4.8 Article

Direct and continuous strain control of catalysts with tunable battery electrode materials

Journal

SCIENCE
Volume 354, Issue 6315, Pages 1031-1036

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aaf7680

Keywords

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Funding

  1. Global Climate Energy Project at Stanford University
  2. Stanford Interdisciplinary Graduate Fellowship
  3. Center on Nanostructuring for Efficient Energy Conversion (CNEEC) at Stanford University, an Energy Frontier Research Center - U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences [DE-SC0001060]
  4. DOE, Office of Basic Energy Sciences
  5. National Science Foundation Graduate Research Fellowship Program (GRFP) grant [DGE-114747]
  6. DOE, Basic Energy Sciences, Materials Sciences and Engineering Division [DE-AC02-76SF00515]
  7. DOE Office of Science, Office of Basic Energy Sciences [DE-AC02-05CH11231]

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We report a method for using battery electrode materials to directly and continuously control the lattice strain of platinum (Pt) catalyst and thus tune its catalytic activity for the oxygen reduction reaction (ORR). Whereas the common approach of using metal overlayers introduces ligand effects in addition to strain, by electrochemically switching between the charging and discharging status of battery electrodes the change in volume can be precisely controlled to induce either compressive or tensile strain on supported catalysts. Lattice compression and tension induced by the lithium cobalt oxide substrate of similar to 5% were directly observed in individual Pt nanoparticles with aberration-corrected transmission electron microscopy. We observed 90% enhancement or 40% suppression in Pt ORR activity under compression or tension, respectively, which is consistent with theoretical predictions.

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