CHEM01200604009 Sreejith Kaniyankandy - Homi Bhabha ...

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53 eliminated by use of standard which is generally a single crystal and has peak near that particular 2 value. The broadening is calculated as given below. (2.6) 2 2 2 D I Here D arises from domain size and L arises from instrumental factors. As mentioned earlier this is a crude method for estimating size as broadening can also arise from stress in the sample. Therefore D is also a function of stress and samples are assumed to be spherical. 2.4. 2. Instrumentation Figure 2.1 shows a schematic of XRD instrument. The first step is creation X-Rays which is accomplished by bombarding high energy electrons on a metal target. By this process, apart from broad distribution of X-rays created due to deceleration on electrons also called Bremsstrahlen, sharp lines are also created which are superimposed on the broad distribution. These sharp lines arise from characteristic X-ray coming from knocking down of core electrons creating a “hole” and subsequent filling of higher electrons. Performing a diffraction experiment requires intense sharp X-ray as the diffraction angle is also dependent on x-ray energies; therefore a broad distribution is ineffective for performing diffraction. The mainly used targets in a set up are metals like copper, molybdenum, chromium etc. The filtering of broad distribution is accomplished by using a filter which has a 1 unit atomic number less than the target material. The resultant beam is further monochromatised by using a single crystal monochromator. In a PXRD, the samples in powdered form are spread over an amorphous substrate (generally glass slides) in presence of a binder like colloidion in amyl alcohol. The detectors are generally scintillation counters. The detector is scanned over
54 different angles and intensities are plotted with respect to angles. The peak position observed are angle where Bragg condition is satisfied. In the present thesis, we have used a Philips X-ray machine, model-PW 1710 with Ni filtered Cu Kα radiation (λ=1.5406Å), using silicon as an external standard. The measurements are performed in a range of 10˚-80˚ in a continuous scan mode, with a step width of 0.02˚, and scan of 1˚ per minute. The measurement of corresponding to each peak position and peak intensity is important for identification of materials. The measured data is compared with database of standards samples with the help of JCPDS-ICDD (Joint Committee on Powder Diffraction Standards-International Centre for Diffraction Data) [2.8]. Figure. 2. 1. Schematic of a typical XRD instrument 2.5. Raman Spectroscopy Raman spectroscopy is a technique complementary to infrared spectroscopy. Raman spectroscopy is used to study mainly vibrational modes in a system [2.9]. Since vibrational peaks positions are fingerprints of a molecular species it can help in characterization of a
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Charge Transfer Dynamics in Quantum
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DECLARATION I, hereby declare that
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ACKNOWLEDGEMENTS It is my privilege
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1.3.5. Defect Mediated Relaxation 2
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2. 8. 4. White Light Generation- 45
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6.2. Experimental 6.2.1.Synthesis o
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devices based on QDs it has been sh
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Furthermore generation of pump (~40
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shell). This clearly indicated that
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12. V. I. Klimov, J. Phys. Chem. B,
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1.13 Reactant and Product Potential
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light. Inset: Kinetic traces monito
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6.5 Transient decay kinetics of gra
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at 670 nm after exciting at 400 nm
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ABBREVIATIONS BET BQ CB CCD CdS CdT
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1 Chapter 1
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3 size dependent optical properties
Page 44 and 45: 5 1.2. Physics of Semiconductors 1.
Page 46 and 47: 7 As seen from the schematic, poten
Page 48 and 49: 9 Substituting this in Schrödinger
Page 50 and 51: 11 ( r, r ) ( r ) ( r ) (1.13) e
Page 52 and 53: 13 E E E 2 2 2 EX ne, le nh,
Page 54 and 55: 15 spherical symmetry of field. The
Page 56 and 57: 17 gE ( ) 2Em 2 3 3 (1.25) For a
Page 58 and 59: 19 1.3.2. Electron-Hole energy tran
Page 60 and 61: 21 Impact Ionization Figure 1.7. Sc
Page 62 and 63: 23 understanding on mechanistic asp
Page 64 and 65: 25 carriers are unable to sample th
Page 66 and 67: 27 CB VB QD Metal Figure. 1. 10. Sc
Page 68 and 69: 29 energy barrier. Therefore it is
Page 70 and 71: 31 1 f q 2 A qB (1.30) 2 In equa
Page 72 and 73: 33 Vibrational contribution can be
Page 74 and 75: 35 1. 7. 1. Electron Injection ET i
Page 76 and 77: 37 Under assumption of invariance o
Page 78 and 79: 39 distribution. To achieve good si
Page 80 and 81: 41 initially achieved monodispersit
Page 82 and 83: 43 and rate of charge transfer acro
Page 84 and 85: 45 1.32 P. V. Kamat, J. Phys. Chem.
Page 87: 47 Chapter 2
Page 90 and 91: 49 chemical species. Since a partic
Page 92 and 93: 51 fluorescence forms an important
Page 96 and 97: 55 sample. Raman spectroscopy is ba
Page 98 and 99: 57 will appear bright and region wi
Page 100 and 101: 59 volatile solvent is drop casted
Page 102 and 103: 61 spots arise from diffraction fro
Page 104 and 105: 63 The electrical signal is then ch
Page 106 and 107: 65 delayed and inverted. The two si
Page 108 and 109: 67 Pump-probe technique is one of t
Page 110 and 111: 69 Amplifier Jade Stretcher fs Osci
Page 112 and 113: 71 Figure 2.6. Optical layout of Ti
Page 114 and 115: 73 Grating Convex Mirror Concave Mi
Page 116 and 117: 75 changes the polarization from ho
Page 118 and 119: 77 Grating Output Input Mirror Grat
Page 120 and 121: 79 μJ has a very high peak power.
Page 122 and 123: 81 2.6. Dynamical Theory of X-Ray D
Page 125: 83 Chapter 3
Page 128 and 129: 85 Therefore the study of interfaci
Page 130 and 131: 87 3. 2. Experimental Section 3.2.1
Page 132 and 133: 89 and intensity show absence of ot
Page 134 and 135: 91 which is also neutral; therefore
Page 136 and 137: 93 electron transfer times. This re
Page 138 and 139: 95 r B a * 0 3.1 me / me Now the
Page 140 and 141: 97 nonadiabatic case the electron t
Page 142 and 143: 99 drastically reduced leading to a
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101 While the study of injection dy
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103 study. Based on the injection d
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105 17. L. E. Brus, J. Phys. Chem.
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107 Chapter 4
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109 of the QDs. As a result surface
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111 4.2.2. Synthesis: The CdTe QDs
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113 lower hole state. In CdSe the l
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115 4.2 inset. The kinetic traces a
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117 growth of the bleach kinetics (
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119 previous section we have discus
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121 lived charge transfer complex w
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123 100 times concentration of the
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125 4.5. References 4.1. Efros, Al.
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127 Chapter 5
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129 been made in the synthesis of t
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131 metallic synthesis by arrested
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133 5.3. Result and discussion: 5.3
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135 indicating a confinement induce
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137 absorption studies that on form
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139 1000 c b PL Intensity 100 10 a
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141 samples due to a very weak exci
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143 dynamical spectrum is negligibl
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145 Earlier authors [5.4] reported
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147 Sample t r(ps) t 1(ps) t 2(ps)
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149 In addition to the cooling dyna
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151 pulse-width time scale followed
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153 5.20. Sreejith Kaniyankandy, Sa
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155 CHAPTER 6 Charge Separation in
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157 Studies by Wang et. al. [6.15]
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159 graphene in a 1M NaOH solution.
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161 Intensity (a.u.) 5 4 3 2 1 CdTe
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163 dynamics of graphene oxide and
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165 GO as shown in the Figure 3 rev
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167 electron acceptor for Graphene.
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169 governs the recombination dynam
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171 Sample τ 1 (ps) τ 2 (ps) τ 3
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173 A (mO.D) 10.0 0.0 -10.0 -20.0 0
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175 involved in the relaxation may
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177 Electron quencher (benzoquinone
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179 Scheme 6.1. Schematic of Electr
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181 6.6. Reina, A.; Jia, X.; Ho, J.
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183 6.26. Kaiser, A. B.; Navarro, C
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185 assigned to injection into diff
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187 transfer from CdSe core to ZnTe
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189 However the position of bands i
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