Search

Chalcogenide solid‐state electrolytes (SSEs) have been receiving growing attentions due to their high ionic conductivity and suitable mechanic properties, especially the Li2S–P2S5 systems incorporated with a second glass network formers (Si, Ge, Sn, and so on) besides P. Although the ionic conductivities are generally enhanced with the second glass network formers, the comprehensive effects of different glass formers on other properties, including electrochemical, cycling, and air stability, remain elusive. To acquire deeper understanding, herein, three common but representative glass network formers (SiS2, GeS2, and SnS2) were introduced into Li2S–P2S5, and their individual effects were investigated systematically. The results of multiscale characterizations before and after lithium stripping/plating cycling confirmed that the introduction of metal cations (Ge, Sn) generally leads to worse electrochemical stability and shorter cycle life of these SSEs toward lithium metal compared with SSEs with nonmetal cation (Si) modification. However, the air stability is related to the binding energy of M–S (M = Si, Ge, Sn), which is consistent with the hard base soft acid theory. This work provides valuable understanding for designing pragmatic Li2S–P2S5–MS2‐based SSEs with high electrochemistry, cycling, and air stability. [ABSTRACT FROM AUTHOR]

High ionic conductivity, low grain boundary impedance, and stable electrochemical property have become the focus for all‐solid‐state lithium–sulfur batteries (ASSLSB). One of the approaches is to promote the rapid diffusion of lithium ions by regulating the chemical bond interactions within the framework. The structure control of P5+ substitution for Sn4+ on lithium‐ion transport was explored for a series of Li3PS4–Li4SnS4 glass–ceramic electrolytes. Results showed that the grain boundary impedance of the glass electrolyte was reduced after heat treatments. The formation of LiSnPS microcrystals, a good superionic conductor, was detected by X‐ray diffraction tests. Electrochemical experiments obtained the highest conductivity of 29.5 S cm−1 at 100°C and stable electrochemical window from –0.1 to 5 V at 25°C. In addition, the cell battery was assembled with prepared electrolyte, which is promoted as a candidate solid electrolyte material with improved performance for ASSLSB. [ABSTRACT FROM AUTHOR]

The glass‐ceramics of AgI‐based electroconductive chalcogenide system was realized using an appropriate heat treatment at a fairly high temperature (Tg + 40°C) and different times ranging from 4 to 20 hours. The crystallization behavior and electroconductive properties of the heat‐treated samples were studied in detail. Transmission study was performed, and the results show that the cut‐off edge of the short wavelength is red‐shifted at prolonged annealing time but remains an excellent transmittance in the mid‐infrared (IR) region. XRD and scanning electron microscopy results indicated that the precipitated crystalline phases are mainly β‐/γ‐AgI. Moreover, a small amount of α‐AgI, which rarely existed at room temperature, is precipitated in the AgI‐rich chalcogenide glass‐ceramics. The ionic conductivity of all glass‐ceramics was enhanced by heat treatment in contrast to that of base glass. Raman analysis exhibited the structure variation in the glass sample after heat treatments. This study provided an observation of crystallization in chalcogenide glass containing large amounts of AgI and be of good guidance to fabricate novel AgI‐based chalcogenide glass‐ceramics that can be candidates in infrared optics and solid electrolyte applications. [ABSTRACT FROM AUTHOR]

A novel family of Ga2S3-Sb2S3-XI (XI = PbI2, CsI, AgI) was investigated to understand the role of metal halides and exploit new chalco-halide glasses for infrared optics. The dependence of the thermal properties, infrared optical properties, and structural information of the novel family on different metal-iodines was investigated. Results showed that metal halides increase the glass stability but decrease the glass network connectivity. The compositional dependence of the short-wave cut-off edge is associated with the electronegativity difference between the cations and anions of the metal halides. Raman study showed that the metal- iodine modified the glass structure mainly through the iodide content, and the cations dissolved in the glass network mostly as charge compensators for the aperiodic network. For the glasses in the series Ga2S3-Sb2S3-XI-Dy3+, Dy3+ emission increased in the PbI2- and CsI-doped glasses but decreased in the AgI-doped glass due to the combined effect of dysprosium and oxygen. For all that, these novel glasses are highly promised for use in infrared optics. [ABSTRACT FROM AUTHOR]

Materials containing rare-earth ions and Ag nanoparticles ( NPs) have been widely applied due to prior demonstration of increase in their luminescence properties. Here, Tm3+ ions-doped bismuth germanate glasses were synthesized by a chemical reduction method based on the conventional melting-quenching technique. The Ag NPs were facilely precipitated in the glass matrix by the chemical reduction method during the annealing process. TEM image shows that the Ag NPs are closely dispersed in the glass matrix. The luminescence properties and energy-transfer mechanism were systematically investigated by means of absorption, emission, and excitation spectra. Significant enhancements of Tm3+ ions emission and a broad emission band centered at 568 nm caused by Ag NPs are observed upon 474-nm excitation. Our research may illustrate the interactions between Tm3+ ions and Ag NPs and provide a simplified way to synthesize the high-efficiency luminescent materials for the blue light-excited W- LEDs. [ABSTRACT FROM AUTHOR]

Diagram of the phase transformation behavior of GeS2- Ga2 S3- CsI glasses is realized in this article and the structure-property dependence of the chalcogenide glasses is elucidated using differential scanning calorimetry and Raman spectroscopy. We observe the compositional threshold of crystallization behavior locates at x = 6-7 mol% in (100− x)(0.8 GeS2-0.2 Ga2 S3)- x CsI glasses, which is confirmed by the thermodynamic studies. Structural motifs are derived from the Raman result that [ Ge( Ga) S4], [ S2 GeI2], [ S3 GaI], and [ S3 Ga- GaS3] were identified to exist in this glass network. Combined with the information of structural threshold, local arrangement of these structural motifs is proposed to explain all the experimental observations, which provides a new way to understand the correlation between crystallization behavior and network structure in chalcogenide glasses. [ABSTRACT FROM AUTHOR]