Two-Dimensional Nonlinear Optical Switching Materials: Molecular Engineering toward High Nonlinear Optical Contrasts

被引:25
|
作者
Haensel, Marc [1 ]
Barta, Christoph [2 ]
Rietze, Clemens [3 ]
Utecht, Manuel [3 ]
Rueck-Braun, Karola [2 ]
Saalfrank, Peter [3 ]
Tegeder, Petra [1 ]
机构
[1] Heidelberg Univ, Phys Chem Inst, Neuenheimer Feld 253, D-69120 Heidelberg, Germany
[2] Tech Univ Berlin, Inst Chem, Organ Chem, Str 17 Juni 135, D-10623 Berlin, Germany
[3] Univ Potsdam, Inst Chem, Theoret Chem, Karl Liebknecht Str 24-25, D-14476 Potsdam, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2018年 / 122卷 / 44期
关键词
2ND HARMONIC-GENERATION; 2ND-HARMONIC GENERATION; THIN-FILMS; AZOBENZENE; SURFACE; DESIGN; PHOTOISOMERIZATION; ISOMERIZATION; MONOLAYERS; BEHAVIOR;
D O I
10.1021/acs.jpcc.8b08212
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Combining photochromism and nonlinear optical (NLO) properties of molecular switches-functionalized self-assembled monolayers (SAMs) represents a promising concept toward novel photonic and optoelectronic devices. Using second harmonic generation, density functional theory, and correlated wave function methods, we studied the switching abilities as well as the NLO contrasts between different molecular states of various fulgimide-containing SAMs on Si(111). Controlled variations of the linker systems as well as of the fulgimides enabled us to demonstrate very efficient reversible photoinduced ring-opening/closure reactions between the open and closed forms of the fulgimides. Thus, effective cross sections on the order of 10(-18) cm(-2) are observed. Moreover, the reversible switching is accompanied by pronounced NLO contrasts up to 32%. Further molecular engineering of the photochromic switches and the linker systems may even increase the NLO contrast upon switching.
引用
收藏
页码:25555 / 25564
页数:10
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