Dissolution Stability: The Major Challenge in the Regenerative Fuel Cells Bifunctional Catalysis

被引:39
作者
da Silva, Gabriel C. [1 ,2 ]
Mayrhofer, Karl J. J. [1 ]
Ticianelli, Edson A. [2 ]
Cherevko, Serhiy [1 ]
机构
[1] Forschungszentrum Julich GmbH, Helmholtz Inst Erlangen Nurnberg Renewable Energy, D-91058 Erlangen, Germany
[2] Univ Sao Paulo, Sao Carlos Inst Chem, BR-13560970 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
OXYGEN EVOLUTION REACTION; THERMALLY TREATED IRIDIUM; PLATINUM DISSOLUTION; PURE IRIDIUM; OXIDE; OXIDATION; NANOPARTICLES; ELECTROCATALYSTS; SURFACE; LAYERS;
D O I
10.1149/2.1201816jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Unitized regenerative fuel cells (URFCs) with Pt and Ir as catalysts can potentially provide required buffering capacity for the intermittent renewable energy. While a relatively good catalytic activity of Pt-Ir catalysts has been shown, data on dissolution stability is less convincing. In this work, two representative oxygen bifunctional catalysts for application in URFCs are synthesized by depositing Pt nanoparticles on hydrous Ir oxide (Pt/IrOx) and rutile Ir oxide (Pt/IrO2). A set of spectroscopy and microscopy techniques is used to characterize the synthesized materials. Regarding the catalytic activity, it is shown that Pt/IrO2 and Pt/IrOx are superior for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), respectively. Further, the catalysts' stability toward dissolution is evaluated using a scanning flow cell coupled to an inductively coupled plasma mass spectrometer (SFC-ICP-MS) setup. Dissolution data reveal that Pt is relatively stable in either ORR or OER potential ranges. On the other hand, dissolution of Ir in the OER protocol is considerable. In the ORR-OER potential range, dissolution of both elements enhances significantly. Especially critical is high dissolution of Pt, which limits lifetime of the catalysts. These results must be considered in the development of novel bifunctional catalyst to be used in URFC. (C) The Author(s) 2018. Published by ECS.
引用
收藏
页码:F1376 / F1384
页数:9
相关论文
共 71 条
[1]   Iridium Oxide for the Oxygen Evolution Reaction: Correlation between Particle Size, Morphology, and the Surface Hydroxo Layer from Operando XAS [J].
Abbott, Daniel F. ;
Lebedev, Dmitry ;
Waltar, Kay ;
Povia, Mauro ;
Nachtegaal, Maarten ;
Fabbri, Emiliana ;
Coperet, Christophe ;
Schmidt, Thomas J. .
CHEMISTRY OF MATERIALS, 2016, 28 (18) :6591-6604
[2]   Activity and Durability of Iridium Nanoparticles in the Oxygen Evolution Reaction [J].
Alia, Shaun M. ;
Rasimick, Brian ;
Ngo, Chilan ;
Neyerlin, K. C. ;
Kocha, Shyam S. ;
Pylypenko, Svitlana ;
Xu, Hui ;
Pivovar, Bryan S. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2016, 163 (11) :F3105-F3112
[3]   Self-assembled IrO2 nanoparticles on a DNA scaffold with enhanced catalytic and oxygen evolution reaction (OER) activities [J].
Anantharaj, S. ;
Karthik, P. E. ;
Kundu, Subrata .
JOURNAL OF MATERIALS CHEMISTRY A, 2015, 3 (48) :24463-24478
[4]   Towards an electricity-powered world [J].
Armaroli, Nicola ;
Balzani, Vincenzo .
ENERGY & ENVIRONMENTAL SCIENCE, 2011, 4 (09) :3193-3222
[5]   XPS AND AES STUDY OF MIXED LAYERS OF RUO2 AND IRO2 [J].
ATANASOSKA, L ;
ATANASOSKI, R ;
TRASATTI, S .
VACUUM, 1990, 40 (1-2) :91-94
[6]   A chimie douce route to pure iridium oxide [J].
Bestaoui, N ;
Prouzet, E .
CHEMISTRY OF MATERIALS, 1997, 9 (04) :1036-1041
[7]  
Cherevko S., 2017, ELECTROCHEMICAL DISS
[8]  
Cherevko S., 2018, CURRENT OPINION ELEC
[9]   Oxygen evolution activity and stability of iridium in acidic media. Part 2. - Electrochemically grown hydrous iridium oxide [J].
Cherevko, Serhiy ;
Geiger, Simon ;
Kasian, Olga ;
Mingers, Andrea ;
Mayrhofer, Karl J. J. .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2016, 774 :102-110
[10]   Oxygen evolution activity and stability of iridium in acidic media. Part 1. - Metallic iridium [J].
Cherevko, Serhiy ;
Geiger, Simon ;
Kasian, Olga ;
Mingers, Andrea ;
Mayrhofer, Karl J. J. .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2016, 773 :69-78