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The document discusses various types of astronomical detectors, focusing on electronic photon detectors, including solid-state detectors and their operational principles. It highlights the differences between metals, semiconductors, and insulators, detailing the behavior of electrons in these materials and their implications for photon detection. Additionally, it covers the structure and functioning of CCDs, their applications in astronomy, and the challenges faced in their manufacturing and performance.

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0% found this document useful (0 votes)
9 views45 pages

Class 3

The document discusses various types of astronomical detectors, focusing on electronic photon detectors, including solid-state detectors and their operational principles. It highlights the differences between metals, semiconductors, and insulators, detailing the behavior of electrons in these materials and their implications for photon detection. Additionally, it covers the structure and functioning of CCDs, their applications in astronomy, and the challenges faced in their manufacturing and performance.

Uploaded by

elbiblionauta.25
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

Astronomical Instrumentation and Observational Methods

Timo Anguita
Detectors and receivers
Electronic
Detectors Photon Detectors:
Solid State Detectors
general
● The most common of detectors: radio to X-ray
● They work by using the interaction of photons with bound electrons in atoms.
The atoms on the other hand are bound in a crystalline lattice.
● Innermost electrons and corresponding lowest energy states essentially not
influenced
● Outer electrons, characterized by overlappingwavefunctions, are strongly
modified.
general
● Interaction with adjacent atoms 🡪 overlapping wavefunctions 🡪 Pauli exclusion
principle 🡪 broad energy bands are formed
● As in the case of discrete energy levels in a free atom, intermediate energy
states are forbidden and empty.
● Highest occupied energy bands (responsible for chemical reactions) = valence
bands
● If an energy band is not fully occupied 🡪 energy supply 🡪 electrons can be
lifted to higher energies 🡪 movement or electric current 🡪 conduction bands
general
● Relative location between the
valence and conduction bands
determines the conductive
properties of a solid:
○ Metal: (no "distance" between
conduction and valence bands)
○ Semiconductor
○ Insulating
● These last two have a "gap"
between the bands
Schematic diagram for different solids:
E F is the Fermi energy.
general
● metals
○ Small number of external electrons that are easily released forming ions
○ They have positive ion structure immersed in a sea of free electrons 🡪 electrons reach the
conduction band with extremely low external stimulation
● insulators, semiconductors
○ V and C bands separated by an energy gap E g
■ Semiconductor: E g < 5eV
○ With a few exceptions, only semiconductors are of interest for photon detection.
■ Metals: reflect most of the radiation
■ Insulators: Photoelectric effect only increases the charges
general
● Probability of finding an electron at an
(allowed) energy level E:
○ The f(E) distribution of electrons follows a
Fermi-Dirac statistic

○ E F : Fermi energy, depends on the material


○ eg: f(E F )=0.5 🡪 E F is the energy at which the
probability that the corresponding energy level
is occupied is 0.5 Probability distribution of an
electron f(E) as a function of T,
compared to the energy band
diagram
general

● T>0: Probability of finding an electron in the conduction band of a


semiconductor or an insulator ≠ 0
● The probability decreases when the energy increases
○ Very low for insulators at low temperatures
● At a sufficient temperature, any crystalline solid will show significant
conductivity.
● Example: Conductivity of glass at 10 3 K ≈ Si 10 2 K
semiconductors
● Spectral response of intrinsic semiconductors is limited to photons that have
energy equal to or greater than the gap.
Cut-off energy (frequency): E cut-off =h ν cut-off ≥E g =h ν g (corresponds to a λ max )
● Above E cut-off : Very efficient process (RQE≤90%)
● Not suitable for λ ≥ 15 μ

Gaps and cut-off wavelengths for


different semiconductors
Semiconductors
● Doped Semiconductors
○ Conductivity can be modified by implanting small concentrations of atoms with different numbers
of valence electrons in the semiconductor lattice.
○ Example: Sb (5 valence e- ) in Si or Ge lattice

○ Only four e - used 🡪 extra electron has very low binding energy (<50 meV) and large orbit
semiconductors
○ The thermal energy of the network is sufficient to release these extra e- to
the conduction band 🡪 increase in conductivity
○ n-type doped semiconductor: One additional electron 🡪 Increased E F
relative to intrinsic semiconductor
○ Called "donor"
semiconductors
● p-type semiconductor: group III atom in group IV lattice
● Acquiring an additional surface electron from the valence band 🡪
creating a positively charged “hole” in the electron distribution in the
valence band 🡪 “unfilled” valence band 🡪 can carry a current that
can be ascribed to the movement of “holes” ” positive.
● Called "acceptor"
● Hole has a very low binding energy (<50meV)
● The Fermi level E F reduced relative to that of the intrinsic
semiconductor.
semiconductors
● n-type “extra electrons” have
extended orbits that overlap even
at very small values of impurity
concentration (up to 10 -8 ) 🡪
doped semiconductors have
additional energy bands
(“impurity bands”) that are
located between the valence and
conduction band
● Extrinsic photoelectric effect
semiconductors
● Low binding energy 🡪 energy gap between impurity and conduction
band always lower than E G
● Cooling is necessary (thermal excitation)
○ ν cut-off : much lower than intrinsic photoelectric effect
○ Especially in the case of IR detectors
● Additional reduction of ν cut-off
○ mechanical pressure
○ composition change
Hg 1-x Cd x Te:
x=0 🡪 metallic properties
x=0.2 🡪 E G =0
x=1 🡪 E G =1.6 eV

Ge:Ga with λ cut-off ~ 240 μμ


semiconductors
● Electrical conductivity of extrinsic material differs fundamentally
from intrinsic material
○ Intrinsic: Charge carriers are created by the absorption of a photon as
electron/hole pairs. Applied voltage 🡪 photon current ∝ photon rate
○ Extrinsic: Individual charge carriers are created, complementary charges
reside on ionized atoms bound to the crystal lattice; immobile, cannot carry
current
● High temperatures 🡪intrinsic mechanism dominates in both
types of materials
● Low temperatures 🡪 carrier contributed by the dominant impurity
is more numerous.
semiconductors
● "Dopants" do not interfere with the intrinsic absorption process; number
of intrinsic atoms >> number of extrinsic atoms
○ Intrinsic absorption is maintained over extrinsic absorption in regions where the
intrinsic effect is efficient.
○ Necessary to use of filters

Energy gaps E G and


wavelengths λ max for
photoconductors used in
astronomy
Basic properties of semiconductors
● Radiation absorption in semiconductors
N=h ν /w
where N: number of electron-hole pairs
w: energy to create torque
● Statistical fluctuations described by the Fano factor (~0.1 in
semiconductors)
● energy resolution

where
σ N : e-hole pairs
σ R : charge loss during transfer
σ A : power loss in the amplifier
Basic properties of semiconductors
● Limits of extrinsic photoconductors
○ Absorption: a(λ) ∝N i ; N i : neutral concentration of impurities
○ Upper limits for N i :
■ Solubility limit for impurity atoms in the crystal: 10 18 -10 21 cm -3
■ Long before the solubility limit: the electrical properties of the crystal
undergo unwanted changes in the form of conduction modes that
cannot be controlled
Typical N i : 10 15 -10 16 for Si, slightly lower Ge
● Problem: absorption coefficients in extrinsic photoconductors ~ 3
orders of magnitude lower than for intrinsic ones
🡪necessary to use a volume large enough to have adequate QE;
typically 1mm in the direction of the photon beam.
applications in astronomy
● Light Sensitive Resistors, Photoconduction:
○ absorption of a photon 🡪 e - lifted from valence band to
valence band to conduction band 🡪 increase in conductivity
○ Now: application of voltage 🡪 current ∝ photon rate
○ If E ph >E bond 🡪 photoelectron is emitted (photoionization,
photomultiplier)
○ Photovoltaic diodes produce lighting depending on the
voltage
Diode (PN)
● Semiconductor crystal where in a
narrow transition zone, the doping
changes from n-type to p-type
● Without voltage the Fermi level
must be constant across the
network
● Fermi level depends on doping 🡪
distorted conduction and valence
bands
● e - (holes) tend to occupy the
lowest allowed energy levels 🡪 e -
(hole) depletion zone forms at the
junction between p- and n-type
materials
Diode (PN)
● The diode has a higher resistance than its p-type and -n components
(with no applied voltage).
● Now external voltage 🡪 Fermi level deformation
● Depending on the polarity the voltage can:
○ Compensate for band distortions and restore conductivity
○ Cause a more resistant depletion zone
● Photons absorbed in the depletion zone 🡪 photoelectrons and holes
separated by a potential gradient across the depletion zone
● The two terminals of a diode connected by a resistor, absorbed
radiation results in current and voltage ∝ light flux
PIN diode
● PIN: positive-intrinsic-negative
● Closely related to PN diodes
● They contain a region of
intrinsic material between the
p-type and n-type layers.
● The extent of the depletion
zone is increased
● Larger photosensitive volume
and higher frequency
response
Schottky diode
● Junction between metal and n-type
semiconductor
● Distortion of the semiconductor bands by
differential doping or by charges trapped
between the surface layers
● Thermal excitation or quantum tunneling 🡪
electrons can cross the barrier formed by the
depletion zone 🡪 DC current can flow without
external voltage
● External voltage: depending on the polarity the
current is significantly reduced or increased
● Schottky diodes have non-linear voltage-current
relationships.
● important in radio
CCD's
● The most important detector in astronomy
● Semiconductor detector, two-dimensional array of small semiconductor
elements
● Pixel size: d ≥ 4 μm
● CCD size: ≤ 8k x 8k pixels
● Larger CCDs are available as CCD arrays (mosaics)
● Initially conceived in 1970 at Bell Laboratories
● In astronomy since the 1980s, for a long time only in the optical spectrum,
today also in X-ray and IR astronomy
● IR: Material InSb or Ge
● They combine good energy and spatial resolution
Structure of a CCD
● Thin monocrystalline rectangular
plate (<0.2mm) of
photoconductive material
● Si pn-type in most cases
● Covered surface of very thin
conductive electrodes (≤ 1μm)
separated from the substrate by
an insulating layer of ~ 0.1μm
layer
● Photosensitive part of the chip:
Lightly doped or practically
intrinsic (≤ 10 μm ) below the
insulating layer
Structure of a CCD
● The “pixel” is created by long, thin “channel
stops” (highly doped p-type material)
● Movement of electrons is prevented by
charge depletion and the resulting negative
charge.
● Reading channels perpendicular to the
electronic strips
● The pixels are defined by “channel stops”
and 3 electrodes (three-phase CCD)
● The channel stops end in the reading
register, which has its own set of electrodes.
● Three-phase device: individual electrodes
are alternately connected to three voltage
lines
Diagram of the arrangement of the
electrodes in a three-phase CCD
(6x6 pix)
Exposure of a CCD
● Creation of electron-hole pairs
● The electrodes are maintained with a positive voltage (little V)
● Electrons accumulate under the electrodes, the holes are attracted to
the substrate
● The exposed chips then show a 2-D distribution of charge that exactly
corresponds to the distribution of absorbed light.
Reading Procedure
● The 2-D charge distribution is read
by periodic changes in electrode
voltage.
● Each complete cycle of voltage
changes moves the entire charge
distribution for a pixel along the read
channels 🡪 the content is read
sequentially
● Line of pixels adjacent to the read
register is moved to the register; read
sequentially through an on-chip
pre-amplifier to the signal line.
Charge transfer in a three-phase
CCD
CCD's
CCDs: Problems
● Lattice defects: The most serious problem in manufacturing
○ trap electrons 🡪 incomplete charge transfer
○ Many charge transfers (each pixel ≤ 10), add up 🡪 even a small loss of charge
at each stage will have serious consequences on an image (particularly at low
exposure levels)
● Particularly critical: Surface or interface layers
● Solution: High-quality CCDs have a very thin (~0.2 μm) n-type zone
under the insulating layer.
○ The minimum of the electrostatic potential is slightly below the Si and insulating
layers.
○ Photoelectrons are accumulated in a potential minimum where the lattice is
more uniform.
○ Electrons can be safely transferred
lighting possibilities
● Absorption through
electrodes, unavoidable light
losses
● Backlight (from the substrate
side)
○ Si absorption coefficient
increases strongly with
decreasing wavelength 🡪
Back-illuminated CCDs have low
sensitivity to blue light

Photon absorption coefficient in


silicon
lighting possibilities
● Possible solution: “Thinning” the Si
plate to ~10 ∝μ → dramatic
change in blue light sensitivity
● UV: Even “thin” CCDs have a
strong decrease in UV RQE (very
high absorption coefficient on Si)
for UV, photons in the surface
layers are absorbed, where
photoelectrons tend to get trapped
in defects 🡪 especially in layers
with treated surfaces.
● Or: phosphor paints 🡪 UV photons Comparison of RQE
(measured) between a thick
are converted to optical photons. and “thin” back-illuminated
CCD
Typical Parameters for CCDs
● Larger chips: 8192 x 8192 pixels
● Typical pixel sizes: 10 - 30μm
● Cooling (liquid nitrogen): negligible
dark current
● Sensitivity limited by read noise
● Very low readout noise (≤ 10 e - ) 🡪
Well-suited to detect weak signals
● Only ~10 5 load capacity

Typical design of a nitrogen cryostat


for photoconductive detectors
Some examples
● FORS1 (ESO VLT)
○ TK2048EB4-1, backlit, AR
coated
○ 2048 x 2048 pixels
○ Pixel size: 24 x 24μm
○ Reading noise: 5 -6.2 e - rms
○ Example of cosmetic
defects:
■ Type: Dark blobs
■ Location (x,y): 268,
1652 Quantum efficiency of FORS1
■ Number of affected
pixels: 6 pixels in
diameter
Some examples
● FORS2
○ MIT/LL CCID-20,
back-illuminated, AR-coated
○ 2048 x 4096 pixels
○ Pixel size 15 x 15μm
○ Reading noise: 2.7 - 4.2 e -
rms

Quantum efficiency of FORS2


Some examples

FORS2 Flat
FORS1
Some examples
● WFI (MPG 2.2m)
● 8 EEV 44.82, backlit
● 2048 x 4096 pixels
● Pixel size: 15 x 15μm
● Reading noise: 2.4 - 5.6 e - rms
● +1 CCD for tracking

Quantum efficiency of the 8 WFI


CCDs
some CCD's
some CCD's
● HST
○ WFPC2
■ 4, front lit, thick, Yes,
800 x 800 pix. Reading
noise ~5e - rms
○ HRC
■ 2, backlit, “thinned out”
SiTe, 4096 x 2048, 15 x
15 μm pixel
○ STIS
■ 1, backlit, 1024 x 1024
pix
X-Ray CCDs
● Problem: X-rays are absorbed very quickly in Si
● Extremely difficult to prepare very thin layers
● Backlit devices thinner (~40μm ) than the depleted region of
front-lit devices ( 60−75μm )
● Used in the ACIS-I and -S detectors of Chandra (Advanced CCD
Imaging Spectrometer). 4 and 6 CCD arrays, 1024 x 1024 pixels
● Energy resolution: 60eV at 1 KeV, 150 eV at 8 keV
● Spatial resolution: ~0.8”
● Both much better than eg ROSAT PSPC
European Photon Imaging Camera
● XMM-Newton
● 2 MOS (Metal Oxide
Semiconductor) cameras
● Front-illuminated, one of three
electrodes “enlarged” to occupy
a larger fraction of pixel, etched
with holes 🡪 “open” fraction of
total pixel area of 40%
● Areas with holes have high
transmission of "soft" X-rays.
● 7 CCD array
epic pn
● New design, made in MPE,
Garching
● Back-illuminated CCDs, X-rays
absorbed in diodes (pn transition)
● Sensitive at full volume
● Very good absorption throughout
the spectral range
● Array of six 400x400 pixels (6x6cm
2
) 🡪the largest X-ray CCD ever
epic pn
IR CCDs
● Not possible with intrinsic semiconductors 🡪 extrinsic material is
necessary
● But: Conduction properties of the different layers of a CCD chip
are based on the thermal excitation of charge carriers 🡪 CCD
design cannot be applied directly on photoconductors with
extrinsic impurity bands
● In IR: hybrid CCDs; array of impurity bands are bonded to Si
CCD

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