Premium
High‐temperature phase and microstructure evolution of polymer‐derived SiZrCN and SiZrBCN ceramic nanocomposites
Author(s) -
Feng Bo,
Peter Johannes,
Fasel Claudia,
Wen Qingbo,
Zhang Yue,
Kleebe HansJoachim,
Ionescu Emanuel
Publication year - 2020
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/jace.17149
Subject(s) - materials science , microstructure , ceramic , zirconium , high resolution transmission electron microscopy , crystallization , amorphous solid , chemical engineering , nanocomposite , thermal stability , transmission electron microscopy , crystallography , composite material , nanotechnology , metallurgy , chemistry , engineering
A zirconium and a zirconium/boron containing single‐source precursor were synthesized via chemical modification of a commercially available polysilazane (Durazane 1800) with tetrakis (dimethylamido) zirconium (IV) (TDMAZ) as well as with both TDMAZ and borane dimethyl sulfide complex, respectively. The polymer‐to‐ceramic transformation of the precursors into SiZrCN and SiZrBCN ceramics as well as the thermal evolution of their phase composition and microstructure was studied. The pyrolysis of the precursors led to the formation of amorphous SiZrCN and SiZrBCN ceramics. Interestingly, the as prepared SiZrBCN ceramic was single‐phasic and fully featureless; whereas SiZrCN exhibited the presence of nano‐sized ZrO 2 particles; however, only very localized in close proximity to internal surfaces. Heat treatment at higher temperatures induced crystallization processes in both prepared ceramics. Thus, at temperatures beyond 1500°C, cubic ZrC x N y , β‐Si 3 N 4 as well as β‐SiC were generated. It was shown that the incorporation of B into SiZrCN suppressed the crystallization of ZrC x N y and, in addition, impeded the reaction of SiN x with C, resulting in an improved thermal stability of SiZrBCN compared to SiZrCN ceramic. Moreover boron was shown to be mainly located in the sp 2 ‐hybridized “free” carbon present in SiZrBCN, forming a turbostratic BCN phase which has been unequivocally detected by means of high‐resolution transmission electron microscopy (HRTEM) and energy‐dispersive X‐ray spectroscopy (EDS).