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   <subfield code="a">Nanostructured Nickelate Oxides as Efficient and Stable Cathode Electrocatalysts for Li-O2 Batteries</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Ayad Nacy, Xianfeng Ma, Eranda Nikolla]</subfield>
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   <subfield code="a">Li-O2 (Li-air) batteries are among the most promising energy storage technologies due to their high theoretical specific capacity and energy density. Key challenges with this technology include high overpotential losses associated with catalyzing the electrochemical reactions (i.e., oxygen reduction and evolution reactions) at the cathode of the battery. In this contribution, we report through the example of La2NiO4+δ that layered nickelate oxide materials with rod-shaped nanostructure exhibit promising electrochemical performance as cathode electrocatalysts for Li-O2 batteries. We demonstrate the ability to control the nanostructure of La2NiO4+δ electrocatalyst at the nanoscale level using a reverse-microemulsion synthesis approach. We show that Li-O2 batteries with cathodes containing rod-shaped La2NiO4+δ electrocatalyst exhibit lower charging potentials and higher reversible capacities when compared to batteries with carbon-only cathodes. Our studies indicate that the enhancement in the battery performance induced by the rod-shaped La2NiO4+δ electrocatalyst can be attributed to the fact that La2NiO4+δ nanorods (i) facilitate the formation of nanosized Li2O2 particles during discharge, and (ii) promote the electrocatalytic activity toward the oxygen evolution reaction during charging. These findings open up avenues for the utilization of (i) reverse-microemulsion method for controlling the nanostructure of layered oxide materials, and (ii) nanorod-structured nickelate oxides as efficient cathode electrocatalysts for Li-O2 batteries.</subfield>
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   <subfield code="a">Nickelate oxides</subfield>
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   <subfield code="t">Topics in Catalysis</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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