中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
In Situ Scanning Tunneling Microscopy Investigation of Subphthalocyanine and Subnaphthalocyanine Adlayers on a Au(111) Electrode

文献类型:期刊论文

作者Gu, Jing-Ying1,2; Cui, Bo1,2; Chen, Ting1; Yan, Hui-Juan1; Wang, Dong1; Wan, Li-Jun1
刊名LANGMUIR
出版日期2013-01-08
卷号29期号:1页码:264-270
ISSN号0743-7463
DOI10.1021/la3042742
英文摘要The adsorption behaviors of subphthalocyanine (SubPc) and subnaphthalocyanine (SubNc) on the Au(111) surface were investigated by electrochemical scanning tunneling microscopy (ECSTM). Two types of ordered adlayer structures of SubPc were observed at 550 mV versus the reversible hydrogen electrode (RHE). All of the Sub Pc molecules take the Cl-down adsorption configuration on Au(111) in both structures. The ordered adlayers exist in the potential range between 350 and 650 mV. The SubNc molecules adsorb on Au(111) in a less-ordered pattern than the Sub Pc molecules. The present work provides direct evidence for understanding the potential-controlled adsorption behaviors of SubPc and SubNc on the Au(111) surface.
语种英语
WOS记录号WOS:000313305900031
出版者AMER CHEMICAL SOC
源URL[http://ir.iccas.ac.cn/handle/121111/42021]  
专题中国科学院化学研究所
通讯作者Wang, Dong
作者单位1.Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Nanostruct & Nanotechnol, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Gu, Jing-Ying,Cui, Bo,Chen, Ting,et al. In Situ Scanning Tunneling Microscopy Investigation of Subphthalocyanine and Subnaphthalocyanine Adlayers on a Au(111) Electrode[J]. LANGMUIR,2013,29(1):264-270.
APA Gu, Jing-Ying,Cui, Bo,Chen, Ting,Yan, Hui-Juan,Wang, Dong,&Wan, Li-Jun.(2013).In Situ Scanning Tunneling Microscopy Investigation of Subphthalocyanine and Subnaphthalocyanine Adlayers on a Au(111) Electrode.LANGMUIR,29(1),264-270.
MLA Gu, Jing-Ying,et al."In Situ Scanning Tunneling Microscopy Investigation of Subphthalocyanine and Subnaphthalocyanine Adlayers on a Au(111) Electrode".LANGMUIR 29.1(2013):264-270.

入库方式: OAI收割

来源:化学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。