To evaluate the role of atmospheric
heterogeneous reactions on
the ice nucleation ability of airborne dust particles, we investigated
the systematic study of ice nucleation microphysics with a suite of
atmospherically relevant metals (10), halides (4), and oxyhalides
(2). Within a minute, a kaolin–iron oxide composite (KaFe)
showed efficient reactions with aqueous mercury salts. Among the different
mercury salts tested, only HgCl
2
reacting with KaFe generated
HgKaFe, a highly efficient ice nucleating particle (HEIN). When added
to water, HgKaFe caused water to freeze at much warmer temperatures,
within a narrow range of −6.6 to −4.7 °C. Using
a suite of optical spectroscopy, mass spectrometry, and microscopy
techniques, we performed various experiments to decipher the physical
and chemical properties of surface and bulk. KaFe was identified as
a mixture of different iron oxides, namely, goethite, hematite, magnetite,
and ε-Fe
2
O
3
, with kaolin. In HgKaFe, HgCl
2
was reduced to Hg
2
Cl
2
and iron was
predominantly in maghemite form. Reduction of Fe
2+
by NaBH
4
, followed by aerial oxidation, helped KaFe to be an exact
precursor for the synthesis of HEIN HgKaFe. Kaolin served as a template
for synthesizing iron oxide, opposing unwanted aggregation. No other
metal or metal halide was found to have more efficient nucleating
particles than HgCl
2
with KaFe composite. The chelation
of Hg(II) hindered the formation of HEIN. This study is useful for
investigating the role of morphology and how inorganic chemical reactions
on the surface of dust change morphology and thus ice nucleation activity.
The understanding of the fundamentals of what makes a particle to
be a good ice nucleating particle is valuable to further understand
and predict the amount and types of atmospheric ice nucleating particles.