sebacate) (PPS) polymer family has been recognized as promising biomaterials for biomedical applications with their characteristics of easy production, elasticity, biodegradation, and cytocompatibility. Poly(xylitol sebacate)-co-poly(ethylene glycol) (PXS-co-PEG) has been developed to fabricate PPS-based hydrogels;however, current PXS-co-PEG hydrogels presented limited properties and functions due to the limitations of the crosslinkers and crosslinking chemistry used in the hydrogel formation. Here, we fabricate a new type of PXS-co-PEG hydrogels through the use of multifunctional crosslinkers as well as dynamic bonds. In our design, polyethyleneimine-polydopamine (PEI-PDA) macromers are utilized to crosslink aldehyde-functionalized PXS-co-PEG (APP) through imine bonds and hydrogen bonds. PEI-PDA/APP hydrogels present multiple functional properties (e.g., fluorescent, elastomeric, biodegradable, self-healing, bioadhesive, antioxidant, and antibacterial behaviors). These properties of PEI-PDA/APP hydrogels can be fine-tuned by changing the PDA grafting degrees in the PEI-PDA crosslinkers. Most importantly, PEI-PDA/APP hydrogels are considered promising wound dressings to promote tissue remodeling and prevent bacterial infection in vivo. Taken together, PEI-PDA/APP hydrogels have been demonstrated as versatile biomaterials to provide multiple tailorable properties and desirable functions to expand the utility of PPS-based hydrogels for advanced biomedical applications. Statement of significance: Various strategies have been developed to fabricate poly(polyol sebacate) (PPS)-based hydrogels. However, current PPS-based hydrogels present limited properties and functions due to the limitations of the crosslinkers and crosslinking chemistry used in the hydrogel formation. This work describes that co-engineering crosslinkers and interfacial crosslinking is a promising approach to synthesizing a new type of poly(xylitol sebacate)-co-poly(ethylene glycol) (PXS-co-

关键词： Polyols

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Gamma(ɣ)‑MnO_(2)/rGO Fibered Cathode Fabrication from Wet Spinning and Dip Coating Techniques for Cable‑Shaped Zn‑Ion Batteries

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Advanced Fiber Materials 2022年第3期4卷 457-474页

作者： Nakarin Subjalearndee Nanfei He Hui Cheng Panpanat Tesatchabut Priew Eiamlamai Pimpa Limthongkul Varol Intasanta Wei Gao Xiangwu Zhang Fiber and Polymer Science Program Wilson College of TextilesNorth Carolina State University1020 Main Campus DriveRaleighNC 27606USA National Nanotechnology Center National Science and Technology Development Agency111 Thailand Science ParkPhahonyothin RoadKhlong NuengKhlong LuangPathum Thani 12120Thailand National Energy Technology Center National Science and Technology Development Agency114 Thailand Science ParkPhahonyothin RoadKhlong NuengKhlong LuangPathum Thani 12120Thailand

Cable/fber-shaped Zn-ion batteries are designed to power wearable electronics that require high fexibility to operate on human ***,one of technical challenges of these devices is the complexity and high cost for manufacturing fbered *** this work,we demonstrated gamma manganese oxide(ɣ-MnO_(2))/reduced graphene oxide(rGO)fbered cathode fabrication using facile and cost-efective fber production and active material coating ***,rGO fbers were fabricated via wet spinning,followed by chemical reduction with hydroiodic acid(HI).The synthesized rGO fber bundle was then dip-coated with a mixture ofɣ-MnO_(2),carbon black or multi-walled carbon nanotubes,and xanthan gum or polyvinylidene fuoride binder to obtainɣ-MnO_(2)/rGO fbered *** studied the efect of binders and conductive materials on physical properties and electrochemical performance of the fbered *** was found that hydrophobic binder had more benefts than hydrophilic binder by providing higher active material loading,better coating layer homogeneity,and more stable electrochemical ***-shaped Zn-ion batteries(CSZIBs)were then assembled by using theɣ-MnO_(2)/rGO fbered cathode,Zn wire anode,and xanthan gum polymeric gel electrolyte with 2 M ZnSO_(4) and 0.2 M MnSO_(4) salts without a *** investigated the battery assembling procedure on a glass slide(prototype ZIB)and in a plastic tube(cable-shaped ZIB),and evaluated their electrochemical *** CSZIB showed promising maximum capacity of~230 mAh/g with moderate cycling stability(80%capacity retention after 200 cycles)and high fexibility by maintaining the potential after consecutive pressing for 200 times under controlled pressing distance,duration,and testing ***,we explored ion intercalation behaviours and proposed a H^(+)/Zn^(2+)co-intercalation mechanism in ZIB withɣ-MnO_(2) active material.

关键词： Zn-ion battery Wet spinning Dip coating Reduced graphene oxide Manganese dioxide Fiber

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Catalytic hydrotreating of palm oil for bio-jet fuel production over Ni supported on mesoporous zeolite

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Materials Today: Proceedings 2022年 57卷 1082-1087页

作者： Panarmasar, N. Hinchiranan, N. Kuchonthara, P. Program in Petrochemistry and Polymer Science Faculty of Science Chulalongkorn University Phayathai Road Bangkok10330 Thailand Fuels Research Center Department of Chemical Technology Faculty of Science Chulalongkorn University Phayathai Road Bangkok10330 Thailand Phayathai Road Bangkok10330 Thailand Chulalongkorn University Phayathai Road Bangkok10330 Thailand

This research was focused on the bio-jet fuel production from hydroprocessing of palm oil over different types of Ni/desilicated mesoporous zeolites (Hbeta, USY, NH4-ZSM-5). Conventional zeolites were modified for mesoporous zeolites by desilication with NaOH. The zeolite supported Ni-catalysts were prepared by a wet impregnation method with 10 wt% of Ni loading. The experiments were carried out in a continuous-flow fixed-bed reactor at different conditions;temperatures of 375–475 °C and hydrogen pressures of 15–25 bar. The findings demonstrated that the reaction temperature has a strong effect on conversion of palm oil and selectivity of jet-fuel range product which has 8–16 carbon atoms per molecule. A high liquid content was achieved at the temperature and pressure of 425 °C and 25 bar, respectively. The conventional zeolite 10 wt% Ni/USY gave the highest liquid product, lowest aromatic content and highest jet-fuel range selectivity of 56.83%, 17.97% and 79.97%, respectively. Moreover, in case of modified-support catalyst, 10 wt% Ni/USY desilicated with 0.5 M NaOH can reach the higher yield of liquid product up to 58.52% and high iso-alkane selectivity. This is due to the highest amount of weak and strong acid sites. © 2021

关键词： Zeolites

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Insightful analysis of physical properties, kinetics, absorption capacity, and regeneration heat duty of monoethanolamine and N-methyl-4-piperidinol blended solvent in post-combustion carbon capture

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Environmental science and Pollution Research 2024年第40期31卷 52868-52885页

作者： Apaiyakul, Rattanaporn Khuenkaew, Wachiramon Sirirathomsud, Ornicha Boonprasop, Sutthichai Liu, Heilei Gao, Hongxia Liang, Zhiwu Tontiwachwuthikul, Paitoon Sema, Teerawat Petrochemistry and Polymer Science Program Faculty of Science Chulalongkorn University Pathumwan Bangkok10330 Thailand Department of Chemical Engineering Faculty of Engineering Mahidol University Nakhon Pathom73170 Thailand Department of Biotechnology Faculty of Science Mahidol University Bangkok10400 Thailand School of Chemistry and Chemical Engineering Beijing Institute of Technology Beijing100081 China Provincial Hunan Key Laboratory for Cost-Effective Utilization of Fossil Fuel Aimed at Reducing CO₂ Emissions College of Chemistry and Chemical Engineering Hunan University Changsha410082 China Faculty of Engineering and Applied Science University of Regina ReginaSKS4S 0A2 Canada Department of Chemical Technology Faculty of Science Chulalongkorn University Pathumwan Bangkok10330 Thailand

In this study, the high potential tertiary N-methyl-4-piperidinol or MPDL (0.25–1.00 M) was blended with 5 M monoethanolamine (MEA) to formulate 5.25–6.00 M MEA-MPDL solvent and compare with the benchmark 5 M MEA. It was found that the density and the Henry’s constant slightly decreased, while the viscosity increased as the MPDL concentration in the blend increased. Even though the equilibrium CO2-loaded viscosity considerably increased (by 34.3–40.2%) as the MPDL content increased, it was still in a great operating region of less than 10 mPa.s. Experimental overall reaction kinetics constant (kov) was well corresponding with the zwitterion mechanism of MEA and the base-catalyze hydration mechanism of MPDL based absorption kinetics model, with %AAD of 0.56%. Interestingly, an addition of MPDL into 5 M MEA slightly enhanced kov (1.2–3.3% increment) and considerably favored absorption capacity (13–31% elevation), and regeneration heat duty (28–47% reduction), respecting 5 M MEA. The proposed strategic blending can maintain the overall solvent reactivity at the same level of the benchmark, while obviously increase the absorption capacity and largely reduce the regeneration heat duty. This highly favors a solvent upgrading for the existing 5 M MEA based CO2 capture plant. According to the recent data, 5 M MEA + 1.00 M MPDL was suggested. Since the blend was formulated at high concentration, its corrosiveness should also be considered. Graphical abstract: (Figure presented.) © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024.

关键词： Carbon capture and utilization

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Sound absorption properties of rigid polyurethane foam composites with rubber-wood sawdust as a natural filler 15

Sound absorption properties of rigid polyurethane foam compo...

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15th Siam Physics Congress, SPC 2020

作者： Chanlert, P. Ruamcharoen, P. Physics Program Faculty of Science and Technology Songkhla Rajabhat University Songkhla90000 Thailand Rubber and Polymer Technology Program Faculty of Science and Technology Songkhla Rajabhat University Songkhla90000 Thailand

Rigid closed-cell polyurethane (PU) foam is well-known for its ability to withstand external force. On the other hand, due to the closed-cell nature, its ability to absorb sound is doubtful since hollowed materials are supposed be better in sound absorption. However, the composites fabrication with non-reactive fillers was thought to improve sound absorption ability since it might prohibit the formation of closed cell in the process. In this research, rigid polyurethane foam was prepared from polyether polyol and polymeric methylene di-isocyanate (p-MDI) formulated with water as a blowing agent. Natural rubber-wood sawdust was used as a filler. The percentages of rubber-wood sawdust in the polyurethane foam composites were varied by 0, 1, 3, 5 and 7%. The measurement of sound absorption coefficient has been done using impedance tube technique. The results showed that the rigid closed-cell polyurethane foam with 0% filler exhibits poor acoustic absorption. Additionally, sound absorption coefficient results showed that a sample with higher amount of rubber-wood sawdust allowed the sound wave to be absorbed at wider frequency range. This could be explained that the rubber-wood sawdust filler played an important role in sound absorption property. © Content from this work may be used under the terms of the Creative Commons Attribution 3.0 licence.

关键词： Fillers

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Block Sequence Effects on the Self-Assembly Behaviors of Polypeptide-Based Penta-Block Copolymer Hydrogels

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ACS Applied Materials and Interfaces 2024年第5期16卷 6674-6686页

作者： Wang, Ke-Hsin Liu, Chung-Hao Tan, Dun-Heng Nieh, Mu-Ping Su, Wei-Fang Department of Materials Science and Engineering National Taiwan University No. 1 Sec. 4 Roosevelt Road Taipei10617 Taiwan Polymer program Institute of Materials Science University of Connecticut 25 King Hill Road Unit 3136 StorrsCT06269-3136 United States Department of Chemical and Biomolecular Engineering University of Connecticut StorrsCT06269 United States Department of Materials Engineering Ming-Chi University of Technology 84 Gungjuan Rd. New Taipei City243303 Taiwan

Peptide-based hydrogels have great potential for applications in tissue engineering, drug delivery, and so on. We systematically synthesize, characterize, and investigate the self-assembly behaviors of a series of polypeptide-based penta-block copolymers by varying block sequences and lengths. The copolymers contain hydrophobic blocks of poly(γ-benzyl-l-glutamate) (PBG, Bx) and two kinds of hydrophilic blocks, poly(l-lysine) (PLL, Ky) and poly(ethylene glycol) (PEG, EG34), where x and y are the number of repeating units of each block, where PBG and PLL blocks have unique functions for nerve regeneration and cell adhesion. It shows that a sufficient length of the middle hydrophilic segment capped with hydrophobic end PBG blocks is required. They first self-assemble into flower-like micelles and sequentially form transparent hydrogels (as low as 2.3 wt %) with increased polymer concentration. The hydrogels contain a microscale porous structure, a desired property for tissue engineering to facilitate the access of nutrient flow for cell growth and drug delivery systems with high efficiency of drug storage. We hypothesize that the structure of Bx-Ky-EG34-Ky-Bx agglomerates is beyond micron size (transparent), while that of Ky-Bx-EG34-Bx-Ky is on the submicron scale (opaque). We establish a working strategy to synthesize a polypeptide-based block copolymer with a wide window of sol-gel transition. The study offers insight into rational polypeptide hydrogel design with specific morphology, exploring the novel materials as potential candidates for neural tissue engineering. © 2024 The Authors. Published by American Chemical Society

关键词： Block copolymers

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