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A perovskite oxide optimized for oxygen evolution catalysis from molecular orbital principles.

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TLDR
The high activity of BSCF was predicted from a design principle established by systematic examination of more than 10 transition metal oxides, which showed that the intrinsic OER activity exhibits a volcano-shaped dependence on the occupancy of the 3d electron with an eg symmetry of surface transition metal cations in an oxide.
Abstract
The efficiency of many energy storage technologies, such as rechargeable metal-air batteries and hydrogen production from water splitting, is limited by the slow kinetics of the oxygen evolution reaction (OER). We found that Ba 0.5 Sr 0.5 Co 0.8 Fe 0.2 O 3–δ (BSCF) catalyzes the OER with intrinsic activity that is at least an order of magnitude higher than that of the state-of-the-art iridium oxide catalyst in alkaline media. The high activity of BSCF was predicted from a design principle established by systematic examination of more than 10 transition metal oxides, which showed that the intrinsic OER activity exhibits a volcano-shaped dependence on the occupancy of the 3d electron with an e g symmetry of surface transition metal cations in an oxide. The peak OER activity was predicted to be at an e g occupancy close to unity, with high covalency of transition metal–oxygen bonds.

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Ultrathin nanosheets constructed CoMoO4 porous flowers with high activity for electrocatalytic oxygen evolution

TL;DR: Benefiting from the high specific surface area and constituent nanosheets with an ultrathin thickness, the CoMoO4 micro-flowers exhibit substantially higher electrocatalytic activity and stability than the IrO2 benchmark for the oxygen evolution reaction.
Journal ArticleDOI

Bifunctional electrocatalysts of MOF-derived Co–N/C on bamboo-like MnO nanowires for high-performance liquid- and solid-state Zn–air batteries

TL;DR: In this article, a highly efficient bifunctional catalyst was fabricated by forming an interconnected and conducting Co-N/C framework on hollow MnO nanowires, which demonstrates prominent ORR/OER activity and promising potential in rechargeable Zn-air batteries.
Journal ArticleDOI

High‐Valence Nickel Single‐Atom Catalysts Coordinated to Oxygen Sites for Extraordinarily Activating Oxygen Evolution Reaction

TL;DR: The bonding between single nickel and oxygen sites results in the extraordinary boosting of OER performance of Ni‐O‐G SACs, which opens numerous opportunities for creating unconventional Sacs via metal–oxygen bonding.
Journal ArticleDOI

Double Perovskite LaFe x Ni 1-x O 3 Nanorods Enable Efficient Oxygen Evolution Electrocatalysis

TL;DR: It is demonstrated that the double perovskite LaFex Ni1-x O3 (LFNO) nanorods (NRs) can be adopted as highly active and stable OER electrocatalysts.
References
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Building better batteries

TL;DR: Researchers must find a sustainable way of providing the power their modern lifestyles demand to ensure the continued existence of clean energy sources.
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Powering the planet: Chemical challenges in solar energy utilization

TL;DR: Solar energy is by far the largest exploitable resource, providing more energy in 1 hour to the earth than all of the energy consumed by humans in an entire year, and if solar energy is to be a major primary energy source, it must be stored and dispatched on demand to the end user.
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Activity benchmarks and requirements for Pt, Pt-alloy, and non-Pt oxygen reduction catalysts for PEMFCs

TL;DR: In this article, the authors quantified the activities and voltage loss modes for state-of-the-art MEAs (membrane electrode assemblies), specifies performance goals needed for automotive application, and provides benchmark oxygen reduction activities for state of the art platinum electrocatalysts.
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Improved Oxygen Reduction Activity on Pt3Ni(111) via Increased Surface Site Availability

TL;DR: It is demonstrated that the Pt3Ni( 111) surface is 10-fold more active for the ORR than the corresponding Pt(111) surface and 90-foldMore active than the current state-of-the-art Pt/C catalysts for PEMFC.
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In Situ Formation of an Oxygen-Evolving Catalyst in Neutral Water Containing Phosphate and Co2+

TL;DR: A catalyst that forms upon the oxidative polarization of an inert indium tin oxide electrode in phosphate-buffered water containing cobalt (II) ions is reported that not only forms in situ from earth-abundant materials but also operates in neutral water under ambient conditions.
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