Block copolymers P(MA4-block -MMA)10 and P(MA4- block -MMA)20 and a random copolymer P(MA4-ran-MMA)10 were prepared from azobenzene methacrylate (MA4) and methyl methacrylate (MMA). The former monomer was introduced as both a photoresponsive and a mesogenic component, and the latter as a transparent non-mesogenic component. Thin films of the copolymers were used to investigate all-optical writing by linear-polarized illumination in the pulsed regime to modify the local birefringence at the microscopic scale. The optical properties of P(MA4- block -MMA)10 were compared with those of P(MA4- ran-MMA)10 having the same chemical composition (10 mol% MA4) but different distributions of the two components. It was found that in the block copolymers relatively intense pulses as short as 100 ms produced a remarkable local increase in the birefringence, stable in the time-scale (up to several days) explored in the experiment. In contrast, efficient and stable optical modifications could not be achieved in the random copolymer.
All-optical pulsed writing in azobenzene copolymer films in the sub-millisecond regime
GALLI, GIANCARLO;FUSO, FRANCESCO;ALLEGRINI, MARIA
2012-01-01
Abstract
Block copolymers P(MA4-block -MMA)10 and P(MA4- block -MMA)20 and a random copolymer P(MA4-ran-MMA)10 were prepared from azobenzene methacrylate (MA4) and methyl methacrylate (MMA). The former monomer was introduced as both a photoresponsive and a mesogenic component, and the latter as a transparent non-mesogenic component. Thin films of the copolymers were used to investigate all-optical writing by linear-polarized illumination in the pulsed regime to modify the local birefringence at the microscopic scale. The optical properties of P(MA4- block -MMA)10 were compared with those of P(MA4- ran-MMA)10 having the same chemical composition (10 mol% MA4) but different distributions of the two components. It was found that in the block copolymers relatively intense pulses as short as 100 ms produced a remarkable local increase in the birefringence, stable in the time-scale (up to several days) explored in the experiment. In contrast, efficient and stable optical modifications could not be achieved in the random copolymer.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.