Title: Probing the active sites of oxide encapsulated electrocatalysts with controllable oxygen evolution selectivity

Journal Article · · EES Catalysis
DOI: https://doi.org/10.1039/d4ey00074a · OSTI ID:2341915

Electrocatalysts encapsulated by nanoscopic overlayers can control the rate of redox reactions at the outer surface of the overlayer or at the buried interface between the overlayer and the active catalyst, leading to complex behavior in the presence of two competing electrochemical reactions. This study investigated oxide encapsulated electrocatalysts (OECs) comprised of iridium (Ir) thin films coated with an ultrathin (2–10 nm thick) silicon oxide (SiOx) or titanium oxide (TiOx) overlayer. The performance of SiOx|Ir and TiOx|Ir thin film electrodes towards the oxygen evolution reaction (OER) and Fe(II)/Fe(III) redox reactions were evaluated. An improvement in selectivity towards the OER was observed for all OECs. Overlayer properties, namely ionic and electronic conductivity, were assessed using a combination of electroanalytical methods and molecular dynamics simulations. SiOx and TiOx overlayers were found to be permeable to H2O and O2 such that the OER can occur at the MOx|Ir (M = Ti, Si) buried interface, which was further supported with molecular dynamics simulations of model SiO2 coatings. In contrast, Fe(II)/Fe(III) redox reactions occur to the same degree with TiOx overlayers having thicknesses less than 4 nm as bare electrocatalyst, while SiOx overlayers inhibit redox reactions at all thicknesses. This observation is attributed to differences in electronic transport between the buried interface and outer overlayer surface, as measured with through-plane conductivity measurements of wetted overlayer materials. These findings reveal the influence of oxide overlayer properties on the activity and selectivity of OECs and suggest opportunities to tune these properties for a wide range of electrochemical reactions.

Research Organization:
National Renewable Energy Laboratory (NREL), Golden, CO (United States); Univ. of California, Irvine, CA (United States)
Sponsoring Organization:
National Science Foundation (NSF); USDOE; USDOE Office of Energy Efficiency and Renewable Energy (EERE), Office of Sustainable Transportation. Hydrogen Fuel Cell Technologies Office (HFTO); USDOE Office of Science (SC)
Grant/Contract Number:
AC36-08GO28308; AC52-07NA27344; EE0008838; SC0023431
OSTI ID:
2341915
Report Number(s):
NREL/JA-5700-89958; MainId:90737; UUID:5ec68401-14c7-4b1a-a715-6f8510859ae3; MainAdminId:72654
Journal Information:
EES Catalysis, Journal Name: EES Catalysis Vol. 2; ISSN 2753-801X
Publisher:
Royal Society of ChemistryCopyright Statement
Country of Publication:
United States
Language:
English