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The History of OLED

Blaze Display Technology Co., Ltd. | Updated: Nov 27, 2018

André Bernanose and co-workers at the Nancy-Université in France made the first observations of electroluminescence in organic materials in the early 1950s. They applied high alternating voltages in air to materials such as acridine orange, either deposited on or dissolved in cellulose or cellophane thin films. The proposed mechanism was either direct excitation of the dye molecules or excitation of electrons.

In 1960, Martin Pope and some of his co-workers at New York University developed ohmic dark-injecting electrode contacts to organic crystals. They further described the necessary energetic requirements (work functions) for hole and electron injecting electrode contacts. These contacts are the basis of charge injection in all modern OLED devices. Pope's group also first observed direct current (DC) electroluminescence under vacuum on a single pure crystal of anthracene and on anthracene crystals doped with tetracene in 1963 using a small area silver electrode at 400 volts. The proposed mechanism was field-accelerated electron excitation of molecular fluorescence.

Pope's group reported in 1965 that in the absence of an external electric field, the electroluminescence in anthracene crystals is caused by the recombination of a thermalized electron and hole, and that the conducting level of anthracene is higher in energy than the exciton energy level. Also in 1965, Wolfgang Helfrich and W. G. Schneider of the National Research Council in Canada produced double injection recombination electroluminescence for the first time in an anthracene single crystal using hole and electron injecting electrodes, the forerunner of modern double-injection devices. In the same year, Dow Chemical researchers patented a method of preparing electroluminescent cells using high-voltage (500–1500 V) AC-driven (100–3000 Hz) electrically insulated one millimetre thin layers of a melted phosphor consisting of ground anthracene powder, tetracene, and graphite powder. Their proposed mechanism involved electronic excitation at the contacts between the graphite particles and the anthracene molecules.

The first Polymer LED (PLED) to be created was by Roger Partridge at the National Physical Laboratory in the United Kingdom. It used a film of poly(N-vinylcarbazole) up to 2.2 micrometers thick located between two charge injecting electrodes. The light generated was readily visible in normal lighting conditions though the polymer used had 2 limitations; low conductivity and the difficulty of injecting electrons. Later development of conjugated polymers would allow others to largely eliminate these problems. His contribution has often been overlooked due to the secrecy NPL imposed on the project. When it was patented in 1974 it was given a deliberately obscure "catch all" name while the government's Department for Industry tried and failed to find industrial collaborators to fund further development. As a result publication was delayed until 1983.


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