In the version of this Article originally published, Liban M. A. Saleh was incorrectly listed as Liban A.
View Article and Find Full Text PDFWe control the chain conformation of a semiconducting polymer by encapsulating it within the aligned nanopores of a silica host. The confinement leads to polarized, low-threshold amplified spontaneous emission from the polymer chains. The polymer enters the porous silica film from only one face and the filling of the pores is therefore graded.
View Article and Find Full Text PDFWe study the photodetachment of electrons from sodium anions in room temperature liquid tetrahydrofuran (THF) using a new type of three-pulse pump-probe spectroscopy. Our experiments use two variably-time-delayed pulses for excitation in what is essentially a resonant 1+1 two-photon ionization: By varying the arrival time of the second excitation pulse, we can directly observe how solvent motions stabilize and trap the excited electron prior to electron detachment. Moreover, by varying the arrival times of the ionization (excitation) and probe pulses, we also can determine the fate of the photoionized electrons and the distance they are ejected from their parent Na atoms.
View Article and Find Full Text PDFThe scavenging of a solvated electron represents the simplest possible electron-transfer (ET) reaction. In this work, we show how a sequence of femtosecond laser pulses can be used to manipulate an ET reaction that has only electronic degrees of freedom: the scavenging of a solvated electron by a single atom in solution. Solvated electrons in tetrahydrofuran are created via photodetachment using the charge-transfer-to-solvent (CTTS) transition of sodide (Na(-)).
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