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正十六烷聚脲微胶囊化相变材料(英文) 被引量:38
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作者 邹光龙 兰孝征 +2 位作者 谭志诚 孙立贤 张涛 《物理化学学报》 SCIE CAS CSCD 北大核心 2004年第1期90-93,共4页
用界面聚合法,合成了直径大约2.5μm可用于热能储存含相变材料的聚脲包覆微胶囊.在含乳化剂的水溶液中,将溶有芯材正十六烷的有机相乳化成微米级油性液滴,随后加入的水溶性单体二胺与甲苯2,4-二异氰酸酯在胶束界面相互反应形成囊壁.分... 用界面聚合法,合成了直径大约2.5μm可用于热能储存含相变材料的聚脲包覆微胶囊.在含乳化剂的水溶液中,将溶有芯材正十六烷的有机相乳化成微米级油性液滴,随后加入的水溶性单体二胺与甲苯2,4-二异氰酸酯在胶束界面相互反应形成囊壁.分别用乙烯二胺,1,6-己二胺和它们的混合物作为水溶性单体进行了研究.并用红外光谱和热分析分别考察了不同胺类对微胶囊化学结构和热性质的影响.红外谱图显示合成了聚脲微胶囊,热重曲线表明含正十六烷的聚脲微胶囊能够耐受大约300℃高温,差示扫描量热测试表明所有样品均具有合适的相转变热,冷热循环实验揭示微胶囊能够维持储热容量不衰减.研究表明微胶囊化的正十六烷作为相变储热材料具有良好的应用前景. 展开更多
关键词 正十六烷 聚脲微胶囊 相变材料 界面聚合 储热材料 热分析
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Preparation and Characterization of Microencapsulated Hexadecane Used for Thermal Energy Storage 被引量:7
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作者 Guang Long ZOU Zhi Cheng TAN +2 位作者 Xiao Zheng LAN Li Xian SUN Tao ZHANG 《Chinese Chemical Letters》 SCIE CAS CSCD 2004年第6期729-732,共4页
Polyurea microcapsules about 2.5 μm in diameter containing phase change material for thermal energy storage application were synthesized and characterized by interfacial polycondensation method with toluene-2,4-diiso... Polyurea microcapsules about 2.5 μm in diameter containing phase change material for thermal energy storage application were synthesized and characterized by interfacial polycondensation method with toluene-2,4-diisocyanate and ethylenediamine as monomers in an emulsion system. Hexadecane was used as a phase change material and OP, which is nonionic surfactant, and used as an emulsifier. The chemical structure and thermal behavior of the microcapsules were investigated by FTIR and thermal analysis respectively. The results show encapsulated hexadecane has a good potential as a solar energy storage material. 展开更多
关键词 Phase change material MICROCAPSULE interfacial polycondensation energy storage.
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Design strategies for rechargeable aqueous metal-ion batteries 被引量:2
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作者 Yang Li Xin Zhao +5 位作者 Yifu Gao Yichen Ding Zhichun Si Liubing Dong Dong Zhou Feiyu Kang 《Science China Chemistry》 SCIE EI CSCD 2024年第1期165-190,共26页
Rechargeable aqueous metal-ion batteries(AMBs)have attracted extensive scientific and commercial interest due to their potential for cost-effective,highly safe,and scalable stationary energy storage.However,their limi... Rechargeable aqueous metal-ion batteries(AMBs)have attracted extensive scientific and commercial interest due to their potential for cost-effective,highly safe,and scalable stationary energy storage.However,their limited output voltage,inadequate energy density,and poor reversibility of ambiguous electrode reactions in aqueous electrolytes strongly limit their practical viability.This review aims to elucidate the challenges of existing AMBs from the material design to whole device applications.We summarize the emerging electrochemistry,fundamental properties,and key issues in interfacial behaviors of various classes of prevailing AMBs,including aqueous alkali metal-ion batteries and multivalent-ion batteries,and present an appraisal of recent advances for addressing the performance deficiency.Specifically,the progress of zinc-ion batteries is highlighted to provide a ubiquitous guideline for their commercialization in the grid-scale energy storage.Finally,we figure out the dominating general challenges for achieving high-performance AMBs,laying out a perspective for future breakthroughs. 展开更多
关键词 aqueous metal-ion batteries aqueous alkali metal-ion batteries zinc-ion batteries interfacial behavior stationary energy storage
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Microencapsulation of n-Eicosane as Energy Storage Material 被引量:4
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作者 蓝孝征 谭志诚 +2 位作者 邹光龙 孙立贤 张涛 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2004年第5期411-414,共4页
For heat energy storage application, polyurea microcapsules containing phase change material, n-eicosane, were synthesized by using interfacial polymerization method with toluene-2,4-diisocyanate (TDI) and diethylenet... For heat energy storage application, polyurea microcapsules containing phase change material, n-eicosane, were synthesized by using interfacial polymerization method with toluene-2,4-diisocyanate (TDI) and diethylenetriamine (DETA) as monomers in an emulsion system. Poly(ethylene glycol)octyl-phenyl ether (OP), a nonionic surfactant, was the emulsifier for the system. The experimental result indicates that TDI was reacted with DETA in a mass ratio of 3 to 1. FT-IR spectra confirm the formation of wall material, polyurea, from the two monomers, TDI and DETA. Encapsulation efficiency of n-eicosane is about 75%. Microcapsule of n-eicosane melts at a temperature close to that of n-eicosane, while its stored heat energy varies with core material n-eicosane when wall material fixed. Thermo-gravimetric analysis shows that core material n-eicosane, micro-n-eicosane and wall material polyurea can withstand temperatures up to 130, 170 and 250 ℃, respectively. 展开更多
关键词 phase change material n-eicosane MICROCAPSULE interfacial polymerization heat energy storage thermal analysis
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Electrolyte design for rechargeable anion shuttle batteries 被引量:5
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作者 Yao Wang Xu Yang +7 位作者 Zhijia Zhang Xia Hu Yuefeng Meng Xia Wang Dong Zhou Hao Liu Baohua Li Guoxiu Wang 《eScience》 2022年第6期573-590,共18页
As an emerging new type of battery chemistry,the anion shuttle battery(ASB),based on the shuttling and storage of anions,is considered a sustainable alternative to gigawatt-scale energy storage due to the associated r... As an emerging new type of battery chemistry,the anion shuttle battery(ASB),based on the shuttling and storage of anions,is considered a sustainable alternative to gigawatt-scale energy storage due to the associated resource abundance,low cost,high safety,and high energy density.Although significant progress has been achieved,practical applications of ASBs are still hindered by tough challenges,such as short lifetime,limited reversible capacity,and low Coulombic efficiency.Therefore,it is very necessary to design and explore new electrolyte systems with high electrochemical/chemical stability,sufficient compatibility towards electrodes,and excellent kinetics/reversibility for anion electrochemical reactions.Here,we review the recent achievements and main challenges in developing electrolytes for ASBs,which include solid,non-aqueous,and aqueous electrolytes.We mainly focus on the unique properties and basic principles of designing these electrolytes,and their various performance parameters.Perspectives on design strategies for ASB electrolytes are also presented,which could facilitate the development of advanced ASBs for grid-scale energy storage. 展开更多
关键词 Anion shuttle batteries Electrolytes Electrochemical stability interfacial compatibility Grid-scale energy storage
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Optimizing the electrolyte salt of aqueous zinc-ion batteries based on a high-performance calcium vanadate hydrate cathode material 被引量:4
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作者 Weijun Zhou Minfeng Chen +4 位作者 Anran Wang Aixiang Huang Jizhang Chen Xinwu Xu Ching-Ping Wong 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2021年第1期377-384,I0012,共9页
It is urgent to develop high-performance cathode materials for the emerging aqueous zinc-ion batteries with a facile strategy and optimize the related components.Herein,a Ca0.23V2O5·0.95 H2O nanobelt cathode mate... It is urgent to develop high-performance cathode materials for the emerging aqueous zinc-ion batteries with a facile strategy and optimize the related components.Herein,a Ca0.23V2O5·0.95 H2O nanobelt cathode material with a rather large interlayer spacing of 13.0 A is prepared via a one-step hydrothermal approach.The battery with this cathode material and 3 M Zn(CF3SO3)2 electrolyte displays high specific capacity(355.2 mAh g^(-1) at 0.2 A g^(-1)),great rate capability(240.8 mAh g^(-1) at 5 A g^(-1)),and excellent cyclability(97.7% capacity retention over 2000 cycles).Such superior performances are ascribed to fast electrochemical kinetics,outstanding electrode/electrolyte interface stability,and nearly dendrite-free characteristic.Instead,when ZnSO4 or Zn(ClO4)2 is used to replace Zn(CF3SO3)2,the electrochemical performances become much inferior,due to the slow electrochemical kinetics,inhomogeneous Zn stripping/plating process,and the formation of large dendrites and byproducts.This work not only discloses a high-performance cathode material for aqueous zinc-ion batteries but also offers a reference for the choice of electrolyte salt. 展开更多
关键词 Calcium vanadate hydrates Electrolytes interfacial stability Zn-ion batteries Aqueous energy storage
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电化学储能界面的核磁共振谱学研究方法
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作者 欧阳意梅 赵蒙蒙 +1 位作者 钟贵明 彭章泉 《储能科学与技术》 CSCD 北大核心 2024年第1期157-166,共10页
深入认识电化学储能体系(如锂离子电池与锂金属电池等)表界面层的组成与结构,以及相关的物质传递、电荷存储与转移机理,对于开发宽温区、长循环与高倍率电化学储能器件具有重要的理论指导价值。电化学表界面层呈现出稀薄、无序和敏感等... 深入认识电化学储能体系(如锂离子电池与锂金属电池等)表界面层的组成与结构,以及相关的物质传递、电荷存储与转移机理,对于开发宽温区、长循环与高倍率电化学储能器件具有重要的理论指导价值。电化学表界面层呈现出稀薄、无序和敏感等特征,直接观测并获取准确信息充满了挑战。在众多表征技术中,核磁共振技术表现出非侵入性和可定量等特点,是物质鉴别以及微观结构与动力学研究的重要手段。利用原位电化学核磁共振技术还能够观测电化学表界面生成的亚稳态中间相或发生的动态结构演变,为电化学储能体系表界面研究提供了独特而关键的见解。本文综述了电化学储能界面的典型核磁共振研究方法,着重介绍了一维与二维核磁共振技术、同位素示踪技术、动态核极化技术和交叉极化技术以及原位电化学核磁共振技术等方法的基本原理与应用策略。通过上述方法在电极与电解质、复合固态电解质等界面的组成结构、离子输运与界面电荷存储机理等电化学储能界面的应用实例,展示了核磁共振技术在电化学储能界面研究中的应用潜力和重要研究成果。 展开更多
关键词 界面电化学 电化学原位核磁共振 离子输运 电化学储能
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基于磁性测试揭示CoO储锂机理
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作者 徐熙祥 赵越 +1 位作者 阮明岳 李强 《储能科学与技术》 CSCD 北大核心 2024年第1期12-23,共12页
当今社会对储能技术需求日益迫切,电化学储能作为储能系统中的“桥梁”极具发展潜力,然而面临电化学储能中微量杂质相检测以及复杂界面储能探测的挑战,传统表征手段已经显示出局限性。储能材料的晶体结构、元素价态、电子能带以及电化... 当今社会对储能技术需求日益迫切,电化学储能作为储能系统中的“桥梁”极具发展潜力,然而面临电化学储能中微量杂质相检测以及复杂界面储能探测的挑战,传统表征手段已经显示出局限性。储能材料的晶体结构、元素价态、电子能带以及电化学特性与其磁学性质密切耦合,因此本文基于磁性测试,通过高低温等温磁化曲线(magnetic hysteresis,M-H)测试、零场冷/场冷(zero-field-cooled/field-cooled,ZFC/FC)变温磁化曲线测试,相较于传统表征手段X射线衍射(X-ray diffraction,XRD)、X射线光电子能谱(X-ray photoelectron spectroscopy,XPS)及高分辨透射电镜(high resolution transmission electron microscope,HRTEM),能够定量、高效、精准地检测出CoO中存在有效降低极化、提升首圈库仑效率(74.3%~83.77%)、提高大电流循环性能(2 A/g 50圈容量保持率116.59%)的微量金属Co杂质相(CoO/Co@20min 0.66%,CoO/Co@40min 2.27%)。同时本文利用原位实时磁学循环伏安法CV测试及恒流充放电测试,直观揭示出CoO在低电压区间里复杂、难以探测的空间电荷与固体电解质界面(solid electrolyte interphase,SEI)膜两种不同类型的界面储能机制,成功解释了CoO远超理论容量的额外容量来源。储能材料的合成制备离不开高度精准的杂质相检测,储能领域的下一步研究发展取决于能否对界面储能深入理解。本工作为杂质相检测及界面储能机理探测提供了一种无伤且高分辨的磁学全新视角,为推动储能领域的创新,解决当今社会面临的能源挑战贡献力量。 展开更多
关键词 磁学测试 杂质相监测 界面储能 原位实时磁学测试 磁电化学
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聚苯胺纳米纤维的共溶剂界面聚合及储能性能研究
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作者 梁浜雷 刘尧 +2 位作者 冯媛 谢凯 司建鑫 《化学研究与应用》 CAS CSCD 北大核心 2022年第3期533-540,共8页
本文采用以盐酸溶液为水相、四氯化碳为有机相的界面聚合法,通过向水相中分别引入具有非对称结构的甲醇和乙醇,以及具有对称结构的异丙醇和丙三醇作为共溶剂,成功制备出聚苯胺纳米纤维。采用场发射扫描电镜、紫外可见光谱和傅里叶红外... 本文采用以盐酸溶液为水相、四氯化碳为有机相的界面聚合法,通过向水相中分别引入具有非对称结构的甲醇和乙醇,以及具有对称结构的异丙醇和丙三醇作为共溶剂,成功制备出聚苯胺纳米纤维。采用场发射扫描电镜、紫外可见光谱和傅里叶红外光谱对其形貌和结构进行了表征分析,并通过循环伏安测试、恒流充放电测试和交流阻抗测试着重研究了不同共溶剂在酸性电解液下对聚苯胺纳米纤维储能性能的影响。研究表明:共溶剂的引入能够提高聚苯胺的质子化程度,有利于改善电化学性能。其中,以具有对称结构的异丙醇为共溶剂所制备的聚苯胺纳米纤维具有最低的电化学阻抗,在5 mV·s^(-1)的扫描速率下的比电容值达928.6 F·g^(-1),500次循环后比电容保留率为62.2%,展现出最高的储能性能。 展开更多
关键词 聚苯胺 纳米纤维 共溶剂 界面聚合 储能性能
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