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Scanning near field optical microscopy SNOM structuring

More recently, the method of scanning near-field optical microscopy (SNOM) has been applied to LB films of phospholipids and has revealed submicron-domain structures [55-59]. The method involves scanning a fiber-optic tip over a surface in much the same way an AFM tip is scanned over a surface. In principle, other optical experiments could be combined with the SNOM, snch as resonance energy transfer, time-resolved flnorescence, and surface plasmon resonance. It is likely that spectroscopic investigation of snbmicron domains in LB films nsing these principles will be pnrsned extensively. [Pg.67]

Fig. 34. dPS volume fraction (J)dPS vs depth z for a 50/50 dPS/PBrxS mixture after annealing for different times at T=180 °C as revealed by TOF-FRES a tA=10 min, b tA=160 min, c tA= 6175 min). In the bottom part, a sketch of the domain structure is shown as revealed from the ion beam and scanning near field optical microscopy (SNOM) results (shaded areas dPS-rich domains white areas dPS-poor domains). From Straub et al. [153]... [Pg.78]


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Field microscopy

Microscopy SNOM)

Microscopy near-field

Near-field

Near-field scanning optical microscopy

Optical fields

Optical microscopy

Optical near-field

Optical structuring

SNOM

SNOM (scanning near-field optical

SNOM Structuring

Scanning near field optical

Scanning near-field optical microscopy SNOM)

Scanning optics

Scanning optics microscopy

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