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Facile dissociation of reactants and weak binding of intermediates are key requirements for
efficient and selective catalysis. However, these two variables are intimately linked in a way
that does not generally allow the optimization of both properties simultaneously. By using
desorption measurements in combination with high-resolution scanning tunneling microscopy,
we show that individual, isolated Pd atoms in a Cu surface substantially lower the energy barrier
to both hydrogen uptake on and subsequent desorption from the Cu metal surface. This facile
hydrogen dissociation at Pd atom sites and weak binding to Cu allow for very selective
hydrogenation of styrene and acetylene as compared with pure Cu or Pd metal alone.

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