Thermal stability of superhard Ti-B-N coatings

被引:69
作者
Mayrhofer, P. H. [1 ]
Stoiber, M.
机构
[1] Mt Uni Leoben, Dept Phys Met & Mat, A-8700 Leoben, Austria
[2] Rhein Westfal TH Aachen, D-52074 Aachen, Germany
[3] Mt Univ Leoben, Mat Ctr Leoben, A-8700 Leoben, Austria
基金
奥地利科学基金会;
关键词
nanostructure; TiBN; TEM; ab initio;
D O I
10.1016/j.surfcoat.2006.08.132
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ternary transition-metal boron nitride Ti-B-N offers outstanding hardness and thermal stability, which are increasingly required for wear resistant applications, as the protective coatings are subjected to high temperature, causing thermal fatigue. Ti-B-N coatings with chemical compositions close to the quasibinary TiN-TiB2 tie line and boron contents below similar to 18 at.% contain a crystalline supersaturated NaCl structure phase, where B substitutes for N. Annealing above the deposition temperature causes precipitation of TiB2, which influence dislocation mobility and hence the hardness of TiB0.40N0.83 remains at a very high level of similar to 43 GPa with annealing temperature T. up to 900 degrees C. Growth of Ti-B-N coatings with B contents above similar to 18 at.% results in the formation of nm sized TiN and TiB2 crystallites embedded in a high volume fraction of disordered boundary layer. The compaction of this disordered phase during annealing results in a hardness increase of TiB0.80N0.83 coatings from the as-deposited value of similar to 37 GPa to similar to 42 GPa at Ta=800 degrees C. Excess B during growth of TiB2.4 coatings causes the formation of bundles of similar to 5 nm wide TiB2 subcolumns encapsulated in a B-rich tissue phase. This nanocolumnar structure is thermally stable up to temperatures of similar to 900 degrees C, and consequently the hardness remains at the very high level of similar to 48 GPa, as nucleation and growth of dislocations is inhibited by the nm sized columns. Furthermore, the high cohesive strength of the B-rich tissue phase prevents grain boundary sliding. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:6148 / 6153
页数:6
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