Volume 9 Issue 3, March 2024

The scarcity of raw materials and complex synthesis procedures have impeded the development of electrolytes for Mg and Ca metal batteries. Research now reports a facile synthesis of organoborate electrolytes through cation replacement reactions, offering highly reversible Mg or Ca electrochemistry.

Injecting hydrogen into subsurface environments could provide seasonal energy storage, but understanding of technical feasibility is limited as large-scale demonstrations are scarce. Now, field tests show that hydrogen can be stored and microbially converted to methane in a depleted underground hydrocarbon reservoir.

Surface reconstruction, chemo-mechanical degradation, and interfacial side reactions are major factors limiting the cyclability of Ni-rich cathodes. A strategy based on entropy-assisted epitaxial coating is now shown to effectively mitigate these issues, leading to improved battery performance and promising advances in electrochemical energy storage.

Development ramifications of global decarbonization efforts for fossil fuel-producing low and lower–middle income countries remain underexplored. This Perspective suggests three transition pathways for navigating these ramifications.

All-solid-state lithium-metal batteries are at the forefront of battery research and development. Here C. Wang and colleagues have developed an interlayer design strategy to address issues associated with lithium dendrite growth and interface resistance, resulting in substantial improvements in battery performance.

The practicality of osmotic energy for portable electronics has been challenging despite recent advancements. Researchers devise a method to store iontronic energy in a polymer film based on osmotic effects, achieving high energy and power density.

Ideal photoelectrochemical systems for hydrogen production should be highly efficient, stable and scalable. Here the authors report that a perovskite-based system with promising efficiency and stability can be scaled to cells of several square centimetres in area as well as formed into mini-modules with overall area >100 cm².

Cost-efficient electrolytes are important for the development of multivalent metal batteries, but expensive precursors and complex synthesis hinder progress. The authors present a cation replacement method for low-cost, high-reversibility magnesium and calcium electrolytes, advancing high-energy-density multivalent metal batteries.

Tin oxidation limits the efficiency of low bandgap perovskite solar cells. Yu et al. synthesize electron-withdrawing chloromethyl phosphonic acid ligand that suppresses tin oxidation, enabling 27%-efficiency perovskite tandem solar cells.

Chemical reactions at the interface between the perovskite and hole transport layer limit the performance of inverted solar cells. Li et al. insert a p-type antimony-doped tin oxide layer that suppresses the reactions, enabling 24.8% efficiency and 500-h operational stability.

Retaining high performance of perovskite solar cells over large areas is a challenge. Yang et al. use a thermotropic liquid crystal with high diffusivity that does not co-crystallize with the perovskite, suppressing defect formation and enabling large-area solar modules with improved stability and efficiency.

The efficiency of perovskite quantum dot solar cells based on organic cations is relatively low. Aqoma et al. develop an alkyl ammonium iodide-based ligand exchange strategy for the replacement of the long-chain oleyl ligands and phase stabilization that enables 18.1%-efficiency solar cells.

Geologic formations could be used for hydrogen storage and conversion to methane, yet technical feasibility is unclear as field-scale data are lacking. Here the authors perform field tests demonstrating that hydrogen can be stored and microbially converted to methane in a depleted underground hydrocarbon reservoir.

Layered Ni-rich oxide cathodes are susceptible to challenges with surface reconstruction and strain propagation, limiting their cyclability. The authors propose a solution involving oriented attachment-driven reactions, utilizing Wadsley–Roth nanocrystals and layered oxide to induce an epitaxial entropy-assisted coating, effectively addressing these issues.