Solar thermochemical hydrogen (STCH) production is one avenue for converting sunlight into hydrogen through concentrating solar thermal technology. STCH is a two-step redox process that begins with concentrated sunlight to thermally reduce a metal oxide around 1500 °C leaving it in an oxygen deficient form. Subsequent exposure of the reduced metal oxide to steam at lower temperature reoxidizes the material and produces hydrogen. The efficiency of this process is dependent on the metal oxide material thermodynamic properties and cycle operating conditions.
Singh, Abhishek; Lapp, Justin; Grobbel, Johannes; Reinhold, Jan P.; Olivera, Lamark; Ermanoski, Ivan; Siegel, Nathan P.; Mcdaniel, Anthony H.; Roeb, Martin; Sattler, Christian
Recently a novel design concept of a reactor—the cascading pressure reactor—for the thermochemical fuel production, using a solar-driven redox cycle, was proposed. In this concept, thermal reduction of metal oxide particles is completed in multiple stages, at successively lower pressures. This leads to an order of magnitude decrease in the pumping power demand as compared to a single stage, which in turn increases the solar to fuel efficiency. An important step in the process is the transfer of heat in the form of concentrated solar radiation to the particles, while providing reducing conditions in the space surrounding the particles. In this context, a novel system for heating and reducing particles, with a focus on operating at the small prototype scale (below 20 kW), is investigated. The key goals of the system are continuous operation, uniform heating of the reactive material, the ability to heat reactive material to 1723 K or higher, and flexibility of control. These criteria have led to the conceptual design of a continuous thin-layer particle conveyor, contained in an apertured, windowed cavity and enclosed in a vacuum chamber. This chamber, in combination with a water-splitting chamber and other system components, allows the possibility of testing multiple redox materials without any significant change in the reactor design. The present work shows a potential design for the proposed component, feasibility tests of the physics of moving particles with relevant materials, and series of interconnected numerical models and calculations that can be used to size such a system for the appropriate scales of power and mass flow rates. The use of a unified design strategy has led to efficient development of the system. Experimental investigations of the horizontal motion plate allowed effective determination of motion profiles and bed uniformity. The most important factors determined through the modeling effort were the aperture diameter, which serves as the coupling point between the solar simulator lamp array and the cavity particle heating, and the particle bed thickness, which has a strong effect on the outlet temperature of the particles.
This research and development project is focused on the advancement of a technology that produces hydrogen at a cost that is competitive with fossil-based fuels for transportation. A twostep, solar-driven WS thermochemical cycle is theoretically capable of achieving an STH conversion ratio that exceeds the DOE target of 26% at a scale large enough to support an industrialized economy [1]. The challenge is to transition this technology from the laboratory to the marketplace and produce hydrogen at a cost that meets or exceeds DOE targets.
In this paper, we offer a perspective on the current state of material research in a part of the solar fuels community that exploits process heat derived from concentrated solar energy to power simple thermochemical gas-splitting cycles. The working fluid in this process is a nonstoichiometric oxide subject to extreme conditions that repeatedly distorts the lattice by forcing oxygen atoms to move in and out of the crystal. This technology is currently challenged by a need to discover optimal materials and derive robust processes to increase cycle efficiency. In the realm of emerging technologies for converting solar insulation to portable and storable energy carriers, this approach has already proven to be scalable with demonstrations that approach 100 kW. Innovations in materials and methods are required to increase solar utilization and process efficiency in order to achieve commercial viability.
Mcdaniel, Anthony H.; Ermanoski, Ivan; Stechell, Ellen; Johnson, Nathan; Siegel, Nathan; Hayre, Michael'; Sanders, Michael; Wolverton, Christopher; Chueh, William
Overall objectives of the project were: Verify the potential for solar thermochemical cycles for hydrogen production to be competitive in the long term and by 2020, develop this technology to produce hydrogen with a projected cost of $3.00/gge at the plant gate; and, Develop a high-efficiency particle bed reactor for producing hydrogen via a thermochemical water-splitting (WS) cycle, and demonstrate eight continuous hours of operation on a solar simulator producing greater than 3 L of H2.
The surface chemical capacitance of ceria and SDC was investigated using in situ ambient pressure X-ray photoelectron spectroscopy (APXPS) in H2 H 2O environments at elevated temperatures. The spectra were collected in situ after equilibrating the samples under oxygen chemical potentials spanning -2.95 and -3.44 eV versus 1 atm O2. Consequently, the volumetric chemical capacitance of the surface, in the range of 103-104Fcm-3, is nearly two orders of magnitude larger than that of the bulk. Addition of Sm leads to a slight decrease of surface Ce3+ concentration, but a 10-fold enhancement in the surface capacitance under H2 H 2O atmospheres. Our hypothesis for this observation is that Sm lowers defect interactions. The areal surface capacitance calculated for SDC is in good agreement with literature values extrapolated from electrochemical measurements.
Recent work regarding the efficiency maximization for solar thermochemical fuel production in two step cycles has led to the design of a new type of reactor - the cascading pressure reactor - in which the thermal reduction step of the cycle is completed in multiple stages, at successively lower pressures. This approach enables lower thermal reduction pressures than in single-staged reactors, and decreases required pump work, leading to increased solar to fuel efficiencies. Here we report on the design and construction of a prototype cascading pressure reactor and testing of some of the key components. We especially focus on the technical challenges particular to the design, and their solutions.
Preparation of sodium zirconium silicate phosphate (NaSICon), Na1+ xZr2SixP3− xO12(0.25 ≤ x ≤ 1.0), thin films has been investigated via a chemical solution approach on platinized silicon substrates. Increasing the silicon content resulted in a reduction in the crystallite size and a reduction in the measured ionic conductivity. Processing temperature was also found to affect microstructure and ionic conductivity with higher processing temperatures resulting in larger crystallite sizes and higher ionic conductivities. The highest room temperature sodium ion conductivity was measured for an x = 0.25 composition at 2.3 × 10−5 S/cm. The decreasing ionic conductivity trends with increasing silicon content and decreasing processing temperature are consistent with grain boundary and defect scattering of conducting ions.
Next generation metal-ion conducting membranes are key to developing energy storage and utilization technologies like batteries and fuel ce lls. Sodium super-ionic conductors (aka NaSICON) are a class of compounds with AM 1 M 2 (PO 4 ) 3 stoichiometry where the choice of "A" and "M" cation varies widely. This report, which de scribes substitutional derivatives of NZP (NaZr 2 P 3 O 12 ), summarizes the accomplishments of a Laboratory D irected Research and Development (LDRD) project to analyze transport mec hanisms using a combination of in situ studies of structure, composition, and bonding, com bined with first principles theory and modeling. We developed an experimental platform and applied methods, such as synchrotron- based X-ray spectroscopies, to probe the electronic structure of compositionally well-controlled NaSICON films while in operation ( i.e ., conducting Na ions exposed to oxygen or water va por atmospheres). First principles theory and modeling were used to interpret the experimental observations and develop an enhanced understanding of atomistic processes that give rise to, and affect, ion conduction.