Nb-doped TiO2 cathode catalysts for oxygen reduction reaction of polymer electrolyte fuel cells

被引:24
作者
Arashi, Takuya [1 ]
Seo, Jeongsuk [1 ]
Takanabe, Kazuhiro [2 ]
Kubota, Jun [1 ,3 ]
Domen, Kazunari [1 ]
机构
[1] Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] King Abdullah Univ Sci & Technol, KAUST Catalysis Ctr, Div Phys Sci & Engn, Thuwal 239556900, Saudi Arabia
[3] Kyoto Univ, Elements Strategy Initiat Catalysts & Batteries, Kyoto 6158520, Japan
基金
日本学术振兴会;
关键词
Cathode catalyst; Polymer electrolyte fuel cells; Non-Pt catalysts; Oxygen reduction reaction; Conductive oxides; ALLOY CATALYSTS; METAL; NANOPARTICLES; ELECTROCATALYSTS; COMPOSITE; NITRIDE; TA;
D O I
10.1016/j.cattod.2013.12.009
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
Nb-doped TiO2 particles were studied as electrocatalysts for the oxygen reduction reaction (ORR) under acidic conditions. The Nb-doped TIN nanoparticles were first synthesized by meso-porous C3N4 and then fully oxidized to Nb-doped TiO2 by immersing in 0.1 M H2SO4 at 353 K for 24 h. Although the ORR activity of the as-obtained sample was low, a H-2 treatment at relatively high temperature (1173K) dramatically improved the ORR performance. An onset potential as high as 0.82 V-RHE was measured. No degradation of the catalysts was observed during the oxidation-reduction cycles under the ORR condition for over 127 h. H-2 treatment at temperatures above 1173 K caused the formation of a Ti4O7 phase, resulting in a decrease in ORR current. Elemental analysis indicated that the Nb-doped TiO2 contained 25 wt% residual carbon. Calcination in air at 673 or 973 K eliminated the residual carbon in the catalyst, which was accompanied by a dramatic decrease in ORR activity. This post-calcination process may reduce the conductivity of the sample by filling the oxygen vacancies, and the carbon residue in the particle aggregates may enhance the electrocatalytic activity for ORR. The feasibility of using conductive oxide materials as electrocatalysts is discussed. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:181 / 186
页数:6
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