Abstract
The relationship between the electrochemical activity of fuel cell catalysts and Pt particle size, as well as the catalyst support and co-catalyst is still unclear. In this work, FESEM, XRD, BET, TEM and CV techniques were adopted to investigate the effects of TiO2 anatase (A)/rutile (R) phases content on the electrochemical activity of Pt electrocatalyst. The results showed that the anatase-rutile phase transformation occurred during the heat treatment of TiO2 at 700 ~ 900 oC accompanied by the growth of two-phase crystalline size, and anatase was completely transformed into rutile at 900 oC. TEM results revealed that the ultrafine Pt electrocatalysts with the particle size of 1.8 ~ 2.8 nm were successfully prepared over the TiO2-CNx supports. The content of TiO2 (A)/(R) phases had a “volcano-type” effect on both the BET surface area of TiO2-CNx supports and the real “effective” electrochemical active surface area (ECSA) of Pt/TiO2-CNx catalysts. When the rutile content was 25%, the TiO2(25%R)-CNx support and Pt/TiO2(25%R)-CNx catalyst had the largest specific surface area and the most electrochemical active sites, respectively. It is speculated that raising the rutile content, there might be a strong metal-support interaction between Pt nanoparticles and TiO2(25%R)-CNx support with the rutile content of 25%, which could anchor the ultrafine Pt nanoparticles, resulting in the highest ECSA of Pt/TiO2(25%R)-CNx catalyst. Therefore, the Pt/TiO2(25%R)-CNx became more suitable as a catalyst for fuel cells.
Graphical Abstract
Keywords
catalyst, TiO2, anatase, rutile, electrochemical active surface area
Publication Date
2022-05-28
Online Available Date
2022-01-02
Revised Date
2021-12-21
Received Date
2021-12-15
Recommended Citation
Ai-Lin Cui, Yang Bai, Hong-Ying Yu, Hui-Min Meng.
Electrocatalytic “Volcano-Type” Effect of Nano-TiO2 (A)/(R) Phase Content in Pt/TiO2-CNx Catalyst[J]. Journal of Electrochemistry,
2022
,
28(5): 2110021.
DOI: 10.13208/j.electrochem.211002
Available at:
https://jelectrochem.xmu.edu.cn/journal/vol28/iss5/3
Included in
Catalysis and Reaction Engineering Commons, Engineering Science and Materials Commons, Materials Chemistry Commons, Materials Science and Engineering Commons, Nanoscience and Nanotechnology Commons, Physical Chemistry Commons, Power and Energy Commons