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Iridium motif linked porphyrins for efficient light-driven hydrogen evolution via triplet state stabilization of porphyrin
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Indexed by:Journal Papers

Date of Publication:2020-02-14

Journal:JOURNAL OF MATERIALS CHEMISTRY A

Included Journals:EI、SCIE

Volume:8

Issue:6

Page Number:3005-3010

ISSN No.:2050-7488

Abstract:Two new iridium motif linked porphyrins, MBPyZnP-Ir and TBPyZnP-Ir are developed for photocatalytic hydrogen evolution (PHE). The tetra-iridium linked one, TBPyZnP-Ir, displayed the highest H-2 production rate (eta H-2) of 16.12 mmol g(-1) h(-1) within 5 h of irradiation, which is over 2.73-fold higher than MBPyZnP-Ir (5.90 mmol g(-1) h(-1)) and much higher than their precursors TBPyZnP (0.12 mmol g(-1) h(-1)) and MBPyZnP (0.06 mmol g(-1) h(-1)) without iridium. The superior eta H-2 of TBPyZnP-Ir could be explained by the iridium motifs linked to the porphyrin, stabilizing the triplet states of the porphyrin through intramolecular energy transfer; thus enhancing electron transfer from the triplet photo-excited porphyrin moiety to the cobaloxime co-catalyst and consequently proton reduction.

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Gender:Male

Alma Mater:Jilin University

Degree:Doctoral Degree

School/Department:School of Chemistry Engineering

Discipline:Organic Chemistry. Applied Chemistry. Physical Chemistry (including Chemical Physics)

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