LiFeOHS is a material with Li(OH) layers intercalated between FeS planes. Its hydrothermal synthesis in various concentrations of LiOH yields materials with a high non-stoichiometry of the Li/Fe ratio which can be explained by partial substitution of Li for Fe in the Li(OH) layers. Thermogravimetry, X-ray diffraction and Mössbauer studies indicate that the charge balance is obtained by substitution of hydroxyl ions OH by oxide ions O. This material has been tested as an electrode for lithium-ion batteries against lithium metal. Specific capacities above 200 mA h g at C/10 are achieved, involving 1 lithium per chemical formula when cycled between 1 V and 3 V lithium. The first irreversible discharge leads to the insertion of one lithium atom and the evolution of hydrogen gas while iron remains in its +2-oxidation state. An original LiOFeS oxysulfide is formed. The following reversible oxidation/reduction cycles involve the Fe/Fe redox couple between the two limiting compositions: LiOFeS and LiOFeS.
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http://dx.doi.org/10.1039/d4dt00405a | DOI Listing |
ACS Appl Mater Interfaces
January 2025
State Key Laboratory of Wide-Bandgap Semiconductor Devices and Integrated Technology, Xidian University, Xi'an 710071, PR China.
Commercial SnO nanocrystals used for producing electron transporting layers (ETLs) of perovskite solar cells (PSC) are prone to aggregation at room temperature and contain many structural defects. Herein, we report that the LiOH additive can simultaneously delay the aggregation and donate the beneficial aging effect to SnO nanocrystals. The resulting SnO ETLs show the desired characteristics, including a broadened absorption range, reduced defects, improved transporting properties, and decreased work function.
View Article and Find Full Text PDFChem Sci
January 2025
Hunan Key Laboratory of Micro & Nano Materials Interface Science, College of Chemistry and Chemical Engineering, Central South University Changsha 410083 P. R. China
The layer-stacking mode of a two-dimensional (2D) material plays a dominant role either in its topology or properties, but remains challenging to control. Herein, we developed alkali-metal ion-regulating synthetic control on the stacking structure of a vinylene-linked covalent triazine framework (termed spc-CTF) for improving hydrogen peroxide (HO) photoproduction. Upon the catalysis of EtONa in Knoevenagel polycondensation, a typical eclipsed stacking mode (spc-CTF-4@AA) was built, while a staggered one (spc-CTF-4@AB) was constructed using LiOH.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
State Key Laboratory of Intelligent Manufacturing Equipment and Technology, School of Mechanical Science and Engineering, Huazhong University of Science and Technology, Wuhan, Hubei 430074, People's Republic of China.
The Ni-rich LiNiCoMnO cathode (NCM, ≥ 0.6) suffers rapid capacity decay due to serious surface degradations from the corrosion of the electrolyte. The processes of the HO- and O-based AlO atomic layer deposition (ALD) on the single-crystal LiNiCoMnO (NCM83) are investigated by measurements to understand the mechanism of their different impacts on the electrochemical performance of NCM83.
View Article and Find Full Text PDFJ Colloid Interface Sci
April 2025
College of Physics, Qingdao University, Qingdao 266071, China. Electronic address:
ACS Appl Mater Interfaces
December 2024
School of Metallurgy and Environment, Central South University, Changsha, Hunan 410083, China.
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