Lithium and lanthanum promoted Ni-Al2O3 as an active and highly coking resistant catalyst layer for solid-oxide fuel cells operating on methane

被引:47
|
作者
Wang, Wei [1 ]
Ran, Ran [1 ]
Shao, Zongping [1 ]
机构
[1] Nanjing Univ Technol, State Key Lab Mat Oriented Chem Engn, Coll Chem & Chem Engn, Nanjing 210009, Peoples R China
关键词
Solid-oxide fuel cells; Anode; Catalyst layer; Methane; Carbon deposition; ALKALI-METAL OXIDE; PARTIAL OXIDATION; CARBON-DIOXIDE; NI/AL2O3; CATALYSTS; THERMAL-STABILITY; NATURAL-GAS; ANODE; SOFC; PERFORMANCE; SYNGAS;
D O I
10.1016/j.jpowsour.2010.07.033
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ni-Al2O3 catalyst is modified with Li2O3, La2O3 and CaO promoters to improve its resistance to coking. These catalysts are used as the materials of the anode catalyst layer in solid-oxide fuel cells operating on methane. Their catalytic activity for the partial oxidation, steam reforming and CO2 reforming of methane at 600-850 degrees C is investigated. Their catalytic stability and carbon deposition properties are also studied. The LiLaNi-Al2O3 catalyst shows a catalytic activity that is comparable to those of LaNi-Al2O3 and LiNi-Al2O3 catalysts for all three reactions. However, it displays a higher catalytic activity than those of CaLaNi-Al2O3 and CaNi-Al2O3 catalysts. Among the various catalysts, the LiLaNi-Al2O3 catalyst presents the highest catalytic stability. O-2-TPO profiles indicate that the modification of the Ni-Al2O3 catalyst with Li and La greatly reduces carbon deposition under pure methane atmosphere. The LiLaNi-Al2O3 catalyst is applied as the anode functional layer of a Ni + ScSZ anode-supported fuel cell. The cell is operated on methane-O-2, methane-H2O or methane-CO2 gas mixtures and yields peak power densities of 538,532 and 529 mW cm(-2) at 850 degrees C, respectively, comparable to that of hydrogen fuel. In sum, the LiLaNi-Al2O3 is highly promising as a highly coking resistant catalyst layer for solid-oxide fuel cells. (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:90 / 97
页数:8
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