Abstract
Protonic ceramic fuel cells, like their higher-temperature solid-oxide fuel cell counterparts, can directly use both hydrogen and hydrocarbon fuels to produce electricity at potentially more than 50 per cent efficiency 1,2 . Most previous direct-hydrocarbon fuel cell research has focused on solid-oxide fuel cells based on oxygen-ion-conducting electrolytes, but carbon deposition (coking) and sulfur poisoning typically occur when such fuel cells are directly operated on hydrocarbon- and/or sulfur-containing fuels, resulting in severe performance degradation over time 3-6 . Despite studies suggesting good performance and anti-coking resistance in hydrocarbon-fuelled protonic ceramic fuel cells 2,7,8, there have been no systematic studies of long-term durability. Here we present results from long-term testing of protonic ceramic fuel cells using a total of 11 different fuels (hydrogen, methane, domestic natural gas (with and without hydrogen sulfide), propane, n-butane, i-butane, iso-octane, methanol, ethanol and ammonia) at temperatures between 500 and 600 degrees Celsius. Several cells have been tested for over 6,000 hours, and we demonstrate excellent performance and exceptional durability (less than 1.5 per cent degradation per 1,000 hours in most cases) across all fuels without any modifications in the cell composition or architecture. Large fluctuations in temperature are tolerated, and coking is not observed even after thousands of hours of continuous operation. Finally, sulfur, a notorious poison for both low-temperature and high-temperature fuel cells, does not seem to affect the performance of protonic ceramic fuel cells when supplied at levels consistent with commercial fuels. The fuel flexibility and long-term durability demonstrated by the protonic ceramic fuel cell devices highlight the promise of this technology and its potential for commercial application.
Original language | English |
---|---|
Pages (from-to) | 217-222 |
Number of pages | 6 |
Journal | Nature |
Volume | 557 |
Issue number | 7704 |
DOIs | |
State | Published - May 10 2018 |
Externally published | Yes |
Funding
This work was supported by Advanced Research Projects Agency-Energy (ARPA-E) for funding under the REBELS program (award DEAR0000493). Additional support was provided by the Army Research Office under grant no. W911NF-17-1-0051 and the Colorado Office of Economic Development and International Trade (COEDIT) under their Advanced Industries Proof-of-Concept grant program. The views and conclusions contained in this document are those of the authors and should not be interpreted as representing the official policies, either expressed or implied, of ARPA-E, the Department of Energy, the Army Research Office or the US Government. This research used resources of the Advanced Light Source, which is a DOE Office of Science User Facility under contract no. DE-AC02-05CH11231. The US Government is authorized to reproduce and distribute reprints for Government purposes notwithstanding any copyright notation herein Acknowledgements This work was supported by Advanced Research Projects Agency–Energy (ARPA-E) for funding under the REBELS program (award DEAR0000493). Additional support was provided by the Army Research Office under grant no. W911NF-17-1-0051 and the Colorado Office of Economic Development and International Trade (COEDIT) under their Advanced Industries Proof-of-Concept grant program. The views and conclusions contained in this document are those of the authors and should not be interpreted as representing the official policies, either expressed or implied, of ARPA-E, the Department of Energy, the Army Research Office or the US Government. This research used resources of the Advanced Light Source, which is a DOE Office of Science User Facility under contract no. DE-AC02-05CH11231. The US Government is authorized to reproduce and distribute reprints for Government purposes notwithstanding any copyright notation herein.
Funders | Funder number |
---|---|
Advanced Research Projects Agency–Energy | |
Colorado Office of Economic Development and International Trade | |
DOE Office of Science | |
DOE Office of Science user facility | DE-AC02-05CH11231 |
US Government | |
U.S. Department of Energy | |
Army Research Office | W911NF-17-1-0051 |
Advanced Research Projects Agency | DEAR0000493 |