Determinants of the efficiency of photon upconversion by triplet–triplet annihilation in the solid state: zinc porphyrin derivatives in PVA. Issue 34 (22nd August 2017)

• Record Type: Journal Article
• Authors: Rautela, Ranjana; Joshi, Neeraj K.; Novakovic, Sacha; Wong, Wallace W. H.; White, Jonathan M.; Ghiggino, Kenneth P.; Paige, Matthew F.; Steer, Ronald P.
• Is Part Of: Physical chemistry chemical physics. Volume 19:Issue 34(2017)
• Page Start: 23471
• Page End: 23482
• Publication Date: 2017-08-22
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c7cp04746k
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Differences in efficiencies of photon upconversion are explained for a series of alkyl-substituted diphenyl and tetraphenyl zinc porphyrins. Abstract : Spectroscopic, photophysical and computational studies designed to expose and explain the differences in the efficiencies of non-coherent photon upconversion (NCPU) by triplet–triplet annihilation (TTA) have been carried out for a new series of alkyl-substituted diphenyl and tetraphenyl zinc porphyrins, both in fluid solution and in solid films. Systematic variations in the alkyl-substitution of the phenyl groups in both the di- and tetraphenyl porphyrins introduces small, but well-understood changes in their spectroscopic and photophysical properties and in their TTA efficiencies. In degassed toluene solution TTA occurs for all derivatives and produces the fluorescent S2 product states in all cases. In PVA matrices, however, none of the di-phenylporphyrins exhibit measurable NCPU whereas all the tetraphenyl-substituted compounds remain upconversion-active. In PVA the NCPU efficiencies of the zinc tetraphenylporphyrins vary significantly with their steric characteristics; the most sterically crowded tetraphenyl derivative exhibits the greatest efficiency. DFT-D computations have been undertaken and help reveal the sources of these differences.