In this study, three commonly used methods for oxidative etching of diamond
{111} faces are compared: gas phase etching using 'dry' oxygen, gas phase
etching using an oxygen/water vapour mixture and liquid etching in molten p
otassium nitrate. The synthetic diamond surfaces are prepared by cleavage.
The morphology of the surfaces is studied using atomic force microscopy and
the kinetics of the reactions is determined by measuring the decrease in t
hickness of the diamond. The atomic arrangement of the {111} surfaces etche
d in oxygen/water is studied using surface X-ray diffraction. Upon dry oxyg
en etching, the {111} faces are roughened and become morphologically unstab
le. This observation conflicts with standard theory, which predicts {111} t
o be a stable F-face that should etch via a layer mechanism. A possible exp
lanation for this is chemical roughening. The addition of water vapour to t
he oxygen has a dramatic effect on the etching mechanism of the {111} faces
. Now etching proceeds via a layer mechanism involving monoatomic steps. Sh
allow etch pits are formed, of which the slope increases for increasing etc
hing temperature. Surface X-ray diffraction experiments show that the surfa
ce is -OH terminated. For potassium nitrate etching, the {111} face etches
also via a layer mechanism and triangular etch pits with rounded corners ar
e formed, hav g point or flat bottoms, This etching technique appears to be
the best method to reveal different types of defects ending on diamond {11
1} surfaces. (C) 2001 Elsevier Science B.V. All rights reserved.