检索结果-南通市图书馆

Building 2D quasicrystals from 5-fold symmetric corannulene molecules

Nano Research 2018年第4期11卷 2129-2138页

作者： nataliya kalashnyk Julian Ledieu Emilie Gaudry Can Cui An-Pang Tsai Vincent Fournee Institut Jean Lamour UMR 7198 CNRS - Universite de Lorraine Campus ARTEM - 2 allde Andre Guinier F-54000 NANCY France Department of Physics Zhejiang Sci-Tech University Hangzhou 310018 China Institute of Multidisciplinary Research for Advanced Materials (IMRAM) Tohoku University 2-1-1 Katahira Aoba-ku Sendai 980-8577 Japan

The formation of long-range ordered aperiodic molecular films on quasicrystalline substrates is a new challenge that provides an opportunity for further surface functionalization. This aim can be realized through the smart selection of molecular building blocks, based on symmetry-matching between the underlying quasicrystal and individual molecules. It was previously found that the geometric registry between the C60 molecules and the 5- and 10-fold surfaces was key to the growth of quasiperiodic organic layers. However, an attempt to form a quasiperiodic C60 network on i-Ag-In-Yb substrates was unsuccessful, resulting in disordered molecular films. Here we report the growth of 5-fold symmetric corannulene C20H10 molecules on the 5-fold surfaces of i-Ag-In-Yb quasicrystals. Low-energy electron diffraction （LEED） and scanning tunneling microscopy （STM） revealed long-range quasiperiodic order and 5-fold rotational symmetry in self-assembled corannulene films. Recurrent decagonal molecular rings were seen, resulting from the decoration of specific adsorption sites with local pentagonal symmetry by corannulenes, adsorbed with their bowl-openings pointing away from the surface. They were identified as （Ag, In）-containing rhombic triacontahedral （RTH） duster centers and pentagonal Yb motifs, which cannot be occupied simultaneously due to steric hindrance. It is proposed that symmetry-matching between the molecule and specific substrate sites drives this organization. Alteration of the molecular rim by the introduction of CH substituents appeared to increase molecule mobility on the potential energy surface and facilitate trapping at these specific sites. This finding suggests that rational selection of molecular moiety enables the templated self-assembly of molecules leading to an ordered aperiodic corannulene layer.

关键词： quasicrystal,surface science 5-fold symmetry molecular self-assembly,corannulene

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Unraveling giant Cu（110） surface restructuring induced by a non-planar phthalocyanine

引用

Nano Research 2018年第5期11卷 2605-2611页

作者： nataliya kalashnyk Luke A. Rochford Dongzhe Li Alexander Smogunov Yannick J. Dappe Tim S. Jones Laurent Guillemot Institut des Sciences Moleculaires d'Orsay CNRS Universite Paris-Sud 11 Orsay 91405 France School of Chemistry The University of Birmingham Birmingham B15 2TT UK Department of Physics University ofKonstanz Konstanz 78457 Germany SPEC CEA CNRS Universite Paris-Saclay CEA Saclay Gif-sur-Yvette Cedex 91191 France

The surface stability of coinage metals is paramount when they are used as electrode materials for functional electronic devices incorporating organic semiconductors. In this work, it is shown that the adsorption of non-planar vanadyl phthalocyanine molecules on Cu（110） drastically restructured the metal surface at room temperature, which was further enhanced upon moderate annealing. Scanning tunneling microscopy imaging demonstrated that the surface was restructured at step edges into sawtooth features that gradually replaced the （110） terraces. The edges of the modified steps were preferentially composed of chiral （1×6） kink sites decorated with vanadyl phthalocyanine molecules adsorbed in a tilted configuration with the oxygen atom pointing downwards. These results can have a strong impact on the optimization of the performance of organic devices integrated with phthalocyanine molecules.

关键词： surface restructuring step-etching chiral kink phthalocyanine

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

欢迎您,

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案：

请选择收藏分类：

通借通还

欢迎您,

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：