Towards a better understanding of atmospheric water harvesting (AWH) technology.

Atmospheric water harvesting (AWH) technology is an emerging sustainable development strategy to deal with global water scarcity. To better understand the current state of AWH technology development, we conducted a bibliometric analysis highlighting three water harvesting technologies (fog harvesting, condensation, and sorption). By comprehensively reviewing the research progress and performing a comparative assessment of these technologies, we summarized past achievements and critically analyzed the different technologies. Traditional fog collectors are more mature, but their efficiency still needs to be improved. External field-driven fog harvesting and active condensation need to be driven by external forces, and passive condensation has high requirements for environmental humidity. Emerging bio-inspired fog harvesting and sorption technology provide new possibilities for atmospheric water collection, but they have high requirements for materials, and their commercial application is still to be further promoted. Based on the key characteristics of each technology, we presented the development prospects for the joint use of integrated/hybrid systems. Next, the water-energy relationship is used as a link to clarify the future development strategy of AWH technology in energy driving and conversion. Finally, we outlined the core ideas of AWH for both basic research and practical applications and described its limitless possibilities for drinking water supply and agricultural irrigation. This review provides an essential reference for the development and practical application of AWH technologies, which contribute to the sustainable utilization of water resources globally.

A Binary Solution Strategy Enables High-Efficiency Quasi-2D Perovskite Solar Cells with Excellent Thermal Stability.

Quasi-two-dimensional (2D) perovskites are highly promising light-harvesting materials for commercialization of perovskite solar cells (PSCs) owing to the excellent materials stability. However, the coexistence of multiple n-value species in 2D perovskites often causes increased complexities in crystallization that can negatively affect the eventual photovoltaic performance. Herein, we present a binary solution based strategy via introducing nontoxic and widely accessible CH3COOH (HAc) as a co-solvent for preparing high-quality 2D perovskite films. Based on a 2D perovskite model system, (AA)2MA4Pb5I16 (n = 5), we show that the prenucleation and grain growth kinetics are appreciably modified with HAc, which benefits from the strong electron-donating ability of HAc with the key component of PbI2, leading to formation of favorable cluster aggregates and resultant modulation of crystal growth. With the HAc-based method, the devices yield a boosted photovoltaic efficiency of 18.55% with an impressive photovoltage of 1.26 V. The champion cells exhibit a supreme thermal stability, showing <3% efficiency degradation under continuous thermal aging for 800 h.

Solvent Effect on Film Formation and Trap States of Two-Dimensional Dion-Jacobson Perovskite.

Two dimensional Dion-Jacobson (2D DJ) perovskite has emerged as a potential photovoltaic material because of its unique optoelectronic characteristics. However, due to its low structural flexibility and high formation energy, extra assistance is needed during crystallization. Herein, we study the solvent effect on film formation and trap states of 2D DJ perovskite. It is found that the nucleation process of 2D DJ perovskite can be retarded by extra coordination, which is proved by in situ optical spectra. As a benefit, out-of-plane oriented crystallization and ordered phase distribution are realized. Finally, in 1,5-pentanediammonium (PeDA) based 2D DJ perovskite solar cells (PSCs), one of the highest reported open-circuit voltage (VOC) values of 1.25 V with state-of-the-art efficiency of 18.41% is obtained due to greatly shallowed trap states and suppressed nonradiative recombination. The device also exhibits excellent heat tolerance, which maintains 80% of its initial efficiency after being kept under 85 °C after 3000 h.