Ordered layered structures serve as essential components in lithium (Li)-ion cathodes^1–3. However, on charging, the inherently delicate Li-deficient frameworks become vulnerable to lattice strain and structural and/or chemo-mechanical degradation, resulting in rapid capacity deterioration and thus short battery life^2,4. Here we report an approach that addresses these issues using the integration of chemical short-range disorder (CSRD) into oxide cathodes, which involves the localized distribution of elements in a crystalline lattice over spatial dimensions, spanning a few nearest-neighbour spacings. This is guided by fundamental principles of structural chemistry and achieved through an improved ceramic synthesis process. To demonstrate its viability, we showcase how the introduction of CSRD substantially affects the crystal structure of layered Li cobalt oxide cathodes. This is manifested in the transition metal environment and its interactions with oxygen, effectively preventing detrimental sliding of crystal slabs and structural deterioration during Li removal. Meanwhile, it affects the electronic structure, leading to improved electronic conductivity. These attributes are highly beneficial for Li-ion storage capabilities, markedly improving cycle life and rate capability. Moreover, we find that CSRD can be introduced in additional layered oxide materials through improved chemical co-doping, further illustrating its potential to enhance structural and electrochemical stability. These findings open up new avenues for the design of oxide cathodes, offering insights into the effects of CSRD on the crystal and electronic structure of advanced functional materials.

The formation of stable interphases on the electrodes is crucial for rechargeable lithium (Li) batteries. However, next-generation high-energy batteries face challenges in controlling interphase formation due to the high reactivity and structural changes of electrodes, leading to reduced stability and slow ion transport, which accelerate battery degradation. Here, we report an approach to address these issues by introducing multicomponent grain-boundary-rich interphase that boosts the rapid transport of ions and enhances passivation toward prolonged lifespan. This is guided by fundamental principles of solid-state ionics and geological crystallization differentiation theory, achieved through improved solvation chemistry. Demonstrations showcase how the introduction of the interphase substantially impacts the Li-ion transport across the interphase and the electrode-electrolyte compatibility in cost-effective electrolyte solutions optimized with multiple Li salts. The resulting interphases feature microstructures rich in inorganic grain boundaries with a diverse array of nanosized grains, presenting enhanced Li-ion transport. Comprehensive analyses revealed that this realizes remarkable electrochemical stability over extended cycling periods by inhibiting electrode corrosion, thus holding promise for high-capacity thin-Li-metal, Si-based anodes, and even Li-free anodes when paired with high-capacity oxide cathodes. This work opens new avenues to customize protective interphases on high-capacity electrodes, promoting the development of batteries with the highest energy density using cost-effective electrolytes.

Interfacial wettability adjustment is a new method for intensifying vapor–liquid mass transfer process. Contact angle effect has been well investigated but not complete due to interfacial wettability consisting of both static behavior (contact angle) and dynamic behavior (contact angle hysteresis). Here, methods of adjusting contact angle hysteresis (CAH) were proposed, and then, the CAH effect on the hydrodynamics was investigated. A multiscale analysis of CAH effect, from interfacial force and wettability to single-bubble and gas–liquid two-phase flow inside the foam to bubble swarm hydrodynamics, was conducted, and thus, the hydrodynamic performance criteria were derived. The interfaces had similar contact angles, whereas a significant difference in the CAH was prepared by using the developed sol dip-coating and spray coating methods. Subsequent experiments revealed that lower CAH can decrease the pressure drop, homogenize the gas distribution, and increase the weeping rate, which are consistent with the derived criteria.

Accurate and reliable flow forecasting form an important basis for efficient real-time river management, including flood control, flood warning and so on. In order to improve the accuracy of flow forecasting, gain matrix of Kalman filter was applied to real-time correction of hydraulic model for spatial distributing the system deviation (called expected value of system noise in Kalman filter). That means Kalman gain matrix is used to distribute model system deviation from measurement cross sections to the entire state of the river system. State functions of Kalman filter were set up based on discretization and linearization Saint-Venant equations by adopting four-point linear implicit form, and the spatial distribution system deviation method (SDM) was used for real-time correction. The calculation of flood forecasting for river section from Cuntan to Fengjie of Yangtze River verifies that SDM is useful in promoting the accuracy of real-time flood forecasting.