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Platinum triplet exciton

Baldo et al. [ 164] used the platinum complex of 2,3,7,8,12,13,17,18-octaethyl-21 //,23//-porphine (PtOEP, 66) as efficient phosphorescent material. This complex absorbs at 530 nm and exhibits weak fluorescence at 580 nm but strong phosphorescence from the triplet state at 650 nm. Triplet transfer from a host like Alq3 was assumed to follow the Dexter mechanism. Dexter-type excitation transfer is a short-range process involving the exchange of electrons. In contrast to Forster transfer, triplet exciton transfer is allowed. [Pg.132]

Roberts ST, Schlenker CW, Barlier VS, McAnally RE, Zhang Y, Mastron JN, Thompson ME, Bradforth SE (2011) Observation of triplet exciton formation in a platinum sensitized organic photovoltaic device. J Phys Chem Lett 2 48... [Pg.206]

These approaches have been adopted more recently to incorporate phosphorescent chromophores into PF in order to make use of the fact that a large proportion (up to 75%) of all excitons formed in LEDs are triplet states, whose energy can only be harvested by using phosphorescent units. The first fluorene copolymers with phosphorescent units 34-35 were made by Holmes and coworkers who added monobrominated red- or green-emitting iridium complexes to an AA-BB Suzuki polycondensation [57]. With short fluorene chains, only emission from the iridium complexes are observed, but with longer fluorene chains some blue emission is also seen. Other groups have since incorporated different phosphorescent units such as platinum [58] or zinc salen [59] units or porphyrins [60,61 ]. [Pg.14]


See other pages where Platinum triplet exciton is mentioned: [Pg.421]    [Pg.542]    [Pg.312]    [Pg.417]    [Pg.138]    [Pg.250]    [Pg.318]    [Pg.341]    [Pg.142]    [Pg.741]    [Pg.382]    [Pg.386]    [Pg.314]    [Pg.11]    [Pg.311]    [Pg.71]    [Pg.71]    [Pg.263]   
See also in sourсe #XX -- [ Pg.437 ]




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