1. Magnifying power and the simple microscope
- Magnifying power : β is the angle subtended at the eye by the final image; α is the angle subtended by the object without the instrument (for a microscope, the object held at the near point, D = 25 cm). Small angles: angle = height/distance.
- Simple microscope (a convex lens held close to the eye, object inside F): virtual, erect, enlarged image.
- Image at D (derivation): v = −D in gives . With the eye at the lens, β = h/|u| and α = h/D, so (equal to the linear magnification v/u).
- Image at infinity (derivation): object at F, rays leave parallel; β = h/f, α = h/D, so (relaxed eye; one less than at D).
- A shorter focal length magnifies more, but very short lenses are tiny, need the object almost touching them and suffer aberrations: in practice M up to about 10.
- image at D: 1 + D/f
- image at infinity: D/f
Formulas
- Simple microscope, image at D
- Simple microscope, image at infinity
Key terms
- Near point (D)
The least distance of distinct vision, about 25 cm for a normal eye: the closest an object can be seen sharply.
- Magnifying power
The ratio of the angle subtended at the eye by the final image to the angle subtended by the object viewed without the instrument.
2. The compound microscope
- Construction: objective of very short focal length f_o and small aperture; eyepiece of short focal length f_e. Object just beyond F_o; the objective forms a real, inverted, enlarged image A′B′ just inside F_e; the eyepiece forms the final virtual image A″B″ (inverted relative to the object, greatly enlarged).
- Final image at D (derivation): β = h′/|u_e| (A″B″ subtends the same angle as A′B′ at the eye), α = h/D, so with and : . Lens separation .
- Approximation: (object near F_o, A′B′ a distance L ≈ tube length from the objective).
- Final image at infinity (expression only, derivation not required): A′B′ at F_e; ; separation .
- High M needs short f_o and short f_e; an object at 2F_o would give m_o = 1.
Formulas
- Compound microscope, image at D
- Compound microscope, image at infinity
Key terms
- Objective
The lens nearer the object; in a microscope it has a very short focal length and forms a real, enlarged image.
- Eyepiece
The lens next to the eye; it acts as a simple microscope on the image formed by the objective.
3. The refracting astronomical telescope
- Construction: objective of long focal length f_o and large aperture (collects light, forms a real image of the distant object at F_o); eyepiece of short focal length f_e. α is the angle the object subtends where it is.
- Normal adjustment (derivation): the image I (height h) lies at F_o and at F_e. α = h/f_o, β = h/f_e, so ; length ; final image at infinity, inverted.
- Final image at D (derivation): I lies |u_e| from the eyepiece with ; β = h/|u_e|, α = h/f_o, so ; length (slightly shorter).
- The objective’s diameter does not change M; the light collected grows with its area (brighter images, finer detail). Terrestrial telescopes add an erecting system.
Formulas
- Telescope, normal adjustment
- Telescope, image at D
Key terms
- Normal adjustment
The setting of a telescope in which the final image is at infinity, the image formed by the objective lying at the focus of the eyepiece.
4. Reflecting telescopes
- Cassegrain type: a large concave paraboloidal primary mirror reflects the light towards its focus; a small convex secondary mirror inside that focus reflects it back through a hole in the primary to a focus behind it, viewed with an eyepiece (or recorded by a camera). Image at infinity: , F being the focal length of the mirror system (the convex secondary makes F several times the primary’s focal length while the tube stays short).
- Advantages over refractors: no chromatic aberration (reflection does not depend on n); no spherical aberration with a paraboloid; a mirror is supported over its whole back, so very large apertures are possible (a lens sags); only one surface to figure and no light absorbed in glass, so cheaper and brighter; greater light-gathering and resolving power; short tube.
- Drawbacks: the secondary blocks a little light (the image stays complete, slightly dimmer); mirrors need re-coating and careful alignment.
Formulas
- Reflecting telescope, image at infinity
Key terms
- Chromatic aberration
Coloured fringes in an image because a lens focuses different colours at different distances, its refractive index depending on wavelength.
- Spherical aberration
Blurring because rays far from the axis are focused at a different point from paraxial rays.
5. Resolving power; uses, advantages and drawbacks
- Resolving power of a microscope (formula only): two points closer than cannot be seen as separate; resolving power . β is the half-angle of the cone of light from the object accepted by the objective; n sin β is the numerical aperture.
- Factors: wavelength (shorter is better), refractive index of the medium between object and objective, and β. To increase it: blue, violet or ultraviolet light (or electrons in an electron microscope); oil immersion (n ≈ 1.5); a wide-aperture objective close to the object. A stronger eyepiece gives only empty magnification.
- Uses: simple microscope — watch and jewellery repair, reading fine print, field biology; compound microscope — cells, bacteria, blood tests, metallurgy, forensic work; telescopes — astronomy, navigation, surveying.
- Advantages and drawbacks: simple microscope cheap and erect but M ≤ about 10; compound microscope high M but inverted image, small field, needs strong light; refractors sealed and simple but chromatic aberration and size limits; reflectors large and colour-free but a central obstruction and upkeep.
- green light, 550 nm
- violet light, 400 nm
Formulas
- Resolving power of a microscope
Key terms
- Resolving power
The reciprocal of the smallest separation between two points that an instrument can show as separate.
- Numerical aperture
The product n sin β for a microscope objective, where β is the half-angle of the accepted cone of light and n the index of the medium in front of the objective.
Exam tips
- Always say what α and β are; D = 25 cm; magnifying powers are quoted as magnitudes.
- Microscopes: simple 1 + D/f (D) and D/f (infinity); compound (v_o/|u_o|)(1 + D/f_e) at D, (v_o/|u_o|)(D/f_e) at infinity (expression only).
- Telescopes: f_o/f_e with L = f_o + f_e; (f_o/f_e)(1 + f_e/D) at D.
- Reflectors: concave primary, convex secondary, hole; no chromatic aberration. Resolving power 2n sin β/λ, not changed by the eyepiece.