Thermal
atomic layer etch (ALE) of W metal can be achieved by sequential
self-limiting oxidation and chlorination reactions at elevated temperatures.
In this paper, we analyze the reaction mechanisms of W ALE using the
first-principles simulation. We show that oxidizing agents such as
O
2
, O
3
, and N
2
O can be used to produce
a WO
x
surface layer in the first step
of an ALE process with ozone being the most reactive. While the oxidation
pulse on clean W is very exergonic, our study suggests that runaway
oxidation of W is not thermodynamically favorable. In the second ALE
pulse, WCl
6
and Cl
2
remove the oxidized surface
W atoms by the formation of volatile tungsten oxychloride (W
x
O
y
Cl
z
) species. In this pulse, each adsorbed WCl
6
molecule was found to remove one surface W atom with a moderate
energy cost. Our calculations further show that the desorption of
the additional etch products is endothermic by up to 4.7 eV. Our findings
are consistent with the high temperatures needed to produce ALE in
experiments. In total, our quantum chemical calculations have identified
the lowest energy pathways for ALE of tungsten metal along with the
most likely etch products, and these findings may help guide the development
of improved etch reagents.