Solar desalination is one of the most promising strategies to address the global freshwater shortage crisis. However, the residual salt accumulated on the top surface of solar evaporators severely reduces light absorption and steam evaporation efficiency, thus impeding the further industrialization of this technology. Herein, a metal–phenolic network (MPN)‐engineered 3D evaporator composed of photothermal superhydrophilic/superhydrophobic sponges and side‐twining hydrophilic threads for efficient desalination with directional salt crystallization and zero liquid discharge is reported. The MPN coatings afford the engineering of alternating photothermal superhydrophilic/superhydrophobic sponges with high heating efficiency and defined vapor escape channels, while the side‐twining threads induce site‐selective salt crystallization. The 3D evaporator exhibits a high and stable indoor desalination rate (≈2.3 kg m−2 h−1) of concentrated seawater (20 wt%) under simulated sun irradiation for over 21 days without the need for salt crystallization inhibitors. This direct desalination is also achieved in outdoor field operations with a production rate of clean water up to ≈1.82 kg m−2 h−1 from concentrated seawater (10 wt%). Together with the high affinity and multiple functions of MPNs, this work is expected to facilitate the rational design of solar desalination devices and boost the research translation of MPN materials in broader applications.

Si, as a narrow bandgap semiconductor with a broadband absorption for sunlight, is considered to be a very competitive photoelectrode material for solar-driven photoelectrochemical (PEC) water splitting. However, there are major barriers in construction of efficient and stable Si-based PEC cell, including low photovoltage, sluggish reaction kinetics, and poor stability in electrolytes. This review focuses on the strategies to solve these issues and summarizes recent progress. The working principles of PEC water splitting are first introduced. Then the strategies for improving Si-based photoelectrode performances are discussed, including (1) the regulation of Si surface morphology for enhancing light harvesting, (2) band structure engineering strategies to reduce recombination of photogenerated carriers, and (3) modification of protection layers for long stability and loading cocatalysts on Si-based photoelectrodes for accelerating water splitting. Lastly, we have presented some issues of Si-based photoelectrode materials, which should be addressed in future research.

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A nonstoichiometric La1.5Sr0.5Ga3O7.25 melilite oxide ion conductor features active interstitial oxygen defects in its pentagonal rings with high mobility. In this study, electron localization function calculated by density functional theory indicated that the interstitial oxide ions located in the pentagonal rings of gallate melilites may be removed and replaced by electron anions that are confined within the pentagonal rings, which would therefore convert the melilite interstitial oxide ion conductor into a zero-dimensional (0D) electride. The more active interstitial oxide ions, compared to the framework oxide ions, make the La1.5Sr0.5Ga3O7.25 melilite structure more reducible by CaH2 using topotactic reduction, in contrast to the hardly reducible nature of parent LaSrGa3O7. The topotactic reduction enhances the bulk electronic conduction (σ ∼ 0.003 S/cm at 400 °C) by ∼ 1 order of magnitude for La1.5Sr0.5Ga3O7.25. The oxygen loss in the melilite structure was verified and most likely took place on the active interstitial oxide ions. The identified confinement space for electronic anions in melilite interstitial oxide ion conductors presented here provides a strategy to access inorganic electrides from interstitial oxide ion conductor electrolytes.