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Temperature-dependent microstructural evolution in a compositionally complex solid electrolyte:The role of a grain boundary transition

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Journal of Advanced Ceramics 2025年第3期14卷 163-176页

作者： Shu-Ting Ko Chaojie Du Huiming Guo Hasti Vahidi Jenna L.Wardini Tom Lee Yi Liu Jingjing Yang Francisco Guzman Timothy J.Rupert William J.Bowman Shen J.Dillon Xiaoqing Pan Jian Luo Aiiso Yufeng Li Family Department of Chemical and Nano Engineering University of California San DiegoLa JollaCalifornia 92093USA Program in Materials Science and Engineering University of California San DiegoLa JollaCalifornia 92093USA Department of Materials Science and Engineering University of California IrvineIrvineCalifornia 92697USA Department of Physics and Astronomy University of California IrvineIrvineCalifornia 92697USA Irvine Materials Research Institute University of California IrvineIrvineCalifornia 92697USA

Compositionally complex solid electrolyte(Li_(0.375)Sr_(0.4375))(Ta_(0.375)Nb_(0.375)Zr_(0.125)Hf_(0.125))O_(3)(LSTNZH)samples are synthesized using different sintering temperatures,durations,and cooling conditions(furnace cooling(FC)*** quenching(AQ)).The temperature-dependent grain growth has been examined to investigate the microstructural evolution and the origin of exaggerated(abnormal)grain *** moderate temperatures,the grain growth of LSTNZH follows a cubic root growth model with an Arrhenius temperature *** increasing temperature,bimodal microstructures develop,and the Arrhenius temperature dependence breaks ***,increasing the temperature induces increased Nb segregation at general grain boundaries(GBs),in contrast to classical GB segregation models but suggesting premelting-like GB disordering,which can explain the observed abnormal grain growth(AGG).In addition,the large grains become faceted with increasing temperature,which occurs concurrently with the temperature-induced transitions in GB segregation and grain growth,thereby further supporting the occurrence of a GB phase-like(complexion)*** impacts on the densification,ionic conductivity,and hardness are also *** work provides a new insight into the fundamental understanding of the grain growth mechanisms of the emergent class of medium-and high-entropy compositionally complex ceramics(CCCs),which is essential for tailoring microstructures and material properties.

关键词： compositionally complex ceramics(CCCs) solid electrolytes perovskite grain growth grain boundary(GB) electron backscatter diffraction(EBSD)

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Design of fluorine-rich poly(arylene amine) membranes for liquid aliphatic hydrocarbon separation

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science China Chemistry 2025年第5期68卷 1635-1636页

作者： Chao Zhang Zhi-Kang Xu MOE Key Lab of Macromolecular Synthesis and Functionalization Key Lab of Adsorption and Separation Materials & Technologies of Zhejiang ProvinceDepartment of Polymer Science and EngineeringZhejiang University The “Belt and Road” Sino-Portugal Joint Lab on Advanced Materials International Research Center for X PolymersZhejiang University

Separation of liquid aliphatic hydrocarbons is of fundamental interest and practical importance in the development of liquid fuels and basic chemical feedstocks [1]. As a classic platform to synthesize high-value hydrocarbons using nonfossil feedstocks, the Fischer-Tropsch process usually produces a broad distribution of aliphatic alkanes, accompanied with some olefin byproducts [2].

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CO_(2)-Sourced Poly(chloropropylene carbonate) with High Flame-Retardant Performance

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Chinese Journal of Polymer science 2025年第1期43卷 110-119,I0010页

作者： Yue Gong Xiao-Feng Zhu Guan-Wen Yang Meng Ma Xu Wang Jie Xu Xin Shu Guang-Peng Wu MOE Key Laboratory of Macromolecular Synthesis and Functionalization Key Laboratory of Adsorption and Separation Materials&Technologies of Zhejiang ProvinceDepartment of Polymer Science and EngineeringZhejiang UniversityHangzhou 310058China Zhejiang Key Laboratory of Plastic Modification and Processing Technology College of Materials Science and EngineeringZhejiang University of Technology Hangzhou 310014China Shanxi Coal Chemical Industry Technology Research Institute Co Ltd.Xi'an 710100China

The alternating copolymer of CO_(2) with epoxide is a green plastic that can efficiently transform CO_(2) into valuable chemicals. Despite the significant advances made, the restricted practical application of CO_(2)-sourced polycarbonates due to their lack of functionality has hindered field development. We successfully demonstrated the flame retardancy of poly(chloropropylene carbonate) (PCPC), a perfectly alternating copolymer of epichlorohydrin (ECH) and CO_(2). This was prepared at a 200-gram scale using a high-efficacy tetranuclear organoborane catalyst. PCPC’s excellent flame-retardant performance has been proven by both the vertical combustion test (UL94 V-0) and the limiting oxygen index (LOI) value (29.1%). The underlaid flame-retardant mechanism of PCPC was clearly elucidated. As a result, we confirmed that the generated cyclic carbonates and concurrently released flame-retardant chlorine radicals, hydrogen chloride, and CO_(2) during combustion render PCPC an excellent flame retardant. Furthermore, we investigated the practicability of PCPC as a halogen-rich polymeric flame retardant by blending it with commercial bisphenol A polycarbonate (BPA-PC). PCPC upgraded the flame retardancy rating of BPA polycarbonate from V-2 to V-0 even with a mere 1 wt% addition. It is our hope that this result will prove useful in future developments of advanced CO_(2)-sourced polymeric materials.

关键词： Carbon dioxide Ring-Opening polymerization Organocatalysis Sustainable materials Flame-retardant polymer

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Unassisted photoelectrochemical CO_(2)reduction by employingⅢ-Ⅴphotoelectrode with 15%solar-to-fuel efficiency

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Carbon Energy 2025年第3期7卷 1-10页

作者： Karthik Peramaiah Purushothaman Varadhan Vinoth Ramalingam Bilawal Khan Pradip Kumar Das Hao Huang Hui-Chun Fu Xiulin Yang Vincent Tung Kuo-Wei Huang Jr-Hau He Chemistry Program Center for Renewable Energy and Storage Technologies(CREST)and Division of Physical Science and EngineeringKing Abdullah University of Science and Technology(KAUST)ThuwalSaudi Arabia Institute of Sustainability for Chemicals Energyand Environment(ISCE2)Agency for ScienceTechnologyand Research(A*STAR)Singapore School of Computing Engineering and TechnologyRobert Gordon UniversityAberdeenUK Department of Materials Science and Engineering City University of Hong KongKowloonSARHong KongChina Guangxi Key Laboratory of Low Carbon Energy Materials School of Chemistry and Pharmaceutical SciencesGuangxi Normal UniversityGuilinChina Department of Chemical System and Engineering University of TokyoTokyoJapan

Solar-driven carbon dioxide reduction reaction(CO_(2)RR)provides an oppor tunity to produce value-added chemical feedstocks and ***,achieving efficient and stable photoelectrochemical(PEC)CO_(2)RR into selec tive products is challenging owing to the difficulties associated with the optical and the electrical configuration of PEC devices and electrocatalyst ***,we construct an efficient,concentrated sunlight-driven CO_(2)RR setup consisting of InGaP/GaAs/Ge triple-junction cell as a photoanode and oxide-derived Au(Ox-Au)as a cathode to perform the unassisted PEC CO_(2)*** one-sun illumination,a maximum operating current density of 11.5 mA cm^(-2) with an impressive Faradaic efficiency(FE)of~98%is achieved for carbon monoxide(CO)production,leading to a solar-to-fuel conversion efficiency of~15%.Under concentrated intensity of 10 sun,the photoanode records a maximum current density of~124 mAcm^(-2) and maintains~60%of FE for CO *** results demonstrate crucial advancements in usingⅢ-Ⅴbased photoanodes for concentrated PEC CO_(2)RR.

关键词： photoelectrochemical oxide derived Au concentrated sunlight selec tive products III V photoelectrode pec devices CO reduction solar fuel efficiency

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Material Design for Durable Lubricant-Infused Surfaces That Can Reduce Liquid and Solid Fouling

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ACS Nano 2025年第19期19卷 18075-18094页

作者： Wang, Fan-Wei Sun, Jianxing Tuteja, Anish Department of Chemical Engineering University of Michigan Ann ArborMI48109 United States Biointerfaces Institute University of Michigan Ann ArborMI48109 United States Department of Materials Science and Engineering University of Michigan Ann ArborMI48109 United States Macromolecular Science and Engineering Program University of Michigan Ann ArborMI48109 United States

Liquid and solid fouling is a pervasive problem in numerous natural and industrial settings, significantly impacting energy efficiency, greenhouse emissions, operational costs, equipment lifespan, and human health. Inspired by pitcher plants, recently developed lubricant-infused surfaces (LISs) demonstrate resistance to both liquid and solid accretion under diverse environmental conditions, offering a potential solution to combat various foulants such as ice, bacteria, and mineral deposits. However, the commercial viability for most fouling-resistant LISs has thus far been compromised due to the challenges associated with maintaining a stable lubricant layer during operation. This review aims to address this important concern by providing systematic material design guidelines for fabricating durable LISs. We discuss fundamental design principles, methods for evaluating fouling resistance, and strategies to prevent lubricant loss. By presenting a comprehensive design methodology for this important class of materials, this review aims to aid future advancements in the field of antifouling surfaces, potentially impacting a variety of industries ranging from marine engineering to medical device manufacturing. © 2025 American Chemical Society.

关键词： Biofouling

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Smartly tuning supramolecular chirality in polymer gels via photoexcitation-induced cooperative self-assembly

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science China Chemistry 2025年第3期68卷 1126-1135页

作者： Bingbing Yue Yulong Shi Fan Yang Danfeng Ye Jian Jin Pilan Zhang Shen Song Yifei Xu Hui Lin Shihui Zhu Liangliang Zhu School of Materials and Chemistry University of Shanghai for Science and TechnologyShanghai 200093China State Key Laboratory of Molecular Engineering of Polymers Department of Macromolecular ScienceFudan UniversityShanghai 200438China College of Material Science and Chemical Engineering Ningbo University of TechnologyNingbo 315211China Shanghai Depeac Biotechnology Co. Ltd.Shanghai 201900China Burn and Plastic Surgery Department Children’s Medical Center Affiliated to Shanghai Jiao Tong University School of MedicineShanghai 200120China

Although supramolecular chirality tuning is prosperous in systems with small molecular building blocks,these systems lack structural strength and have limited practical ***,polymer systems do not exhibit these drawbacks but suffer from topological chain entanglement,which often leads to large dynamic obstacles and therefore limits the tunability of supramolecular ***,we report that by manipulating stoichiometry and employing light to alter the H-bond crosslinking between a photoexcitation-induced aggregatable molecule and high molecular weight poly(L-lactic acids),supramolecular chirality tuning of the polymer gel systems can be achieved in different ways through a cooperative ***,the Cotton effects of the examined systems can be negatively tuned by varying their stoichiometry,while positive tuning can be realized by *** deexcitation,negative Cotton effect tuning occurs again spontaneously in some *** supramolecular chirality tuning is accompanied by rheological property tuning,demonstrating that our strategy can overcome polymer chain entanglement *** proposed strategy inspires further works on the precise control of polymer chirality and,hence,development of asymmetric materials with changeable optical activity and modulus.

关键词： supramolecular chirality polymer gels phototuning self-assembly rheological property

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Distance Learning at the MS and PhD Levels in the Nuclear and Radiation engineering program, Nuclear and Applied Robotics, materials science and engineering and Walker department of Mechanical engineering at the University of Texas at Austin

Distance Learning at the MS and PhD Levels in the Nuclear an...

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2023 Transactions of the American Nuclear Society Winter Conference and Expo, ANS 2023

作者： Landsberger1, Sheldon Charlton, William Clamo, Kevin Ezekoye, Ofodike Kovar, Desiderio Haas, Derek Pryor, Mitchell University of Texas at Austin Nuclear and Radiation Engineering Program Nuclear Engineering Teaching Lab 10100 Burnet Road Pickle Research Campus R-9000 AustinTX United States Walker Department of Mechanical Engineering University of Texas at Austin 204.Dean Keeton ETC II 5.160 AustinTX United States The University of Texas at Austin Materials Science and Engineering Walker Department of Mechanical Engineering 204 Dean Keeton ETC II 5.100 AustinTX United States

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Enhancing the high-temperature stability of OFETs by inducing D-A stacking in P(NDI2OD-T2) films

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science China materials 2025年第1期68卷 117-124页

作者： Xuetao Xiao Wenhao Li Qing Zhou Zeng Wu Xiaochan Zuo Rong Ma Yifei Xu Sichun Wang Yan Zhao Laboratory of Molecular Materials and Devices Department of Materials ScienceFudan UniversityShanghai 200433China State Key Laboratory of Molecular Engineering of Polymers and Department of Macromolecular Science Fudan UniversityShanghai 200433China

High-temperature stability of organic field-effect transistors(OFETs)is critical to ensure its long-term reliable operation under various environmental *** molecular packing of donor-acceptor(D-A)conjugated polymers is closely related to the electrical performance stability in ***,we choose poly[[N,N′-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5′-(2,2′-bithiophene)]as a modal system to reveal the relationship between the molecular stacking and electrical stability in high-temperature *** results demonstrate that the films with D-A moieties in alternate stacking have better electrical thermal stability compared to normal donor-donor(D-D)*** D-A stacking configuration alternates donor and acceptor units along the out-of-plane direction,while the D-D stacking involves D-D and A-A stacking *** structural transition from D-D to D-A is captured at a treated temperature range of 225±250°*** to the tighter packing arrangement along theπ-πand lamellar directions,the electron mobility of the D-A stacked films reaches up to 0.23 cm^(2)/V·s,a 50%increase as compared to the D-D stacking ***,the D-A stacked films indicate superior electrical performance stability with mobility retaining 100%at 250°C during high-temperature cycling *** result highlights that the manipulation of conjugated polymer closely stacked structures can significantly enhance the thermal stability and durability of semiconductor devices.

关键词： high-temperature stability D-A stacking P(NDI2OD-T2) electrical properties OFETs

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Biobased Poly(ester amide)s as Sustainable Coating materials for Vegan Leather with Improved Haptic Sensation

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ACS Sustainable Chemistry and engineering 2025年第20期13卷 7585-7597页

作者： Ryu, Jieun Hao, Lam Tan Kim, Hyeri Lee, Somyong Jeon, Hyeonyeol Hwang, Dong Soo Park, Jeyoung Park, Cheol Hun Oh, Dongyeop X. Koo, Jun Mo Park, Sung Bae Ulsan44429 Korea Republic of Pohang37673 Korea Republic of Ulsan44429 Korea Republic of Pohang37673 Korea Republic of Daejeon34113 Korea Republic of Department of Chemical and Biomolecular Engineering Sogang University Seoul04107 Korea Republic of Department of Polymer Science and Engineering and Program in Environmental and Polymer Engineering Inha University Incheon22212 Korea Republic of Department of Organic Materials Engineering Chungnam National University Daejeon34134 Korea Republic of Department of Materials Science and Engineering Chungnam National University Daejeon34134 Korea Republic of

Increased consumer awareness of animal welfare and environmental sustainability has driven the development of vegan leather alternatives to natural leather. Fossil-derived leather substitutes offer superior strength and thermal stability but often lack biodegradability, carbon neutrality and aesthetics. Biorenewable alternatives are more eco-friendly but typically suffer from insufficient thermal and mechanical properties and poor moisture resistance. This study presents the synthesis of mechanically reinforced, thermally enhanced and biodegradable poly(ester amide)s (PEAs) incorporating hydrogen bonds as vegan leather coating materials. Synthesized from biobased 1,4-butanediol, adipic acid and nylon 46 via a two-step transesterification/polycondensation process, the resulting PEAs exhibit over eight times higher tensile strength, 3-fold greater toughness, and enhanced thermal stability compared to their constituting homopolymers, poly(butylene adipate) and nylon 46. All PEAs disintegrate within 18 weeks and achieve over 60% biodegradation rate relative to cellulose under composting conditions within one month. When applied to mushroom fabrics, the PEA coating provides haptic sensations (slipperiness and softness) comparable to commercially available leather. Life-cycle assessment indicates that PEA-coated leather imposes considerably lower environmental impacts than both bovine and polyurethane-based leather. This novel material holds promise as a sustainable, high-performance vegan leather substitute. © 2025 American Chemical Society.

关键词： Biodegradability

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Dense carbon nanofiber self-supporting electrode fabricated by orientation/compaction strategy for high volumetric lithium storage capacity

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Progress in Natural science:materials International 2025年第1期35卷 229-237页

作者： Haihui Liu Chaoqun Chen Qiang Xu Yan Song Xiangwu Zhang Chang Ma Tianjin Municipal Key Lab of Advanced Fiber and Energy Storage Technology Tiangong University CAS Key Laboratory of Carbon Materials Institute of Coal Chemistry Chinese Academy of Sciences Fiber and Polymer Science Program Department of Textile Engineering Chemistry and Science Wilson College of Textiles North Carolina State University

Low bulk density greatly restricts the large-scale application of electrospun carbon-based fiber membrane as electrode in energy storage devices. To solve the above challenges, herein an orientation-compaction densification strategy is proposed to enhance the bulk density and volumetric capacity of PAN-based carbon nanofiber membranes as self-supporting electrode used in lithium-ion batteries（LIBs）. Specifically, highly-oriented fibers are achieved by high-speed roller collecting during electrospinning, and compaction densification is conducted by hot-pressing treatment. The effects of collecting speed and hot-pressing pressure on the morphology, conductivity,bulk density, tensile strength, and flexibility of the obtained carbon nanofiber membrane are *** to conventional fiber membranes, of which fibers are disorderly stacked, the oriented fiber membrane is much easier to achieve dense stacking by compaction. The obtained dense carbon nanofiber membrane demonstrates a bulk density of 0.566 g cm-3, and shows a significantly-enhanced volumetric capacity(318.3 mA h cm-3), high-rate performance(86.6 mA h cm-3at 5 A g-1), and satisfactory cycling stability when used as selfsupporting electrode of LIBs.

关键词： Bulk density Densification Electrospinning Orientation-compaction Volumetric capacity

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