Chapter Fourteen SEMICONDUCTOR ELECTRONICS:

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Chapter FourteenSEMICONDUCTORELECTRONICS:MATERIALS, DEVICESAND SIMPLE CIRCUITS14.1 INTRODUCTIONDevices in which a controlled flow of electrons can be obtained are thebasic building blocks of all the electronic circuits. Before the discovery oftransistor in 1948, such devices were mostly vacuum tubes (also calledvalves) like the vacuum diode which has two electrodes, viz., anode (oftencalled plate) and cathode; triode which has three electrodes – cathode,plate and grid; tetrode and pentode (respectively with 4 and 5 electrodes).In a vacuum tube, the electrons are supplied by a heated cathode andthe controlled flow of these electrons in vacuum is obtained by varyingthe voltage between its different electrodes. Vacuum is required in theinter-electrode space; otherwise the moving electrons may lose theirenergy on collision with the air molecules in their path. In these devicesthe electrons can flow only from the cathode to the anode (i.e., only in onedirection). Therefore, such devices are generally referred to as valves.These vacuum tube devices are bulky, consume high power, operategenerally at high voltages ( 100 V) and have limited life and low reliability.The seed of the development of modern solid-state semiconductorelectronics goes back to 1930’s when it was realised that some solidstate semiconductors and their junctions offer the possibility of controllingthe number and the direction of flow of charge carriers through them.Simple excitations like light, heat or small applied voltage can changethe number of mobile charges in a semiconductor. Note that the supply2021–22

Physicsand flow of charge carriers in the semiconductor devices are within thesolid itself, while in the earlier vacuum tubes/valves, the mobile electronswere obtained from a heated cathode and they were made to flow in anevacuated space or vacuum. No external heating or large evacuated spaceis required by the semiconductor devices. They are small in size, consumelow power, operate at low voltages and have long life and high reliability.Even the Cathode Ray Tubes (CRT) used in television and computermonitors which work on the principle of vacuum tubes are being replacedby Liquid Crystal Display (LCD) monitors with supporting solid stateelectronics. Much before the full implications of the semiconductor deviceswas formally understood, a naturally occurring crystal of galena (Leadsulphide, PbS) with a metal point contact attached to it was used asdetector of radio waves.In the following sections, we will introduce the basic concepts ofsemiconductor physics and discuss some semiconductor devices likejunction diodes (a 2-electrode device) and bipolar junction transistor (a3-electrode device). A few circuits illustrating their applications will alsobe described.14.2 CLASSIFICATION OF METALS, CONDUCTORSSEMICONDUCTORS468ANDOn the basis of conductivityOn the basis of the relative values of electrical conductivity (σ ) or resistivity( ρ 1/σ ), the solids are broadly classified as:(i) Metals: They possess very low resistivity (or high conductivity).ρ 10–2 – 10–8 Ω mσ 102 – 108 S m–1(ii) Semiconductors: They have resistivity or conductivity intermediateto metals and insulators.ρ 10–5 – 106 Ω mσ 105 – 10–6 S m–1(iii)Insulators: They have high resistivity (or low conductivity).ρ 1011 – 1019 Ω mσ 10–11 – 10–19 S m–1The values of ρ and σ given above are indicative of magnitude andcould well go outside the ranges as well. Relative values of the resistivityare not the only criteria for distinguishing metals, insulators andsemiconductors from each other. There are some other differences, whichwill become clear as we go along in this chapter.Our interest in this chapter is in the study of semiconductors whichcould be:(i) Elemental semiconductors: Si and Ge(ii) Compound semiconductors: Examples are: Inorganic: CdS, GaAs, CdSe, InP, etc. Organic: anthracene, doped pthalocyanines, etc. Organic polymers: polypyrrole, polyaniline, polythiophene, etc.Most of the currently available semiconductor devices are based onelemental semiconductors Si or Ge and compound inorganic2021–22

Semiconductor Electronics:Materials, Devices andSimple Circuitssemiconductors. However, after 1990, a few semiconductor devices usingorganic semiconductors and semiconducting polymers have beendeveloped signalling the birth of a futuristic technology of polymerelectronics and molecular-electronics. In this chapter, we will restrictourselves to the study of inorganic semiconductors, particularlyelemental semiconductors Si and Ge. The general concepts introducedhere for discussing the elemental semiconductors, by-and-large, applyto most of the compound semiconductors as well.On the basis of energy bandsAccording to the Bohr atomic model, in an isolated atom the energy ofany of its electrons is decided by the orbit in which it revolves. But whenthe atoms come together to form a solid they are close to each other. Sothe outer orbits of electrons from neighbouring atoms would come veryclose or could even overlap. This would make the nature of electron motionin a solid very different from that in an isolated atom.Inside the crystal each electron has a unique position and no twoelectrons see exactly the same pattern of surrounding charges. Becauseof this, each electron will have a different energy level. These differentenergy levels with continuous energy variation form what are calledenergy bands. The energy band which includes the energy levels of thevalence electrons is called the valence band. The energy band above thevalence band is called the conduction band. With no external energy, allthe valence electrons will reside in the valence band. If the lowest level inthe conduction band happens to be lower than the highest level of thevalence band, the electrons from the valence band can easily move intothe conduction band. Normally the conduction band is empty. But whenit overlaps on the valence band electrons can move freely into it. This isthe case with metallic conductors.If there is some gap between the conduction band and the valenceband, electrons in the valence band all remain bound and no free electronsare available in the conduction band. This makes the material aninsulator. But some of the electrons from the valence band may gainexternal energy to cross the gap between the conduction band and thevalence band. Then these electrons will move into the conduction band.At the same time they will create vacant energy levels in the valence bandwhere other valence electrons can move. Thus the process creates thepossibility of conduction due to electrons in conduction band as well asdue to vacancies in the valence band.Let us consider what happens in the case of Si or Ge crystal containingN atoms. For Si, the outermost orbit is the third orbit (n 3), while for Geit is the fourth orbit (n 4). The number of electrons in the outermostorbit is 4 (2s and 2p electrons). Hence, the total number of outer electronsin the crystal is 4N. The maximum possible number of electrons in theouter orbit is 8 (2s 6p electrons). So, for the 4N valence electrons thereare 8N available energy states. These 8N discrete energy levels can eitherform a continuous band or they may be grouped in different bandsdepending upon the distance between the atoms in the crystal (see boxon Band Theory of Solids).At the distance between the atoms in the crystal lattices of Si and Ge,the energy band of these 8N states is split apart into two which areseparated by an energy gap Eg (Fig. 14.1). The lower band which is2021–22469

Physicscompletely occupied by the 4N valence electrons at temperature of absolutezero is the valence band. The other band consisting of 4N energy states,called the conduction band, is completely empty at absolute zero.BANDTHEORY OF SOLIDSConsider that the Si or Ge crystalcontains N atoms. Electrons of eachatom will have discrete energies indifferent orbits. The electron energywill be same if all the atoms areisolated, i.e., separated from eachother by a large distance. However,in a crystal, the atoms are close toeach other (2 to 3 Å) and thereforethe electrons interact with eachother and also with theneighbouring atomic cores. Theoverlap (or interaction) will be morefelt by the electrons in theoutermost orbit while the innerorbit or core electron energies mayremain unaffected. Therefore, for understanding electron energies in Si or Ge crystal, weneed to consider the changes in the energies of the electrons in the outermost orbit only.For Si, the outermost orbit is the third orbit (n 3), while for Ge it is the fourth orbit(n 4). The number of electrons in the outermost orbit is 4 (2s and 2p electrons). Hence,the total number of outer electrons in the crystal is 4N. The maximum possible number ofouter electrons in the orbit is 8 (2s 6p electrons). So, out of the 4N electrons, 2N electronsare in the 2N s-states (orbital quantum number l 0) and 2N electrons are in the available6N p-states. Obviously, some p-electron states are empty as shown in the extreme right ofFigure. This is the case of well separated or isolated atoms [region A of Figure].Suppose these atoms start coming nearer to each other to form a solid. The energiesof these electrons in the outermost orbit may change (both increase and decrease) due tothe interaction between the electrons of different atoms. The 6N states for l 1, whichoriginally had identical energies in the isolated atoms, spread out and form an energyband [region B in Figure]. Similarly, the 2N states for l 0, having identical energies inthe isolated atoms, split into a second band (carefully see the region B of Figure) separatedfrom the first one by an energy gap.At still smaller spacing, however, there comes a region in which the bands merge witheach other. The lowest energy state that is a split from the upper atomic level appears todrop below the upper state that has come from the lower atomic level. In this region (regionC in Figure), no energy gap exists where the upper and lower energy states get mixed.Finally, if the distance between the atoms further decreases, the energy bands againsplit apart and are separated by an energy gap Eg (region D in Figure). The total numberof available energy states 8N has been re-apportioned between the two bands (4N stateseach in the lower and upper energy bands). Here the significant point is that there areexactly as many states in the lower band (4N ) as there are available valence electronsfrom the atoms (4N ).Therefore, this band ( called the valence band ) is completely filled while the upperband is completely empty. The upper band is called the conduction band.4702021–22

Semiconductor Electronics:Materials, Devices andSimple CircuitsThe lowest energy level in theconduction band is shown as EC andhighest energy level in the valence bandis shown as EV . Above EC and below EVthere are a large number of closely spacedenergy levels, as shown in Fig. 14.1.The gap between the top of the valenceband and bottom of the conduction bandis called the energy band gap (Energy gapEg ). It may be large, small, or zero,depending upon the material. Thesedifferent situations, are depicted in Fig.14.2 and discussed below:Case I: This refers to a situation, asshown in Fig. 14.2(a). One can have ametal either when the conduction bandFIGURE 14.1 The energy band positions in ais partially filled and the balanced bandsemiconductorat 0 K. The upper band, called theis partially empty or when the conductionconductionband,consists of infinitely large numberand valance bands overlap. When thereof closely spaced energy states. The lower band,is overlap electrons from valence band cancalled the valence band, consists of closely spacedeasily move into the conduction band.completely filled energy states.This situation makes a large number ofelectrons available for electrical conduction. When the valence band ispartially empty, electrons from its lower level can move to higher levelmaking conduction possible. Therefore, the resistance of such materialsis low or the conductivity is high.FIGURE 14.2 Difference between energy bands of (a) metals,(b) insulators and (c) semiconductors.2021–22471

PhysicsCase II: In this case, as shown in Fig. 14.2(b), a large band gap Eg exists(Eg 3 eV). There are no electrons in the conduction band, and thereforeno electrical conduction is possible. Note that the energy gap is so largethat electrons cannot be excited from the valence band to the conductionband by thermal excitation. This is the case of insulators.Case III: This situation is shown in Fig. 14.2(c). Here a finite but smallband gap (Eg 3 eV) exists. Because of the small band gap, at roomtemperature some electrons from valence band can acquire enoughenergy to cross the energy gap and enter the conduction band. Theseelectrons (though small in numbers) can move in the conduction band.Hence, the resistance of semiconductors is not as high as that of theinsulators.In this section we have made a broad classification of metals,conductors and semiconductors. In the section which follows you willlearn the conduction process in semiconductors.14.3 INTRINSIC SEMICONDUCTORWe shall take the most common case of Ge and Si whose lattice structureis shown in Fig. 14.3. These structures are called the diamond-likestructures. Each atom is surrounded by four nearest neighbours. Weknow that Si and Ge have four valence electrons. In its crystallinestructure, every Si or Ge atom tends to share one of its four valenceelectrons with each of its four nearest neighbour atoms, and also to takeshare of one electron from each such neighbour. These shared electronpairs are referred to as forming a covalent bond or simply a valencebond. The two shared electrons can be assumed to shuttle back-andforth between the associated atoms holding them together strongly.Figure 14.4 schematically shows the 2-dimensional representation of Sior Ge structure shown in Fig. 14.3 which overemphasises the covalentbond. It shows an idealised picture in which no bonds are broken (allbonds are intact). Such a situation arises at lowtemperatures. As the temperature increases, morethermal energy becomes available to these electronsand some of these electrons may break–away(becoming free electrons contributing to conduction).The thermal energy effectively ionises only a few atomsin the crystalline lattice and creates a vacancy in thebond as shown in Fig. 14.5(a). The neighbourhood,from which the free electron (with charge –q ) has comeout leaves a vacancy with an effective charge ( q ). Thisvacancy with the effective positive electronic charge iscalled a hole. The hole behaves as an apparent freeparticle with effective positive charge.In intrinsic semiconductors, the number of freeFIGURE 14.3 Three-dimensional diaelectrons,ne is equal to the number of holes, nh. That ismond-like crystal structure for Carbon,n n(14.1)Silicon or Germanium witheh ective lattice spacing a equaliSemiconductors posses the unique property into 3.56, 5.43 and 5.66 Å.472which, apart from electrons, the holes also move.2021–22

Semiconductor Electronics:Materials, Devices andSimple CircuitsSuppose there is a hole at site 1 as shown inFig. 14.5(a). The movement of holes can bevisualised as shown in Fig. 14.5(b). An electronfrom the covalent bond at site 2 may jump tothe vacant site 1 (hole). Thus, after such a jump,the hole is at site 2 and the site 1 has now anelectron. Therefore, apparently, the hole hasmoved from site 1 to site 2. Note that the electronoriginally set free [Fig. 14.5(a)] is not involvedin this process of hole motion. The free electronmoves completely independently as conductionelectron and gives rise to an electron current, Ieunder an applied electric field. Remember thatthe motion of hole is only a convenient way ofFIGURE 14.4 Schematic two-dimensionaldescribing the actual motion of bound electrons,representation of Si or Ge structure showingwhenever there is an empty bond anywhere incovalent bonds at low temperature(all bonds intact). 4 symbolthe crystal. Under the action of an electric field,indicatesinner cores of Si or Ge.these holes move towards negative potentialgiving the hole current, Ih. The total current, I isthus the sum of the electron current Ie and thehole current Ih:I Ie Ih(14.2)It may be noted that apart from the process of generation of conductionelectrons and holes, a simultaneous process of recombination occurs inwhich the electrons recombine with the holes. At equilibrium, the rate ofgeneration is equal to the rate of recombination of charge carriers. Therecombination occurs due to an electron colliding with a hole.(a)(b)FIGURE 14.5 (a) Schematic model of generation of hole at site 1 and conduction electrondue to thermal energy at moderate temperatures. (b) Simplified representation ofpossible thermal motion of a hole. The electron from the lower left hand covalent bond(site 2) goes to the earlier hole site1, leaving a hole at its site indicating an473apparent movement of the hole from site 1 to site 2.2021–22

PhysicsFIGURE 14.6 (a) An intrinsic semiconductor at T 0 Kbehaves like insulator. (b) At T 0 K, four thermally generatedelectron-hole pairs. The filled circles ( ) represent electronsand empty circles ( ) represent holes.An intrinsic semiconductorwill behave like an insulator atT 0 K as shown in Fig. 14.6(a).It is the thermal energy athigher temperatures (T 0K),which excites some electronsfrom the valence band to theconduction band. Thesethermally excited electrons atT 0 K, partially occupy theconduction band. Therefore,the energy-band diagram of anintrinsic semiconductor will beas shown in Fig. 14.6(b). Here,some electrons are shown inthe conduction band. Thesehave come from the valenceband leaving equal number ofholes there.EXAMPLE 14.1Example 14.1 C, Si and Ge have same lattice structure. Why is Cinsulator while Si and Ge intrinsic semiconductors?Solution The 4 bonding electrons of C, Si or Ge lie, respectively, inthe second, third and fourth orbit. Hence, energy required to takeout an electron from these atoms (i.e., ionisation energy Eg ) will beleast for Ge, followed by Si and highest for C. Hence, number of freeelectrons for conduction in Ge and Si are significant but negligiblysmall for C.14.4 EXTRINSIC SEMICONDUCTOR474The conductivity of an intrinsic semiconductor depends on itstemperature, but at room temperature its conductivity is very low. Assuch, no important electronic devices can be developed using thesesemiconductors. Hence there is a necessity of improving theirconductivity. This can be done by making use of impurities.When a small amount, say, a few parts per million (ppm), of a suitableimpurity is added to the pure semiconductor, the conductivity of thesemiconductor is increased manifold. Such materials are known asextrinsic semiconductors or impurity semiconductors. The deliberateaddition of a desirable impurity is called doping and the impurity atomsare called dopants. Such a material is also called a doped semiconductor.The dopant has to be such that it does not distort the original puresemiconductor lattice. It occupies only a very few of the originalsemiconductor atom sites in the crystal. A necessary condition to attainthis is that the sizes of the dopant and the semiconductor atoms shouldbe nearly the same.There are two types of dopants used in doping the tetravalent Sior Ge:(i) Pentavalent (valency 5); like Arsenic (As), Antimony (Sb), Phosphorous(P), etc.2021–22

Semiconductor Electronics:Materials, Devices andSimple Circuits(ii) Trivalent (valency 3); like Indium (In),Boron (B), Aluminium (Al), etc.We shall now discuss how the dopingchanges the number of charge carriers (andhence the conductivity) of semiconductors.Si or Ge belongs to the fourth group in thePeriodic table and, therefore, we choose thedopant element from nearby fifth or thirdgroup, expecting and taking care that thesize of the dopant atom is nearly the same asthat of Si or Ge. Interestingly, the pentavalentand trivalent dopants in Si or Ge give twoentirely different types of semiconductors asdiscussed below.(i) n-type semiconductorSuppose we dope Si or Ge with a pentavalentelement as shown in Fig. 14.7. When an atomof 5 valency element occupies the positionof an atom in the crystal lattice of Si, four ofits electrons bond with the four siliconneighbours while the fifth remains veryweakly bound to its parent atom. This isbecause the four electrons participating inbonding are seen as part of the effective core FIGURE 14.7 (a) Pentavalent donor atom (As, Sb,P, etc.) doped for tetravalent Si or Ge giving nof the atom by the fifth electron. As a resulttype semiconductor, and (b) Commonly usedthe ionisation energy required to set thisschematic representation of n-type materialelectron free is very small and even at roomwhich shows only the fixed cores of thetemperature it will be free to move in thesubstituent donors with one additional effectivelattice of the semiconductor. For example, the positive charge and its associated extra electron.energy required is 0.01 eV for germanium,and 0.05 eV for silicon, to separate thiselectron from its atom. This is in contrast to the energy required to jumpthe forbidden band (about 0.72 eV for germanium and about 1.1 eV forsilicon) at room temperature in the intrinsic semiconductor. Thus, thepentavalent dopant is donating one extra electron for conduction andhence is known as donor impurity. The number of electrons madeavailable for conduction by dopant atoms depends strongly upon thedoping level and is independent of any increase in ambient temperature.On the other hand, the number of free electrons (with an equal numberof holes) generated by Si atoms, increases weakly with temperature.In a doped semiconductor the total number of conduction electronsne is due to the electrons contributed by donors and those generatedintrinsically, while the total number of holes nh is only due to the holesfrom the intrinsic source. But the rate of recombination of holes wouldincrease due to the increase in the number of electrons. As a result, thenumber of holes would get reduced further.Thus, with proper level of doping the number of conduction electrons475can be made much larger than the number of holes. Hence in an extrinsic2021–22

Physicssemiconductor doped with pentavalent impurity, electronsbecome the majority carriers and holes the minority carriers.These semiconductors are, therefore, known as n-typesemiconductors. For n-type semiconductors, we have,n e nh(14.3)(ii) p-type semiconductorThis is obtained when Si or Ge is doped with a trivalent impuritylike Al, B, In, etc. The dopant has one valence electron less thanSi or Ge and, therefore, this atom can form covalent bonds withneighbouring three Si atoms but does not have any electron tooffer to the fourth Si atom. So the bond between the fourthneighbour and the trivalent atom has a vacancy or hole as shownin Fig. 14.8. Since the neighbouring Si atom in the lattice wantsan electron in place of a hole, an electron in the outer orbit ofan atom in the neighbourhood may jump to fill this vacancy,leaving a vacancy or hole at its own site. Thus the hole isavailable for conduction. Note that the trivalent foreign atombecomes effectively negatively charged when it shares fourthelectron with neighbouring Si atom. Therefore, the dopant atomof p-type material can be treated as core of one negative chargealong with its associated hole as shown in Fig. 14.8(b). It isobvious that one acceptor atom gives one hole. These holes arein addition to the intrinsically generated holes while the sourceof conduction electrons is only intrinsic generation. Thus, forsuch a material, the holes are the majority carriers and electronsFIGURE 14.8 (a) Trivalentare minority carriers. Therefore, extrinsic semiconductors dopedacceptor atom (In, Al, B etc.)with trivalent impurity are called p-type semiconductors. Fordoped in tetravalent Si or Gep-type semiconductors, the recombination process will reducelattice giving p-type semiconthe number (n i )of intrinsically generated electrons to n e. Weductor. (b) Commonly usedhave, for p-type semiconductorsschematic representation ofn h ne(14.4)p-type material which showsonly the fixed core of theNote that the crystal maintains an overall charge neutralitysubstituent acceptor withas the charge of additional charge carriers is just equal andone effective additionalopposite to that of the ionised cores in the lattice.negative charge and itsIn extrinsic semiconductors, because of the abundance ofassociated hole.majority current carriers, the minority carriers producedthermally have more chance of meeting majority carriers andthus getting destroyed. Hence, the dopant, by adding a large number ofcurrent carriers of one type, which become the majority carriers, indirectlyhelps to reduce the intrinsic concentration of minority carriers.The semiconductor’s energy band structure is affected by doping. Inthe case of extrinsic semiconductors, additional energy states due to donorimpurities (ED ) and acceptor impurities (EA ) also exist. In the energy banddiagram of n-type Si semiconductor, the donor energy level E D is slightlybelow the bottom EC of the conduction band and electrons from this levelmove into the conduction band with very small supply of energy. At roomtemperature, most of the donor atoms get ionised but very few ( 1012)atoms of Si get ionised. So the conduction band will have most electrons476coming from the donor impurities, as shown in Fig. 14.9(a). Similarly,2021–22

Semiconductor Electronics:Materials, Devices andSimple Circuitsfor p-type semiconductor, the acceptor energy level EA is slightly abovethe top EV of the valence band as shown in Fig. 14.9(b). With very smallsupply of energy an electron from the valence band can jump to the levelEA and ionise the acceptor negatively. (Alternately, we can also say thatwith very small supply of energy the hole from level EA sinks down intothe valence band. Electrons rise up and holes fall down when they gainexternal energy.) At room temperature, most of the acceptor atoms getionised leaving holes in the valence band. Thus at room temperature thedensity of holes in the valence band is predominantly due to impurity inthe extrinsic semiconductor. The electron and hole concentration in asemiconductor in thermal equilibrium is given bynenh ni2(14.5)Though the above description is grossly approximate andhypothetical, it helps in understanding the difference between metals,insulators and semiconductors (extrinsic and intrinsic) in a simplemanner. The difference in the resistivity of C, Si and Ge depends uponthe energy gap between their conduction and valence bands. For C(diamond), Si and Ge, the energy gaps are 5.4 eV, 1.1 eV and 0.7 eV,respectively. Sn also is a group IV element but it is a metal because theenergy gap in its case is 0 eV.FIGURE 14.9 Energy bands of (a) n-type semiconductor at T 0K, (b) p-typesemiconductor at T 0K.Example 14.2 Suppose a pure Si crystal has 5 1028 atoms m–3. It isdoped by 1 ppm concentration of pentavalent As. Calculate thenumber of electrons and holes. Given that ni 1.5 1016 m–3. 4.5 109 m–32021–22EXAMPLE 14.2Solution Note that thermally generated electrons (ni 1016 m–3 ) arenegligibly small as compared to those produced by doping.Therefore, ne ND.Since nenh ni2, The number of holesnh (2.25 1032 )/(5 1022 )477

Physics14.5 p-n /solids/pnjun.htmlA p-n junction is the basic building block of many semiconductor deviceslike diodes, transistor, etc. A clear understanding of the junction behaviouris important to analyse the working of other semiconductor devices.We will now try to understand how a junction is formed and how thejunction behaves under the influence of external applied voltage (alsocalled bias).14.5.1 p-n junction formationFormation and working of p-n junction diodeConsider a thin p-type silicon (p-Si) semiconductor wafer. By addingprecisely a small quantity of pentavelent impurity, part of the p-Si wafercan be converted into n-Si. There are several processes by which asemiconductor can be formed. The wafer now contains p-region andn-region and a metallurgical junction between p-, and n- region.Two important processes occur during the formation of a p-n junction:diffusion and drift. We know that in an n-type semiconductor, theconcentration of electrons (number of electrons per unit volume) is morecompared to the concentration of holes. Similarly, in a p-typesemiconductor, the concentration of holes is more than the concentrationof electrons. During the formation of p-n junction, and due to theconcentration gradient across p-, and n- sides, holes diffuse from p-sideto n-side (p n) and electrons diffuse from n-side to p-side (n p). Thismotion of charge carries gives rise to diffusion current across the junction.When an electron diffuses from n p, it leaves behind an ioniseddonor on n-side. This ionised donor (positive charge) is immobile as it isbonded to the surrounding atoms. As the electrons continue to diffusefrom n p, a layer of positive charge (or positive space-charge region) onn-side of the junction is developed.Similarly, when a hole diffuses from p n due to the concentrationgradient, it leaves behind an ionised acceptor (negative charge) which isimmobile. As the holes continue to diffuse, a layer of negative charge (ornegative space-charge region) on the p-side of the junction is developed.This space-charge region on either side of the junction together is knownas depletion region as the electrons and holes taking part in the initialmovement across the junction depleted the region of itsfree charges (Fig. 14.10). The thickness of depletion regionis of the order of one-tenth of a micrometre. Due to thepositive space-ch

Semiconductor Electronics: Materials, Devices and Simple Circuits semiconductors. However , after 1990, a few semiconductor devices using organic semiconductors and semiconducting polymers have been developed signalling the birth of a futuristic technology of polymer-electronics and molecular-electronics. In this chapter, we will restrict

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