Using scanning transmission electron microscopy it was possible, by directly imaging single atoms, to investigate the motion of heavy atoms deposited onto the surfaces of thin films. Here, U, Pt, Au, In, Cd, Ag and Pd were deposited onto 15Å-thick amorphous carbon substrates. It is found that adatom motion was strongly dependent upon the local substrate structure and adatom specie (table 1). Diffusion coefficients and activation energies for single atoms, as well as dimers, trimers, etc., were obtained by directly measuring the motion of atoms. Pair-density and nearest-neighbor distributions were measured and used to derive the interatomic potential and the rate of adatom nucleation. It was found that the interatomic potential was very weak and long-ranged.

Direct Observation of the Behavior of Heavy Single Atoms on Amorphous Carbon Substrates. Utlaut, M.: Physical Review B, 1980, 22[10], 4650–60

 

Table 1

Surface diffusion of various

species on amorphous C film

 

Species

Region

E (eV)

D (Å2/s)

Ag

area

0.83

0.021

Ag

terrace

0.87

0.016

Ag

ledge

0.83

0.026

Au

area

0.88

0.013

Au

terrace

0.88

0.012

Au

ledge

0.87

0.014

AuCl3

area

0.88

0.009

AuCl3

terrace

0.88

0.004

AuCl3

ledge

0.88

0.011

CdCl2

area

0.86

0.029

CdCl2

terrace

0.88

0.026

CdCl2

ledge

0.87

0.031

In

area

0.84

0.040

In

terrace

0.87

0.032

In

ledge

0.83

0.044

UO2Ac2

area

0.86

0.036

UO2Ac2

terrace

0.88

0.029

UO2Ac2

ledge

0.85

0.039

UO2Cl2

area

0.89

0.010

UO2Cl2

terrace

0.93

0.005

UO2Cl2

ledge

0.89

0.012