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Figure 17 High-resolution TEMs of CdSe tetrapods. (a) Image down the [001]direction of one of the four arms. All arms are wurtzite phase, as confirmed byanalysis of lattice spacings. (b) ‘‘Dendritic’’ tetrapod, where branches have grownfrom each arm. Some stacking faults are present in the branches, and zinc-blendelayers are present at the ends of the original four arms. (From Ref. 38, reprintedwith permission.)particles, and synthetic steps unique to rod overcoating have been employedin the most successful preparations [40]. As discussed previously (Sect. III),spherical nanoparticle systems benefit from having highly curved surfaces,compared to less strain-tolerant planar systems. Nanorods provide anintermediate case. The average curvature of rods lies between that of dotsand films, and, due to their larger size/surface area compared to dots, moreinterfacial strain can accumulate, leading to the formation of dislocations.The 12% lattice mismatch between ZnS and CdSe is, therefore, less welltolerated in rods. CdS can be used as a lattice-mismatch ‘‘buffer layer’’between CdSe and ZnS (only f4% lattice mismatch with CdSe and f8%with ZnS). The addition of a small amount of Cd precursor to the shellprecursor solution (Cd : Zn of 0.12 : 1.0) appears to lead to the preferentialformation of CdS at the surface of the rods. ZnS growth then proceeds on theCdS. High-resolution TEM images demonstrate uniform and epitaxialgrowth. Interestingly, QYs remain low, and the benefits of inorganic overcoatingin the graded epitaxial approach are only fully realized followingphotochemical annealing (via laser irradiation) of the rod particles (Fig. 18)[40].Solution-phase preparations of unusually shaped and highly anisotropicparticles that are soluble, relatively monodisperse, and sufficientlysmall to exhibit quantum-confinement effects are thus far limited, but notexclusive to CdSe. CdS and CdTe rods can be prepared using phosphonic-Copyright 2004 by Marcel Dekker, Inc. All Rights Reserved.
Figure 18 Absorption (solid line) and PL (dashed line) spectra for medium-length(3.3 21 nm) CdSe nanorods; (a) core nanorods without ZnS shell; (b) (core)shellnanorods with thin CdS–ZnS shells (f2 monolayers of shell material, where the CdS‘‘buffer’’ shell comprises f35% of the total shell); (c) (core)shell nanorods withmedium CdS–ZnS shells (f4.5 monolayers of shell material, where the CdS ‘‘buffer’’shell comprises f22% of the total shell). PL spectra were recorded followingphotoannealing of the samples. (From Ref. 40 reprinted with permission.)acid-controlled reactions. In addition, CdS rods and multipods can beprepared in a monosurfactant system in which hexadecylamine (HDA) servesboth as the stabilizing ligand and as the shape-determining ligand [41]. Here,rod and multipod formation is temperature dependent. Rods form at hightemperatures (f300jC), whereas bipods, tripods, and tetrapods dominate atlower temperature (120–180jC). The dependence of shape on temperaturelikely results from preferential formation of wurtzite CdS nuclei (thermodynamicphase) at high temperatures and zinc-blende nuclei (kinetic phase) atlower temperatures. As in the CdSe system, the zinc-blende {111} faces cansupport fast growth of (001 ) wurtzite ‘‘arms.’’ Significantly, this methodCopyright 2004 by Marcel Dekker, Inc. All Rights Reserved.
Page 1: Copyright 2004 by Marcel Dekker, In
Page 4 and 5: Copyright 2004 by Marcel Dekker, In
Page 6 and 7: Copyright 2004 by Marcel Dekker, In
Page 8 and 9: This book covers several topics of
Page 10 and 11: esult, some exciting topics were no
Page 12 and 13: 3. Fine Structure and Polarization
Page 14 and 15: 9. III-V Quantum Dots and Quantum D
Page 16 and 17: ContributorsUri BaninThe Hebrew Uni
Page 18 and 19: 1‘‘Soft’’ Chemical Synthesi
Page 20 and 21: structure of energy states leads to
Page 22 and 23: growth can proceed by Ostwald ripen
Page 24 and 25: Figure 3 Transmission electron micr
Page 26 and 27: Figure 4 Temporal evolution of the
Page 28 and 29: No. 26, are f85% (Fig. 6) [21]. Alt
Page 30 and 31: tion spectra and broad PL spectra.
Page 32 and 33: ing surface-to-volume ratio with di
Page 34 and 35: Figure 8 Photoluminescence spectra
Page 36 and 37: lattice mismatch. Such a large latt
Page 38 and 39: match between InAs and ZnS of f11%.
Page 40 and 41: successfully repeated for up to thr
Page 42 and 43: Under a different growth regime, on
Page 44 and 45: Figure 14 Atomic model of the CdSe
Page 46 and 47: ‘‘Teardrop-shaped’’ particl
Page 50 and 51: allows isolation of tetrapods in f8
Page 52 and 53: ligand concentrations yield a reduc
Page 54 and 55: een determined and quantitatively c
Page 56 and 57: tion volumes were also shown to be
Page 58 and 59: synthesis temperatures of z400jC ar
Page 60 and 61: Figure 23 (a) Photoluminescence spe
Page 62 and 63: levels (fV1 Mn per NQD). Despite in
Page 64 and 65: Figure 25 X-ray diffraction pattern
Page 66 and 67: Figure 27 Transmission electron mic
Page 68 and 69: An additional factor that strongly
Page 70 and 71: Figure 30 (a,b) Schematics illustra
Page 72 and 73: Slow, controlled precipitation of h
Page 74 and 75: Figure 34 Schematic illustrating th
Page 76 and 77: Figure 36 Transmission electron mic
Page 78 and 79: achieving biological compatibility
Page 80 and 81: 47. Yu H.; Gibbons P.C.; Kelton K.F
Page 82 and 83: 2Electronic Structure inSemiconduct
Page 84 and 85: Figure 2 (a) Simple model of a nano
Page 88 and 89: electron and hole to be treated as
Page 90 and 91: independently, Eq. (13) is commonly
Page 92: a better description of the bulk ba
Page 95 and 96: investigated. For optical experimen
Page 97 and 98: Figure 4 (a) Absorption (solid line
Page 99 and 100:
Figure 6 Normalized PLE scans for s
Page 101 and 102:
Figure 8 A simplistic model for des
Page 103 and 104:
Figure 10 Theoretically predicted p
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Figure 12 Schematics depicting the
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Figure 14 Calculated band-edge exci
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Figure 15 Absorption (solid line) a
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Figure 18 (a) Calculated band-edge
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IV.BEYOND CdSeA. Indium Arsenide Na
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the six-band Luttinger Hamiltonian.
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11. Norris, D.J.; Efros, Al.L.; Ros
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69. Gaponenko, S.V.; Woggon, U.; Sa
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formation of a long-lived dark exci
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where the constant A is determined
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In crystals for which the function
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The respective wave functions areC
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passive, as was shown in Ref. 12. T
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square of the matrix element of the
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where e F = e F ieV and e F F = e x
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see that for all nanocrystal shapes
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optical recombination of the excito
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B. Recombination of the Dark Excito
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where x = cos h and f = l B g e H/3
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The theory of the polarization memo
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Figure 7 The size dependence of the
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state would have an infinite lifeti
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crystal axis [see Eq. (40)]. As a r
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time of the exciton momentum relaxa
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One must also account for the influ
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observed in one of the first studie
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REFERENCES1. Bawendi, M.G.; Wilson,
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4Intraband Spectroscopyand Dynamics
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The solid line in Fig. 1 shows the
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Figure 2 FTIR spectra of n-type CdS
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of the center frequency. The experi
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limit given by radiative relaxation
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from a long lifetime due to the pho
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are two natural approaches to study
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32. Inoshita, T.; Sakaki, H. Physic
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continuous spectral tunability over
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function and envelope function mome
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ottleneck’’ [14,28]. Further re
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in NQDs is dominated by nonphonon e
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Figure 4 Dynamics of the IR postpum
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Figure 5 (a) Time-resolved PL spect
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Figure 6 (a) The time delay of the
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and due to Auger-type e-h interacti
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Figure 9 Dynamics of the 1S bleachi
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significantly greater than the fast
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Figure 11 (a) Pump-intensity-depend
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NQD size. For small NQD sizes (R =
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Figure 14 Nonlinear absorption/gain
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sorption change associated with a s
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where n h em is the hole ‘‘emit
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ultrafast (subpicosecond to picosec
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Figure 18 Schematic of transitions
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Figure 19 Dynamics of pump-induced
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where n i (i=1, 2 . . . , N ) is th
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Figure 21 (a) Two-e-h-pair (biexcit
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the volume fraction (filling factor
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intensity dependence of this peak (
Page 219 and 220:
Copyright 2004 by Marcel Dekker, In
Page 221 and 222:
can contribute to the saturation of
Page 223 and 224:
Page 225 and 226:
coupling between ‘‘volume’’
Page 227 and 228:
numerous discussions on the photoph
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53. Kang, K.; Kepner, A.; Gaponenko
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the ‘‘on-off ’’ emission in
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parallel form of data acquisition i
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Figure 3 (a) Spectral time trace of
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transition energies. In fact, these
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distribution (dark line) does not d
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exposure to only room light. In our
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statistics for the off times are in
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230Shimizu and BawendiCopyright 200
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Figure 10 (a) Time trace of a CdSe(
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and excited QD core states to fluct
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arrows indicate the on-time truncat
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W. K. Woo and V. C. Sundar for assi
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size allows the electron affinity a
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II.THEORY OF ELECTRON TRANSFER BETW
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For the specific case of charge tra
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dominates, the mobility is often fi
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where the constant A and the temper
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components of modulation which are
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nanocrystals [41], understanding ph
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and ionization potential through tw
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quantum dots. Furthermore, because
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For many applications, a host mater
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form blends with morphologies that
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Figure 11 Photoluminescence efficie
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Figure 12 (a) Room-temperature PIA
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discussed briefly in Section IV. Ch
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dithiolates to thiol-terminated DNA
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Films of passivated CdSe nanocrysta
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Figure 16 Photocurrent action spect
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decay with stretched exponential ki
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siderably larger than might be esti
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dispersing CdSe nanocrystal chromop
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memory and charge storage effects [
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all) of the optically excited elect
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composites of nanocrystals and conj
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55. Asbury, J.B.; Hao, E.C.; Wang,
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108. Morgan, N.Y.; Leatherdale, C.A
Page 305 and 306:
The approaches to fabrication of se
Page 307 and 308:
Figure 1 Experimental realization o
Page 309 and 310:
Due to this voltage division, the m
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Figure 3 Simulated tunneling spectr
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electron charging. In both positive
Page 315 and 316:
Figure 5 shows the typical features
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Figure 7 Map of levels for InAs nan
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Figure 8 Scanning electron microsco
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D CB = 0.31 eV is thus obtained. On
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Figure 11 Correlation of optical an
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atomistic approach based on pseudop
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charging indicated that the tunneli
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capacitance values were also kept t
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could not be detected in the QD/DT/
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Figure 18 Tunneling conductanceF sp
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data in the inset of Fig. 19 repres
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corresponding to the s-like wave fu
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7. Grabert, H.; Devoret, M.H., Eds.
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66. Su, B.; Goldman, V.J.; Cunningh
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dimensional confinement are created
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Figure 1 Transmission electron micr
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The room-temperature absorption and
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narrower in samples with larger mea
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GaInP 2 QDs from a plot of the squa
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crystal, indicating lattice-matched
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Figure 5 Evolution of Stranski-Kras
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Figure 7 Photoluminescence spectra
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Figure 8 Photoluminescence spectra
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C. Efficient Anti-Stokes Photolumin
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Because HF treatment has been shown
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intensity of the PL when it is on a
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eV stems from recombining carriers
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Figure 16 Model to explain two-colo
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although this term is not rigorousl
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10 ps (about an order of magnitude
Page 377 and 378:
electron relaxation is inhibited an
Page 379 and 380:
Figure 18 Transmission electron mic
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QDs, the nature of the QD capping s
Page 383 and 384:
QD solution. For an interdot distan
Page 385 and 386:
emission spectra of the two individ
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Figure 23 Change of the PL intensit
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(viz. the absorbed light intensity)
Page 391 and 392:
Figure 25Impact ionization in QDs.m
Page 393 and 394:
prevent electron-hole recombination
Page 395 and 396:
36. Miller, R.D.J.; McLendon, G.; N
Page 397 and 398:
91. Vurgaftman, I.; Singh, J. Appl.
Page 399 and 400:
139. Mićić, O.I.; Ahrenkiel, S.P.
Page 401 and 402:
10Synthesis and Fabrication of Meta
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Figure 2 (A-C) Progression of HR-TE
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Figure 3 Schematic for gold nanocry
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Nanocrystal growth can occur by two
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on the other hand, provide an ensem
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Figure 6 (a) SAXS patterns for disp
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Figure 8 The gold nanocrystal film
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of the stabilizing ligand, and the
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successfully modeled the 2D island
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2. Steric Stabilization and a Soft
Page 421 and 422:
are fully extended. Moving away fro
Page 423 and 424:
Figure 11 High-resolution SEM image
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Figure 13 (A) Transmission electron
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function of the density of localize
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Figure 15 High-resolution SEM image
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thiol-capped nanocrystals [2]. The
Page 433 and 434:
41. Ackerson, B.J. Nature 1993, 365
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with the effect of the particle com
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Figure 1a shows the surface plasmon
Page 439 and 440:
Figure 2 (a) Ultraviolet-visible ab
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agents [34]. The short-wavelength b
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Figure 4 (a) Plot of the plasmon ab
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the framework of traditional Mie’
Page 447 and 448:
show that effects due to the surrou
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is located at the position of the g
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Figure 8 Ultraviolet-visible absorp
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laser pulses while being mixed in t
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Figure 10 shows HR-TEM images of go
Page 459 and 460:
Figure 11 Transmission electron mic
Page 461 and 462:
final irradiation product. At the s
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following the laser excitation appe
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36. Papavassiliou, G.C. Prog. Solid
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particles to expand. Because the he
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was frequency doubled in a 1-mm B-
Page 471 and 472:
Figure 2 Frequency of the acoustic
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Figure 3 Change in radius (DR/R) ve
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In this model, the electrons couple
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Figure 5 Transient bleach data for
Page 479 and 480:
Figure 7 (a) Transient bleach data
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that the particles with >80% Au hav
Page 483 and 484:
3. Del Fatti, N.; Valle´e, F.; Fly
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