Electrically enhanced thermochemical cycles for hydrogen generation

Conference · Thu Aug 17 04:00:00 EDT 2023

DOI:https://doi.org/10.2172/1997415· OSTI ID:1997415

Miller, James E. ^[1]; Ermanoski, Ivan ^[1]; Milcarek, Ryan; Rahimipetroudi, Iman; Stechel, Ellen B. ^[1]; Ambrosini, Andrea ^[2]; Babiniec, Sean ^[2]

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1. Arizona State Univ., Tempe, AZ (United States)
2. Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

In two-step metal-oxide (MO) solar thermochemical cycles, high temperature solar thermal energy is first converted to chemical energy in the form of a reduced MO. The reduced MO is then reoxidized in a second step with steam (or carbon dioxide) to produce hydrogen (or carbon monoxide) at a lower temperature. Solar thermochemical cycles of this type circumvent heat-to-electrical conversion required for electrochemical water splitting and promise high efficiencies. However, significant challenges remain to implementation. Ultra-high temperatures and efficiency-sapping low per-cycle conversion stand out as particularly difficult hurdles. Hybrid approaches utilizing both thermal and electrical energy provide some of the advantages of each, and can facilitate lower temperature operation and offer better per-pass utilization than thermochemical alone. However, early concepts for implementing the thermo-electrochemical approach introduced substantial new challenges including difficult separations, corrosive environments, and energy losses from large temperature swings and phase changes. We are currently investigating two different options for implementation. In the first, a MO that reduces at lower temperature is selected. As the reduced MO lacks the full thermodynamic driving force to effectively split water, the reaction is driven forward by an electrically-assisted proton-conducting membrane that separates and recovers hydrogen as it is produced. This approach produces a pure hydrogen stream, is mechanically simple, and has unique thermodynamic advantages. The second option seeks to more directly couple the electrical boost to the solid MO to drive either the reduction or oxidation step, or both, through the utilization of layered MO materials and advanced reactors. This approach could be applied to both water and carbon dioxide splitting. The results of process modeling and optimization will be presented, and progress towards demonstrating the concepts at the laboratory scale will be discussed.

• Research Organization: Arizona State University
• Sponsoring Organization: USDOE Office of Energy Efficiency and Renewable Energy (EERE), Renewable Power Office. Solar Energy Technologies Office
• DOE Contract Number: EE0009818
• OSTI ID: 1997415
• Report Number(s): DOE-ASU-09818-1
• Country of Publication: United States
• Language: English

Related Subjects

08 HYDROGEN
14 SOLAR ENERGY