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Molecular origin for toughness of hydrogel artificial spider silk for surgical sutures

Science China Chemistry 2025年

作者： Jiatian Li Abdul Qadeer Khan Weiqiang Zhao Zhipeng Lai Qiankun Bao Muhammad Rafique Fazhi Ye Jie Bai Qiang Zhou Liqiang Mai Zongqian Wang Enzhao Liu Xiang Zhou Zunfeng Liu Chemical Engineering College Inner Mongolia University of Technology Tianjin Key Laboratory of Ionic-Molecular Function of Cardiovascular Disease Department of Cardiology Tianjin Institute of CardiologyThe Second Hospital of Tianjin Medical University State Key Laboratory of Medicinal Chemical Biology Key Laboratory of Functional Polymer Materials Tianjin Key Laboratory of Functional Polymer Materials College of Chemistry Nankai University School of Biomedical Engineering and Med-X Research Institute Shanghai Jiao Tong University State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Tianjin First Central Hospital School of Textile and Garment Anhui Polytechnic University Department of Science School of Traditional Chinese Pharmacy China Pharmaceutical University

The pursuit of biomimetic fibers with simultaneous high toughness and strength persists, despite their inherent ***, for artificial spider silk based on gel fiber, it is still unclear for the molecular chain attributes related to the improvement of the strength and toughness. Here, a hydrogel fiber was prepared by mimicking the molecular structure of natural spider silk, and we delved into the molecular chain structure characteristics related to the strength, toughness and damping capacity of gel fiber, such as crosslinking density, molecular chain orientation and hydrogen bond interaction. The results indicate that a certain increase in crosslinking density and molecular chain orientation contributes to the enhancement of tensile strength, while the toughness and damping remain essentially unaltered. The thermal dissociation of hydrogen bond could enhance the toughness in a specific range, while the humidity destruction of hydrogen bond would reduce the *** well-regulation control of the weight ratio of polyacrylamide （PAM） to poly（acrylic acid）(PAA), the PAM@PAA gel fibers could reach maximum breaking strength of 1.02 GPa, maximum toughness of 149 MJ m-3, and damping capacity of 95%.PAM@PAA gel fiber has demonstrated excellent wound healing performance and biocompatibility in vivo evaluation as a surgical suture, which indicates its potential in biomedical applications.

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Flexible three-dimensional-networked iron vanadate nanosheet arrays/carbon cloths as high-performance cathodes for magnesium ion batteries

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Science China materials 2022年第8期65卷 2197-2206页

作者： Han Tang Chunli Zuo Fangyu Xiong Cunyuan Pei Shuangshuang Tan Ping Luo Wei Yang Qinyou An Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China Hubei Provincial Key Laboratory of Green Materials for Light Industry Collaborative Innovation Center of Green Light-Weight Materials and ProcessingSchool of Materials and Chemical EngineeringHubei University of TechnologyWuhan 430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan 528200China

Owing to their safety and low cost,magnesium ion batteries(MIBs)have attracted much attention in recent ***,the sluggish diffusion dynamics of magnesium ions hampers the search for appropriate cathode materials with excellent electrochemical ***,we design and synthesize a novel flexible three-dimensional-networked composite of iron vanadate nanosheet arrays/carbon cloths(3 D FeVO/CC)as a binder-free cathode for *** to bare FeVO nanosheets,the 3 D binder-free electrode with designed architecture enables a full range of electrochemical potential,including a high specific capacity of270 mA h g^(-1) and an increased life span(over 5000 cycles).Such achievable high-density energy originates from the synergistic optimization of electron and ion kinetics,while the durability benefits from the robust structure that prevents degradation in *** single-phase reaction mechanism of FeVO in the magnesium ion storage process is also explored by in-situ X-ray diffraction and Raman ***,a flexible MIB pouch cell(3 D FeVO/CCIMgNaTi_(3)O_(7)) is assembled and exhibits practical application *** work verifies that 3 D FeVO/CC is a potential candidate cathode material that can satisfy the requirements of highperformance *** also opens a new avenue to improve the electrochemical performance of cathode materials for MIBs.

关键词： iron vanadate nanosheet arrays flexibility cathode materials magnesium ion batteries

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Designing polymer nanocomposites with high energy density using machine learning

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npj Computational materials 2021年第1期7卷 999-1007页

作者： Zhong-Hui Shen Zhi-Wei Bao Xiao-Xing Cheng Bao-Wen Li Han-Xing Liu Yang Shen Long-Qing Chen Xiao-Guang Li Ce-Wen Nan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and DevicesWuhan University of TechnologyWuhanChina International School of Materials Science and Engineering Wuhan University of TechnologyWuhanChina Hefei National Laboratory for Physical Sciences at the Microscale Department of Physics and CAS Key Laboratory of Strongly-Coupled Quantum Matter Physics University of Science and Technology of China HefeiChina Department of Materials Science and Engineering The Pennsylvania State UniversityUniversity ParkPAUnited States School of Materials Science and Engineering State Key Lab of New Ceramics and Fine ProcessingTsinghua UniversityBeijingChina

Addressing microstructure-property relations of polymer nanocomposites is vital for designing advanced dielectrics for electrostatic energy ***,we develop an integrated phase-field model to simulate the dielectric response,charge transport,and breakdown process of polymer ***,based on 6615 high-throughput calculation results,a machine learning strategy is schemed to evaluate the capability of energy *** find that parallel perovskite nanosheets prefer to block and then drive charges to migrate along with the interfaces in x-y plane,which could significantly improve the breakdown strength of polymer *** verify our predictions,we fabricate a polymer nanocomposite P(VDF-HFP)/Ca_(2)Nb_(3)O_(10),whose highest discharged energy density almost doubles to 35.9 J cm^(−3) compared with the pristine polymer,mainly benefit from the improved breakdown strength of 853 MVm^(−1).This work opens a horizon to exploit the great potential of 2D perovskite nanosheets for a wide range of applications of flexible dielectrics with the requirement of high voltage endurance.

关键词： polymer energy perovskite

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Enhanced Photocatalytic H_(2)-production Activity of CdS Nanoflower using Single Atom Pt and Graphene Quantum Dot as Dual Cocatalysts

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Chinese Journal of Structural Chemistry 2022年第6期41卷 6-14页

作者： Yi Yang Jinsong Wu Bei Cheng Liuyang Zhang Ahmed Abdullah Al-Ghamdi Swelm Wageh Youji Li State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Nanostructure Research Centre(NRC)Wuhan University of TechnologyWuhan 430070China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430074China Department of Physics Faculty of ScienceKing Abdulaziz UniversityJeddah 21589Saudi Arabia College of Chemistry and Chemical engineering Jishou UniversityJishouHunan 416000China

Single-atom catalysts have high catalytic activity due to their unique quantum size effects and optimal atom ***,visi-ble-light-responsive photocatalysts were designed by coupling CdS with graphene quantum dots(GQDs)and platinum single atoms(PtSAs).GQDs and PtSAs were successively loaded on ultrathin CdS nanosheets through freeze-drying and in-situ photocatalytic *** synergistic effect between PtSAs and GQDs results in superior photocatalytic activity with a hydrogen production rate of 13488μmol h^(-1)g^(-1)as well as the maximum apparent quantum efficiency(AQE)of 35.5%in lactic acid aqueous solution,which is 62 times higher than that of pristine CdS(213μmol g^(-1)h^(-1)).The energy conversion efficiency is ca.13.05%.As a photosensitizer and an electron reservoir,GQDs can not only extend the light response of CdS to the visible-light region(400-800 nm),but also promotes the separation of photoinduced electron-hole ***,PtSAs,with unique electronic and geometric features,can provide more efficient proton reduction *** finding provides an effective strategy to remarkably improve the photocatalytic H_(2) production performance.

关键词： hierarchical nanostructure single-atom catalysts graphene quantum dots CdS nanosheets hydrogen production

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Perfluorosulfonic acid proton exchange membrane with double proton site side chain for high-performance fuel cells at low humidity

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Journal of materials Science & technology 2023年第35期166卷 155-163页

作者： Hongyun Tan Shengqiu Zhao S.Eltahir Ali Shuhong Zheng Abdullah K.Alanazi Rui Wang Haining Zhang Hala M.Abo-Dief Ben Bin Xu Hassan Algadi Handong Li Priyanka Wasnik Zhanhu Guo Haolin Tang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Science and Technology University College-RanyahTaif UniversityP.O.Box 11099Taif 21944Saudi Arabia Department of Chemistry College of ScienceTaif UniversityP.O.Box 11099Taif 21944Saudi Arabia Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen ValleyFoshan 528200China Integrated Composites Laboratory(ICL) Mechanical and Construction EngineeringNorthumbria UniversityNewcastle Upon Tyne NE18STUK College of Materials Science and Engineering Taiyuan University of Science and TechnologyTaiyuan 030024China Department of Electrical Engineering Faculty of EngineeringNajran UniversityNajran11001Saudi Arabia

Structural optimization of ionomers is an effective strategy for achieving high-performance proton ex-change membranes(PEMs)under low relative humidity(RH)*** this study,sulfonimide group and trifluoromethanesulfonate acid(TFSA)ionic liquids were introduced to the perfluorosulfonic acid(PFSA)side chain,resulting in polymer membranes with varying chain lengths(i.e.,PFC_(2)-TF-SI,PFC_(4)-TF-SI,and PFC_(5)-TF-SI).This dual proton-conducting structure extended the length of the hydrophilic side chain and enhanced the hydrophobic-hydrophilic phase separation,aiding in the formation of proton transport ***,the proton conductivity of PFC_(5)-TF-SI and PFC_(2)-TF-SI membranes reached 7.1 and 10.6 mS/cm at 30%RH and 80℃,respectively,which were approximately 29.1%and 92.7%higher than that of the pristine PFC_(5)-SA membrane(5.5 mS/cm).Furthermore,the maximum power density of the PFC_(5)-TF-SI and PFC_(2)-TF-SI membranes from the built single fuel cell achieved 649 and 763 mW/cm^(2) at 30%RH and 80℃,respectively,which were higher than that of the pristine PFC_(5)-SA membrane(567 mW/cm^(2))by about 14.5%and 34.6%,***,this study provides a strategy for PEM design under low RH conditions.

关键词： Proton exchange membrane Structural design Dual proton conduction Hydrophilic channel Proton conductivity Fuel cells

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Oriented Growth for Efficient and Scalable Perovskite Solar Cells by Vapor-Solid Reaction

SSRN

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SSRN 2023年

作者： Duan, Changyu Zhong, Jialing Hu, Shenghan Dou, Yichen Lu, Jianfeng Cheng, Yi-Bing Ku, Zhiliang State Key Laboratory of Advanced Technologies for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China State Key Laboratory of Silicate Materials for Architectures Wuhan University of Technology Wuhan430070 China

The precise control and understanding of crystal orientation in perovskite polycrystalline films are crucial for the development of efficient and stable devices. However, achieving this control remains a significant challenge. Herein, we have developed a PbI2 oriented growth strategy, combining with in-situ vapor-solid reaction transformations, to achieve oriented growth of full-vacuum perovskite films. GIWAXS analysis revealed the general pattern of PbI2 oriented vapor growth and in-situ vapor-solid reaction transformation in this two-step process. The resulting preferred orientation has effectively reduced trap states density, optimizing the carrier dynamics. As a result, champion efficiencies of 22.11% (0.148 cm2), 20.60% (1 cm2) and 19.41% (5 × 5 cm2 mini-modules) are achieved, which are the highest value for perovskite based on vapor-solid reaction. Additionally, the oriented growth method is applicable to a variety of guide layers and is extended to 30 × 30 cm2 film, demonstrating the universality and scalability of the method. © 2023, The Authors. All rights reserved.

关键词： Perovskite solar cells

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A review of efficient electrocatalysts for the oxygen evolution reaction at large current density

DeCarbon

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DeCarbon 2024年第3期5卷 24-40页

作者： Youtao Yao Jiahui Lyu Xingchuan Li Cheng Chen Francis Verpoort John Wang Zhenghui Pan Zongkui Kou State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070PR China Sanya Science and Education Innovation Park of Wuhan University of Technology Sanya572000PR China Hubei Key Laboratory of Fuel Cell Wuhan University of TechnologyWuhan430070PR China Department of Materials Science and Engineering National University of Singapore117574SingaporeSingapore Institute of Materials Research and Engineering(IMRE) A*STAR(Agency for ScienceTechnology and Research)2 Fusionopolis WaySingapore138634Singapore National University of Singapore(Chongqing)Research Institute Chongqing401123PR China School of Materials Science and Engineering Tongji UniversityShanghai201804PR China

Within the framework of achieving global carbon neutrality,utilizing electrocatalytic water splitting to produce“green hydrogen”holds significant promise as an effective *** strategic development of economic,efficient,and robust anode oxygen evolution reaction(OER)catalysts is one of the imminent bottlenecks for scalable application of electrolyzing water into hydrogen and oxygen,particularly under actual yet harsh operating conditions such as large current density(LCD).In this review,we intend to summarize the advances and challenges in the understanding of the electrocatalytic OER at ***,the impact of LCD on the electron transfer,mass transportation efficiency and catalyst stability is identified and ***,five basic principles for catalyst design,namely the dimension of the materials,surface chemistry,creation of electron transfer pathways,synergy among nano-,micro-,and macroscale structures,and catalyst-support interaction,are systematically ***,the correlation between the synergistic function of the multiscale structures and the catalyst-support interaction is highlighted to direct improvements in catalyst efficiency and durability at the ***,an outlook is prospected to further our understanding of these topics and provide related researchers with potential research areas.

关键词： Oxygen evolution reaction Electrocatalyst Large current density Green hydrogen Water splitting

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在导电陶瓷基体中加入hBN薄片来创制材料性能的各向异性

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Science China materials 2023年第11期66卷 4317-4325页

作者：梁华岳邹冀刘晶晶顾熠涵季伟王子涵王为民傅正义 Hubei Longzhong Laboratory Wuhan University of Technology Xiangyang Demonstration ZoneXiangyang 441000China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China Jingdezhen Huaxun Special Ceramics Co. Ltd.Jingdezhen 333000China

导电陶瓷的物理性能由连续的导电基体所决定,调控困难.在这项研究中,通过在陶瓷基体中引入hBN薄片,成功实现了导电陶瓷力学和物理性能各向异性的调控.以包含TiN、Al、硼和hBN的混合粉末为原料,通过放电等离子烧结制备了两种hBN含量不同... 详细信息

导电陶瓷的物理性能由连续的导电基体所决定,调控困难.在这项研究中,通过在陶瓷基体中引入hBN薄片,成功实现了导电陶瓷力学和物理性能各向异性的调控.以包含TiN、Al、硼和hBN的混合粉末为原料,通过放电等离子烧结制备了两种hBN含量不同的导电TiB_(2)-AlNhBN陶瓷.在垂直于烧结压力的方向上,TiB_(2)-AlN-60vol%hBN陶瓷在室温下的弯曲强度、断裂韧性、电导率和热导率分别为151±6.34MPa、2.62±0.31MPam^(1/2)、5.3×10^(5)S m^(−1)和77.87Wm^(-1)K^(-1).而在平行于烧结压力的方向上,室温电导率和热导率分别降低到2.0×10^(5)S m^(−1)和32.25Wm^(-1)K^(-1).这些差异是通过在导电基体中加入少量额外排列的hBN薄片而产生的,为材料选择和设计提供了新的机会.

关键词： hexagonal boron nitride texture microstructure mechanical property physical property

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Mg-Based Micromotors with Motion Responsive to Dual Stimuli

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Research 2020年第1期2020卷 966-977页

作者： Kang Xiong Leilei Xu Jinwei Lin Fangzhi Mou Jianguo Guan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China

Mg-based micromotors have emerged as an extremely attractive artificial micro/nanodevice,but suffered from uncontrollable propulsion and limited motion lifetime,restricting the fulfillment of complex ***,we have demonstrated Mg-based micromotors composed of Mg microspheres asymmetrically coated with Pt and temperature-sensitive poly(N-isopropylacrylamide)(PNIPAM)hydrogel layers in *** can implement different motion behaviors stemming from the driving mechanism transformation when encountering catalyzed substrates such as H_(2)O_(2) and respond to both H_(2)O_(2) concentration and temperature in aqueous *** as-constructed Mg-based micromotors are self-propelled by Pt-catalyzed H_(2)O_(2) decomposition following the self-consuming Mg-H_(2)O *** this case,they could further generate bilateral bubbles and thus demonstrate unique self-limitation motion like hovering when the phase transformation of PNIPAM is triggered by decreasing temperature or when the H_(2)O_(2) concentration after permeating across the PNIPAM hydrogel layer is high enough to facilitate bubble *** work for the first time provides a stimuli-induced“hovering”strategy for self-propelled micromotors,which endows Mg-based micromotors with an intelligent response to the surroundings besides the significant extension of their motion lifetime.

关键词： transformation consuming attractive

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Awakening the oxygen evolution activity of MoS_(2) by oxophilic-metal induced surface reorganization engineering

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Journal of Energy Chemistry 2021年第11期30卷 546-551,I0013页

作者： Xueqin Mu Yang Zhu Xiangyao Gu Shipeng Dai Qixin Mao Lintao Bao Wenxuan Li Suli Liu Jianchun Bao Shichun Mu Jiangsu Key Laboratory of Biofunctional Materials School of Chemistry and Materials ScienceNanjing Normal UniversityNanjing 210023JiangsuChina Key Laboratory of Advanced Functional Materials of Nanjing Nanjing Xiaozhuang UniversityNanjing 211171JiangsuChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu hydrogen ValleyFoshan 528200GuangdongChina

Although molybdenum disulfide (MoS_(2))-based materials are generally known as active electrocatalysts for the hydrogen evolution reaction (HER), the inert performance for the oxygen evolution reaction (OER) seriously limits their wide applications in alkaline electrolyzers due to there exists too strong metal-sulfur (M−S) bond in MoS_(2). Herein, by means of surface reorganization engineering of bimetal Al, Co-doped MoS_(2) (devoted as AlCo_(3)-MoS_(2)) through in situ substituting partial oxidation, we successfully significantly activate the OER activity of MoS_(2), which affords a considerably low overpotential of 323 mV at −30 mA cm^(−2), far lower than those of MoS_(2), Al-MoS_(2) and Co-MoS_(2) catalysts. Essentially, the AlCo_(3)-MoS_(2) substrate produces lots of M−O (M=Al, Co and Mo) species with oxygen vacancies, which trigger the surface self-reconstruction of pre-catalysts and simultaneously boost the electrocatalytic OER activity. Moreover, benefiting from the moderate M−O species formed on the surface, the redistribution of surface electron states is induced, thus optimizing the adsorption of OH* and OOH* intermediates on metal oxyhydroxides and awakening the OER activity of MoS_(2).

关键词： Surface reorganization engineering Porous nanosheets Oxygen evolution reaction MoS_(2) Oxophilic-metal

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