2009
DOI: 10.1063/1.3125244
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Transient absorption and higher-order nonlinearities in silver nanoplatelets

Abstract: We show that the imaginary parts of higher-order optical nonlinearities and their decay times can be determined by a time-intensity domain analysis of the conventional transient absorption data. Using this method we have measured the values and decay times of third, fifth and seventh-order nonlinear susceptibilities of silver nanoplatelets in water. The origin of these higher-order nonlinearities is explained using a two-temperature model.

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Cited by 19 publications
(15 citation statements)
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“…Since the measurement of third-, fifth-, and seventh-order nonlinearities of silver nanoplatelet colloids using a femtosecond laser [26], an extension of nonlinear Schrödinger equation including the cubic-quintic-septic nonlinearity was used to model the propagation of spatial solitons. In [27], for example, the authors performed numerical calculations based on higher-order nonlinearity parameters including seventh-order susceptibility χ 7 ðÞ (a chalcogenide glass is an example).…”
Section: Introductionmentioning
confidence: 99%
“…Since the measurement of third-, fifth-, and seventh-order nonlinearities of silver nanoplatelet colloids using a femtosecond laser [26], an extension of nonlinear Schrödinger equation including the cubic-quintic-septic nonlinearity was used to model the propagation of spatial solitons. In [27], for example, the authors performed numerical calculations based on higher-order nonlinearity parameters including seventh-order susceptibility χ 7 ðÞ (a chalcogenide glass is an example).…”
Section: Introductionmentioning
confidence: 99%
“…Such variations can lead to deviation in the measurement of the true optical response of the sample. Further, in many samples the decay time also depends on the excited carrier density and hence the pump power [21][22][23]. In such cases averaging over large number of data with larger deviation in pump power would result in a wrong estimation for the response time.…”
Section: Introductionmentioning
confidence: 99%
“…When the sample is excited by the pump pulse its optical response changes. For sufficiently small excitation conditions, the change in the absorption coefficient will be proportional to the third-order nonlinear absorption coefficient [2,22]. Consider an instantaneously responding sample having a relaxation time much longer than the pulse width, the absorption coefficient after excitation by the pump pulse can be written as,…”
Section: Introductionmentioning
confidence: 99%
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“…[13][14][15] Such transient measurements can throw some light on the origin and time response of the optical nonlinearity. In pump-probe experiments on silver nanoplatelet water colloids, the nonlinear response was observed to peak a few hundred fs after the peak of the 100 fs excitation pulse.…”
Section: Introductionmentioning
confidence: 99%