@article{26885,
  author = {Lei Tang and Byungchan Han and Kristin A Persson and Cody Friesen and Ting He and Karl Sieradzki and Gerbrand Ceder},
  title = {Electrochemical stability of nanometer-scale Pt particles in acidic environments},
  abstract = {<p>Understanding and controlling the electrochemical stability or corrosion behavior of nanometerscale solids is vitally important in a variety of applications such as nanoscale electronics, sensing, and catalysis. For many applications, the increased surface to volume ratio achieved by particle size reduction leads to lower materials cost and higher efficiency, but there are questions as to whether the intrinsic stability of materials also decreases with particle size. An important example of this relates to the stability of Pt catalysts in, for example, proton exchange fuel cells. In this Article, we use electrochemical scanning tunneling microscopy to, for the first time, directly examine the stability of individual Pt nanoparticles as a function of applied potential. We combine this experimental study with ab initio computations to determine the stability, passivation, and dissolution behavior of Pt as a function of particle size and potential. Both approaches clearly show that smaller Pt particles dissolve well below the bulk dissolution potential and through a different mechanism. Pt dissolution from a nanoparticle occurs by direct electro-oxidation of Pt to soluble Pt2+ cations, unlike bulk Pt, which dissolves from the oxide. These results have important implications for understanding the stability of Pt and Pt alloy catalysts in fuel cell architectures, and for the stability of nanoparticles in general.</p>},
  year = {2009},
  journal = {Journal of the American Chemical Society},
  volume = {132},
  pages = {596-600},
  month = {12/2009},
  doi = {10.1021/ja9071496},
  language = {eng},
}