Light Switching of Molecules on Surfaces

被引:253
作者
Browne, Wesley R. [1 ]
Feringa, Ben L.
机构
[1] Univ Groningen, Fac Math & Nat Sci, Stratingh Inst Chem, NL-9747 AG Groningen, Netherlands
关键词
self-assembled monolayer; polymer immobilization; bilayers; photochemistry; photoswitching; SELF-ASSEMBLED MONOLAYERS; ELECTRON-TRANSFER; GOLD NANOPARTICLES; SINGLE-CRYSTAL; DIARYLETHENES; PHOTOISOMERIZATION; CONDUCTANCE; AZOBENZENE; PHOTOCHEMISTRY; AU(111);
D O I
10.1146/annurev.physchem.040808.090423
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
Smart surfaces, surfaces that respond to an external stimulus in a defined manner, hold considerable potential as components in molecular-based devices, not least as discrete switching elements. Many stimuli can be used to switch surfaces between different states, including redox, light, pH, and ion triggers. The present review focuses on Molecular switching through die electronic excitation of molecules on surfaces with light. In developing light-responsive surfaces, investigators face several challenges, not only in achieving high photostationary states and fully reversible switching, but also in dealing with fatigue resistance and the effect of immobilization itself on molecular properties. The immobilization of light-responsive molecules requires the design and synthesis of functional molecular components both to achieve light switching and to anchor the molecular entity onto a surface. This review discusses several demonstrative examples of photoswitchable molecular systems in which the photochemistry has been explored in the immobilized State under ambient conditions and especially on electroactive surfaces, including self-assembled monolayers, bilayers, and polymer films.
引用
收藏
页码:407 / 428
页数:22
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