当前位置：
X-MOL 学术
›
J. Am. Chem. Soc.
›
论文详情
Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Lanthanum-Promoted Electrocatalyst for the Oxygen Evolution Reaction: Unique Catalyst or Oxide Deconstruction?
Journal of the American Chemical Society ( IF 14.4 ) Pub Date : 2024-12-19 , DOI: 10.1021/jacs.4c14696 Alaina C. Hartnett, Ryan J. Evenson, Agnes E. Thorarinsdottir, Samuel S. Veroneau, Daniel G. Nocera
Journal of the American Chemical Society ( IF 14.4 ) Pub Date : 2024-12-19 , DOI: 10.1021/jacs.4c14696 Alaina C. Hartnett, Ryan J. Evenson, Agnes E. Thorarinsdottir, Samuel S. Veroneau, Daniel G. Nocera
|
A conventional performance metric for electrocatalysts that promote the oxygen evolution reaction (OER) is the current density at a given overpotential. However, the assumption that increased current density at lower overpotentials indicates superior catalyst design is precarious for OER catalysts in the working environment, as the crystalline lattice is prone to deconstruction and amorphization, thus greatly increasing the concentration of catalytic active sites. We show this to be the case for La3+ incorporation into Co3O4. Powder X-ray diffraction (PXRD), Raman spectroscopy and extended X-ray absorption fine structure (EXAFS) reveal smaller domain sizes with decreased long-range order and increased amorphization for La-modified Co3O4. This lattice deconstruction is exacerbated under the conditions of OER as indicated by operando spectroscopies. The overpotential for OER decreases with increasing La3+ concentration, with maximum activity achieved at 17% La incorporation. HRTEM images and electron diffraction patterns clearly show the formation of an amorphous overlayer during OER catalysis that is accelerated with La3+ addition. O 1s XPS spectra after OER show the loss of lattice-oxide and an increase in peak intensities associated with hydroxylated or defective O-atom environments, consistent with Co(O)x(OH)y species in an amorphous overlayer. Our results suggest that improved catalytic activity of oxides incorporated with La3+ ions (and likely other metal ions) is due to an increase in the number of terminal octahedral Co(O)x(OH)y edge sites upon Co3O4 lattice deconstruction, rather than enhanced intrinsic catalysis.
更新日期：2024-12-20
京公网安备 11010802027423号