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Pb metallic nanospheres embedded within conductive carbon frameworks (Pb@C) are prepared by a facile coprecipitation and pyrolysis method using MOFs as the precursor and template. The Pb@C electrode presents a high reversible capacity of 379.1 mAh/g at 2 A/g and capacity retention of 88.2% after 6000 cycles, corresponding to a capacity loss of 0.00748% per cycle. [Display omitted] Alloying-type anode materials are considered promising candidates for sodium-ion batteries (SIBs) due to their high theoretical capacities. However, their application is limited by the severe capacity decay stemming from dramatic volume changes during Na+ insertion/extraction processes. Here, Pb nanospheres encapsulated in a carbon skeleton (Pb@C) were successfully synthesized via a facile metal–organic frameworks (MOFs)-derived method and used as anodes for SIBs. The nanosized Pb particles are uniformly incorporated into the porous carbon framework, effectively mitigating volume changes and enhancing Na+ ion transport during discharging/charging. Benefiting from this unique architecture, a reversible capacity of 334.2 mAh g−1 at 2 A g−1 is achieved after 6000 cycles corresponding to an impressive 88.2 % capacity retention and a minimal capacity loss of 0.00748 % per cycle. Furthermore, a high-performance full sodium-ion battery of Pb@C//NVPF was constructed, demonstrating a high energy density of 291 Wh kg−1 and power density of 175 W kg−1. This facile MOFs-derived method offers insights into the design of high-capacity alloy-type anode materials using Pb sources, opening up new possibilities for innovative approaches to Pb recycling and pollution prevention. [ABSTRACT FROM AUTHOR]

Abstract: Potassium‐ion batteries (KIBs) are plagued by a lack of materials for reversible accommodation of the large‐sized K+ ion. Herein we present, the Bi anode in combination with the dimethoxyethane‐(DME) based electrolyte to deliver a remarkable capacity of ca. 400 mAh g−1 and long cycle stability with three distinct two‐phase reactions of Bi↔ KBi2↔K3Bi2↔K3Bi. These are ascribed to the gradually developed three‐dimensional (3D) porous networks of Bi, which realizes fast kinetics and tolerance of its volume change during potassiation and depotassiation. The porosity is linked to the unprecedented movement of the surface Bi atoms interacting with DME molecules, as suggested by DFT calculations. A full KIB of Bi//DME‐based electrolyte//Prussian blue of K0.72Fe[Fe(CN)6] is demonstrated to present large energy density of 108.1 Wh kg−1 with average discharge voltage of 2.8 V and capacity retention of 86.5 % after 350 cycles. [ABSTRACT FROM AUTHOR]

Abstract: Potassium‐ion batteries (KIBs) are plagued by a lack of materials for reversible accommodation of the large‐sized K+ ion. Herein we present, the Bi anode in combination with the dimethoxyethane‐(DME) based electrolyte to deliver a remarkable capacity of ca. 400 mAh g−1 and long cycle stability with three distinct two‐phase reactions of Bi↔ KBi2↔K3Bi2↔K3Bi. These are ascribed to the gradually developed three‐dimensional (3D) porous networks of Bi, which realizes fast kinetics and tolerance of its volume change during potassiation and depotassiation. The porosity is linked to the unprecedented movement of the surface Bi atoms interacting with DME molecules, as suggested by DFT calculations. A full KIB of Bi//DME‐based electrolyte//Prussian blue of K0.72Fe[Fe(CN)6] is demonstrated to present large energy density of 108.1 Wh kg−1 with average discharge voltage of 2.8 V and capacity retention of 86.5 % after 350 cycles. [ABSTRACT FROM AUTHOR]