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Highly robust zinc metal anode directed by organic–inorganic synergistic interfaces for wearable aqueous zinc battery

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SmartMat 2024年第1期5卷 135-146页

作者： Xixi Zhang Chuanlin Li Guangmeng Qu Chenggang Wang Shunshun Zhao Tongkai Wang Na Li Xiaojuan Li Xijin Xu School of physics and Technology University of JinanJinanChina School of chemistry and Chemical Engineering Shandong UniversityJinanChina State Key Laboratory of Chemical Resource Engineering Beijing Key Laboratory of Electrochemical Process and Technology of MaterialsBeijing University of Chemical TechnologyBeijingChina

Flexible aqueous zinc batteries(FAZBs)with high safety and environmental friendliness are promising smart power sources for smart wearable ***,the bare zinc anode usually suffers from damnable dendrite growth and rampant side reaction on the surface,greatly impeding practical applications in ***,a composite polymer interface layer is artificially self‐assembled on the surface of the zinc anode by graft‐modified fluorinated monomer(polyacrylic acid‐2‐(Trifluoromethyl)propenoic acid,PAA‐TFPA),on which an organic–inorganic hybrid(PAA‐Zn/ZnF2)solid electrolyte interface(SEI)with excellent ionic conductivity is formed by interacting with Zn2+.Both the pouch cell and fiber zinc anode exhibit excellent plating/stripping reversibility after protecting by this organic–inorganic SEI,which can be stably cycled more than 3000 h in symmetric Zn||Zn cells or 550 h in fiber Zn||Zn ***,this interface layer preserves zinc anode with excellent mechanical durability under various mechanical deformation(stably working for another 1200 h after bending 100 h).The corresponding PAA‐Zn/ZnF2@Zn||MnO2 full cell displays an ultra‐long life span(79%capacity retention after 3000 cycles)and mechanical robustness(85%of the initial capacity for another 3000 cycles after bending 100 times).More importantly,the as‐assembled cells can easily power smart wearable devices to monitor the user's health condition.

关键词： hybrid SEI mechanical durability wearable zinc battery zinc anode

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Unleashing the Power of Bio-based Thermotropic Liquid Crystal Modifiers:Toughening and Reinforcing Petroleum-based Epoxy Resin without Compromising Other Properties

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Chinese Journal of polymer Science 2024年第8期42卷 1093-1102页

作者： Qing-Yun Lu Hong-Wei Gu Jia-Hui Li Qian-Qian Fan Bei-Tao Liu Yan Kou Xi-Gao Jian Zhi-Huan Weng State Key Laboratory of Fine Chemicals Frontiers Science Center for Smart MaterialsLiaoning Technology Innovation Center of High Performance Resin MaterialsDepartment of Polymer Science&EngineeringDalian University of TechnologyDalian 116024China Thermochemistry Laboratory Liaoning Province Key Laboratory of Thermochemistry for Energy and MaterialsDalian National Laboratory for Clean EnergyDalian Institute of Chemical PhysicsChinese Academy of SciencesDalian 116023China

Toughening the petroleum-based epoxy resin blends with bio-based modifiers without compromising their modulus,mechanical strength,and other properties is still a big challenge in view of the *** this study,a bio-based liquid crystal epoxy resin(THMT-E P)with an s-triazine ring structure was utilized to modify a petroleum-based bisphenol A epoxy resin(E51)with 4,4'-diaminodiphenylsulfone(DDS)as a curing agent,and the blended systems were evaluated for their thermal stability,mechanical properties,and flame *** results showed that the impact strength of the blended system initially increased and then decreased with the increase in THMT-EP content,and it reached the a maximum value of 26.5 kJ/m^(2)when the THMT-EP content was 5%,which was 31.2%higher than that of E51/***,the flexural strength,modulus,and glass transition tem perature of the blended system were all simultaneously improved with the addition of *** the same time,the addition of THMT-EP enhanced the flame retardancy of the system by increasing the char yield at 700℃and decreasing the peak heat release rate and total heat release *** work paves the way for a more sustainable improvement in the comprehensive performance of epoxy resin.

关键词： Epoxy resin Toughening Bio-based Thermotropic liquid crystal

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Reinforced concrete-like Na_(3.5)V_(1.5)Mn_(0.5)(PO_(4))_(3)@graphene hybrids with hierarchical porosity as durable and high-rate sodium-ion battery cathode

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Chinese Chemical Letters 2024年第4期35卷 214-219页

作者： Tao Long Peng Chen Bin Feng Caili Yang Kairong Wang Yulei Wang Can Chen Yaping Wang Ruotong Li Meng Wu Minhuan Lan Wei Kong Pang Jian-Fang Wu Yuan-Li Ding College of Materials Science and Engineering Hunan UniversityChangsha 410082China Department of physics Xiamen UniversityXiamen 361005China College of chemistry and Chemical Engineering Central South UniversityChangsha 410083China Institute for Superconducting&Electronic Materials Faculty of EngineeringUniversity of WollongongWollongongNSW 2522Australia

Realizing high-rate capability and high-efficiency utilization of polyanionic cathode materials is of great importance for practical sodium-ion batteries(SIBs) since they usually suffer from extremely low electronic conductivity and limited ionic diffusion kinetics. Herein, taking Na_(3.5)V_(1.5)Mn_(0.5)(PO_(4))_(3)(NVMP) as an example, a reinforced concrete-like hierarchical and porous hybrid(NVMP@C@3DPG) built from 3D graphene(“rebar”) frameworks and in situ generated carbon coated NVMP(“concrete”) has been developed by a facile polymer assisted self-assembly and subsequent solid-state method. Such hybrids deliver superior rate capability(73.9 m Ah/g up to 20 C) and excellent cycling stability in a wide temperature range with a high specific capacity of 88.4 m Ah/g after 5000 cycles at 15 C at room temperature, and a high capacity retention of 97.1% after 500 cycles at 1 C(-20 ℃), and maintaining a high reversible capacity of 110.3 m Ah/g in full cell. This work offers a facile and efficient strategy to develop advanced polyanionic cathodes with high-efficiency utilization and 3D electron/ion transport systems.

关键词： Sodium-ion battery Polyanionic cathode Hybrid structure Interconnected structure Energy storage

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High-performance Ti_(3)C_(2)T_(x)achieved by polyaniline intercalation and gelatinization as a high-energy cathode for zinc-ion capacitor

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Nano Research 2024年第6期17卷 5305-5316页

作者： Peng Liao ZiYu Geng Xin Zhang Wenjie Yan Zenghui Qiu Haijun Xu College of Mathematics and physics Beijing University of Chemical TechnologyBeijing 100029China

The actual manufacture of supercapacitors(SCs)is restricted by the inadequate energy density,and the energy density of devices can be properly promoted by assembling zinc-ion capacitors(ZICs)which used capacitive cathode and battery-type ***-dimensional(2D)MXene has brought great focuses in the electrode research on the foundation of large redox-active surface,but the specific capacitance is still affected by the tight stacking of ***_(3)C_(2)T_(x)@polyaniline(PANI)heterostructures are prepared by uniformly depositing the conductive polymer PANI nanorods as the intercalation agent into the external of Ti_(3)C_(2)T_(x)nanosheets to inhibit ***,by using graphene oxide(GO)-assisted low-temperature hydrothermal self-assembly manufacture,2D heterostructures are assembled into the three-dimensional(3D)porous crosslinked Ti_(3)C_(2)T_(x)@PANI-reduced graphene oxide(RGO)*** to the synergistic work of PANI nanorods,Ti_(3)C_(2)T_(X)nanosheets,and 3D crosslinking frameworks of RGO to match capacitive and battery effects,3D porous hierarchical Ti_(3)C_(2)T_(x)@PANI-RGO heterostructure hydrogels have rich ion transport channels,a large number of active sites,and excellent reaction *** is assembled by using Ti_(3)C_(2)T_(x)@PANI-RGO heterostructure hydrogels as cathodes and zinc foil as *** this work,Ti_(3)C_(2)T_(x)@PANI-RGO//Zn ZIC exhibits a wide working window(2.0 V),marked specific capacitance(589.89 F·g^(−1)at 0.5 A·g−1),salient energy density(327.71 Wh·kg^(−1)at 513.61 W·kg^(−1)and 192.20 Wh·kg^(−1)at 13,005.87 W·kg^(−1)),and durable cycling stability(97.87%capacitance retention after 10,000 cycles at 10 A·g^(−1)).This study emphasizes the device design of ZICs and the broad prospect of Ti_(3)C_(2)T_(x)-based hydrogels as viable cathodes for ZICs.

关键词： polyaniline(PANI) Ti_(3)C_(2)T_(x)@PANI heterostructure intercalation process three-dimensional(3D)porous hydrogel high energy density zinc-ion capacitor

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Responsive Composite Janus Cages

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Chinese Journal of polymer Science 2015年第10期33卷 1462-1469页

作者： Qi-guang Wang 梁福鑫 Qian Wang Xiao-zhong Qu 杨振忠 State Key Laboratory of polymer physics and chemistry Institute of Chemistry Chinese Academy of Sciences

pH responsive composite Janus cages of PS-silica-PEO are prepared using silica nanoparticles to crosslink two PAA contained di-block copolymers at an emulsion interface sequentially. Transverse channels are in situ created across the shell, which facilitates mass transfer. Shell is pH responsive owing to the presence of residual PAA chains tethered onto the silica nanoparticles. The Janus cages are capable to preferentially capture oil from their aqueous surroundings. The saturation absorption capacity is determined by pH and oil property. Other composite Janus cages are expected by extension the method using other copolymers and functional nanoparticles.

关键词： Janus cages Block copolymer Composited pH response Emulsion.

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One-dimensional Janus polymeric Vehicles

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Chinese Journal of polymer Science 2015年第9期33卷 1344-1350页

作者： Dong-mei Lv Wei Ni 梁福鑫 Qian Wang Xiao-zhong Qu 杨振忠 State Key Laboratory of polymer physics and chemistry Institute of Chemistry Chinese Academy of Sciences

We herein report a novel approach to fabricate poly（DVB-co-VBC） one-dimentional nanomaterials with varied composition. By adjusting the monomer DVB/VBC ratio and using inert solvents, after internal cavity of the nanotubes disappears and length of the nanotubes is decreased, thus nanorods are achieved. After quaternary ammoniation from the benzyl chloride group, the exterior surface becomes hydrophilic while the interiority preserves hydrophobic. The Janus nanorods can serve as a specific vehicle to selectively collect oils from their aqueous surroundings.

关键词： Poly(DVB-co-VBC) Janus Nanotube Nanorod.

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Application of different fiber structures and arrangements by electrospinning in triboelectric nanogenerators

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Chinese Journal of Chemical Engineering 2024年第5期69卷 177-191页

作者： Hebin Li Zifei Meng Dehua Wang Ye Lu Longlong Jiang Le Zhang Hanbin Wang Xiaoxiong Wang College of physics Qingdao UniversityQingdao 266071China School of physics and Electronic Engineering Jiangsu Normal UniversityXuzhouJiangsu 221000China Microsystem&Terahertz Research Center China Academy of Engineering Physics(CAEP)Chengdu 610200China Institute of Electronic Engineering China Academy of Engineering Physics(CAEP)Mianyang 621900China University-Industry Joint Center for Ocean Observation and Broadband Communication College of PhysicsQingdao UniversityQingdao 266071China Weihai Innovation Research Institute of Qingdao University Weihai 264200China Collaborative Innovation Center for Eco-Textiles of Shandong Province and State Key Laboratory of Bio-Fibers and Eco-TextilesQingdao UniversityQingdao 266071China

In recent years,nanogenerators(NGs)have attracted wide attention in the energy field,among which triboelectric nanogenerators(TENGs)have shown superior *** reports of electrospinning(ES)-based TENGs have been reported,but there is a lack of deep analysis of the designing method from microstructure,limiting the creative of new ES-based *** TENGs use polymer materials to achieve corresponding design,which requires structural design of polymer *** existing polymer molding design methods include macroscopic molding methods,such as injection,compression,extrusion,calendering,etc.,combined with liquid-solid changes such as soluting and melting;it also includes micro-nano molding technology,such as melt-blown method,coagulation bath method,ES method,and nanoimprint *** fact,ES technology has good controllability of thickness dimension and rich means of nanoscale structure *** present,these characteristics have not been ***,in this paper,we combine recent reports with some microstructure regulation functions of ES to establish a more general TENGs design *** on the rich microstructure research results in the field of ES,much more new types of TENGs can be designed in the future.

关键词： Triboelectric nanogenerators Electrospinning Fiber microstructure regulation Nanomaterials Membranes Global optimization

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Fluorinated semi-interpenetrating polymer networks for enhancing the mechanical performance and storage stability of polymer-bonded explosives by controlling curing and phase separation rates

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Defence Technology（防务技术） 2024年第8期38卷 58-66页

作者： Chao Deng Huihui Liu Yongping Bai Zhen Hu School of chemistry and Chemical Engineering Harbin Institute of TechnologyHarbin 150000China Wuxi HIT New Material Research Institute Co. Ltd.Wuxi 214000China Institute of Chemical Materials China Academy of Engineering PhysicsMianyang 621900China

Herein, the effect of fluoropolymer binders on the properties of polymer-bonded explosives(PBXs) was comprehensively investigated. To this end, fluorinated semi-interpenetrating polymer networks(semiIPNs) were prepared using different catalyst amounts(denoted as F23-CLF-30-D). The involved curing and phase separation processes were monitored using Fourier-transform infrared spectroscopy, differential scanning calorimetry, a haze meter and a rheometer. Curing rate constant and activation energy were calculated using a theoretical model and numerical method, respectively. Results revealed that owing to its co-continuous micro-phase separation structure, the F23-CLF-30-D3 semi-IPN exhibited considerably higher tensile strength and elongation at break than pure fluororubber F2314 and the F23-CLF-30-D0 semi-IPN because the phase separation and curing rates matched in the initial stage of *** arc Brazilian test revealed that F23-CLF-30-D-based composites used as mock materials for PBXs exhibited excellent mechanical performance and storage stability. Thus, the matched curing and phase separation rates play a crucial role during the fabrication of high-performance semi-IPNs;these factors can be feasibly controlled using an appropriate catalyst amount.

关键词： Semi-interpenetrating polymer networks Fluoropolymer Curing rate Phase separation rate polymer-bonded explosives

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Thermal and Redox Dual Responsive Poly(L-glutamate)with Oligo(ethylene glycol)Side-chains

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Chinese Journal of polymer Science 2016年第12期34卷 1436-1447页

作者： Xiao-hui Fu Yi-nan Ma 孙静李志波 School of polymer Science and Engineering Qingdao University of Science and Technology Laboratory of polymer physics and chemistry Institute of Chemistry Chinese Academy of Sciences

A series of poly（L-glutamate）s grafted with oligo（ethylene glycol）（OEG） side-chains through the thioether linkages （PALGn-g-EGx, x = 2, 3 and 4） were prepared by ring-opening polymerization （ROP） of γ-allyl-L-glutamate N-carboxyanhydride （ALG-NCA） and thiol-ene photoaddition. The chemical structures and physical properties were characterized by 1H-NMR, Fourier transform infrared （FTIR）, circular dichroism （CD）, etc. The PALGn-g-EGx samples with x = 3 and 4 displayed lower critical solution temperature （LCST） in water due to the presence of OEG units. The clouding point （CP） of polypeptides can be finely tuned by changing the side chain structures, molecular weights and sample concentrations. In addition, the thioether linkages in the side chains offer additional redox-responsive properties. The influence of both OEG units and thioether linkages on the LCST behavior was systematically investigated. This work provides an efficient way to prepare multi-stimuli responsive materials with highly tunable properties.

关键词： N-carboxyanhydride (NCA) Polypeptide Ring-opening polymerization Click chemistry Stimuli-responsive.

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Tunable supramolecular hydrogels from polypeptidePEG-polypeptide triblock copolymers

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Science China chemistry 2015年第6期58卷 1005-1012页

作者： Xiaohui Fu Yong Shen Yinan Ma Wenxin Fu Zhibo Li Laboratory of polymer physics and chemistry Institute of chemistry Chinese Academy of Sciences School of polymer Science and Engineering Qingdao University of Science and Technology

A series of ABA triblock copolymers of poly(?-(2-methoxy ethoxy)esteryl-glutamate)-block-poly(ethylene glycol)-blockpoly(?-(2-methoxy ethoxy)esteryl-glutamate) with poly(ethylene glycol) as middle hydrophilic B block and oligo(ethylene glycol)-functionalized polyglutamate(poly-L-EG2Glu) as terminal A blocks were prepared via ring-opening polymerization of EG2 Glu N-carboxyanhydride(NCA). The resulting P(EG2Glu)-b-PEG-b-P(EG2Glu) triblocks can spontaneously form hydrogels in water. The intermolecular hydrogen bonding interactions between polypeptides blocks were responsible for the formation of gel network structure. These hydrogels displayed shear-thinning and rapid recovery properties, which endowed them potential application as injectable drug delivery system. The mechanical strength of hydrogels can be modulated by copolymer composition, molecular weight and concentrations. Also, it was found that the hydrogels' strength decreased with temperature due to dehydration of polypeptide segments. Atomic force microscopy and scanning electron microscopy images revealed that these hydrogels were formed through micelle packing mechanism. Circular dichroism and Fourier transform infrared spectroscopy characterizations suggested the poly-L-EG2 Glu block adopted mixed conformation. A preliminary assessment of drug release in vitro demonstrated the hydrogels can offer a sustained release of doxorubicin(DOX) and the release rate could be controlled by varying chemical composition.

关键词： hydrogel polypeptide N-carboxyanhydride (NCA) ring-opening polymerization (ROP) drug delivery

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