Platinum–Nickel Nanowires with Improved Hydrogen Evolution Performance in Anion Exchange Membrane-Based Electrolysis
[1];
[3]
- Chemistry and Nanoscience Center, National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States
- Computational Science Center, National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States
- Department of Chemistry, Colorado School of Mines, 1012 14th Street, Golden, Colorado 80401, United States
Platinum–nickel (Pt–Ni) nanowires were developed as hydrogen evolving catalysts for anion exchange membrane electrolyzers. Following synthesis by galvanic displacement, the nanowires had Pt surface areas of 90 m2 gPt–1. The nanowire specific exchange current densities were 2–3 times greater than commercial nanoparticles and may benefit from the extended nanostructure morphology that avoids fringe facets and produces higher quantities of Pt{100}. Hydrogen annealing was used to alloy Pt and Ni zones and compress the Pt lattice. Following annealing, the nanowire activity improved to 4 times greater than the as-synthesized wires and 10 times greater than Pt nanoparticles. Density functional theory calculations were performed to investigate the influence of lattice compression and exposed facet on the water-splitting reaction; it was found that at a lattice of 3.77 Å, the (100) facet of a Pt-skin grown on Ni3Pt weakens hydrogen binding and lowers the barrier to water-splitting as compared to pure Pt(100). Moreover, the activation energy of water-splitting on the (100) facet of a Pt-skin grown on Ni3Pt is particularly advantageous at 0.66 eV as compared to the considerably higher 0.90 eV required on (111) surfaces of pure Pt or Pt-skin grown on Ni3Pt. This favorable effect may be slightly mitigated during further optimization procedures such as acid leaching near-surface Ni, necessary to incorporate the nanowires into electrolyzer membrane electrode assemblies. Exposure to acid resulted in slight dealloying and Pt lattice expansion, which reduced half-cell activity, but exposed Pt surfaces and improved single-cell performance. Membrane electrode assembly performance was kinetically 1–2 orders of magnitude greater than Ni and slightly better than Pt nanoparticles while at one tenth the Pt loading. These electrocatalysts potentially exploit the highly active {100} facets and provide an ultralow Pt group metal option that can enable anion exchange membrane electrolysis, bridging the gap to proton exchange membrane-based systems.
- Research Organization:
- National Renewable Energy Laboratory (NREL), Golden, CO (United States)
- Sponsoring Organization:
- USDOE Office of Energy Efficiency and Renewable Energy (EERE)
- Grant/Contract Number:
- AC36-08GO28308
- OSTI ID:
- 2317690
- Alternate ID(s):
- OSTI ID: 1660241
- Report Number(s):
- NREL/JA-5900-77118
- Journal Information:
- ACS Catalysis, Journal Name: ACS Catalysis Vol. 10 Journal Issue: 17; ISSN 2155-5435
- Publisher:
- American Chemical SocietyCopyright Statement
- Country of Publication:
- United States
- Language:
- English
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