journal article·2012-01-12

Self-Assembly and Photomechanical Switching of an Azobenzene Derivative on GaAs(110): Scanning Tunneling Microscopy Study

Ivan V. Pechenezhskiy, Jongweon Cho, Giang D. Nguyen, Luis Berbil-Bautista, Brandon L. Giles, Daniel A. Poulsen, Jean M. J. Fréchet, Michael F. Crommie

Publisher page

Abstract

Self-assembly and light-induced mechanical switching of azobenzene derivatives deposited on GaAs(110) were explored at the single molecule level using scanning tunneling microscopy (STM). 3,3′,5,5′-Tetra- tert -butylazobenzene (TTB-AB) molecules in the trans isomer configuration were found to form well-ordered islands on GaAs(110). After exposure to ultraviolet (UV) light, the TTB-AB molecules exhibited conformational changes attributed to trans to cis photoisomerization. Photoisomerization of TTB-AB/GaAs is observed to occur preferentially in one-dimensional (1D) stripes. This 1D cascade behavior differs significantly from optically induced switching behavior observed when TTB-AB molecules are placed on a gold surface.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Molecular Junctions and Nanostructures · Surface Chemistry and Catalysis · Force Microscopy Techniques and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Physics, University of California at Berkeley, Berkeley, California 94720, United States

Center of Integrated Nanomechanical Systems, University of California at Berkeley, Berkeley, California 94720, United States

Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States

Department of Chemistry, University of California at Berkeley, Berkeley, California 94720, United States

References (27)

Show source-provided references
1. Balzani V. · 200810.1002/9783527621682 ↗
2. Zhang C. · Phys. Rev. Lett. · 2004 · 92 · 15830110.1103/PhysRevLett.92.158301 ↗
3. Rau, H.InPhotochromism: Molecules and Systems;Dürr, H.; Bouas-Laurent, H., Eds.; Studies in Organic Chemistry;Elsevier:Amsterdam, 1990; pp165–192.
4. Banghart M. R. · Biochemistry · 2006 · 45 · 1512910.1021/bi0618058 ↗
5. Chambers J. J. · J. Neurophysiol. · 2006 · 96 · 279210.1152/jn.00318.2006 ↗
6. Óvári L. · J. Phys. Chem. C · 2007 · 111 · 1537010.1021/jp075274o ↗
7. Hagen S. · Chem. Phys. Lett. · 2007 · 444 · 8510.1016/j.cplett.2007.07.005 ↗
8. Hagen S. · J. Chem. Phys. · 2008 · 129 · 16410210.1063/1.2997343 ↗
9. Feng C. L. · Surf. Sci. · 2002 · 513 · 11110.1016/S0039-6028(02)01695-3 ↗
10. Yasuda S. · J. Am. Chem. Soc. · 2003 · 125 · 1643010.1021/ja038233o ↗
11. Comstock M. J. · Phys. Rev. Lett. · 2007 · 99 · 03830110.1103/PhysRevLett.99.038301 ↗
12. Kumar A. S. · Nano Lett. · 2008 · 8 · 164410.1021/nl080323+ ↗
13. Cho J. · J. Chem. Phys. · 2010 · 133 · 23470710.1063/1.3519557 ↗
14. Bazarnik M. · Chem. Commun. · 2011 · 47 · 776410.1039/c1cc11578b ↗
15. Morgenstern K. · Prog. Surf. Sci. · 2011 · 86 · 11510.1016/j.progsurf.2011.05.002 ↗
16. Feenstra R. M. · Phys. Rev. Lett. · 1987 · 58 · 119210.1103/PhysRevLett.58.1192 ↗
17. Johnson M. B. · Appl. Phys. Lett. · 1993 · 63 · 292310.1063/1.110274 ↗
18. Johnson M. B. · Appl. Phys. Lett. · 1994 · 64 · 145410.1063/1.111999 ↗
19. Zheng J. F. · Phys. Rev. Lett. · 1994 · 72 · 149010.1103/PhysRevLett.72.1490 ↗
20. Chao K.-J. · Phys. Rev. B · 1996 · 53 · 693510.1103/PhysRevB.53.6935 ↗
21. Pozhidaeva N. · Bioconjugate Chem. · 2004 · 15 · 129710.1021/bc049855h ↗
22. Alemani M. · J. Am. Chem. Soc. · 2006 · 128 · 1444610.1021/ja065449s ↗
23. Comstock M. J. · Appl. Phys. Lett. · 2008 · 92 · 12310710.1063/1.2901877 ↗
24. Alemani M. · J. Phys. Chem. C · 2008 · 112 · 1050910.1021/jp711134p ↗
25. Levy N. · Nano Lett. · 2009 · 9 · 93510.1021/nl802632g ↗
26. Wolf M. · Surf. Sci. · 2009 · 603 · 150610.1016/j.susc.2008.11.049 ↗
27. Comstock M. J. · Phys. Rev. Lett. · 2010 · 104 · 17830110.1103/PhysRevLett.104.178301 ↗