Photoelectrochemical water oxidation improved by pyridine N-oxide as a mimic of tyrosine-Z in photosystem IIShow others and affiliations
2022 (English)In: Chemical Science, ISSN 2041-6520, E-ISSN 2041-6539, Vol. 13, no 17, p. 4955-4961Article in journal (Refereed) Published
Abstract [en]
Artificial photosynthesis provides a way to store solar energy in chemical bonds with water oxidation as a major challenge for creating highly efficient and robust photoanodes that mimic photosystem II. We report here an easily available pyridine N-oxide (PNO) derivative as an efficient electron transfer relay between an organic light absorber and molecular water oxidation catalyst on a nanoparticle TiO2 photoanode. Spectroscopic and kinetic studies revealed that the PNO/PNO+˙ couple closely mimics the redox behavior of the tyrosine/tyrosyl radical pair in PSII in improving light-driven charge separation via multi-step electron transfer. The integrated photoanode exhibited a 1 sun current density of 3 mA cm−2 in the presence of Na2SO3 and a highly stable photocurrent density of >0.5 mA cm−2 at 0.4 V vs. NHE over a period of 1 h for water oxidation at pH 7. The performance shown here is superior to those of previously reported organic dye-based photoanodes in terms of photocurrent and stability.
Place, publisher, year, edition, pages
Royal Society of Chemistry (RSC) , 2022. Vol. 13, no 17, p. 4955-4961
Keywords [en]
Artificial photosynthesis, Bond strength (chemical), Electron transitions, Free radical reactions, Oxidation, Pyridine, Redox reactions, Sodium compounds, Solar energy, Titanium dioxide, Electron transfer, Organics, Photo-anodes, Photoelectrochemical water oxidation, Photosystem-II, Pyridine N-oxide, Pyridine N-oxides, Pyridine-N-oxides, Water oxidation, Amino acids
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-323502DOI: 10.1039/d2sc00443gISI: 000781872400001PubMedID: 35655895Scopus ID: 2-s2.0-85129331219OAI: oai:DiVA.org:kth-323502DiVA, id: diva2:1734269
Note
QC 20230206
2023-02-062023-02-062023-02-06Bibliographically approved