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Nitrogen doping induced by intrinsic defects of recycled polyethylene terephthalate-derived carbon nanotubes

SusMat 2023年第3期3卷 431-440页

作者： Chuanping Li Lijuan Tong Shuling Wang Qian Liu Yaxin Wang Xuan Li Manxi Wang Manxian Li Xiaochuan Chen Junxiong Wu Qinghua Chen Yiu-Wing Mai Weiwei Fan Yuming Chen Xiaoyan Li Engineering Research Center of Polymer Green Recycling of Ministry of Education Fujian Key Laboratory of Pollution Control&Resource ReuseCollege of Environmental and Resource Sciences and College of Carbon Neutral Modern IndustryFujian Normal UniversityFuzhouFujianChina Hebei International Joint Research Center for Computational Optical Imaging and Intelligent Sensing School of Mathematics and Physics Science and EngineeringHebei University of EngineeringHandanHebeiChina Centre for Advanced Materials Technology(CAMT) School of AerospaceMechanical and Mechatronics Engineering J07The University of SydneySydneyNew South WalesAustralia Department of Materials Science and Engineering and Department of Nuclear Science and Engineering Massachusetts Institute of TechnologyCambridgeMassachusettsUSA

The indiscriminate utilization of nondegradable polyethylene terephthalate(PET)-based products has triggered serious environmental pollution that has to be resolved vigorously.A simple synthesis of N-doped carbon nanotubes from recycled PET(NCNTs_(r-PET))was developed by a nitric acid-assisted hydrothermal *** results and theoretical calculations show that the intrinsic defects in CNTs_(r-PET)would induce N-doping by NH_(3)generated from nitric acid during the hydrothermal process,thus producing the NCNTs_(r-PET).The life cycle assessment proves that the developed method for N-doped CNTs using r-PET as the carbon source is more environmentally friendly than the conventional chemical vapor deposition using acetylene as the carbon *** a typical application,the NCNTs_(r-PET)delivered an impressive sodium storage capacity with an ultralong *** work not only provides a new route to upcycling waste plastics into valuable carbonaceous materials in an ecofriendly manner,but also reveals a basic understanding of the N-doping mechanism in carbonaceous materials.

关键词： carbon nanotubes defect-induced N-doping life cycle assessment rechargeable batteries recycled PET

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Interfacial Diffusion Manipulation by Amphiphilic Cellulose Nanocrystal Having Antibacterial Property for Asymmetric Polyamide Layer

SSRN

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SSRN 2023年

作者： Seo, Huiran Shin, Huiseob Kong, Saerom Jung, Kyung Hwa Kim, Mun Hyeon Kim, Jae Jun Lee, Changha Kim, Hee Joong Lee, Jong-Chan Department of Chemical and Biological Engineering Institute of Chemical Processes Seoul National University 1 Gwanak-ro Seoul08826 Korea Republic of Department of Polymer Science and Engineering & Program in Environmental and Polymer Engineering Inha University Incheon22212 Korea Republic of

Polyamide (PA) thin-film composite (TFC) membranes, fabricated by interfacial polymerization (IP) process, have been widely used for the desalination process due to high water permeability with high water/salt selectivity. A number of advanced PA TFC membranes have been developed as more efficient alternatives to further improve separation performance, scalability, and address the surface contamination problem of commercial membranes. Here, we utilized amphiphilic functionalized cellulose nanocrystal (f-CNC) having antibacterial property as a nanofiller material for the preparation of an advanced PA membrane system, featuring improved water permeability with high salt rejection ability. This strategy is inexpensive, scalable, environmentally friendly, and practically relevant, given that typical IP process with a renewable nanofiller was employed. The amphiphilic f-CNC manipulates interfacial diffusion of monomers upon IP process, thereby decreasing the effective PA layer thickness by 30 % and increasing water permeability by 44 %. In addition, the PA membrane with f-CNC showed improved antibacterial and antifouling properties due to the specific nature of f-CNC. This study provides insights for the development of thin, effective, and antibacterial, yet more green and scalable PA membrane alternatives to the conventional desalination membranes. © 2023, The Authors. All rights reserved.

关键词： Cellulose

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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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Photolithography Patterning of Organic Light-Emitting Diodes Using Solvent Resistant Electron Transport Materials

Photolithography Patterning of Organic Light-Emitting Diodes...

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International Symposium, Seminar, and Exhibition, Display Week 2024

作者： Yu, Hyunjin Yeong So, Eun Eun, Kyunghyun Jun Jung, Byung Kim, Myungwoong Lee, Jin-Kyun Yeob Lee, Jun School of Chemical Engineering Sungkyunkwan University 2066 Seobu-ro Jangan-gu Suwon-si Gyeonggi-do16419 Korea Republic of Department of Materials Science and Engineering University of Seoul Seoul02504 Korea Republic of Department of Chemistry and Chemical Engineering Inha University Incheon22212 Korea Republic of Program in Environment and Polymer Engineering Inha University 100 Inha-ro Michuhol-gu Incheon22212 Korea Republic of

In this paper, we develop a novel approach to achieve ultra-high resolution in organic light-emitting diodes (OLEDs) through a photolithography patterning process. It is important to apply a solvent resistant electron transport layer (ETL) in the photolithography pattering of OLED because of solution coating process of photoresist on the ETL. Therefore, a solvent resistant ETL named 2,7-bis(4,6-diphenyl-1,3,5-triazin-2-yl)-9,9′-spirobi[fluorene] (SBF-Trz) was developed and employed as the ETL of OLEDs. The SBF-Trz demonstrated excellent solvent resistance during photolithography process and enabled device performances comparable to those of the conventional OLED without any photolithography process. It was found that the SBF-Trz ETL is appropriate as the ETL of the OLED patterned by photolithography due to good electron transport property, good stability, and good solvent resistance. © 2024, John Wiley and Sons Inc. All rights reserved.

关键词： Reactive ion etching

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Two-dimensional MXenes:New frontier of wearable and flexible electronics

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InfoMat 2022年第4期4卷 1-28页

作者： Abbas Ahmed Sudeep Sharma Bapan Adak Md Milon Hossain Anna Marie LaChance Samrat Mukhopadhyay Luyi Sun Polymer Program Institute of Materials ScienceUniversity of ConnecticutStorrsConnecticutUSA Advanced Sensor and Energy Research(ASER)Lab Department of Electronic EngineeringKwangwoon UniversitySeoulSouth Korea Department of Textile and Fiber Engineering Indian Institute of TechnologyNew DelhiIndia Department of Textile Engineering Chemistry and ScienceNorth Carolina State UniversityRaleighNorth CarolinaUSA Department of Textile Engineering Khulna University of Engineering&TechnologyKhulnaBangladesh Department of Chemical and Biomolecular Engineering University of ConnecticutStorrsConnecticutUSA

Wearable electronics offer incredible benefits in mobile healthcare monitoring,sensing,portable energy harvesting and storage,human-machine interactions,etc.,due to the evolution of rigid electronics structure to flexible and stretchable ***,transition metal carbides and nitrides(MXenes)are highly regarded as a group of thriving two-dimensional nanomaterials and extraordinary building blocks for emerging flexible electronics platforms because of their excellent electrical conductivity,enriched surface functionalities,and large surface *** article reviews the most recent developments in MXene-enabled flexible electronics for wearable *** MXeneenabled electronic devices designed on a nanometric scale are highlighted by drawing attention to widely developed nonstructural attributes,including 3D configured devices,textile and planer substrates,bioinspired structures,and printed ***,the unique progress of these nanodevices is highlighted by representative applications in healthcare,energy,electromagnetic interference(EMI)shielding,and humanoid control of *** emerging prospects of MXene nanomaterials as a key frontier in nextgeneration wearable electronics are envisioned and the design challenges of these electronic systems are also discussed,followed by proposed solutions.

关键词： flexible electronics MXene nanostructures wearable electronics

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Dielectric polymer based electrolytes for high-performance all-solid-state lithium metal batteries

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Journal of Energy Chemistry 2022年第6期31卷 194-204,I0006页

作者： Qi Kang Yong Li Zechao Zhuang Dingsheng Wang Chunyi Zhi Pingkai Jiang Xingyi Huang Department of Polymer Science and Engineering Shanghai Key Laboratory of Electrical Insulation and Thermal AgeingState Key Laboratory of Metal Matrix CompositesShanghai Jiao Tong UniversityShanghai 200240China Institute of Applied and Physical Chemistry and Center for Environmental Research and Sustainable Technology University of BremenBremen 28359Germany Department of Chemistry Tsinghua UniversityBeijing 100084China Department of Materials Science and Engineering City University of Hong KongHong Kong 999077China

Solid polymer electrolytes (SPEs) are urgently required for achieving practical all-solid-state lithium metal batteries (ASSLMBs) but remain plagued by low ionic ***,we propose a strategy of salt polarization to fabricate a highly ion-conductive SPE by employing a high-dielectric polymer that can interact strongly with lithium *** a polymer with large dipole moments can guide lithium cations (Li^(+)) to be arranged along the chain,forming a continuous pathway for Li^(+) hopping within the *** as-fabricated SPE,poly(vinylidene difluoride)(PVDF)-LiN(SO_(2)F)_(2)(LiFSI),has an extraordinarily high dielectric constant (up to 10^(8)) and ultrahigh ionic conductivity (0.77×10^(-3)S cm^(-1)).Based on the PVDF–LiFSI SPE,the assembled Li metal symmetrical cell shows excellent Li plating/stripping reversibility at 0.1 m A cm^(-2),0.1 m Ah cm^(-2)over 1500 h^(-1) the ASS LiFePO_(4) batteries deliver long-term cycling stability at 1 C over 350 cycles (2.74 mg cm^(-2)) and an ultralong cycling lifespan of over 2600 h(100 cycles) with high loading (11.5 mg cm^(-2)) at 28°***-principles calculations further reveal the ion-dipole interactions-controlled conduction of Li^(+) in PVDF–LiFSI SPE along the PVDF *** work highlights the critical role of dielectric permittivity in SPE,and provides a promising path towards high-energy,long-cycling lifespan ASSLMBs.

关键词： Salt polarization High dielectric High-loading All-solid-state Lithium metal battery 2600 h lifespan

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Interfacial Diffusion Manipulation by Amphiphilic Cellulose Nanocrystal Having Antibacterial Property for Asymmetric Polyamide Layer

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SSRN 2023年

作者： Seo, Huiran Shin, Huiseob Kong, Saerom Jung, Kyung Hwa Kim, Mun Hyeon Kim, Jae Jun Suh, Dongwoo Baek, Youngbin Lee, Changha Kim, Hee Joong Lee, Jong-Chan Department of Chemical and Biological Engineering Institute of Chemical Processes Seoul National University Seoul08826 Korea Republic of Department of Biological Engineering Inha University Incheon22212 Korea Republic of Department of Polymer Science and Engineering Program in Environmental and Polymer Engineering Inha University Incheon22212 Korea Republic of

Polyamide (PA) thin-film composite (TFC) membranes, fabricated by interfacial polymerization (IP) process, have been widely used for the desalination process due to high water permeability with high water/salt selectivity. A number of advanced PA TFC membranes have been developed as more efficient alternatives to further improve separation performance and address the surface contamination problem of commercial membranes. Here, we utilized amphiphilic functionalized cellulose nanocrystal (f-CNC) having antibacterial property as a nanofiller material for the preparation of an advanced PA membrane system, featuring improved water permeability with high salt rejection ability. This strategy is inexpensive, scalable, environmentally friendly, and practically relevant, given that typical IP process with a renewable nanofiller was employed. The amphiphilic f-CNC manipulates interfacial diffusion of monomers upon IP process, thereby decreasing the effective PA layer thickness by 30% (from ~377 nm to ~268 nm) and increasing water permeability by 44% (from 1.26 Lm-2h-1bar-1 to 1.82 Lm-2h-1bar-1). In addition, the PA membrane with f-CNC showed improved antibacterial (~90%) and antifouling properties (~84%, FRR) due to the specific nature of f-CNC. This study provides insights for the development of thin, effective, and antibacterial, yet more green and scalable PA membrane alternatives to the conventional desalination membranes. © 2023, The Authors. All rights reserved.

关键词： Cellulose

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Effects of nanopores and sulfur doping on hierarchically bunched carbon fibers to protect lithium metal anode

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Carbon Energy 2021年第5期3卷 784-794页

作者： Ji In Jung Sunwoo Park Son Ha Se Youn Cho Hyoung-Joon Jin Young Soo Yun Program in Environmental and Polymer Engineering Inha UniversityIncheonSouth Korea KU-KIST Graduate School of Converging Science and Technology Korea UniversitySeoulSouth Korea Carbon Composite Materials Research Center Korea Institute of Science and TechnologyWanju-gunJeollabuk-doSouth Korea Department of Polymer Science and Engineering Inha UniversityIncheonSouth Korea Department of Integrative Energy Engineering Korea UniversitySeoulSouth Korea

Studies on three-dimensional structured carbon templates have focused on how to guide homogeneous lithium metal nucleation and growth for lithium metal anodes(LMAs).However,there is still insufficient evidence for a key factor to achieve their high electrochemical ***,the effects of nanopores and sulfur doping on carbon-based nanoporous host(CNH)electrode materials for LMAs were investigated using natural polymer-derived *** pore-filling behaviors of lithium metal in the nanopores of the CNH electrode materials were first observed by ex situ scanning electron microscopy analysis,where the protective lithium metal nucleation and growth process led to significantly high Coulombic efficiency(CE)of~99.4%and stable 600 *** addition,a comparison study of CNH and sulfurdoped CNH(S-CNH)electrodes,which differ only in the presence or absence of sulfur,revealed that sulfur doping can cause lower electrochemical series resistance,higher CE value,and better cycling stability in a wide range of current densities and number of ***,S-CNH-based LMAs showed high electrochemical performance in full-cell Li-S battery tests using a sulfur copolymer cathode,where a high energy density of 1370Wh kgelectrode−1 and an excellent power density of 4120Wkgelectrode−1 were obtained.

关键词： carbon template Li-S batteries lithium metal anode lithium metal batteries nanoporous carbon sulfur doping

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Porous PVA skin-covered thin Zirfon-type separator as a new approach boosting high-rate alkaline water electrolysis beyond 1000 hours’lifespan

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escience 2024年第6期4卷 127-137页

作者： Xi Luo Nengneng Xu Yongnan Zhou Xiaohui Yang Woochul Yang Guicheng Liu Joong Kee Lee Jinli Qiao State Key Laboratory for Modification of Chemical Fibers and Polymer Materials College of Environmental Science and EngineeringDonghua UniversityShanghai 201620China Shanghai Institute of Pollution Control and Ecological Security Shanghai 200092China Department of Physics Dongguk UniversitySeoul 04620Republic of Korea School of Energy Power and Mechanical Engineering North China Electric Power UniversityBeijing 100096China Dept.of Chemical&Biochemical Eng Gachon University1342 Seongnam-daeroSeongnam-si 13120Republic of Korea

Regulating the pore structure of a zirfon-based diaphragm is critical to promoting a high-rate alkaline electrolyzer,but it is still a big challenge to respond“trade-off”between the thickness of the diaphragm and the current density/gas barrier *** this work,a porous hydrophilic skin layer with~μm thick of polyvinyl alcohol(PVA)has been successfully constructed and casted onto the thin zirfon-type separator composite(V-Zirfon-350μm).The V-Zirfon-350μm separator generates a high KOH uptake(>90%),low area resistance(0.2026Ωcm^(2))but a low electrolyte permeation flux density(5.2×10^(-4) mL cm^(-2) s^(-1) at 0.5 bar),which largely surpasses the state-of-the-art commercial Zirfon UTP-500μm *** coupled with Raney Ni cathode and NiCoMo-LDH anode catalysts,the V-Zirfon-350μm separator offers a high current density over 1300 mA cm^(-2)@2.0 V(80℃ in 30%KOH)and a superior stability of 300 h under 800 mA cm^(-2) for alkaline water electrolysis(AWE).Specifically,the voltage is merely~3.5 V for two electrolytic cells connected in series,which can be even conducted for more than 1300 h at different operational *** work provides a novel methodology for the practical application of a thin Zirfon-based diaphragm.

关键词： Alkaline water electrolysis Porous separator Zirfon type Polyvinyl alcohol Skin layer

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Assessing the Potential of Biodegradable Plastics in a Circular Economy: A Methodological Outlook

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Circular Economy and Sustainability 2025年第2期5卷 1291-1305页

作者： Scheers, Quinten Nimmegeers, Philippe Galant, Or Spatari, Sabrina Van den Brande, Niko Brancart, Joost Billen, Pieter Faculty of Applied Engineering Intelligence in Processes Advanced Catalysts and Solvents (iPRACS) University of Antwerp Groenenborgerlaan 171 Antwerp 2020 Belgium Faculty of Business and Economics Department of Engineering Management Environmental Economics (EnvEcon) University of Antwerp Prinsstraat 13 Antwerp 2000 Belgium Flanders Make@UAntwerp Antwerp 2000 Belgium Faculty of Civil and Environmental Engineering Technion– Israel Institute of Technology Haifa 3200003 Israel Grand Technion Energy Program Technion– Israel Institute of Technology Haifa 3200003 Israel Physical Chemistry and Polymer Science (FYSC) Vrije Universiteit Brussel Pleinlaan 2 Brussels 1050 Belgium IVL Swedish Environmental Research Institute Valhallavägen 81 Stockholm 11428 Sweden

Increased biodegradability, in other words reduced environmental recalcitrance, has the potential to be an important asset in the battle against plastics pollution. It can partially mitigate global plastic leakages into the environment, which is next to their impact on climate change the biggest concern regarding plastics use. Biodegradation should be regarded as an optimal safety net in many applications and should often not be the targeted waste management option for biodegradable plastics. Biodegradability should not preclude reuse or proper recyclability, which are impactful means to reduce the carbon intensity of plastics lifecycles. Despite the added advantages, the market penetration of biodegradable plastics is only very slowly growing. Moreover, policy recommends its use only in limited applications, driven by sometimes-higher cost and limited recyclability. In this article, we posit that arguments against widespread application of biodegradable plastics are largely driven by misperceptions arising from intrinsic limitations of contemporary sustainability assessments and offer an alternative viewpoint that could compensate for this. In general, sustainability assessments fail to properly assess learning curves, often do not take littering potential into account, and are rather conservative with respect to background systems. Hence, recyclability– or better: circularity– judgements often do not resolve the paradoxical situation in which increased market shares lead to easier and more profitable recycling schemes and vice versa. Judging disruptive innovations by incorporating thermodynamics-inspired, less data-intensive, state-based methods, based on, e.g., statistical entropy analysis, into the decision support framework could allow to forecast packaging markets with performant materials that are intrinsically circular, having reduced environmental recalcitrance. © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2024.

关键词： Biodegradable Plastics Decision Making Statistical Entropy Sustainability Assessments

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