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Ir nanodendrites on ATO for acid OER

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TTAB-grown Ir nanodendrites on mesoporous ATO outperform Ir black for oxygen evolution in acid and in a PEM electrolyzer.

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Oxide-supported Ir nanodendrites with high activity and durability for the oxygen evolution reaction in acid PEM water electrolyzers

Oh HS, Nong HN, Reier T, et al. · Chemical science · 2015

doi.org/10.1039/c5sc00518cRead the full paper ↗117 citationscc by

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Ir nanodendrites on ATO for acid OER

These passages occur verbatim in the stored paper text. They support the points listed below; they do not verify every statement in the explanation.

Ir-ND particles are 15–20 nm by TEM

The low resolution TEM image of the as-synthesized material revealed a largely dendritic structure with a narrow size range of 15–20 nm () and high-yield formation.

Crystallite size of Ir-ND is 1.7 nm versus 3.2 nm for Ir black

The crystallite size of Ir-ND and Ir black was estimated to 1.7 nm and 3.2 nm, respectively.
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What they did

They reduced H2IrCl6 with NaBH4 in TTAB to make 15–20 nm Ir nanodendrites, deposited them on high-area ATO (or carbon), oxidized the surface electrochemically, and measured OER in 0.05 M H2SO4 and in a 5 cm2 PEMWE single cell.

What they found

Ir-ND crystallites are 1.7 nm versus 3.2 nm for Ir black; BET area is 39.2 versus 18.2 m2 g–1; electrochemical porosity is 34.2% versus 20%. Mass activity is 8 times Ir black at 1.51 V. Ir-ND/ATO reaches 1.50 A cm–2 at 1.8 V in the cell, versus 0.80 A cm–2 for Ir black, and is the most durable in 15 h chronopotentiometry.

The limits

What it doesn't show

Long-term stack lifetime and Ir dissolution rates are not quantified beyond 15 h RDE holds. The 8-fold mass-activity claim is at one overpotential in liquid acid, not a full Tafel comparison across pH. Carbon-supported Ir-ND still faces support corrosion in PEM anodes.

Key terms

Oxygen evolution reaction (OER)
Anodic 2 H2O → O2 + 4 H+ + 4 e–; the slow electrode reaction in acid water electrolyzers.
Nanodendrite
Branched nanoparticle with many edges/corners, here assembled from tiny Ir seeds.
ATO
Antimony-doped tin oxide, a corrosion-resistant oxide support used instead of carbon at the anode.
PEMWE
Polymer-electrolyte-membrane water electrolyzer operating in acid with a solid Nafion-type membrane.
Electrochemical porosity
Fraction of charge associated with inner, more porous oxide versus outer surface; 34.2% for Ir-ND.

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Ir-ND mass activity versus commercial Ir black at 1.51 VRHE is about

Common questions

Why support Ir-ND on ATO instead of carbon?

The anode sees high potential and acid; ATO is more corrosion-resistant than carbon black while still conducting.

How much more active is Ir-ND than Ir black?

About 8 times the Ir-mass activity at 1.51 VRHE (280 mV overpotential).

What cell current does Ir-ND/ATO reach?

1.50 A cm–2 at 1.8 V, versus 0.80 A cm–2 for unsupported Ir black.

How are the dendrites made?

Fast NaBH4 reduction of Ir(IV) in TTAB water at 70 °C self-assembles tiny seeds into 15–20 nm dendrites.

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