The two polymorphs of lithium cobalt oxide, LiCoO 2 , present an opportunity to contrast the structural requirements for reversible charge storage (battery function) vs. catalysis of water oxidation/oxygen evolution (OER; 2H 2 O → O 2 + 4H + + 4e − ). Previously, we reported high OER electrocatalytic activity from nanocrystals of the cubic phase vs. poor activity from the layered phase – the archetypal lithium-ion battery cathode. Here we apply transmission electron microscopy, electron diffraction, voltammetry and elemental analysis under OER electrolysis conditions to show that labile Li + ions partially deintercalate from layered LiCoO 2 , initiating structural reorganization to the cubic spinel LiCo 2 O 4 , in parallel with formation of a more active catalytic phase. Comparison of cubic LiCoO 2 (50 nm) to iridium (5 nm) nanoparticles for OER catalysis (commercial benchmark for membrane-based systems) in basic and neutral electrolyte reveals excellent performance in terms of Tafel slope (48 mV dec −1 ), overpotential ( η = ∼420 mV@10 mA cm −2 at pH = 14), faradaic yield (100%) and OER stability (no loss in 14 hours). The inherent OER activity of cubic LiCoO 2 and spinel LiCo 2 O 4 is attributed to the presence of [Co 4 O 4 ] n+ cubane structural units, which provide lower oxidation potential to Co 4+ and lower inter-cubane hole mobility. By contrast, the layered phase, which lacks cubane units, exhibits extensive intra-planar hole delocalization which entropically hinders the four electron/hole concerted OER reaction. An essential distinguishing trait of a truly relevant catalyst is efficient continuous operation in a real electrolyzer stack. Initial trials of cubic LiCoO 2 in a solid electrolyte alkaline membrane electrolyzer indicate continuous operation for 1000 hours (without failure) at current densities up to 400 mA cm −2 and overpotential lower than proven PGM (platinum group metal) catalysts.
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Enhanced oxygen evolution over dual corner-shared cobalt tetrahedra
Abstract Developing efficient catalysts is of paramount importance to oxygen evolution, a sluggish anodic reaction that provides essential electrons and protons for various electrochemical processes, such as hydrogen generation. Here, we report that the oxygen evolution reaction (OER) can be efficiently catalyzed by cobalt tetrahedra, which are stabilized over the surface of a Swedenborgite-type YBCo 4 O 7 material. We reveal that the surface of YBaCo 4 O 7 possesses strong resilience towards structural amorphization during OER, which originates from its distinctive structural evolution toward electrochemical oxidation. The bulk of YBaCo 4 O 7 composes of corner-sharing only CoO 4 tetrahedra, which can flexibly alter their positions to accommodate the insertion of interstitial oxygen ions and mediate the stress during the electrochemical oxidation. The density functional theory calculations demonstrate that the OER is efficiently catalyzed by a binuclear active site of dual corner-shared cobalt tetrahedra, which have a coordination number switching between 3 and 4 during the reaction. We expect that the reported active structural motif of dual corner-shared cobalt tetrahedra in this study could enable further development of compounds for catalyzing the OER.
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- NSF-PAR ID:
- 10425537
- Date Published:
- Journal Name:
- Nature Communications
- Volume:
- 13
- Issue:
- 1
- ISSN:
- 2041-1723
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1038/s41467-022-33000-w
