TY - JOUR
T1 - Low-Temperature controlled synthesis of nanocast mixed metal oxide spinels for enhanced OER activity
AU - Guggenberger, Patrick
AU - Priamushko, Tatiana
AU - Patil, Prathamesh
AU - Florek, Justyna
AU - Garstenauer, Daniel
AU - Mautner, Andreas
AU - Won Shin, Jae
AU - Ryoo, Ryong
AU - Pichler, Christian M.
AU - Kleitz, Freddy
N1 - Accession Number
WOS:001178741800001
PubMed ID
38308896
PY - 2024/5
Y1 - 2024/5
N2 - The controlled cation substitution is an effective strategy for optimizing the density of states and enhancing the electrocatalytic activity of transition metal oxide catalysts for water splitting. However, achieving tailored mesoporosity while maintaining elemental homogeneity and phase purity remains a significant challenge, especially when aiming for complex multi-metal oxides. In this study, we utilized a one-step impregnation nanocasting method for synthesizing mesoporous Mn-, Fe-, and Ni-substituted cobalt spinel oxide (Mn0.1Fe0.1Ni0.3Co2.5O4, MFNCO) and demonstrate the benefits of low-temperature calcination within a semi-sealed container at 150–200 °C. The comprehensive discussion of calcination temperature effects on porosity, particle size, surface chemistry and catalytic performance for the alkaline oxygen evolution reaction (OER) highlights the importance of humidity, which was modulated by a pre-drying step. The catalyst calcined at 170 °C exhibited the lowest overpotential (335 mV at 10 mA cm−2), highest current density (433 mA cm−2 at 1.7 V vs. RHE, reversible hydrogen electrode) and further displayed excellent stability over 22 h (at 10 mA cm−2). Furthermore, we successfully adapted this method to utilize cheap, commercially available silica gel as a hard template, yielding comparable OER performance. Our results represent a significant progress in the cost-efficient large-scale preparation of complex multi-metal oxides for catalytic applications.
AB - The controlled cation substitution is an effective strategy for optimizing the density of states and enhancing the electrocatalytic activity of transition metal oxide catalysts for water splitting. However, achieving tailored mesoporosity while maintaining elemental homogeneity and phase purity remains a significant challenge, especially when aiming for complex multi-metal oxides. In this study, we utilized a one-step impregnation nanocasting method for synthesizing mesoporous Mn-, Fe-, and Ni-substituted cobalt spinel oxide (Mn0.1Fe0.1Ni0.3Co2.5O4, MFNCO) and demonstrate the benefits of low-temperature calcination within a semi-sealed container at 150–200 °C. The comprehensive discussion of calcination temperature effects on porosity, particle size, surface chemistry and catalytic performance for the alkaline oxygen evolution reaction (OER) highlights the importance of humidity, which was modulated by a pre-drying step. The catalyst calcined at 170 °C exhibited the lowest overpotential (335 mV at 10 mA cm−2), highest current density (433 mA cm−2 at 1.7 V vs. RHE, reversible hydrogen electrode) and further displayed excellent stability over 22 h (at 10 mA cm−2). Furthermore, we successfully adapted this method to utilize cheap, commercially available silica gel as a hard template, yielding comparable OER performance. Our results represent a significant progress in the cost-efficient large-scale preparation of complex multi-metal oxides for catalytic applications.
KW - Electrochemical stability
KW - Low-energy ion scattering
KW - Mixed metal oxides
KW - Nanocasting
KW - Oxygen evolution reaction
KW - Spinel
KW - Water electrolysis
UR - http://www.scopus.com/inward/record.url?scp=85184002552&partnerID=8YFLogxK
U2 - 10.1016/j.jcis.2024.01.056
DO - 10.1016/j.jcis.2024.01.056
M3 - Article
C2 - 38308896
AN - SCOPUS:85184002552
SN - 0021-9797
VL - 661
SP - 574
EP - 587
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -