Abstract
We take advantage of the dual emission properties of up-conversion fluorescence (UCF) and second harmonic generation (SHG) in Er3+-doped perovskite Na0.95Er0.05Nb0.9Ti0.1O3 to fully temporally characterize the ultrashort laser pulse that excites Er3+-ion fluorescence. The chirped pulses from a broadband Ti:Sa oscillator are temporally characterized using the dispersion scan (d-scan) technique by using the SHG signal in the host perovskite at the same point where UCF is being produced by the same pulse. The pulse durations obtained range from ~45 fs to ~8 fs and positive and negative spectral phases are unambiguously identified. The temporal characterization is compared using a standard non-linear crystal and perfect agreement is obtained. These results show that it is possible to temporally characterize in-situ ultrashort laser pulses while they are inducing a UCF process, as long as the host generates second-harmonic signal.
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