The paper summarizes the current understanding of laserinduced damage in polymeric material systems. A detailed literature review including macroscopic and microscopic models for high optical intensity induced degradation and damage of polymeric systems is given. This is followed with experimental results and discussion on degradation of two different commonly used polymeric systems (acrylic and epoxy) due to exposure to medium optical intensity infrared light. We show that in acrylic systems, degradation occurs slowly over time at infrared wavelengths as high as 1480nm and optical power densities as low as 5X104 W/cm2. In this syaem degradation occurs via a multi-photon absorption pro:ess. In cases where no catastrophic damage occurs, it is possible to completely and repeatedly anneal out any optically induced changes in the acrylic systems. The recovery process for these systems oc&-s via a 1.7 eV process. Moisture appears to accelerate !the degradation rate in these systems. We show that in bisphenol based epoxy systems (bisphenol baxd epoxies are widely used as structural adhesives in many opt1 cal devices), degradation also occurs via a multi-photon absorption process. In all cases, degradation in the bisphenol sysl ems was catastrophic. The time dependent degradation data for this epoxy system indicates that a three-photon absorption process is responsible for degradation in these epoxies. Therefore, the degradation process is very sensitive to both wavelength and optical power density. We did not observe degradation after hundreds of hours of exposure to optical power densities as high at 6MW/cm2 at 1480nm between 25C and 175C in this material system. Degradation was observed in less than 10 hours when the material was exposed to 6MW/cm2 optical power at 1060nm at room temperature. We find the degradation is thermally accelerated with an effective activation energy of > 0.5eV. Finally, we give preliminary design guidelines for the use of bisphenolbased epoxies in high optical power density applications.
I IintroductionMany polymeric systems exhibit good transparency in the near infrared region of the electromagnetic spectrum that is of greiit importance in the telecommunications and data communication industry, approximately 800nm to 1650nm. Typical hydrocarbon based systems have a linear absorption betmeen 1 and 4dB/cm in the 1000nm-1600nm region of the electromagnetic spectrum. This absorption is primarily due to C-E[ stretching (v -1720 nm) and stretching and deformation overtones (v -1350-1500 nm) and 0-H stretching overtones (v .-+ 1430 nm).' Because these materials have losses that are greater than ldB/cm in this region of the spectrum, they are not readily used to transmit light over long distances in the wat elength region. However, in many applications these mat1:rials are used in thin joint configurations, where the joint I thickness is less than 100 pm (typically the actual joint thickness is 10-30 pm). In this configuration the loss per joint is less than 0.04dE3 (4% signal loss). In addition, ...