The Oxygen Evolution Reaction on Platinum
Imagine a future where our energy comes from a clean, abundant source: hydrogen. This vision hinges on a deceptively simple process—splitting water into hydrogen and oxygen using electricity, ideally from renewable sources like solar and wind.
Hydrogen produced through water electrolysis using renewable electricity, creating a truly carbon-free energy carrier.
The oxygen evolution reaction is the primary efficiency-limiting step in water electrolyzers, consuming significant energy due to sluggish kinetics.
The oxygen evolution reaction is the process that creates oxygen gas at the positive electrode (the anode) during water electrolysis. In alkaline environments, this involves a delicate dance of four electrons and four hydroxyl ions coming together to form a single oxygen molecule and two water molecules.
The complexity of this four-electron transfer process, with its multiple intermediate steps, is what makes the reaction inherently slow. It's this slowness that demands extra voltage—known as overpotential—to drive the reaction forward, directly impacting the energy efficiency and cost of hydrogen production.
Complex multi-step reaction requiring precise coordination
Platinum has long been a cornerstone of electrocatalysis, renowned for its stability and activity across numerous reactions. For the oxygen evolution reaction in alkaline media, it serves as a critical benchmark against which all new catalysts are measured.
What transformations does the platinum surface itself undergo during the reaction, and how do these changes influence its catalytic activity?
Benchmark catalyst for OER studies with unmatched stability and activity.
Ex-situ methods failed to capture dynamic surface transformations during reaction conditions.
Platinum surface evolves in response to electrical potential and chemical environment.
Like photographing hummingbird wings - traditional methods miss the crucial motion.
A pivotal 2017 study broke new ground by applying ambient pressure X-ray photoelectron spectroscopy (AP-XPS) to probe platinum surfaces during active OER 1 .
Polycrystalline platinum foil was prepared as the working electrode for the experiment.
Custom-designed cell with alkaline electrolyte (KOH solution) to mimic real operating conditions.
Controlled electrical potential was applied, gradually increasing into the OER range.
Surface probed using synchrotron X-rays while reaction was actively occurring.
| Material | Function |
|---|---|
| Platinum Electrode | Benchmark OER catalyst |
| KOH Electrolyte | Alkaline environment |
| Synchrotron X-ray | Surface chemical analysis |
| Squaric Acid Anions | Interface modification 3 |
| Species | Role in OER |
|---|---|
| Pt-OH | Initial intermediate |
| Pt-O | Key oxidized species |
| Pt-OOH | O-O bond formation |
MOF-derived Fe-Co-Se-O with abundant vacancies lowers overpotential to 280 mV 2
Squaric acid anions stabilize interface, boost durability 10-fold at high currents 3
Mobile Fe species act as co-catalysts in NiFe systems 8
CoFe spinel oxides optimize intermediate binding 6
The journey to unravel the mechanism of the alkaline oxygen evolution reaction on platinum exemplifies the power of fundamental science to illuminate a path toward technological advancement.
The application of advanced operando techniques like AP-XPS has transformed our understanding, moving it from theoretical models to direct observation of the dynamic catalyst surface. The insights gained from studying benchmark materials like platinum have provided an essential framework for evaluating and designing new catalytic systems.
Developing efficient, stable electrolyzers for competitive green hydrogen production