A 3.2 V Binary Layered Oxide Cathode for Potassium-Ion Batteries.

Potassium-ion batteries (KIBs) can offer high energy density, cyclability, and operational safety while being economical due to the natural abundance of potassium. Utilizing graphite as an anode, suitable cathodes can realize full cells. Searching for potential cathodes, this work introduces P3-type K0.5Ni1/3Mn2/3O2 layered oxide as a potential candidate synthesized by a simple solid-state method. The material works as a 3.2 V cathode combining Ni redox at high voltage and Mn redox at low voltage and exhibits highly reversible K+ ion (de)insertion at ambient and elevated (40-50 °C) temperatures. First-principles calculations suggest the ground state in-plane Mn-Ni ordering in the MO2 sheets is strongly correlated to the K-content in the framework, leading to an interwoven and alternative row ordering of Ni-Mn in K0.5Ni1/3Mn2/3O2. Postmortem and electrochemical titration reveal the occurrence of a solid solution mechanism during K+ (de)insertion. The findings suggest that the Ni addition can effectively tune the electronic and structural properties of the cathode, leading to improved electrochemical performance. This work provides new insights in the quest to develop potential low-cost Co-free KIB cathodes for practical applications in stationary energy storage.

Role of Co Content on the Electrode Properties of P3-Type K0.5Mn1-xCoxO2 Potassium Insertion Materials.

Potassium-ion batteries are widely being pursued as potential candidates for stationary (grid) storage, where energy dense K+ insertion cathodes are central to economic and energy efficient operation. To develop robust K-based cathodes, it is key to correlate their underlying electronic states to the final electrochemical performance. Here, we report the synthesis and structure-electrochemical property correlation in P3-type K0.5Mn1-xCoxO2 binary layered oxide cathodes. Spectroscopic analyses revealed a random distribution of Mn and Co in transition metal layers in the oxygen anion framework. In this solid-solution family, Co substitution improved the electronic conductivity and structural stability of P3 phases by minimizing local lattice distortion. Co substitution led to a systematic shift of the Co4+/Co3+ and Mn4+/Mn3+ redox potentials. Galvanostatic cycling showed that the Co substitution reduced the initial capacity while improving the cycling stability. The role of Co on final electrochemical properties of P3-layered oxides has been elucidated as a design tool to develop practical potassium-ion batteries.

Phosphorus distribution in the water and sediments of the Ganga and Yamuna Rivers, Uttar Pradesh, India: insights into pollution sources, bioavailability, and eutrophication implications.

River nutrient enrichment is a significant issue, and researchers worldwide are concerned about phosphorus. The physicochemical characteristics and phosphorus (P) fractions of 36 sediment and water samples from the Ganga (Kanpur, Prayagraj, Varanasi) and Yamuna (Mathura, Agra, Prayagraj) rivers were examined. Among the physicochemical parameters, pH exceeded the permissible limit in Ganga and Yamuna River water and sediment samples. Electrical conductivity (EC) and alkalinity were within the permissible limits, whereas total nitrogen (TN) exceeded the limit in Yamuna water. The analysis of phosphorus fractions indicated the dominance of inorganic phosphorus (IP) (76% in Ganga and 96% in Yamuna) over organic phosphorus in both rivers, suggesting the mineralization and microbial degradation as major processes responsible for transforming OP to IP. The positive correlation of pH with IP, AP (apatite phosphorus), and NAIP (non-apatite inorganic phosphorus) explains the release of inorganic phosphorus under alkaline conditions. The correlation between total organic carbon (TOC), TN, and organic phosphorus (OP) indicated the organic load in the rivers from allochthonous and autochthonous sources. Phosphorus released from river sediments and the concentration of phosphate in overlying river water show a positive correlation, suggesting that river sediments may serve as phosphorus reservoirs. The average phosphorus pollution index (PPI) was above one in both rivers, with relatively higher PPI values observed in the Yamuna River, indicating the contamination of sediment with phosphorus, indicating the contamination of sediment with phosphorus. This study revealed variations in the P fractionation of the sediment in both rivers, primarily as a result of contributions from different P sources. This information will be useful for applying different mitigation techniques to lower the phosphorus load in both river systems.