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作 者:Ying-Xin Ma Song Chen Hong-Tao Lin Shu-Ping Zhuo Xue-Dong Wang 马英鑫;陈松;蔺红桃;禚淑萍;王雪东(School of Chemistry and Chemical Engineering,Shandong University of Technology,Zibo 255000,China;Institute of Functional Nano&Soft Materials(FUNSOM),Jiangsu Key Laboratory for Carbon-Based Functional Materials&Devices,Soochow University,Suzhou 215123,China)
机构地区:[1]School of Chemistry and Chemical Engineering,Shandong University of Technology,Zibo 255000,China [2]Institute of Functional Nano&Soft Materials(FUNSOM),Jiangsu Key Laboratory for Carbon-Based Functional Materials&Devices,Soochow University,Suzhou 215123,China
出 处:《Science Bulletin》2022年第16期1632-1635,M0003,共5页科学通报(英文版)
基 金:supported by the National Natural Science Foundation of China(21703148 and 21971185);the Natural Science Foundation of Shandong Province(ZR2020MB054);Jiangsu Key Laboratory for Carbon-Based Functional Materials&Devices,Soochow University(KJS2156);the Collaborative Innovation Center of Suzhou Nano Science and Technology(CIC-Nano).
摘 要:One dimensional(1D)organic axial micro/nanocrystals serving as the building block towards integrated nanostructures have been demonstrated in various nanosystems[1-3].As an emerging solidstate platform,these micro/nanostructures are increasingly being regarded as potential candidates for constructing optoelectronic circuits.Despite remarkable achievements,pioneering works simultaneously revealed the shortage of non-guidance for molecular nucleation in these 1D axial micro/nanostructures[4-6],posing a great challenge for the practical applications.From this perspective,there is urgent to develop special 1D axial micro/nanostructures to promote the generation of highly ordered integrated structures.一维有机轴向微/纳米晶体作为构建复杂纳米结构的基石已在多种纳米系统中得到证实.尽管取得了显著的成就,但先前的工作同时揭示了这些一维轴向微/纳米结构中分子成核的有序性不足,这给实际应用带来了很大的挑战.本文提出了在一维有机轴向微米结构中引入基于分子重排的孪生变形现象,其弯曲(~50°)形成的相对活性表面为晶体的进一步外延生长提供了潜在的成核位点.此工作将促进高度有序的集成微/纳米结构的基础研究和实际应用方面的发展.
关 键 词:微/纳米结构 分子重排 活性表面 孪生变形 外延生长 微/纳米晶体 高度有序 微米结构
分 类 号:TB383.1[一般工业技术—材料科学与工程]
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