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Nanostructured boron doped diamond electrodes with increased reactivity for solar-driven CO₂ reduction in room temperature ionic liquids

: Knittel, Peter; Buchner, Franzsika; Hadzifekzovic, Emina; Giese, Christian; Quellmalz, Patricia; Seidel, Robert; Petit, Tristan; Iliev, Boyan; Schubert, Thomas J.S.; Nebel, Christoph E.; Foord, John S.

Volltext urn:nbn:de:0011-n-6057346 (2.8 MByte PDF)
MD5 Fingerprint: 33a524ab6ee2242fb5968170bf0e893e
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Erstellt am: 17.10.2020

ChemCatChem 12 (2020), Nr.21, S.5548-5557
ISSN: 1867-3880
ISSN: 1867-3899
European Commission EC
H2020-H2020-FETOPEN-2014-2015-RIA; 665085; DIACAT
Diamond materials for the photocatalytic conversion of CO2 to fine chemicals and fuels using visible light
Zeitschriftenaufsatz, Elektronische Publikation
Fraunhofer IAF ()

Conductive, boron doped diamond (BDD) is an extraordinary material with many applications in electrochemistry due to its wide potential window, outstanding robustness, low capacitance and resistance to fouling. However, in photoelectrochemistry, BDD usually requires UV light for excitation, which impedes e. g., usage in CO2 to fuel reduction. In this work, a heavily boron doped, nanostructured diamond electrode with enhanced light absorption has been developed. It is manufactured from BDD by reactive ion etching and presents a coral‐like structure with pore diameters in the nanometer range, ensuring a huge surface area. The strong light absorbance of this material is clearly visible from its black color. Consequently, the material is called Diamond Black (DB). Electrochemical and X‐ray photoelectron spectroscopy measurements performed at near‐ambient pressure conditions of water vapor demonstrate increased surface reactivity for the hydrogen‐terminated DB compared to oxidized surfaces. Depending on the surface termination, the wettability and hence the electrochemically accessible area can be changed. Photoelectrochemical conversion of CO2 was demonstrated using a Cu2O‐modified electrode in ionic liquids under solar illumination. High formic acid production rates at low catalyst deposition times can be obtained paired with an increased catalyst stability on the DB surface.