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- ItemElectrocatalytic fuel cell desalination for continuous energy and freshwater generation(Maryland Heights, MO : Cell Press, 2021) Zhang, Yuan; Wang, Lei; Presser, VolkerAdvanced hydrogen technologies contribute essentially to the decarbonization of our industrialized world. Large-scale hydrogen production would benefit from using the abundantly available water reservoir of our planet’s oceans. Current seawater-desalination technologies suffer from high energy consumption, high cost, or low performance. Here, we report technology for water desalination at seawater molarity, based on a polymer ion-exchange membrane fuel cell. By continuously supplying hydrogen and oxygen to the cell, a 160-mM concentration decrease from an initial value of 600 mM is accomplished within 40 h for a 55-mL reservoir. This device’s desalination rate in 600 mM NaCl and substitute ocean water are 18 g/m2/h and 16 g/m2/h, respectively. In addition, by removing 1 g of NaCl, 67 mWh of electric energy is generated. This proof-of-concept work shows the high application potential for sustainable fuel-cell desalination (FCD) using hydrogen as an energy carrier.
- ItemIonophobicity of carbon sub-nanometer pores enables efficient desalination at high salinity(Maryland Heights, MO : Cell Press, 2022) Zhang, Yuan; Prehal, Christian; Jiang, Huili; Liu, Yang; Feng, Guang; Presser, VolkerElectrochemical seawater desalination has drawn significant attention as an energy-efficient technique to address the global issue of water remediation. Microporous carbons, that is, carbons with pore sizes smaller than 2 nm, are commonly used for capacitive deionization. However, micropores are ineffective for capacitive deionization at high molar strength because of their inability to permselectively uptake ions. In our work, we combine experimental work with molecular dynamics simulation and reveal the ability of sub-nanometer pores (ultramicropores) to effectively desalinate aqueous media at seawater-like molar strength. This is done without any ion-exchange membrane. The desalination capacity in 600 mM reaches 12 mg/g, with a charge efficiency of 94% and high cycling stability over 200 cycles (97% of charge efficiency retention). Using molecular dynamic simulations and providing experimental data, our work makes it possible both to understand and to calculate desalination capacity and charge efficiency at high molar strength as a function of pore size.
- ItemBest practice for electrochemical water desalination data generation and analysis(Maryland Heights, MO : Cell Press, 2023) Torkamanzadeh, Mohammad; Kök, Cansu; Burger, Peter Rolf; Ren, Panyu; Zhang, Yuan; Lee, Juhan; Kim, Choonsoo; Presser, VolkerElectrochemical desalination shows promise for ion-selective, energy-efficient water desalination. This work reviews performance metrics commonly used for electrochemical desalination. We provide a step-by-step guide on acquiring, processing, and calculating raw desalination data, emphasizing informative and reliable figures of merit. A typical experiment uses calibrated conductivity probes to relate measured conductivity to concentration. Using a standard electrochemical desalination cell with activated carbon electrodes, we demonstrate the calculation of desalination capacity, charge efficiency, energy consumption, and ion selectivity metrics. We address potential pitfalls in performance metric calculations, including leakage current (charge) considerations and aging of conductivity probes, which can lead to inaccurate results. The relationships between pH, temperature, and conductivity are explored, highlighting their influence on final concentrations. Finally, we provide a checklist for calculating performance metrics and planning electrochemical desalination tests to ensure accuracy and reliability. Additionally, we offer simplified spreadsheet tools to aid data processing, system design, estimations, and upscaling.
- ItemAn engineered coccolith-based hybrid that transforms light into swarming motion(Maryland Heights, MO : Cell Press, 2021) Lomora, Mihai; Larrañaga, Aitor; Rodriguez-Emmenegger, Cesar; Rodriguez, Brian; Dinu, Ionel Adrian; Sarasua, Jose-Ramon; Pandit, AbhayTranslating energy into swarming motion for miniature entities remains a challenge. This translation requires simultaneously breaking the symmetry of the system to enable locomotion and a coupling effect between the objects that are part of the population to induce the collective motion. Here, we report on Robocoliths, engineered Emiliania huxleyi (EHUX) coccolith-based miniature hybrid entities capable of swarming behavior. EHUX coccoliths are characterized by an asymmetric morphology that allows breaking symmetry, playing a central role in generating a net force and directed motion. Their activation with the bioinspired material polydopamine not only endows the asymmetric coccoliths with advanced functionalities, such as thermal- and energy-harvesting responsiveness under visible light exposure to display a collective behavior (i.e., swarming), but it also provides a functional surface from which antifouling polymer brushes are grown. In this context, Robocoliths pave the way for the next generation of multifunctional swarming bio-micromachines. © 2021 The Author(s)Establishment of controlled nano- and mesoscopic energized entities that gather, in a concerted effort, into motile aggregated patterns is at the forefront of scientific discovery. Lomora et al. report on coccolith-polydopamine hybrids (Robocoliths) that heat and move collectively upon light excitation and accommodate antifouling brushes on their surface. © 2021 The Author(s)
- ItemEngineered living hydrogels for robust biocatalysis in pure organic solvents(Maryland Heights, MO : Cell Press, 2022) Gao, Liang; Feng, Lilin; Sauer, Daniel F.; Wittwer, Malte; Hu, Yong; Schiffels, Johannes; Li, XinEngineered living hydrogels that can protect cells from harsh environments have achieved preliminary successes in biomedicine and environmental remediation. However, their biocatalytic applications in pure organic solvents have not been explored. Here, living hydrogels were engineered by integrating genetically modified Escherichia coli cells into alginate hydrogels for robust biocatalysis in pure organic solvents. The biocompatible hydrogels could not only support cell growth and diminish cell escape but could also act as protective matrices to improve organic solvent tolerance, thereby prolonging catalytic activity of whole-cell biocatalysts. Moreover, the influence of hydrogel microenvironments on biocatalytic efficiency was thoroughly investigated. Importantly, the versatility of engineered living hydrogels paves the way to achieve robust biocatalytic efficiency in a variety of pure organic co-solvents. Overall, we are able to engineer living hydrogels for regio-selective synthesis in pure organic solvents, which may be particularly useful for the innovation of living hydrogels in biocatalysis.