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The pairing of ions of opposite charge is a central principle of chemistry. Even though the ability to intercalate anions is desirable for many applications, it remains a key challenge for numerous host materials with their outmost layers beingn anions. In this work, we introduce a hydrothermal ion-exchange synthesis to intercalate oxidative S and Se anions between the Se layers of FeSe, which leads to single crystals of novel compounds (Se/S)(NH)FeSe. In particular, the unusual anion-anion bonding between the intercalated S (or Se) and Se layers exhibits strong ionic characteristics. The charge transfer through the Se layer to S (or Se) intercalants is further confirmed by the elevated oxidation state of Fe ions and the dominant hole carriers in the intercalated compounds. By intercalating S, for the first time superconductivity emerged in hole-doped iron chalcogenides. The generality of this chemical approach was further demonstrated with layered FeS and NiSe. Our findings thus open an avenue to exploring diverse aspects of anionic intercalation in similar materials.
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http://dx.doi.org/10.1021/jacs.9b05899 | DOI Listing |
Langmuir
September 2025
Biophysical Chemistry Laboratory, Physical Chemistry Section, Department of Chemistry, Jadavpur University, Raja S. C. Mullick Road, Jadavpur, Kolkata 700032, India.
Photophysical studies on the interaction of small molecules with various forms of nucleic acids are attracting attention nowadays in order to delineate the molecular level mechanism of various biological processes occurring in vivo. Herein, we employed vivid steady-state and time-resolved spectroscopic techniques to elucidate the detailed characterization of the binding interaction of a biologically active cationic dye thioflavin T (ThT) with double and triple helical forms of RNA - A.U duplex and U.
View Article and Find Full Text PDFChem Sci
August 2025
ARC Ctr. Excellence Electromat Sci., University of Wollongong Innovation Campus, North Wollongong NSW 2500 Australia.
Hard carbon is the most commercially viable anode material for sodium-ion batteries (SIBs), yet its application in ester-based electrolytes is hindered by sluggish interfacial ion diffusion and limited sodium nucleation kinetics. After comprehensive evaluation, an interfacial chemistry regulation strategy was proposed based on orbital hybridization between bismuth and electrolyte ions, which was realized through the introduction of ammonium bismuth citrate. The surface bismuth particles regulate the formation of a NaF-rich SEI through improved anion affinity.
View Article and Find Full Text PDFSmall
September 2025
Shanghai Key Laboratory for R&D and Application of Metallic Functional Materials, Institute of New Energy for Vehicles, School of Materials Science and Engineering, Tongji University, Shanghai, 201804, China.
Significant efforts have been devoted to optimizing the morphology and synthesizing composite materials to activate SnO for sodium-ion batteries. However, challenges arising from its intrinsic crystal structure remain insufficiently addressed. This study aims to introduce both oxygen vacancies and fluorine ions into the SnO lattice, yielding a modified compound with a chemical composition of SnO£F.
View Article and Find Full Text PDFNano Lett
August 2025
National Innovation Center for Industry-Education Integration of Energy Storage Technology, MOE Key Laboratory of Low-grade Energy Utilization Technologies and Systems, CQU-NUS Renewable Energy Materials & Devices Joint Laboratory, School of Energy & Power Engineering, Chongqing University, Chongqin
Two-dimensional vanadium disulfide (VS) is widely used in electrode materials for aqueous batteries but still suffers from limited capacity and rate. We designed an interlayer reaction based on VS in synergy of Mg with conventional cations or anions (H, NH, OH, NO, F, Cl, and SO) (dividing these ions' workings into dual-ion batteries, Mg-anion co-(de)intercalation, and gap-filling). Relatively more suitable paired ions were recommended for each of the three mechanisms.
View Article and Find Full Text PDFAdv Mater
August 2025
Division of Energy Storage, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.
Halide cathode active materials (CAMs) with high ionic conductivities have attracted significant attention. However, their capacity and energy density are limited by the large molar weight of the Li⁺ transport-dependent MCl anionic framework. In this study, a low-cost amorphous iron-based oxyhalide LFFOC-0.
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