In this Progress Report we provide an update on recent developments in inkjet printing technology and its applications, which include organic thin-film transistors, light-emitting diodes, solar cells, conductive structures, memory devices, sensors, and biological/pharmaceutical tasks. Various classes of materials and device types are in turn examined and an opinion is offered about the nature of the progress that has been achieved.
Organic light-emitting devices (OLEDs) are a promising technology for flat-panel displays and solid-state lighting. While OLED efficiencies have increased dramatically in recent years, further progress is complicated by the fact that the vast majority of organic materials are fluorescent and therefore emit only from molecular excited states ('excitons') with spin 0, or 'singlet' spin symmetry. Here, we demonstrate the ability to manipulate the fraction of excitons which form as singlets in fluorescent materials by altering the OLED structure. We insert a mixing layer that affects only charge-transfer (CT) states, which are the precursors to excitons. As a result, we triple the singlet fraction and the efficiency of the red fluorophore DCM2. We term fluorescence enhanced by CT spin mixing 'extrafluorescence', and show that its origin is in part an inversion of the usual energetic ordering of the singlet and triplet CT states.
In this review, we survey several recent developments in printing of nanomaterials for contacts, transistors, sensors of various kinds, light-emitting diodes, solar cells, memory devices, and bone and organ implants. The commonly used nanomaterials are classified according to whether they are conductive, semiconducting/insulating or biological in nature. While many printing processes are covered, special attention is paid to inkjet printing and roll-to-roll printing in light of their complexity and popularity. In conclusion, we present our view of the future development of this field.
The performance of a phthalocyanine-based photovoltaic is boosted in the absorption gap between the phthalocyanine Q and Soret bands. Light absorption is decoupled from exciton diffusion using a light absorbing "antenna" layer external to the conventional charge generating layers. Radiation absorbed by the antenna is transferred into the charge generating layers via surface plasmon polaritons in an interfacial thin silver contact. The peak efficiency of energy transfer is measured to be at least ͑51± 10͒%.
The authors demonstrate that thin film organic photovoltaic cells are efficient detectors of surface plasmon polaritons ͑SPPs͒. For = 532 nm radiation in a Kretschmann configuration, the external quantum efficiency in fullerene-copper phthalocyanine photovoltaic cells is doubled at resonance to 12%. In thin heterojunction organic photovoltaics, SPP detection relies on a substantial increase in absorption when the incoming radiation is coupled to guided SPPs rather than unguided photons. SPP scattering and nonradiative losses are negligible; however, optical modeling shows that cathode metal penetration into the neighboring organic semiconductor is a major source of loss for SPP or photonic excitation.
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