Zeolites as Scaffolds for Metal Nanoclusters

This chapter critically reviews the studies related to structural and photophysical properties of metal clusters within zeolites matrices and summarizes the progress made in understanding the host-guest interactions. The goal is to provide useful insight into the nature of such interactions and experiments used in identifying the excited state dynamics and the reaction mechanisms leading to the emitting species. Especially interesting are the combined experimental and computational approaches used to elucidate the structures and electronic transition of clusters inside the cavity. Although a number of excellent research articles have been published in the last years they only cover rather specific areas like organic photochemistry, confinement, charge transfer, theoretical modeling or photostimulated luminescence.

Organic photostimulated luminescence associated with persistent spin-correlated radical pairs

Photostimulated luminescence allows energy or data to be stored and released using electromagnetic waves as both the input and output, and has attracted considerable interest in the fields of biomedical and information technologies. However, this phenomenon is mostly limited to solid inorganic materials. Here, we report photostimulated luminescence from purely organic blend films, composed of electron donor, acceptor, and trap/emitter molecules. Charges in the films are accumulated as radical ions by ultraviolet light irradiation and then extracted by near-infrared light irradiation. Even after storage in the dark for one week they produce visible light with good repeatability, color tunability, and are responsive to weak external magnetic fields. These findings might broadly impact existing applications and provide new prospects for innovative flexible devices.

Multilevel Optical Data Storage in Eu2+/Ho3+ doped Ba2SiO4 Phosphor with Linear Mapping between Ultraviolet Excitation and Thermoluminescence/Photostimulated Luminescence Response

Persistent luminescence phosphors are regarded as one of the promising candidates for optical storage media. However, most optical storages using phosphors can only realize single-bit-data recording, limiting the storage capacity....

Organic Photostimulated Luminescence

Photostimulated luminescence, which allows energy or data to be stored and released using electromagnetic waves as both the input and output, has attracted considerable interest in the fields of biomedical and informatics technologies, but this phenomenon is mostly limited to solid inorganic materials. Here, we report photostimulated luminescence from purely organic blend films composed of electron donor, acceptor, and trap/emitter molecules. In the films, charges are accumulated as radical ions by ultraviolet light irradiation and then extracted by near infrared light irradiation to produce visible light. Films are capable of multiple cycles (>10 times) of organic photostimulated luminescence, which was still observable from films left in the dark at room temperature for one week after excitation, and emission color could be varied by changing the trap/emitter molecules. These findings will broadly impact existing applications and provide new prospects for innovative flexible devices.

Organic Photostimulated Luminescence

Photostimulated luminescence, which allows energy or data to be stored and released using electromagnetic waves as both the input and output, has attracted considerable interest in the fields of biomedical and informatics technologies, but this phenomenon is mostly limited to solid inorganic materials. Here, we report photostimulated luminescence from purely organic blend films composed of electron donor, acceptor, and trap/emitter molecules. In the films, charges are accumulated as radical ions by ultraviolet light irradiation and then extracted by near infrared light irradiation to produce visible light. Films are capable of multiple cycles (>10 times) of organic photostimulated luminescence, which was still observable from films left in the dark at room temperature for one week after excitation, and emission color could be varied by changing the trap/emitter molecules. These findings will broadly impact existing applications and provide new prospects for innovative flexible devices.