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Frequency response                         229

            indices n 1 and n 2 respectively. At each interface there will be some light re-
            flected and some transmitted. The reflection coefficient, from electromagnetic
            theory, at an interface like (a) in Fig. 10.5 is
                                          n 2 – n 1
                                      r a =     .                    (10.17)
                                          n 2 + n 1
            By symmetry, the reflection coefficient at (b) will be the reverse of this,

                                        n 1 – n 2
                                    r b =     =–r a .                (10.18)
                                        n 1 + n 2
            Now suppose that all the layers are a quarter wavelength thick—their actual
            thickness will be n 1 (λ/4) and n 2 (λ/4) respectively. Then the wave reflected
            back from (b) will be π radians out of phase with the wave reflected back from
            (a) because of its extra path length, and another π radians because of the phase
            difference in eqn (10.18). So the two reflected waves are 2π radians different;
            that is, they add up in phase. A large number of these layers, often as many as
            17, makes an excellent mirror. In fact, provided good dielectrics (ones with low  The two reflections have a phase
            losses, that is), are used, an overall reflection coefficient of 99.5% is possible,  difference of π radians.
            whereas the best metallic mirror is about 97–98% reflecting. This great re-
            duction in losses with dielectric mirrors has made their use with low-gain gas
                                                                                        λ/4
            lasers almost universal. I shall return to this topic when discussing lasers.
               Another application of this principle occurs when the layer thickness is one
            half wavelength. Successive reflections then cancel, and we have a reflec-
            tionless or ‘bloomed’ coating, much used for the lenses of microscopes and
            binoculars. A simpler form of ‘blooming’ uses only one intermediate layer on
            the glass surface (Fig. 10.6) chosen so that
                                                                               Air
                                            √
                                       n 1 =  n 2 .                  (10.19)

            The layer of the material of refractive index n 1 is this time one quarter          Glass
                                                                                                refractive
            wavelength, as can be seen by applying eqn (10.17).                                 index n
                                                                                                     2
            10.6 Frequency response                                            Blooming
                                                                               layer, refractive
            Most materials are polarizable in several different ways. As each type has a dif-  index
            ferent frequency of response, the dielectric constant will vary with frequency
                                                                             Fig. 10.6
            in a complicated manner; for example at the highest frequencies (light waves)
                                                                             Simple coating for a ‘bloomed’ lens.
            only the electronic polarization will ‘keep up’ with the applied field. Thus, we
            may measure the electronic contribution to the dielectric constant by measur-
            ing the refractive index at optical frequencies. An important dielectric, water
            has a dielectric constant of about 80 at radio frequencies, but its refractive in-
            dex is 1.3, not (80) 1/2 . Hence we may conclude that the electronic contribution
            is about 1.7, and the rest is probably due to the orientational polarizability of
            the H 2 O molecule.
               The general behaviour is shown in Fig. 10.7. At every frequency where

            varies rapidly, there tends to be a peak of the   curve. In some cases this is
            analogous to the maximum losses that occur at resonance in a tuned circuit:
            the molecules have a natural resonant frequency because of their binding in
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