Photoexcited carrier relaxation and localization in Bi2Sr2Ca1yYyCu2O8 and YBa2Cu3O7δ: A study by femtosecond time-resolved spectroscopy

Abstract
Ultrafast time-resolved optical absorption has been measured as a function of doping and temperature in Bi2 Sr2 Ca1y Yy Cu2 O8 (0<y<1) and YBa2 Cu3 O7δ (0.06 <δ <1). A fast transient response is observed, which changes sign as a function of y in Bi2 Sr2 Ca1y Yy Cu2 O8 and δ in YBa2 Cu3 O7δ. Careful consideration of the possible mechanisms for the observed behavior leads us to suggest that two independent mechanisms are operating, whereby the two observed positive photoinduced absorption components are due to the electrodynamic response of photoinduced carriers, while the negative signal arises due to spectral hole burning. In the metallic samples a long-lived component is observed, which we suggest comes from photoinduced localized states intrinsic only to the superconducting species of the high-Tc materials. A very significant increase in the scattering rate at temperatures just above Tc signifies coupling to charge and possibly spin fluctuations just above Tc. A large reduction in scattering rate is observed below Tc, similar to that observed previously in YBa2 Cu3 O6.9 and Tl2 Ba2 CaCu2 O8. © 1996 The American Physical Society.