Y. Shacham-diamand et al., Electroless deposition of thin-film cobalt-tungsten-phosphorus layers using tungsten phosphoric acid (H-3[P(W3O10)(4)]) for ULSI and MEMS applications, J ELCHEM SO, 148(3), 2001, pp. C162-C167
This paper describes an electroless deposition method for the formation of
thin metallic films that contain mainly cobalt with significant amount of t
ungsten (up to similar to 11 atom % ) and phosphorus (in the range of 1-3 a
tom % ). The Ca(W, P) films can be applied for microelectronics multilevel
metallization or for ultralage-scale integrated (ULSI) and microelectromech
anical systems (MEMS) applications. The film was deposited from an aqueous
electrolyte that contained tungsten phosphoric acid, H-3[P(W3O10)(4)], as a
source for tungsten. Cobalt sulfate was used as a source for the cobalt io
ns and sodium hypophosphite as the reducing agent and a source for phosphor
us. The Co(W, P) thin films from solutions with tungsten phosphoric acid we
re studied and compared to Co(W, P) films that had been obtained from solut
ions wherein the tungsten was supplied by tungstate ions. The use of tungst
en phosphoric acid allowed higher tungsten content and lower deposition rat
e when compared to solutions with Na2WO4 and (NH4)(2)WO4. The deposition wi
th tungsten phosphoric acid was studied for 20-200 nm thick layers and was
found to ire reproducible. The deposited layers were bright colored and the
ir specific resistance was in the rang of 48-90 mu Ohm cm. The process para
meters of typical solutions are presented and discussed. The film sheer res
istance, composition, and surface morphology are presented for various solu
tions and process conditions. The deposition process involves several react
ions that occur simultaneously and are described in this work. Finally, var
ious applications are proposed for copper metallization as a barrier layer,
to confine the copper, or as a capping layer to prevent copper oxidation a
nd improve adhesion of the inlaid copper to upper interlevel dielectric lay
ers. (C) 2001 The Electrochemical Society. All rights reserved.