TY - JOUR
T1 - On the Origin of the OER Activity of Ultrathin Manganese Oxide Films
AU - Plate, Paul
AU - Höhn, Christian
AU - Bloeck, Ulrike
AU - Bogdanoff, Peter
AU - Fiechter, Sebastian
AU - Abdi, Fatwa F.
AU - van de Krol, Roel
AU - Bronneberg, Aafke C.
PY - 2021/1/20
Y1 - 2021/1/20
N2 - There is an urgent need for cheap, stable, and abundant catalyst materials for photoelectrochemical water splitting. Manganese oxide is an interesting candidate as an oxygen evolution reaction (OER) catalyst, but the minimum thickness above which MnOx thin films become OER-active has not yet been established. In this work, ultrathin (<10 nm) manganese oxide films are grown on silicon by atomic layer deposition to study the origin of OER activity under alkaline conditions. We found that MnOx films thinner than 1.5 nm are not OER-active. X-ray photoelectron spectroscopy shows that this is due to electrostatic catalyst-support interactions that prevent the electrochemical oxidation of the manganese ions close to the interface with the support, while in thicker films, MnIII and MnIV oxide layers appear as OER-active catalysts after oxidation and electrochemical treatment. From our investigations, it can be concluded that one MnIII,IV-O monolayer is sufficient to establish oxygen evolution under alkaline conditions. The results of this study provide important new design criteria for ultrathin manganese oxide oxygen evolution catalysts. © 2021 American Chemical Society.
AB - There is an urgent need for cheap, stable, and abundant catalyst materials for photoelectrochemical water splitting. Manganese oxide is an interesting candidate as an oxygen evolution reaction (OER) catalyst, but the minimum thickness above which MnOx thin films become OER-active has not yet been established. In this work, ultrathin (<10 nm) manganese oxide films are grown on silicon by atomic layer deposition to study the origin of OER activity under alkaline conditions. We found that MnOx films thinner than 1.5 nm are not OER-active. X-ray photoelectron spectroscopy shows that this is due to electrostatic catalyst-support interactions that prevent the electrochemical oxidation of the manganese ions close to the interface with the support, while in thicker films, MnIII and MnIV oxide layers appear as OER-active catalysts after oxidation and electrochemical treatment. From our investigations, it can be concluded that one MnIII,IV-O monolayer is sufficient to establish oxygen evolution under alkaline conditions. The results of this study provide important new design criteria for ultrathin manganese oxide oxygen evolution catalysts. © 2021 American Chemical Society.
KW - ALD
KW - electrocatalysis
KW - electrochemistry
KW - MnO x
KW - oxygen evolution
KW - X-ray photoelectron spectroscopy
UR - http://www.scopus.com/inward/record.url?scp=85099948009&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85099948009&origin=recordpage
U2 - 10.1021/acsami.0c15977
DO - 10.1021/acsami.0c15977
M3 - RGC 21 - Publication in refereed journal
C2 - 33426879
SN - 1944-8244
VL - 13
SP - 2428
EP - 2436
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 2
ER -