TY - JOUR
T1 - Long-term stable Ti/BDD electrode fabricated with HFCVD method using two-stage substrate temperature
AU - Guo, Liang
AU - Chen, Guohua
N1 - Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].
PY - 2007
Y1 - 2007
N2 - Boron-doped diamond-film-coated titanium (TiBDD) has become increasingly attractive because of the combined properties of these two unique materials. The challenge for the composite material is stability, especially when it is used as an electrode. In order to meet this challenge, a two-temperature (2-T)-stage hot-filament chemical vapor deposition (HFCVD) method was employed in this study. The accelerated working lifetime was significantly increased to 804 h for the 2-T electrode, compared with 244 h for the diamond-film electrode fabricated under the one-temperature (1-T)-stage method. With the characterization of micro-Raman, X-ray diffraction, and cross-sectional scanning electron microscopy, a multilayer of Ti/TiC/(diamond + amorphous carbon)/diamond could be found in the 2-T sample and the structure of TiTiCdiamond in the 1-T sample. There was less void space observed in the interlayer of the 2-T sample. The multilayered compact structure played an important role in improving the adhesion of diamond film to the titanium substrate, which in turn increased the electrode working lifetime by over two times. © 2007 The Electrochemical Society.
AB - Boron-doped diamond-film-coated titanium (TiBDD) has become increasingly attractive because of the combined properties of these two unique materials. The challenge for the composite material is stability, especially when it is used as an electrode. In order to meet this challenge, a two-temperature (2-T)-stage hot-filament chemical vapor deposition (HFCVD) method was employed in this study. The accelerated working lifetime was significantly increased to 804 h for the 2-T electrode, compared with 244 h for the diamond-film electrode fabricated under the one-temperature (1-T)-stage method. With the characterization of micro-Raman, X-ray diffraction, and cross-sectional scanning electron microscopy, a multilayer of Ti/TiC/(diamond + amorphous carbon)/diamond could be found in the 2-T sample and the structure of TiTiCdiamond in the 1-T sample. There was less void space observed in the interlayer of the 2-T sample. The multilayered compact structure played an important role in improving the adhesion of diamond film to the titanium substrate, which in turn increased the electrode working lifetime by over two times. © 2007 The Electrochemical Society.
UR - http://www.scopus.com/inward/record.url?scp=35548930245&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-35548930245&origin=recordpage
U2 - 10.1149/1.2790798
DO - 10.1149/1.2790798
M3 - RGC 21 - Publication in refereed journal
SN - 0013-4651
VL - 154
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 12
ER -