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Small nanoparticles of ceria deposited on a powder of CuO display a very high selectivity for the production of methanol via CO2 hydrogenation. CeO2/CuO catalysts with ceria loadings of 5%, 20%, and 50% were investigated. Among these, the system with 5% CeOx showed the best catalytic performance at temperatures between 200 and 350 °C. The evolution of this system under reaction conditions was studied using a combination of environmental transmission electron microscopy (E-TEM), in situ X-ray absorption spectroscopy (XAS), and time-resolved X-ray diffraction (TR-XRD). For 5% CeOx/Cu, the in situ studies pointed to a full conversion of CuO into metallic copper, with a complete transformation of Ce4+ into Ce3+. Images from E-TEM showed drastic changes in the morphology of the catalyst when it was exposed to H2, CO2, and CO2/H2 mixtures. Under a CO2/H2 feed, there was a redispersion of the ceria particles that was detected by E-TEM and in situ TR-XRD. These morphological changes were made possible by the inverse oxide/metal configuration and facilitate the binding and selective conversion of CO2 to methanol. 

Solar-thermal evaporation is a promising technology for energy-efficient desalination, but salt accumulation on solar absorbers and system longevity are the major challenges that hinder its widespread application. In this study, we present a sustainable Janus wood evaporator that overcomes these challenges and achieves a record-high evaporation efficiencies in hypersaline water, one of the most difficult water sources to treat via desalination. The Janus wood evaporator has asymmetric surface wettability, where the top layer acts as a hydrophobic solar absorber with water blockage and salt resistance, while the bottom hydrophilic wood layer allows for rapid water replenishment and superior thermal insulation. An evaporation efficiency of 82.0% is achieved for 20% NaCl solution under 1 sun, and persistent salt-resistance is observed during a 10-cycle long-term test. To ensure the environmental impact of the Janus wood evaporator, for the first time, a life cycle assessment (LCA) is conducted to compare this Janus wood evaporator with the emerging Janus evaporators, indicating a functional and more sustainable opportunity for off-grid desalination and humanitarian efforts. 

Hydrogen evolution is not a spontaneous reaction, so current electrochemical H 2 systems either require an external power supply or use complex photocathodes. We present in this study that by using electrical decoupling, H 2 can be produced spontaneously from wastewater. A power management system (PMS) circuit was deployed to decouple bioanode organic oxidation from abiotic cathode proton reduction in the same electrolyte. The special PMS consisted of a boost converter and an electromagnetic transformer, which harvested energy from the anode followed by voltage magnification from 0.35 V to 2.2–2.5 V, enabling in situ H 2 evolution for over 96 h without consuming any external energy. This proof-of-concept demonstrated a cathode faradaic efficiency of 91.3% and a maximum overall H 2 conversion efficiency of 28.9%. This approach allows true self-sustaining wastewater to H 2 evolution, and the system performance can be improved via the PMS and reactor optimization.