A clean air act at the quantum scale takes place inside state-of-the-art
fuel cells. Environmentally friendly technologies have become a necessity
for dealing with increasing levels of air pollution. For example, catalytic
converters reduce the amount of toxic species in automobile exhausts.
Meanwhile, researchers are intensively developing potential new sources
of low-emission power generation, such as solid-oxide fuel cells, which
use a solid material to supply migrating ions for an electricity-producing
chemical reaction.
To a large extent, many of these devices exploit an amazing property
of solid cerium oxide (CeO2) to release oxygen under oxygen-poor
conditions. To shed oxygen, cerium ions in cerium oxide gain electrons,
and a series of "reduced" compounds, with Ce2O3
as an end product, is formed.
In turn, the final product Ce2O3 easily takes
up oxygen under oxygen-rich conditions. However, the fundamental microscopic
origin of this phenomenon has not been elucidated--until now.
Researchers from Chalmers and Uppsala Universities in Sweden now offer
a detailed quantum-mechanical description of how this reaction occurs.
The pivotal transition from CeO2 to Ce2O3,
they show, results from the formation of an oxygen vacancy, in which
an oxygen atom leaves a spot it normally occupies on the cerium oxide
crystal lattice. In order to vacate the CeO2 lattice, oxygen
has to leave behind two electrons, so that it can transform from an
ion with a charge of -2 to a free oxygen atom.
Quantum effects make this process possible. They enable the electrons
to "localize" on two nearby cerium ions, which initially have
a charge of +4. Gaining these electrons allows the two Ce ions each
to acquire a charge of +3 and allow a series of "reduced"
compounds and eventually Ce2O3 to form.
This makes the oxygen storage-and-release ability of solid cerium oxide
a remarkable example of the quantum process of electron localization,
directly manifesting itself in a macroscopic property used in many modern
environmental friendly applications. (N.V.
Skorodumova, S.I. Simak, B.I. Lundqvist, I.A. Abrikosov, B. Johansson,
Physical Review Letters, 14 Oct 2002; contact Sergei Simak, Uppsala
University, 011-46-18-471-5739, Sergei.Simak@fysik.uu.se).