Surface reactions and carbon layer formation on clean metallic beryllium ar
e investigated in situ by X-ray photoelectron spectroscopy (XPS) and Ruther
ford backscattering spectroscopy (RBS). The carbon is supplied by an electr
on beam evaporation device. The deposited films are successively heated to
temperatures between 373 and 873 K in steps of 100 K and analysed after eac
h step. After deposition at room temperature an amount of Be2C up to 6 x 10
(15) cm(-2) is present at the beryllium/carbon interface with elementary ca
rbon on top. A first additional carbide formation takes place after heating
to 473 K. For deposited amounts below 5 x 10(16) cm(-2) almost all carbon
has reacted to carbide after the 673 K step. The carbidisation is complete
at 773 K. Applying annealing times between 10 and 30 min characteristic Be2
C amounts build up for each temperature. Carbon diffusion into the bulk ber
yllium does not take place for temperatures below 773 K. (C) 2001 Elsevier
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