Reversible all-optical control of optical microcavities by a self-assembled azobenzene monolayer

Azobenzene is capable of reversibly switching its conformation upon the UV/Visible optical exposure due to its reversible trans/cis photoisomerization. By merging this organic material with conventional photonic devices, new architectures can be developed. In our study, we developed hybrid organic/inorganic whispering gallery mode microcavities consisting of a self-assembled 4-(4-diethylaminophenylazo)pyridine (Aazo) monolayer anchored on an integrated SiO2 optical microtoroid. As the Aazo monolayer changed conformations, the resonant wavelength was tuned. The surface density of Aazo was modified by introducing CH3 spacer molecules providing control over the magnitude of the shift. Owing to the uniformity of Aazo monolayer, cavity quality factors reached above 1 million in the near-IR range. Two optical lasers were simultaneously coupled into the Aazo-coated devices with a single waveguide. The 1300 nm laser is used to excite and monitor a single resonant wavelength of the cavity, and the 410 nm laser triggers the thermodynamically stable trans-Aazo to photoswitch to the thermodynamically unfavored cis-Aazo. When the Aazo photoswitches, the cavity resonant wavelength at near-IR wavelength shifts due to a change of refractive index in the Aazo layer. To revert the molecule back to trans-Aazo, a CO2 laser is used to heat the device system. Even after storage in air, the switching behavior is unchanged. Theoretical analyses are conducted based on density functional theory of the Aazo isomers combined with finite element method simulations of the optical mode. The theoretical results agree with the experimental findings.