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Bifunctional Liquid Metals Allow Electrical Insulating Phase Change Materials to Dual-Mode Thermal Manage the Li-Ion Batteries

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Nano-Micro Letters 2022年第12期14卷 224-238页

作者： Cong Guo Lu He Yihang Yao Weizhi Lin Yongzheng Zhang Qin Zhang Kai Wu Qiang Fu College of Polymer Science and Engineering State Key Laboratory of Polymer Materials EngineeringSichuan UniversityChengdu 610065People’s Republic of China Department of Polymer Science and Engineering School of Chemical EngineeringNanjing University of Science and TechnologyNanjing 210094People’s Republic of China

Phase change materials(PCMs)are expected to achieve dual-mode thermal management for heating and cooling Li-ion batteries(LIBs)according to real-time thermal conditions,guaranteeing the reliable operation of LIBs in both cold and hot ***,we report a liquid metal(LM)modified polyethylene glycol/LM/boron nitride PCM,capable of dual-mode thermal managing the LIBs through photothermal effect and passive thermal *** geometrical conformation and thermal pathways fabricated through ice-template strategy are conformable to the LIB’s structure and heat-conduction ***,soft and deformable LMs are modified on the boron nitride surface,serving as thermal bridges to reduce the contact thermal resistance among adjacent fillers to realize high thermal conductivity of 8.8 and 7.6 W m^(−1) K^(−1) in the vertical and in-plane directions,*** addition,LM with excellent photothermal performance provides the PCM with efficient battery heating capability if employing a controllable lighting *** a proof-of-concept,this PCM is manifested to heat battery to an appropriate temperature range in a cold environment and lower the working temperature of the LIBs by more than 10℃ at high charging/discharging rate,opening opportunities for LIBs with durable working performance and evitable risk of thermal runaway.

关键词： Phase change materials Liquid metal Thermal conductivity Photothermal conversion Battery thermal management

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Multifunctional Structure-Modified Quaternary Compounds Co9Se8-CuSe2-WSe2 Mixed with MWCNT as a Counter Electrode Material for Dye-Sensitized Solar Cells

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ACS Applied Materials and Interfaces 2024年第3期16卷 3476-3488页

作者： Liu, Rih-Jia Chang, Ling-Yu Lin, Fang-Sian Lee, Yu-Hsin Yeh, Min-Hsin Ho, Kuo-Chuan Department of Chemical Engineering National Taiwan University Taipei10617 Taiwan Institute of Polymer Science and Engineering National Taiwan University Taipei10617 Taiwan Department of Chemical Engineering National Taiwan University of Science and Technology Taipei10607 Taiwan Advanced Research Center for Green Materials Science and Technology National Taiwan University Taipei10617 Taiwan

In this study, a trimetallic selenide material with a hollow spherical structure (Co9Se8-CuSe2-WSe2) was synthesized through two consecutive solvothermal reactions. The synergistic effect between the quaternary elements, the benefits of the selenization of metals, and the unique morphology led to the prominent electrocatalytic ability of Co9Se8-CuSe2-WSe2 hollow spheres. Co9Se8-CuSe2-WSe2 hollow spheres were then mixed with oxygen plasma-treated multiwalled carbon nanotubes (MWCNT) as counter electrode (CE) material for dye-sensitized solar cells (DSSCs), achieving a photoelectric conversion efficiency (η) of 9.23% under one sun condition (AM 1.5G, 100 mW cm-2), surpassing the 8.08% of devices with platinum counter electrodes (PtCEs). For indoor conditions, a T5 light source was applied to the DSSCs with Co9Se8-CuSe2-WSe2 + MWCNT CE, and the efficiency increased to 14.14% under 3600 lx irradiance. Finally, Co9Se8-CuSe2-WSe2 + MWCNT CE demonstrated good stability with 92.23% retention after 1000 cycles of cyclic voltammetry, exceeding the 82.49% of PtCE. Therefore, Co9Se8-CuSe2-WSe2 + MWCNT shows potential as a substitute for platinum as CE material for DSSCs. © 2024 American chemical Society

关键词： Dye-sensitized solar cells

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Surface-modified Ag@Ru-P25 for photocatalytic CO_(2) conversion with high selectivity over CH_(4) formation at the solid–gas interface

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Carbon Energy 2024年第1期6卷 182-196页

作者： Chaitanya B.Hiragond Sohag Biswas Niket SPowar Junho Lee Eunhee Gong Hwapyong Kim Hong Soo Kim Jin-Woo Jung Chang-Hee Cho Bryan M.Wong Su-Il In Department of Energy Science&Engineering Daegu Gyeongbuk Institute of Science and Technology(DGIST)DaeguRepublic of Korea Department of Chemical&Environmental Engineering Materials Science&Engineering ProgramDepartment of ChemistryDepartment of Physics&AstronomyUniversity of California-RiversideRiversideCaliforniaUSA Department of Physics and Chemistry Daegu Gyeongbuk Institute of Science and Technology(DGIST)DaeguRepublic of Korea NiceScience Corporation DaeguRepublic of Korea

Systematic optimization of the photocatalyst and investigation of the role of each component is important to maximizing catalytic activity and comprehending the photocatalytic conversion of CO_(2) reduction to solar fuels.A surface-modified Ag@Ru-P25 photocatalyst with H_(2)O_(2) treatment was designed in this study to convert CO_(2) and H_(2)O vapor into highly selective *** doping followed by Ag nanoparticles(NPs)cocatalyst deposition on P25(TiO_(2))enhances visible light absorption and charge separation,whereas H_(2)O_(2) treatment modifies the surface of the photocatalyst with hydroxyl(–OH)groups and promotes CO_(2) ***-resonance transmission electron microscopy,X-ray photoelectron spectroscopy,X-ray absorption near-edge structure,and extended X-ray absorption fine structure techniques were used to analyze the surface and chemical composition of the photocatalyst,while thermogravimetric analysis,CO_(2) adsorption isotherm,and temperature programmed desorption study were performed to examine the significance of H_(2)O_(2) treatment in increasing CO_(2) reduction *** optimized Ag1.0@Ru1.0-P25 photocatalyst performed excellent CO_(2) reduction activity into CO,CH4,and C2H6 with a~95%selectivity of CH4,where the activity was~135 times higher than that of pristine TiO_(2)(P25).For the first time,this work explored the effect of H_(2)O_(2) treatment on the photocatalyst that dramatically increases CO_(2) reduction activity.

关键词： gas-phase CO_(2) reduction H_(2)O_(2) treatment plasmonic nanoparticles solar fuel photocatalyst surface modification

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Ring-Opening Copolymerization of Biorenewable δ-Caprolactone with trans-Hexahydro-(4,5)-benzofuranone toward Closed-Loop Recyclable Copolyesters and Their Application as Pressure- Sensitive Adhesives

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Chinese Journal of Chemistry 2024年第17期42卷 2035-2042页

作者： Haining Niu Liying Wang Zihan Zhang Yalei Liu Yong Shen Zhibo Li State Key Laboratory Base of Eco-Chemical Engineering College of Chemical EngineeringQingdao University of Science and TechnologyQingdaoShandong266042China Key Laboratory of Biobased Polymer Materials Shandong Provincial Education DepartmentQingdao University of Science and TechnologyQingdaoShandong266042China

Copolymerization as an efficient strategy can provide an opportunity to create new closed-loop recyclable polymeric materials with tailored properties that are generally inaccessible to the individual *** this contribution,the bulk ring-opening copolymerization of bio-renewable-caprolactone and trans-hexahydro-(4,5)-benzofuranone was achieved to produce closed-loop recyclable copolyesters by using an organobase/urea binary catalyst at room *** obtained copolyesters exhibited composition-dependent thermal ***,the obtained copolyesters were able to depolymerize back to recover the corresponding monomers under mild conditions.

关键词： Recyclable polymers Ring-opening polymerization Copolymerization Pressure-sensitive adhesives Aliphatic polyesters

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Harnessing mechanochemical fluorescence toward autonomous damage-reporting coatings

RSC Applied Polymers

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RSC Applied polymers 2025年第3期3卷 592-597页

作者： Wang, Zeyu Zhou, Junfeng Ling, Zichen Zhou, Qixin Wang, Junpeng School of Polymer Science and Polymer Engineering The University of Akron Akron 44325 OH United States Department of Chemical Biomolecular and Corrosion Engineering The University of Akron Akron 44325 OH United States

Protective coatings are essential for shielding engineering materials from environmental and mechanical damage. A significant endeavor in this regard is detecting the damage in coatings and implementing necessary repairs. However, conventional detection methods often require specialized equipment and expertise, rendering them impractical for real-time monitoring. This work introduces an autonomous damage-reporting coating system based on a stress-responsive polymer network containing a Diels-Alder adduct mechanophore. When subjected to mechanical damage, the mechanophore undergoes a retro-Diels-Alder reaction, liberating a fluorescent π-extended anthracene moiety. The mechanically triggered “off-to-on” optical signal allows for highly sensitive detection of material damage preceding failure. A quantitative relationship between the extent of impact damage and the mechanochemically generated fluorescence is established, facilitating the prediction of material failure. Remarkably, the damage-reporting functionality is maintained even after incorporating pigments into the coating formulation, thereby broadening the applicability of this smart coating system in real-world scenarios. © 2025 RSC.

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Boroxine Crystalline Covalent Organic Frameworks Based Single-ion Quasi-solid-state Conductor in Lithium-ion Battery

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Chinese Journal of polymer science 2025年第1期43卷 177-187,I0012页

作者： Hao-Min Wu Wen-Can Ma Yi-Feng Cai Xin Huang Jun-Heng Li Xi Kai Qiu-Hong Zhang Xu-Dong Jia Key Laboratory of High-Performance Polymer Material and Technology of MOE Department of Polymer Science and EngineeringSchool of Chemistry and Chemical EngineeringNanjing UniversityNanjing 210023China Institute of Chemical Industry of Forest Products Chinese Academy of Forestry DepartmentNanjing 210018China School of Chemistryand Chemical Engineering Frontiers Science Center for Transformative MoleculesShanghai Jiao Tong UniversityShanghai 200240China Executive in Low Carbon Management Division of QHSE Department Sinochem Holdings Corporation LtdCentral TowerChemsunny World Trade CenterBejing 100031China State Key Laboratory of Coordination Chemistry Nanjing UniversityNanjing 210023China

Solid-state electrolytes are considered to be the vital part of the next-generation solid-state batteries(SSBs),due to their high safety and long operation life ***,the two major factors that impede the expected performance of batteries are:the easy formation of lithium dendrites due to the concentration gradient of anions,and the low ionic conductivity at room temperature,which prevents reaching ideal electrochemical ***-ion quasi-solid-state electrolytes(SIQSSEs)could provide higher safety and energy density,owing to absence of anion concentration gradient and solvent,as well as good lithium-ion transport *** porous covalent organic frameworks(COFs)are beneficial for con-structing appropriate lithium-ion transport pathway,due to the ordered 1D *** addition,the boroxine COFs(COF-5)offers strong ability of withdrawing anion part of lithium *** but not the least,boron atom could play the role of coordinate site due to its electron *** advantages afford an opportunity to obtain a SIQSSE with high ionic conductivity and high lithium transference number(LTN)*** COF-5 based SIQSSEs delivered a high ionic conductivity of 6.3×10^(-4)S·cm^(-1),with a high LTN of 0.92 and a wide electrochemical stable window(ESW)of 4.7 V at room *** LiFePO4(LFP)/Li cells,which was assembled with COF-5 based SIQSSE,exhibited outstanding long cycle stability,high initial capacity and favorable rate *** results indicated COFs could be an ideal material for single-ion solid-state electrolytes in next-generation batteries.

关键词： Covalent organic framework Quasi-solid-state electrolyte Single-ion Lithium metal batteries

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Interfacial reactions in the Sn-9.0 wt.% Zn/Cu-Ti alloy (C1990 HP) couple

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Soldering and Surface Mount Technology 2024年第1期36卷 30-38页

作者： Laksono, Andromeda Dwi Chen, Chih-Ming Yen, Yee-Wen Department of Materials Science and Engineering National Taiwan University of Science and Technology Taipei Taiwan Department of Chemical Engineering National Chung Hsing University Taichung Taiwan Study Program of Material and Metallurgical Engineering Institut Teknologi Kalimantan Balikpapan Indonesia

Purpose: The purpose of this study was to examine the influence of adding a small amount of Ti to a Cu-based alloy, specifically the commercial Hyper Titanium Copper alloy (C1990 HP), which contains Cu-3.28 wt.% Ti, on its interfacial reaction with Sn-9.0 wt.% Zn (SnZn) solder, using the liquid/solid reaction couple technique. Design/methodology/approach: The SnZn/C1990 HP couples were subjected to a reaction temperature of 240–270°C for a duration of 0.5–5 h. The resulting reaction couple was characterized using a scanning electron microscope, energy dispersive spectrometer, electron probe microanalyzer and X-ray diffractometer. Findings: It was observed that the scallop-shaped CuZn5 and planar Cu5Zn8 phases were formed in almost all SnZn/C1990 HP couples. With increased reaction duration and temperature, the Cu-rich intermetallic compound (IMC)-Cu5Zn8 phase became a dominant IMC formed at the interface. The total thickness of the IMCs was increased with the increase in the reaction duration and temperature. The IMC growth obeyed the parabolic law, and the IMC growth mechanism was diffusion controlled. The activation energy of the SnZn/C1990 HP couple was 64.71 kJ/mol. Originality/value: This article presents an analysis of the IMC thickness in each sample using ImageJ software, followed by kinetic analysis using Origin software at various reaction temperatures of SnZn/C1990 HP in liquid/solid couples. The study also includes detailed reports on the morphology, interface composition and X-ray diffraction analysis, as well as the activation energy. The findings can serve as a valuable reference for electronic packaging companies that utilize C1990 HP substrates. © 2023, Emerald Publishing Limited.

关键词： Binary alloys

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Porphyrin-Grafted Poly(ethylene terephthalate) as a Reusable and Highly Selective Colorimetric Probe for Mercuric Ion Contaminants in Aqueous Samples

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ACS Applied Materials and Interfaces 2024年第30期16卷 39195-39205页

作者： Atayde, Eduardo C. Takenaka, Yasumasa Abe, Hideki Wu, Ming-Rou Wu, Kevin C.-W. Molecular Science and Technology Program Taiwan International Graduate Program Academia Sinica Department of Chemistry National Tsing Hua University Department of Chemical Engineering National Taiwan University Bioplastic Research Team RIKEN Center for Sustainable Resource Science Department of Chemical Engineering and Materials Science Yuan Ze University Department of Chemical Engineering Chung Yuan Christian University

Heavy metals are the most hazardous water pollutants, with severe health and environmental consequences. Among these, mercuric (Hg2+) ions are known to cause detrimental health issues in both humans and aquatic life. ... 详细信息

Heavy metals are the most hazardous water pollutants, with severe health and environmental consequences. Among these, mercuric (Hg²⁺) ions are known to cause detrimental health issues in both humans and aquatic life. Due to this, several analytical techniques have been devised to detect and quantify the amount of this ion. However, most of these require advanced instrumentation, prolonged analysis time, and sample preparation. In this study, a low-cost and highly reusable colorimetric probe was developed by grafting porphyrin to poly(ethylene terephthalate) sheets using an oxazoline polymer as covalent adhesive. Upon exposure to trace amounts of Hg²⁺ in solution, the fabricated material visually transitioned from faint brownish pink to green by the complexation mechanism. Additionally, the transparency of this probe allowed the quantitative spectrophotometric determination of the Hg²⁺ concentration in aqueous samples. It was also shown that the material is highly stable, which can be reused for more than 50 times without significant decline in its performance, hence, making it suitable for the onsite monitoring of mercuric ion contamination in different bodies of water. © 2024 The Authors. Published by American chemical Society.

关键词： colorimetric probe mercuric ion oxazoline PET porphyrin

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Rechargeable Multivalent-Ion Batteries

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Energy Material Advances 2024年第1期5卷 283-284页

作者： Juchen Guo Jennifer LSchaefer Yuyan Shao Department of Chemical and Environmental Engineering Materials Science and Engineering ProgramUniversity of CaliforniaRiversideRiversideCA 92521USA Department of Chemical and Biomolecular Engineering University of Notre DameNotre DameIN 46556USA Pacific Northwest National Laboratory RichlandWA 99352USA

Rechargeable batteries based on multivalent metal anodes including earth-abundant magnesium(Mg),calcium(Ca),zinc(Zn),and aluminum(Al)are potential new“beyond lithium(Li)”electrochemical energy storage technologies for large-scale energy storage *** multivalent elements are more earth abundant,and therefore promising candidates for reducing global dependence on Li for our growing energy storage *** the seminal work by Aurbach and coworkers[1]demonstrating the first prototype rechargeable Mg batteries,tremendous efforts have been made to the research and development of rechargeable multivalent-ion batteries.

关键词： energy storage calcium batteries rechargeable batteries multivalent elements multivalent metal anodes energy storage technologies magnesium batteries

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A highly visible-transparent thermochromic smart window with broadband infrared modulation for all-season energy savings

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国家科学评论（英文版） 2025年第2期12卷 191-201页

作者： Yi Jiang Yunlong Wang Deshuo Kong Zipeng Chen Zhengwei Yang Ningning Cao Haowen Chi Shining Zhu Qiuhong Zhang Jia Zhu Bin Zhu National Laboratory of Solid State Microstructures College of Engineering and Applied SciencesJiangsu Key Laboratory of Artificial Functional MaterialsFrontiers Science Center for Critical Earth Material CyclingCollaborative Innovation Center of Advanced MicrostructuresNanjing UniversityNanjing 210093China Key Laboratory of High Performance Polymer Material and Technology of MOE Department of Polymer Science and EngineeringSchool of Chemistry and Chemical EngineeringNanjing UniversityNanjing 210093China

Thermochromic smart windows effectively reduce the energy consumption for buildings through passive light modulation including the transmission ofvisible(TVis)and near-infrared(TNIR)light,and the emissivity of mid-infrared light(εMIR)in response to ambient temperature ***,thermochromic windows that maintain high TVis while modulating TNIR and εMIR simultaneously are highly desirable but still ***,we develop a thermochromic smart window based on a two-way shape memory polymer to enable reversible transformation and achieve TNIR modulation of 44.0％andεMIR modulation of 76.5％while maintaining high TVis(＞50％).Compared to traditional windows based on silica glass,this device shows 4℃ lower temperature in summer daytime,2℃ higher in winter daytime,and 1℃ higher in spring *** is expected that our device can achieve greater annual energy savings in comparison with commercial glass anywhere in the world and promote the progress of thermochromic windows for energy-efficient buildings.

关键词： thermochromic smart window visible transparency infrared modulation two-way shape memory polymer

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