A combination of the unique hosting properties of cyclodextrins (CDs) and the peculiar UV-responsive trans-cis isomerization of the guest molecule azobenzene has endowed light-responsibility of the inclusion complex (IC). The IC of 4-aminoazobenzene (AAB) and hydroxypropyl-b-cyclodextrin (HPbCD), with its inherent viscosity from hydrogen bondings between CDs and p-p stacking between AABs, was electrospun into nanofibers from water without using any carrier polymer matrix. The integrity of electrospun ICs was proven by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), together with Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The homogeneous distribution of HPbCD-AAB-IC was confirmed by surface chemistry mapping using timeof-flight secondary ion mass spectrometry (ToF-SIMS). The UV response of ICs prior to, during and post electrospinning was investigated. UV irradiation prior to electrospinning caused precipitation of AAB from the aqueous IC solution. UV irradiation during electrospinning flight demonstrated the interruption of ICs and consequently broader diameter distributions were obtained. Post-spinning UV irradiation induced topography and adhesion force changes on the electrospun nanofiber surfaces, demonstrated by in situ atomic force microspectroscopy (AFM) quantitative nanomechanical mapping. The present study is the first case where the supramolecule with stimuli response was electrospun into nanofibers with retained activity.

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X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry were used to investigate the aging effects on the aminopropylsilane (APS) and quaternary ammonium surfactant-treated mineral fibers. APS-coated mineral fiber samples were treated with cationic surfactant and mineral oil and aged at 70 C temperature and 95% humidity. From quantitative XPS measurements, an increase in the atomic composition of oxygen, nitrogen, and silicon is observed after aging. An increase in the protonated amino groups in the N1s high-resolution spectra and C-N group in the C1s high-resolution spectra is also observed. These results indicate that the concentration of hydrocarbon groups decreases after aging due to the partial removal of the long hydrocarbon chains of the surfactant and mineral oil and/or hydrolysis and segregation of APS to the fiber surface. The principle component analysis was applied to the time-of-flight secondary ion mass spectrometry spectra, and an increase in the intensities of APS characteristic peaks were observed after aging. The observed increase in the signals of APS originates from underlying silanized fibers after the removal of the surfactant and mineral oil from the surface.