Reversible solid-oxide cell stack based power-to-x-to-power systems: Comparison of thermodynamic performance
Creators
- 1. Group of Energy Materials and Industrial Process and Energy Systems Engineering, Swiss Federal Institute of Technology in Lausanne, Switzerland
- 2. National Research Center for Thermal Power Engineering and Technology, North China Electric Power University, China
- 3. Group of Energy Materials, Swiss Federal Institute of Technology in Lausanne, Switzerland
- 4. Institute of Biomedical Engineering, National Chiao Tung University, Republic of China
- 5. Industrial Process and Energy Systems Engineering, Swiss Federal Institute of Technology in Lausanne, Switzerland
Description
The increasing penetration of variable renewable energies poses new challenges for grid management. The economic feasibility of grid-balancing plants may be limited by low annual operating hours if they work either only for power generation or only for power storage. This issue might be addressed by a dual-function power plant with power-to-x capability, which can produce electricity or store excess renewable electricity into chemicals at different periods. Such a plant can be uniquely enabled by a solid-oxide cell stack, which can switch between fuel cell and electrolysis with the same stack. This paper investigates the optimal conceptual design of this type of plant, represented by power-to-x-to-power process chains with x being hydrogen, syngas, methane, methanol and ammonia, concerning the efficiency (on a lower heating value) and power densities. The results show that an increase in current density leads to an increased oxygen flow rate and a decreased reactant utilization at the stack level for its thermal management, and an increased power density and a decreased efficiency at the system level. The power-generation efficiency is ranked as methane (65.9%), methanol (60.2%), ammonia (58.2%), hydrogen (58.3%), syngas (53.3%) at 0.4 A/cm2, due to the benefit of heat-to-chemical-energy conversion by chemical reformulating and the deterioration of electrochemical performance by the dilution of
hydrogen. The power-storage efficiency is ranked as syngas (80%), hydrogen (74%), methane (72%), methanol (68%), ammonia (66%) at 0.7 A/cm2, mainly due to the benefit of co-electrolysis and the chemical energy loss occurring in the chemical synthesis reactions. The lost chemical energy improves plant-wise heat integration and compensates for its adverse effect on power-storage efficiency. Combining these efficiency numbers of the two modes results in a rank of round-trip efficiency: methane (47.5%) > syngas (43.3%) ≈ hydrogen (42.6%) > methanol (40.7%) > ammonia (38.6%). The pool of plant designs obtained lays the basis for the optimal deployment of this balancing technology for specific applications.
Notes
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Wang_et_al_2020_APEN.pdf
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Additional details
Funding
- European Commission
- WASTE2WATTS - Unlocking unused bio-WASTE resources with loW cost cleAning and Thermal inTegration with Solid oxide fuel cells 826234
- European Commission
- WASTE2GRIDS - Converting WASTE to offer flexible GRID balancing Services with highly-integrated, efficient solid-oxide plants 826161
- European Commission
- BALANCE - Increasing penetration of renewable power, alternative fuels and grid flexibility by cross-vector electrochemical processes 731224
- European Commission
- CH2P - Cogeneration of Hydrogen and Power using solid oxide based system fed by methane rich gas 735692