Tunable Organic Photocatalysts for Visible-Light-Driven Hydrogen Evolution
Author(s) -
Reiner Sebastian Sprick,
JiaXing Jiang,
Baltasar Bonillo,
Shijie Ren,
Thanchanok Ratvijitvech,
Pierre Guiglion,
Martijn A. Zwijnenburg,
Dave J. Adams,
Andrew I. Cooper
Publication year - 2015
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja511552k
Subject(s) - chemistry , photochemistry , visible spectrum , microporous material , polymer , photocatalysis , ultraviolet , monomer , hydrogen production , hydrogen , amorphous solid , ultraviolet light , chemical engineering , optoelectronics , materials science , organic chemistry , catalysis , engineering
Photocatalytic hydrogen production from water offers an abundant, clean fuel source, but it is challenging to produce photocatalysts that use the solar spectrum effectively. Many hydrogen-evolving photocatalysts are active in the ultraviolet range, but ultraviolet light accounts for only 3% of the energy available in the solar spectrum at ground level. Solid-state crystalline photocatalysts have light absorption profiles that are a discrete function of their crystalline phase and that are not always tunable. Here, we prepare a series of amorphous, microporous organic polymers with exquisite synthetic control over the optical gap in the range 1.94-2.95 eV. Specific monomer compositions give polymers that are robust and effective photocatalysts for the evolution of hydrogen from water in the presence of a sacrificial electron donor, without the apparent need for an added metal cocatalyst. Remarkably, unlike other organic systems, the best performing polymer is only photoactive under visible rather than ultraviolet irradiation.
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