Enhancing the sensitization efficiency of erbium doped organic complexes by heavy halogen substitution

J. X. Hu, S. Karamshuk, J. Gorbaciova, H. Q. Ye, H. Lu, Y. P. Zhang, Y. X. Zheng, X. Liang, M. Motevalli, I. Abrahams, I. Hernández, P. B. Wyatt, W. P. Gillin

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Abstract

Lanthanide complexes with organic ligands have been of interest due to the possibility of sensitising lanthanide ions through the antenna effect. We have recently shown that the zinc(ii) salt of 2-(3,4,5,6-tetrafluoro-2-hydroxyphenyl)-4,5,6,7-tetrafluorobenzothiazole, Zn(FBTZ)2, can provide very high levels of sensitisation to organic erbium complexes whilst maintaining very high quantum yields for the erbium near-infra-red luminescence. We now report the spectroscopic properties of the zinc(ii) salts of 2-(3,4,5,6-tetrafluoro-2-hydroxyphenyl)-6-chloro-4,5,7-trifluorobenzothiazole and 2-(3,4,5,6-tetrafluoro-2-hydroxyphenyl)-6-bromo-4,5,7-trifluorobenzothiazole. The substitution of a single chlorine atom into the chromophore is sufficient to double the sensitisation efficiency compared to the fully fluorinated chromophore. This result implies a 50% reduction in the pump intensity needed to achieve population inversion in the erbium ions.

Original languageEnglish
Pages (from-to)7012-7017
Number of pages6
JournalJournal of Materials Chemistry C
Volume6
Issue number26
DOIs
StatePublished - 2018
Externally publishedYes

Funding

J. X. H., H. Q. Y., H. L. and Y. P. Z. were financially supported by the China Scholarship Council and Queen Mary University of London (QMUL). S. K. was supported by a Proof of Concept grant funded by QMUL and the EPSRC through the Silicon Photonics for Future Systems grant EP/L00044X. J. G. was financially supported by QMUL. I. H. acknowledges financial support from the Spanish Ministerio de Economia y Competi-tividad (Grant: MAT2016-80438-P). Y. Z. acknowledges financial support from the Major State Basic Research Development Program (2013CB922101) and NSFC (21371093). W. P. G. acknowledges financial support from EPSRC (EP/L020114/1 and EP/P007767/1) and from NSFC (61574095). We are grateful to the EPSRC UK National Mass Spectrometry Facility at Swansea University for spectra.

FundersFunder number
Spanish Ministerio de Economia y Competi-tividadMAT2016-80438-P
Queen Mary University of London
Engineering and Physical Sciences Research CouncilEP/L00044X, EP/L020114/1, EP/P007767/1
National Natural Science Foundation of China61574095, 21371093
China Scholarship Council
Major State Basic Research Development Program of China2013CB922101

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