SnS-based materials have attracted considerable attention in energy storage and conversion owing to their high lithium activity and theoretical capacity. However, the practical application is severely limited by the low coulombic efficiency and short cycle life due to irreversible side reactions, low conductivity, and serious pulverization in the discharge/charge process. In this study, sheet-like stacking SnS/reduced graphene oxide (rGO) heterostructures were developed using a facile solvothermal method. It was found that the composites between SnS nanoplates and rGO nanosheets are closely coupled through van der Waals interactions, providing efficient electron/ion paths to ensure high electrical conductivity and sufficient buffer space to alleviate volume expansion. Therefore, the SnS/rGO heterostructure anode can obtain a high capacity of 840 mA h g after 120 cycles at a current density of 200 mA g and maintain a capacity of 450 mA h g after 1000 cycles at 1000 mA g. In situ X-ray diffraction tests showed that SnS/rGO undergoes typical initial intercalation, conversion, and subsequent alloying reactions during the first discharge, and most of the reactions are dealloying/alloying in the subsequent cycles. The galvanostatic intermittent titration technique showed that the diffusion of lithium ions in the SnS/rGO heterostructures is faster in the intercalation and conversion reactions than in the alloying reactions. These observations help to clarify the reaction mechanism and ion diffusion behavior in the SnS anode materials, thus providing valuable insights for improving the energy efficiency of lithium-ion batteries.
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http://dx.doi.org/10.1021/acsami.1c18268 | DOI Listing |
Nat Commun
October 2024
MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.
Enantioselective synthesis governed by chiral catalysts has been extensively developed, but that without any chiral auxiliaries or chiral catalysts is rare, particularly when remote stereogenic centers are involved. Here we report an enantioselectivity of heterochiral coupling in the one-pot reaction of racemic hydrazides with achiral 1,4-bis(isothiocyanine)benzene, yielding preferentially the heterochiral bilateral azapeptides over the homochiral ones. Despite bearing two hydrogen-bonded β-turn structures that allow intramolecular chiral transfer, the bilateral azapeptide products have two chiral centers separated by 14 atoms or 15 bonds, which prevent the direct intramolecular asymmetric communication between the two chiral centers.
View Article and Find Full Text PDFJ Fluoresc
October 2024
Reproductive Medicine Center, Zhongshan Hospital Affiliated to Fudan University, Shanghai, China.
Polycystic ovary syndrome (PCOS) is a multifactorial disease characterized by oxidative stress and follicular dysfunction, leading to menstrual irregularities, hyperandrogenism, and infertility. Traditional drug delivery methods often result in drug loss and side effects on normal tissues. To address these issues, we synthesized two novel Co(II)-containing coordination polymers (CPs), {[Co(L)(HO)]·2HO}n (1) and {[Co(L)(HO)]·1.
View Article and Find Full Text PDFActa Crystallogr C Struct Chem
November 2024
Department of Chemistry, Howard University, Washington, DC 20059, USA.
Acc Chem Res
September 2024
Center for Electron Microscopy, School of Emergent Soft Matter, South China University of Technology, Guangzhou, Guangdong 510640, China.
ConspectusIn the development of 2D metal-organic frameworks (MOFs) and 2D covalent organic frameworks (COFs), obtaining structural details at the atomic level is crucial to understanding their properties and related mechanisms in potential applications. However, since 2D-MOFs and COFs are composed of layered structures and often exhibit sheet-like morphologies, it is challenging to grow large crystals suitable for single-crystal X-ray diffraction (SCXRD). Therefore, structure determination, which refers to solving the structure directly from experimental data without using any prior knowledge or computational input, is extremely rare for 2D-MOFs and COFs.
View Article and Find Full Text PDFJ Phys Chem Lett
August 2024
Materials Chemistry Department, CSIR-Institute of Minerals and Materials Technology, Bhubaneswar 751013, Odisha, India.
A key limitation of supramolecular force-driven molecular assembly in aggregation-induced emission (AIE) materials is the need to precisely regulate molecular interactions within the assembly. Achieving such assemblies with in situ manipulable molecular arrangements could provide valuable insights into the role of molecular forces in AIE. Herein, by using glutathione-protected gold nanoclusters (AuNCs) as a model AIE material and a naturally occurring polyphenol, tannic acid (TA), as the assembling agent, we demonstrate that assemblies dominated by covalent bonds and hydrogen bonding show enhanced AIE, while those dominated by π-π stacking promote charge transfer, resulting in significant photoluminescence (PL) quenching.
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