Abstract

Organic lasers came into existence via the introduction of the pulsed optically-pumped liquid organic dye laser by Sorokin and Lankard (1966) and Schafer et al. (1966). An additional momentous contribution was the discovery of the continuous wave (CW) liquid organic dye laser by Peterson et al. (1970) which opened the way for the development of narrow-linewidth tunability in the CW regime plus the eventual introduction of femtosecond lasers (see, for example, Dietel et al. (1983) and Diels, (1990)). The narrowlinewidth tunable pulsed dye laser was demonstrated by Hansch (1972) and improved by Shoshan et al. (1977), Littman and Metcalf (1978), Duarte and Piper (1980, 1981). All these developments in practical organic tunable lasers, spanning the visible spectrum, “created a renaissance in diverse applied fields such as medicine, remote sensing, isotope separation, spectroscopy, photochemistry, and other analytical tasks” (Duarte et al. (1992)). An early development, in the field of tunable lasers, was also the discovery of solid-state pulsed optically-pumped organic dye lasers by Soffer and McFarland (1967) and Peterson and Snavely (1968). However, it was not until the 1990s that, due to improvements in the dye-doped polymer gain media, this class of lasers would again be the focus of research attention (see, for example, Duarte (1994), Maslyukov et al. (1995), Costela et al. (2003)). An additional effort in optically-pumped tunable laser research is the work on organic semiconductor lasers based on thin-film conjugated polymers (see, for example, Holzer et al. (2002)). All this activity has been conducted on optically-pumped organic lasers although researchers from the onset have also been interested on the direct electronic excitation of tunable organic lasers (Steyer and Schafer, 1974; Marowsky et al., 1976). Some recent reviews mentioning efforts towards realizing coherent emission from direct electrical excitation of organic semiconductors, include Kranzelbinder and Leising (2000), Baldo et al. (2002), Samuel and Turnbull (2007), and Karnutsch (2007). Most of these reviews give ample attention to conjugated polymer gain media. In this chapter, experimental results demonstrating coherent emission from electricallyexcited pulsed dye-doped organic semiconductors, in microcavity configurations, are reviewed. The reported emission is single-transverse-mode, and given the 300 nm cavity length, also single-longitudinal mode. In the spectral domain the emission is indistinguishable

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