Reversible photo-switching of single azobenzene molecules in controlled nanoscale environments

被引:265
作者
Kumar, Ajeet S. [3 ,4 ]
Ye, Tao [3 ,4 ]
Takami, Tomohide [5 ]
Yu, Byung-Chan [1 ,2 ]
Flatt, Austen K. [1 ,2 ]
Tour, James M. [1 ,2 ]
Weiss, Paul S. [3 ,4 ]
机构
[1] Rice Univ, Dept Chem, Houston, TX 77005 USA
[2] Rice Univ, Smalley Inst Nanoscale Sci & Technol, Houston, TX 77005 USA
[3] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[4] Penn State Univ, Dept Phys, University Pk, PA 16802 USA
[5] Visionarts Res Inc, Tokyo 1070062, Japan
基金
美国国家科学基金会;
关键词
D O I
10.1021/nl080323+
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We drive reversible photoinduced switching of single azobenzene-functionalized molecules isolated in tailored alkanethiolate monolayer matrices on Au{111}. We designed molecular tethers to suppress excited-state quenching from the metal substrate and formed rigid assemblies of single tethered azobenezene molecules in the domains of monolayer to limit steric constraints and tip-induced and stochastic switching effects. Single molecules were reversibly photoisomerized between trans and cis conformations by cycling exposure to visible and UV light. Trans and cis conformations were imaged as high (2.1 +/- 0.3 angstrom) and low (0.7 +/- 0.2 angstrom) protrusions in STM images and were assigned to the on and off states of the molecule, respectively.
引用
收藏
页码:1644 / 1648
页数:5
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