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Silicon Photovoltaic Cells: 
An Introduction 
Gavin D. J. 
Harper 
g.harper@glyndwr.ac.uk 
@gavindjharper 
www.gavindjharper.com 
http://orcid.org/0000-0002-4691-6642 
Welsh Energy Sector Training (WEST) 
OpTIC Glyndwr 
Ffordd William Morgan, St Asaph, Wales 
October 2014
Structure of Silicon 
• Matter is composed of atoms. 
• Atoms in turn are made up of 
• Protons (which are positively charged) 
• Electrons, (which are negatively charged) 
• Neutrons (which are neither positively nor negatively charged). 
• If we took an atom of silicon, and examined how it was 
composed, we would see a dense central “core” which is known 
as the ‘nucleus’ which consists of Protons and Neutrons; 14 of 
each to be exact. 
• Around this core are electrons that orbit in a ‘cloud’. Some of 
these electrons orbit at different distances from the central 
nucleus. We call these distances ‘shells’
Structure of Silicon 
• If you think of a shell as an imaginary sphere surrounding the 
nucleus of an atom; these shells are arranged concentrically. 
Each shell only has room for so many electrons, therefore as 
each shell fills up, the next shell in line must be filled with 
electrons. 
• When a molecule has eight electrons in its outer shell (known as 
the valence shell), then it is stable; which is to say not very 
chemically reactive. The ‘Noble Gases’ which reside on the far 
right of the Periodic Table are very stable and as such have little 
tendency to participate in chemical reactions – all atoms strive 
to fill their outer shells and reach this unreactive state.
Structure of Silicon 
As we can tell from its number on the periodic table, “14” we can tell that silicon has 
14 electrons. 
A little knowledge as to the pattern in which electrons are arranged in tells us that 
these electrons are arranged in three ‘shells’. 
The first two ‘shells’ are completely full with electrons, however, the outermost shell 
only has half of the total number of electrons possible.
Structure of Silicon 
• Silicon is what is known as “tetravalent”, this is to say that there are 
four electrons available in the outer shell which can form ‘covalent’ 
bonds. A covalent bond is one where electrons are “shared” between 
pairs of atoms. 
• The natural tendency in chemicals is for them to work towards filling 
their outer shells with eight electrons by forming bonds with other 
chemicals. 
• Silicon is no exception, and fills its outer shell by bonding with other 
silicon atoms and “sharing” electrons. 
• Silicon forms a regular crystalline structure. This is to say that the 
forces between the atoms of silicon are such that they arrange 
themselves in the most compact pattern that the forces between 
atoms will allow.
Crystalline 
Silicon 
• This is what silicon 
looks like when 
represented in 
three dimensions. 
• For the purposes of 
the rest of this 
presentation, we 
will represent 
silicon in two 
dimensions for 
simplicity.
Metalloids 
Silicon is a metalloid. We can classify most chemicals easily into either “metals” 
or “non-metals”, however, silicon is one of a small group of elements that 
occupy a ‘staircase’ diagonal line on the periodic table, where the elements 
chemical properties fit neither description completely. Some metalloids are 
semiconductors.
Semiconductors 
• Silicon is part of a class of materials called ‘semiconductors’ that 
is to say, that it isn’t a conductor, and it isn’t an insulator. 
• It has electrical resistivity that is somewhere in between a 
conductor and an insulator. 
• In its regular state, silicon isn’t all that conductive, as none of its 
electrons can move (and movement of electrons is essential for 
conductivity); the electrons are locked into the crystalline 
structure – each atom sharing electrons with its neighbour.
Doping Silicon 
• We can control and enhance this semiconducting 
property by adding other chemicals to change 
the way silicon behaves. 
• This is known as “doping”, because the silicon is 
“doped” with a small quantity of a different 
chemical. 
• By introducing free electrons, or creating gaps 
into which free electrons can go, we can create 
useful devices.
To give you an example of how doping 
affects the silicon atoms, replacing one in 
every one-hundred and six silicon atoms 
with a gallium atom increases the 
conductivity of the solid silicon by a factor 
of five million as can replacing one in every 
one hundred and six silicon atoms with 
Phosphorus.
The Photoelectric Effect 
• As far back as 1839, Edmond Becquerel discovered 
that sunlight could induce an electrical current in 
solid material; however, it was many years before this 
process became well understood. 
• We now have a more complex understanding of the 
photoelectric effect through understanding of 
Quantum mechanics. 
• Einstein won the Nobel Prize for physics, by 
theorizing that in each quantum of light (think of a 
quantum as a ‘little package’), the frequency of the 
light (or it’s colour in simple terms), multiplied by a 
constant number (known as Planck’s constant) 
determines the energy that little parcel of light has.
Photovoltaic 
Effect 
• Certain materials 
can convert 
incoming 
electromagnetic 
radiation (in this 
case photons) into 
‘free electrons’.
Electron Work Function 
• Electrons have a property known as the “work function”, which is 
the amount of energy they need to stay bound in their place. 
• As photons hit the electrons, they may absorb some of their 
energy. 
• Once an electron garners more energy than it’s work function, it 
is ejected from its position in the ‘valence band’, which is to say 
the outer shell of the atom, into the higher energy ‘conduction 
band’, where the electron can travel and create an electric 
current. 
• However, if the photon has less energy than the electrons work 
function, it will stay in the position.
PN Junctions 
• The two types of doped silicon have slightly different electrical 
properties, and we can take advantage of this by creating a 
“junction”. 
• We are joining a piece of “P-Type” silicon and a piece of “N-Type” 
silicon; so the junction we create is known as a “PN 
junction”. 
• Those of you who are familiar with electronics, will recognise 
that a “PN junction” is effectively a diode – our photovoltaic cell 
is effectively a large, planar diode with a big surface area.
Changing Irradiance 
• If you make the light source more 
intense (i.e. increase the irradiance), 
then it has the effect of increasing 
the number of photons in the light 
beam 
• Whilst it increases the quantity, it still 
does not affect the fundamental energy 
that each photon possesses 
• This is determined by its frequency (or 
colour in simple terms). So, we need the 
right wavelength light for a given 
electron energy, and making it brighter 
increases the number of interactions 
that occur.
Silicon Photovoltaic Cell 
Construction
Photovoltaic Cell Construction 
• The “PN Junction” is the “sandwich” of silicon. 
• We have looked at the chemical properties of this 
sandwich already and how it generates electricity.
Photovoltaic Cell Construction 
• There is a need to make a physical connection between our single 
photovoltaic cell, other photovoltaic cells in the circuit, and the 
world. 
• This is accomplished with an electrode which can harness the 
moving electrons that the cell produces on each side of the cell.
Photovoltaic Cell Construction 
• The rear surface contact can be of relatively simple construction – all it needs to 
do is provide a connection with the P type silicon wafer. 
• The electrode on the front surface which contacts the N type silicon needs to be a 
little bit more sophisticated. In addition to making contact with the N type silicon, 
it also needs to permit the passage of light so that photons can hit the PN 
junction.
Photovoltaic Cell Construction 
• There are a number of different types of electrode – one of 
the simplest is simply screen-printed on top of the cell. 
More advanced electrodes might be ‘grooved’ into the 
cell. A good electrode design will make good contact with 
the silicon whilst obscuring as little light as possible.
Photovoltaic Cell Construction 
• The cell is given an anti-reflection coating. 
• We’ll see later in this chapter that reflection is one of the 
enemies of good photovoltaic cell performance.
Measuring PV Performance
Standard Test Conditions 
In order to make clear comparisons between 
different photovoltaic cells we use a standard set 
of test conditions. 
Standard Test Conditions are taken to be: 
• Vertical Irradiance of 1000 W/m2 
• Cell Temperature of 25°C +/- 2°C 
• A ‘light spectrum’ equivalent to AM = 1.5
Testing PV 
Cells 
We can make a 
circuit with a 
voltmeter, ammeter 
and variable resistor 
for a load in order to 
test a solar cells 
performance.
Testing PV Cells 
• As we change the load on the solar cell, the voltage and current 
readings will also change. We can make a plot of these readings. 
• Modern photovoltaic inverters are able to match the 
characteristics of the solar cell with the load that they present to 
the cell, this helps to extract the most energy from the device. 
• This is known as “Maximum Power Point Tracking”. 
• We will see the “Maximum Power Point” on the graphs on the 
slides to follow.
PV Power Curve 
• The brown line represents 
the plot of current against 
voltage, current is read 
from the left hand scale. 
• Current multiplied by 
voltage gives us ‘power’; It’s 
useful to plot this at the 
same time. 
• The purple line is power 
against voltage. 
• The scale for power can be 
read from the right hand 
side.
Maximum Power 
Point 
• The blue dot which 
indicates the ‘Maximum 
Power Point’ denotes that 
at this point the load is 
matched well to the output 
of the photovoltaic cell, and 
as such the photovoltaic 
cell is delivering maximum 
power into the load. It 
should be noted that the 
units for the Maximum 
Power Point are “Peak 
Watts”.
Fill Factor 
Now, if we draw an imaginary line 
from the MPP straight across to the X 
and Y axis and enclose a square – then 
– draw another two lines from the 
short circuit current and open circuit 
voltage back until they meet enclosing 
another square; we can look at the 
difference between the two areas. The 
smaller area divided by the larger 
gives us what is known as the ‘Fill 
Factor’. The fill factor is a number 
between 0 and 1 which can be used to 
describe the quality of photovoltaic 
cells.
Short Circuit Current 
If you look to the left of the 
graph where the brown line 
crosses the Y axis; the reading 
on the Y axis when voltage is 
zero is the “short circuit 
current” This is the current that 
flows when there is no load but 
one terminal of the panel is 
connected directly to the other. 
The short circuit current will be 
in the region of 5-15% higher 
than the current that flows at 
the maximum power point. 
Short circuit Current
Short Circuit Current 
If you look to the left of the 
graph where the brown line 
crosses the Y axis; the reading 
on the Y axis when voltage is 
zero is the “short circuit 
current” This is the current that 
flows when there is no load but 
one terminal of the panel is 
connected directly to the other. 
The short circuit current will be 
in the region of 5-15% higher 
than the current that flows at 
the maximum power point. 
Short circuit Current
Open Circuit 
Voltage 
Now look at the bottom 
right of the graph where 
the brown and purple 
lines cross the X-axis. Here 
we can take the reading 
for “Open Circuit Voltage”, 
which is the potential 
difference between the 
two terminals of the 
photovoltaic cell when no 
load is connected and no 
circuit is present. 
Short circuit Current 
Open circuit voltage
Factors affecting 
photovoltaic cell efficiency
Conduction 
• Important to ensure that 
electrons can move to the 
conduction layer and to the 
electrodes. 
• Also that holes can migrate 
to the rear contact of the 
photovoltaic cell as smoothly 
as possible without 
resistance.
Absorption 
• Photons are absorbed in the p-layer 
of a photovoltaic cell. 
• It is important that this layer 
absorbs as many photons as 
possible in order to create ‘free 
electrons’. 
• In designing photovoltaic cells, 
engineers try to maximise 
absorption.
Reflection 
• If light reflects off an element of 
the solar cell before it gets the 
chance to pass through and do 
useful work, then it is a wasted 
electron! 
• Want to try and minimise 
reflection as far as possible in 
order to ensure that we absorb as 
much light in the photovoltaic cell 
as possible.
Recombination 
• An electron, once free, meets up with a 
hole and recombines before it gets the 
chance to do useful work and travel 
around the circuit. 
• This is known as “recombination” and is an 
undesirable property that we want to try 
to minimise. 
• We can control and minimise 
recombination, by designing the PN 
junction in such a way that the electrons 
are ‘freed’ as near to the junction – the 
space charge region, as possible
Amorphous Silicon 
• Amorphous silicon is a ‘thin film’ device. 
• It is not a “crystalline” form of silicon. 
• Rather than the tetrahedral crystalline structure carrying on over 
a long range, it is disordered, there are ‘dangling bonds’. 
• These dangling bonds can be “passivated” by bonding hydrogen to 
them. 
• This is known as a-Si:H, hydrogenated amorphous silicon. 
• This hydrogen reduces the number of “dangling bonds” by several 
orders of magnitude. 
• However, it also leads to light-induced degradation over time. 
• This is known as the Staebler-Wronski effect.
Amorphous Silicon 
• “Amorphous Silicon” solar cells 
commonly use a technology called “P-I-N”. 
• Here, inbetween the P and N type 
silicon, is an intermediate layer of silicon 
called “I-Type” which stands for 
“Intrinsic-Silicon”. 
• This I-type silicon is undoped. 
• When light hits the intrinsic region free 
electrons and holes are generated 
which are the divided by the electrical 
field created by the adjacent N and P 
type silicon.
If you found any of this interesting… 
Please stay in touch 
Gavin Harper 
g.harper@glyndwr.ac.uk 
www.gavindharper.com 
http://www.cser.org.uk/ 
https://www.westproject.org.uk/ 
@gavindjharper 
@CSER_PV 
@LCRI_WEST

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Silicon Photovoltaic Basics

  • 1. Silicon Photovoltaic Cells: An Introduction Gavin D. J. Harper g.harper@glyndwr.ac.uk @gavindjharper www.gavindjharper.com http://orcid.org/0000-0002-4691-6642 Welsh Energy Sector Training (WEST) OpTIC Glyndwr Ffordd William Morgan, St Asaph, Wales October 2014
  • 2. Structure of Silicon • Matter is composed of atoms. • Atoms in turn are made up of • Protons (which are positively charged) • Electrons, (which are negatively charged) • Neutrons (which are neither positively nor negatively charged). • If we took an atom of silicon, and examined how it was composed, we would see a dense central “core” which is known as the ‘nucleus’ which consists of Protons and Neutrons; 14 of each to be exact. • Around this core are electrons that orbit in a ‘cloud’. Some of these electrons orbit at different distances from the central nucleus. We call these distances ‘shells’
  • 3. Structure of Silicon • If you think of a shell as an imaginary sphere surrounding the nucleus of an atom; these shells are arranged concentrically. Each shell only has room for so many electrons, therefore as each shell fills up, the next shell in line must be filled with electrons. • When a molecule has eight electrons in its outer shell (known as the valence shell), then it is stable; which is to say not very chemically reactive. The ‘Noble Gases’ which reside on the far right of the Periodic Table are very stable and as such have little tendency to participate in chemical reactions – all atoms strive to fill their outer shells and reach this unreactive state.
  • 4.
  • 5. Structure of Silicon As we can tell from its number on the periodic table, “14” we can tell that silicon has 14 electrons. A little knowledge as to the pattern in which electrons are arranged in tells us that these electrons are arranged in three ‘shells’. The first two ‘shells’ are completely full with electrons, however, the outermost shell only has half of the total number of electrons possible.
  • 6. Structure of Silicon • Silicon is what is known as “tetravalent”, this is to say that there are four electrons available in the outer shell which can form ‘covalent’ bonds. A covalent bond is one where electrons are “shared” between pairs of atoms. • The natural tendency in chemicals is for them to work towards filling their outer shells with eight electrons by forming bonds with other chemicals. • Silicon is no exception, and fills its outer shell by bonding with other silicon atoms and “sharing” electrons. • Silicon forms a regular crystalline structure. This is to say that the forces between the atoms of silicon are such that they arrange themselves in the most compact pattern that the forces between atoms will allow.
  • 7. Crystalline Silicon • This is what silicon looks like when represented in three dimensions. • For the purposes of the rest of this presentation, we will represent silicon in two dimensions for simplicity.
  • 8. Metalloids Silicon is a metalloid. We can classify most chemicals easily into either “metals” or “non-metals”, however, silicon is one of a small group of elements that occupy a ‘staircase’ diagonal line on the periodic table, where the elements chemical properties fit neither description completely. Some metalloids are semiconductors.
  • 9. Semiconductors • Silicon is part of a class of materials called ‘semiconductors’ that is to say, that it isn’t a conductor, and it isn’t an insulator. • It has electrical resistivity that is somewhere in between a conductor and an insulator. • In its regular state, silicon isn’t all that conductive, as none of its electrons can move (and movement of electrons is essential for conductivity); the electrons are locked into the crystalline structure – each atom sharing electrons with its neighbour.
  • 10.
  • 11. Doping Silicon • We can control and enhance this semiconducting property by adding other chemicals to change the way silicon behaves. • This is known as “doping”, because the silicon is “doped” with a small quantity of a different chemical. • By introducing free electrons, or creating gaps into which free electrons can go, we can create useful devices.
  • 12.
  • 13.
  • 14. To give you an example of how doping affects the silicon atoms, replacing one in every one-hundred and six silicon atoms with a gallium atom increases the conductivity of the solid silicon by a factor of five million as can replacing one in every one hundred and six silicon atoms with Phosphorus.
  • 15. The Photoelectric Effect • As far back as 1839, Edmond Becquerel discovered that sunlight could induce an electrical current in solid material; however, it was many years before this process became well understood. • We now have a more complex understanding of the photoelectric effect through understanding of Quantum mechanics. • Einstein won the Nobel Prize for physics, by theorizing that in each quantum of light (think of a quantum as a ‘little package’), the frequency of the light (or it’s colour in simple terms), multiplied by a constant number (known as Planck’s constant) determines the energy that little parcel of light has.
  • 16. Photovoltaic Effect • Certain materials can convert incoming electromagnetic radiation (in this case photons) into ‘free electrons’.
  • 17. Electron Work Function • Electrons have a property known as the “work function”, which is the amount of energy they need to stay bound in their place. • As photons hit the electrons, they may absorb some of their energy. • Once an electron garners more energy than it’s work function, it is ejected from its position in the ‘valence band’, which is to say the outer shell of the atom, into the higher energy ‘conduction band’, where the electron can travel and create an electric current. • However, if the photon has less energy than the electrons work function, it will stay in the position.
  • 18. PN Junctions • The two types of doped silicon have slightly different electrical properties, and we can take advantage of this by creating a “junction”. • We are joining a piece of “P-Type” silicon and a piece of “N-Type” silicon; so the junction we create is known as a “PN junction”. • Those of you who are familiar with electronics, will recognise that a “PN junction” is effectively a diode – our photovoltaic cell is effectively a large, planar diode with a big surface area.
  • 19.
  • 20. Changing Irradiance • If you make the light source more intense (i.e. increase the irradiance), then it has the effect of increasing the number of photons in the light beam • Whilst it increases the quantity, it still does not affect the fundamental energy that each photon possesses • This is determined by its frequency (or colour in simple terms). So, we need the right wavelength light for a given electron energy, and making it brighter increases the number of interactions that occur.
  • 22.
  • 23. Photovoltaic Cell Construction • The “PN Junction” is the “sandwich” of silicon. • We have looked at the chemical properties of this sandwich already and how it generates electricity.
  • 24. Photovoltaic Cell Construction • There is a need to make a physical connection between our single photovoltaic cell, other photovoltaic cells in the circuit, and the world. • This is accomplished with an electrode which can harness the moving electrons that the cell produces on each side of the cell.
  • 25. Photovoltaic Cell Construction • The rear surface contact can be of relatively simple construction – all it needs to do is provide a connection with the P type silicon wafer. • The electrode on the front surface which contacts the N type silicon needs to be a little bit more sophisticated. In addition to making contact with the N type silicon, it also needs to permit the passage of light so that photons can hit the PN junction.
  • 26. Photovoltaic Cell Construction • There are a number of different types of electrode – one of the simplest is simply screen-printed on top of the cell. More advanced electrodes might be ‘grooved’ into the cell. A good electrode design will make good contact with the silicon whilst obscuring as little light as possible.
  • 27. Photovoltaic Cell Construction • The cell is given an anti-reflection coating. • We’ll see later in this chapter that reflection is one of the enemies of good photovoltaic cell performance.
  • 29. Standard Test Conditions In order to make clear comparisons between different photovoltaic cells we use a standard set of test conditions. Standard Test Conditions are taken to be: • Vertical Irradiance of 1000 W/m2 • Cell Temperature of 25°C +/- 2°C • A ‘light spectrum’ equivalent to AM = 1.5
  • 30. Testing PV Cells We can make a circuit with a voltmeter, ammeter and variable resistor for a load in order to test a solar cells performance.
  • 31. Testing PV Cells • As we change the load on the solar cell, the voltage and current readings will also change. We can make a plot of these readings. • Modern photovoltaic inverters are able to match the characteristics of the solar cell with the load that they present to the cell, this helps to extract the most energy from the device. • This is known as “Maximum Power Point Tracking”. • We will see the “Maximum Power Point” on the graphs on the slides to follow.
  • 32. PV Power Curve • The brown line represents the plot of current against voltage, current is read from the left hand scale. • Current multiplied by voltage gives us ‘power’; It’s useful to plot this at the same time. • The purple line is power against voltage. • The scale for power can be read from the right hand side.
  • 33. Maximum Power Point • The blue dot which indicates the ‘Maximum Power Point’ denotes that at this point the load is matched well to the output of the photovoltaic cell, and as such the photovoltaic cell is delivering maximum power into the load. It should be noted that the units for the Maximum Power Point are “Peak Watts”.
  • 34. Fill Factor Now, if we draw an imaginary line from the MPP straight across to the X and Y axis and enclose a square – then – draw another two lines from the short circuit current and open circuit voltage back until they meet enclosing another square; we can look at the difference between the two areas. The smaller area divided by the larger gives us what is known as the ‘Fill Factor’. The fill factor is a number between 0 and 1 which can be used to describe the quality of photovoltaic cells.
  • 35. Short Circuit Current If you look to the left of the graph where the brown line crosses the Y axis; the reading on the Y axis when voltage is zero is the “short circuit current” This is the current that flows when there is no load but one terminal of the panel is connected directly to the other. The short circuit current will be in the region of 5-15% higher than the current that flows at the maximum power point. Short circuit Current
  • 36. Short Circuit Current If you look to the left of the graph where the brown line crosses the Y axis; the reading on the Y axis when voltage is zero is the “short circuit current” This is the current that flows when there is no load but one terminal of the panel is connected directly to the other. The short circuit current will be in the region of 5-15% higher than the current that flows at the maximum power point. Short circuit Current
  • 37. Open Circuit Voltage Now look at the bottom right of the graph where the brown and purple lines cross the X-axis. Here we can take the reading for “Open Circuit Voltage”, which is the potential difference between the two terminals of the photovoltaic cell when no load is connected and no circuit is present. Short circuit Current Open circuit voltage
  • 39. Conduction • Important to ensure that electrons can move to the conduction layer and to the electrodes. • Also that holes can migrate to the rear contact of the photovoltaic cell as smoothly as possible without resistance.
  • 40. Absorption • Photons are absorbed in the p-layer of a photovoltaic cell. • It is important that this layer absorbs as many photons as possible in order to create ‘free electrons’. • In designing photovoltaic cells, engineers try to maximise absorption.
  • 41. Reflection • If light reflects off an element of the solar cell before it gets the chance to pass through and do useful work, then it is a wasted electron! • Want to try and minimise reflection as far as possible in order to ensure that we absorb as much light in the photovoltaic cell as possible.
  • 42. Recombination • An electron, once free, meets up with a hole and recombines before it gets the chance to do useful work and travel around the circuit. • This is known as “recombination” and is an undesirable property that we want to try to minimise. • We can control and minimise recombination, by designing the PN junction in such a way that the electrons are ‘freed’ as near to the junction – the space charge region, as possible
  • 43. Amorphous Silicon • Amorphous silicon is a ‘thin film’ device. • It is not a “crystalline” form of silicon. • Rather than the tetrahedral crystalline structure carrying on over a long range, it is disordered, there are ‘dangling bonds’. • These dangling bonds can be “passivated” by bonding hydrogen to them. • This is known as a-Si:H, hydrogenated amorphous silicon. • This hydrogen reduces the number of “dangling bonds” by several orders of magnitude. • However, it also leads to light-induced degradation over time. • This is known as the Staebler-Wronski effect.
  • 44.
  • 45. Amorphous Silicon • “Amorphous Silicon” solar cells commonly use a technology called “P-I-N”. • Here, inbetween the P and N type silicon, is an intermediate layer of silicon called “I-Type” which stands for “Intrinsic-Silicon”. • This I-type silicon is undoped. • When light hits the intrinsic region free electrons and holes are generated which are the divided by the electrical field created by the adjacent N and P type silicon.
  • 46. If you found any of this interesting… Please stay in touch Gavin Harper g.harper@glyndwr.ac.uk www.gavindharper.com http://www.cser.org.uk/ https://www.westproject.org.uk/ @gavindjharper @CSER_PV @LCRI_WEST