Efficiency Enhancement of an Ammonia-Based Solar Thermochemical Energy Storage System Implemented with Hydrogen Permeation Membrane

The ammonia-based solar thermochemical energy storage (TCES) is one of the most promising solar TCESs. However, the solar-to-electric efficiency is still not high enough for further commercialization. The efficiency is limited by the high ammonia decomposition reaction temperature, which does not only increase the exergy loss through the heat recuperation but also causes a large re-radiation loss. Nonetheless, lowering the reaction temperature would impact the conversion and the energy storage capacity. Thanks to the recent development of the membrane technology, the hydrogen permeation membrane has the potential to enhance the conversion of ammonia decomposition under the moderate operating temperature. In this paper, an ammonia-based solar thermochemical energy storage system implemented with hydrogen permeation membrane is proposed for the first time. The system model has been developed using the Aspen Plus software implemented with user-defined Fortran subroutines. The model is validated by comparing model-generated reactor temperatures and conversions profiles with data from references. With the validated model, an exergy analysis is performed to investigate the main exergy losses of the system. Furthermore, the effects of the membrane on system efficiency improvement are studied. The results show that exergy loss in the charging loop is dominant, among which the exergy losses of Heat Exchanger Eh,A, together with that of the re-radiation Er, play important roles. Compared with the conventional system, i.e., the system without the membrane, the Eh,A and Er of the proposed system are more than 30% lower because the hydrogen permeation membrane can improve ammonia conversion at a lower endothermic reaction outlet temperature. Consequently, the proposed system, presumably realized by the parabolic trough collector at ~400 °C, has a theoretical solar-to-electric efficiency of ηste, which is 4.4% higher than the conventional ammonia-based solar thermochemical energy storage system. Last but not least, the efficiency is 3.7% higher than that of a typical parabolic trough solar power plant, which verifies the thermodynamic feasibility of further commercialization

Copper-coordinated cellulose ion conductors for solid-state batteries

Although solid-state lithium (Li)-metal batteries promise both high energy density and safety, existing solid ion conductors fail to satisfy the rigorous requirements of battery operations. Inorganic ion conductors allow fast ion transport, but their rigid and brittle nature prevents good interfacial contact with electrodes. Conversely, polymer ion conductors that are Li-metal-stable usually provide better interfacial compatibility and mechanical tolerance, but typically suffer from inferior ionic conductivity owing to the coupling of the ion transport with the motion of the polymer chains1,2,3. Here we report a general strategy for achieving high-performance solid polymer ion conductors by engineering of molecular channels. Through the coordination of copper ions (Cu2+) with one-dimensional cellulose nanofibrils, we show that the opening of molecular channels within the normally ion-insulating cellulose enables rapid transport of Li+ ions along the polymer chains. In addition to high Li+ conductivity (1.5 × 10−3 siemens per centimetre at room temperature along the molecular chain direction), the Cu2+-coordinated cellulose ion conductor also exhibits a high transference number (0.78, compared with 0.2–0.5 in other polymers2) and a wide window of electrochemical stability (0–4.5 volts) that can accommodate both the Li-metal anode and high-voltage cathodes. This one-dimensional ion conductor also allows ion percolation in thick LiFePO4 solid-state cathodes for application in batteries with a high energy density. Furthermore, we have verified the universality of this molecular-channel engineering approach with other polymers and cations, achieving similarly high conductivities, with implications that could go beyond safe, high-performance solid-state batteries