Polyanionic Cathode Materials: A Comparison Between Na‐Ion and K‐Ion Batteries
Hanjiao Huang,
Xiaowei Wu,
Yanjun Gao
et al.
Abstract:Sodium‐ion batteries (SIBs) and potassium‐ion batteries (PIBs) are considered the next‐generation candidates for future energy storage systems to partially substitute commercial lithium‐ion batteries because of their abundant sodium/potassium reserves, cost‐effectiveness, and high safety. Polyanionic cathode materials are widely used in alkali ion batteries due to their stable structural framework, high thermal stability, excellent alkali ion diffusion kinetics, and adjustable working voltage. Generally, the p… Show more
“…The incorporation of weakly acidic carbonate ions into the phosphate matrix substantially bolsters the material’s stability. The stabilization is complemented by an extensive network of robust covalent bonds, which concurrently elevate the material’s surface electronegativity [ 32 ]. Furthermore, within the robust framework of carbonate and phosphate groups lies a substantial population of labile sodium ions, which can generate a plethora of ion exchange sites in solution.…”
The efficient segregation of radioactive nuclides from low-level radioactive liquid waste (LLRW) is paramount for nuclear emergency protocols and waste minimization. Here, we synthesized Na3FePO4CO3 (NFPC) via a one-pot hydrothermal method and applied it for the first time to the selective separation of Sr2+ from simulated LLRW. Static adsorption experimental results indicated that the distribution coefficient Kd remained above 5000 mL·g−1, even when the concentration of interfering ions was more than 40 times that of Sr2+. Furthermore, the removal efficiency of Sr2+ showed no significant change within the pH range of 4 to 9. The adsorption of Sr2+ fitted the pseudo-second-order kinetic model and the Langmuir isotherm model, with an equilibrium time of 36 min and a maximum adsorption capacity of 99.6 mg·g−1. Notably, the adsorption capacity was observed to increment marginally with an elevation in temperature. Characterization analyses and density functional theory (DFT) calculations elucidated the adsorption mechanism, demonstrating that Sr2+ initially engaged in an ion exchange reaction with Na+. Subsequently, Sr2+ coordinated with four oxygen atoms on the NFPC (100) facet, establishing a robust Sr-O bond via orbital hybridization.
“…The incorporation of weakly acidic carbonate ions into the phosphate matrix substantially bolsters the material’s stability. The stabilization is complemented by an extensive network of robust covalent bonds, which concurrently elevate the material’s surface electronegativity [ 32 ]. Furthermore, within the robust framework of carbonate and phosphate groups lies a substantial population of labile sodium ions, which can generate a plethora of ion exchange sites in solution.…”
The efficient segregation of radioactive nuclides from low-level radioactive liquid waste (LLRW) is paramount for nuclear emergency protocols and waste minimization. Here, we synthesized Na3FePO4CO3 (NFPC) via a one-pot hydrothermal method and applied it for the first time to the selective separation of Sr2+ from simulated LLRW. Static adsorption experimental results indicated that the distribution coefficient Kd remained above 5000 mL·g−1, even when the concentration of interfering ions was more than 40 times that of Sr2+. Furthermore, the removal efficiency of Sr2+ showed no significant change within the pH range of 4 to 9. The adsorption of Sr2+ fitted the pseudo-second-order kinetic model and the Langmuir isotherm model, with an equilibrium time of 36 min and a maximum adsorption capacity of 99.6 mg·g−1. Notably, the adsorption capacity was observed to increment marginally with an elevation in temperature. Characterization analyses and density functional theory (DFT) calculations elucidated the adsorption mechanism, demonstrating that Sr2+ initially engaged in an ion exchange reaction with Na+. Subsequently, Sr2+ coordinated with four oxygen atoms on the NFPC (100) facet, establishing a robust Sr-O bond via orbital hybridization.
“…Moreover, the availability of lithium (Li) and cobalt (Co), typically utilized in lithium-ion batteries (LIBs), is severely limited in the Earth's crust. 2 The high cost associated with lithium, coupled with its substantial consumption, presents a significant barrier to the widespread adoption of LIBs in the future. 2 In that regard, SIBs present a notable alternative to LIBs due to the comparable physicochemical properties of sodium to lithium.…”
Section: Introductionmentioning
confidence: 99%
“…2 The high cost associated with lithium, coupled with its substantial consumption, presents a significant barrier to the widespread adoption of LIBs in the future. 2 In that regard, SIBs present a notable alternative to LIBs due to the comparable physicochemical properties of sodium to lithium. 3 Additionally, sodium resources are abundantly available on Earth to supplant LIBs for large-scale applications in the near future.…”
This Highlight explores advancements in Ni-rich cathode materials for sodium-ion batteries, which offer practical synthesis methods, high specific capacity, and environmental benefits while addressing energy density and cycle life challenges.
Prussian blue analogues represent as a class of materials with an open framework structure and have been explored as the potential active materials for alkaline‐ion batteries. Here, we present the synthesis of Prussian blue nanoplates (PBN) designed for use as high performance cathode materials in potassium‐ion batteries (KIBs). PBNs were synthesized through a facile solution precipitation, yielding potassium‐rich PBNs with horizontal crystals growth. The PBNs characterized with a larger particle size of 600 nm and a reduced specific surface area of 6.8 m2 g‐1, compared to conventional prepare Prussian blue hexahedrons. Half‐cell tests demonstrated that the PBNs exhibited a high gravimetric capacity of 152.5 mAh g‐1 with a nominal voltage 3.952 V at a C‐rate of 0.1 C, yielding an energy density of 602.7 Wh kg‐1. Cycling tests demonstrated a capacity of 122.7 mAh g‐1 and a nominal voltage of 3.923 V after 200 cycles at 0.2 C. In a full‐cell configuration with graphite anodes, a gravimetric capacity changed from 134.1 mAh g‐1 to 108.9 mAh g‐1 after 100 cycles at 0.2 C, demonstrating a good cycling stability. This work provides a new insight into the electrochemical properties of PBNs and highlights their potential as high‐performing cathode materials for KIBs.
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