Highly active and thermally stable single-atom catalysts for high-temperature electrochemical devices
- Authors
- Shin, Jisu; Lee, Young Joo; Jan, Asif; Choi, Sung Min; Park, Mi Young; Choi, Sungjun; Hwang, Jun Yeon; Hong, Seung ki; Park, Seung Gyu; Chang, Hye Jung; Cho, Min Kyung; Singh, Jitendra Pal; Chae, Keun Hwa; Yang, Sungeun; Ji, Ho-Il; Kim, Hyoungchul; Son, Ji-Won; Lee, Jong-Ho; Kim, Byung-Kook; Lee, Hae-Weon; Hong, Jongsup; Lee, Yun Jung; Yoon, Kyung Joong
- Issue Date
- 2020-12
- Publisher
- Royal Society of Chemistry
- Citation
- Energy & Environmental Science, v.13, no.12, pp.4903 - 4920
- Abstract
- Single-atom catalysts provide unique catalytic properties and maximize the atom utilization efficiency. While utilizing them at elevated temperatures is highly desirable, their operating temperature is usually kept below 300 degrees C to prevent isolated atoms from agglomerating. Moreover, their applications in high-temperature electrochemical devices have been hindered by the lack of suitable processing techniques for catalyst loading. Herein, we report single-atom Pt/ceria nanocatalysts that are highly active and thermally stable in solid oxide cells (SOCs) operating at 600-800 degrees C. Our urea-based chemical solution process creates strong Pt-O-Ce interactions that securely anchor isolated Pt atoms to the surface of ceria nanoparticles and suppress their high-temperature migration. These single-atom Pt/ceria nanocatalysts are loaded in the oxide fuel electrode of a SOC via an in situ synthetic process, which reduces the polarization resistance from 28.2 to 0.82 Ohm cm(2) at 600 degrees C. This electrode outperforms the state-of-the-art Ni-based fuel electrode by up to 10 times and delivers extremely high performance in full SOCs in fuel cell and electrolysis modes. Furthermore, it stably operates at 700 degrees C for over 500 h under realistic operating conditions. Our results provide guidance to resolve the critical issues for the practical use of single-atom catalysts in various industrial processes and accelerate the commercial development of next-generation high-temperature energy devices.
- Keywords
- WATER-GAS SHIFT; OXIDE FUEL-CELLS; ATOMICALLY DISPERSED PALLADIUM; ACCESSIBLE METALLIC SURFACE; CO OXIDATION; IN-SITU; STABILIZED ZIRCONIA; SUPPORTED PLATINUM; LATTICE OXYGEN; SELECTIVE HYDROGENATION; solid oxide fuel cell; solid oxide electrolysis cell; single atom catalyst
- ISSN
- 1754-5692
- URI
- https://pubs.kist.re.kr/handle/201004/117745
- DOI
- 10.1039/d0ee01680b
- Appears in Collections:
- KIST Article > 2020
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