Doped Ceria Nanoparticles with Reduced Solubility and Improved Peroxide Decomposition Activity for PEM Fuel Cells

被引:27
作者
Baker, Andrew M. [1 ,4 ]
Stewart, S. Michael [1 ,2 ,5 ]
Ramaiyan, Kannan P. [2 ]
Banham, Dustin [3 ,6 ]
Ye, Siyu [3 ,7 ]
Garzon, Fernando [2 ]
Mukundan, Rangachary [1 ]
Borup, Rod L. [1 ]
机构
[1] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
[2] Univ New Mexico, Albuquerque, NM 87131 USA
[3] Ballard Power Syst, Burnaby, BC V5J 5J8, Canada
[4] Nikola Motor Co, Phoenix, AZ 85040 USA
[5] Wake Tech Community Coll, Raleigh, NC 27603 USA
[6] Guangdong Dowstone Technol Co Ltd, Shenzhen, Guangdong, Peoples R China
[7] SinoHyKey Corp, Guangzhou, Guangdong, Peoples R China
关键词
Fuel Cells; PEM; Nanoscale materials; Radical scavengers; Peroxide decomposition catalysts; MEMBRANE CHEMICAL DEGRADATION; POLYMER ELECTROLYTE MEMBRANES; OXYGEN REDUCTION REACTION; NANOCRYSTALLINE CERIA; HYDROGEN-PEROXIDE; DURABILITY; MITIGATION; SITU; OXIDE; SIMULATION;
D O I
10.1149/1945-7111/abdee6
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Ceria nanoparticles (NPs) have unique catalytic properties which make them suited to scavenge degrading radical species and their precursor peroxides during PEM fuel cell operation. However, in the acidic environment of the fuel cell, ceria dissolves and the resulting cations migrate within the MEA, causing performance and durability losses. In this work, ex situ testing was used to evaluate the peroxide decomposition, selectivity towards radical generation, and solubility of Gd, Pr, and Zr-doped ceria NPs over a range of crystallite sizes and dopant levels. These doped materials exhibit better peroxide scavenging activity and dissolution resistance than undoped ceria. In these materials, activity is largely governed by increased surface area due to high internal porosity at smaller crystallite sizes compared to undoped ceria. Of the compounds tested, ceria NPs doped with 15 at% Zr (10 nm) and 5 at% Pr (17 nm) exhibited greater dissolution resistance than undoped ceria. Stabilization of the former doped NPs is attributed to crystallite agglomeration, while the increased stability of the latter is proposed to be due to its internally-porous, mesoscale structure suggested by its sorption isotherm. Both materials are more dissolution-resistant and active peroxide decomposers compared to undoped ceria but exhibit increased byproduct radical generation.
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页数:8
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共 46 条
[41]   CeO2 Surface Oxygen Vacancy Concentration Governs in Situ Free Radical Scavenging Efficacy in Polymer Electrolytes [J].
Trogadas, Panagiotis ;
Parrondo, Javier ;
Ramani, Vijay .
ACS APPLIED MATERIALS & INTERFACES, 2012, 4 (10) :5098-5102
[42]   Observation of fuel cell membrane degradation by ex situ and in situ electron paramagnetic resonance [J].
Vogel, B. ;
Aleksandrova, E. ;
Mitov, S. ;
Krafft, M. ;
Dreizler, A. ;
Kerres, J. ;
Hein, M. ;
Roduner, E. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2008, 155 (06) :B570-B574
[43]   A Model to Understand the Oxygen Vacancy Formation in Zr-Doped CeO2: Electrostatic Interaction and Structural Relaxation [J].
Wang, Hai-Feng ;
Gong, Xue-Qing ;
Guo, Yang-Long ;
Guo, Yun ;
Lu, Guan Zhong ;
Hu, P. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (23) :10229-10232
[44]   Engineering the defect state and reducibility of ceria based nanoparticles for improved anti-oxidation performance [J].
Wang, Yan-Jie ;
Dong, Hao ;
Lyu, Guang-Ming ;
Zhang, Huai-Yuan ;
Ke, Jun ;
Kang, Li-Qun ;
Teng, Jia-Li ;
Sun, Ling-Dong ;
Si, Rui ;
Zhang, Jing ;
Liu, Yan-Jun ;
Zhang, Ya-Wen ;
Huang, Yun-Hui ;
Yan, Chun-Hua .
NANOSCALE, 2015, 7 (33) :13981-13990
[45]   In-Situ Modeling of Chemical Membrane Degradation and Mitigation in Ceria-Supported Fuel Cells [J].
Wong, Ka Hung ;
Kjeang, Erik .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2017, 164 (12) :F1179-F1186
[46]   A study of cerium-manganese mixed oxides for oxidation catalysis [J].
Zhou, Gong ;
Shah, Parag R. ;
Gorte, Raymond J. .
CATALYSIS LETTERS, 2008, 120 (3-4) :191-197