02408nas a2200265   4500008004100000022001400041245013100055210006900186260000900255300001400264490000600278520151800284653001401802653001801816653002601834653001201860653002101872100001801893700001701911700002001928700002101948700002101969700002101990856013102011       2020                        eng d  a2196-021600aElectrochemical evaluation of the stability and capacity of r-GO-wrapped copper antimony chalcogenide anode for Li-ion battery0 aElectrochemical evaluation of the stability and capacity of rGOw  cAUG   a3291-33000 v73 a<p>Poor cycling stability and capacity fade are primary concerns for next-generation anode materials for Li-ion batteries. In non-carbonaceous anode materials, alloying with Li leads to volume increase that affects practical applications, and increase in particle size, amorphization and reduced conductivity can all lead to a loss of performance. In this work, binary antimony sulfide (Sb2S3) and ternary copper antimony sulfide (CuSbS2) are synthesized by a convenient solvothermal process. These materials are used to study the Li-active/inactive concept, by incorporating Cu into Sb(2)S(3)forming CuSbS(2)wherein Cu is Li inactive whereas Sb is Li active. By direct comparison, we have shown that incorporating Cu into binary antimony sulfide (Sb2S3) resulting into ternary copper antimony sulfide (CuSbS2) addresses the problem of poor conductivity and capacity loss, as Cu provides conductivity leading to enhanced charge transfer and prevents Sb particle aggregation while charge-discharge by exhibiting spectator or diluent ion effect. The better performance of CuSbS(2)is associated with the better Li(+)ion diffusion in the CuSbS2(D=8.97x10(-15) cm(2) s(-1)) compared to Sb2S3(D=2.76x10(-15) cm(2) s(-1)) and lower series resistance of CuSbS2(R=4.70x10(5) omega) compared to Sb2S3(R=5.81x10(8) omega). We have also investigated the composite with the addition of rGO. The CuSbS2-rGO delivered a reversible capacity of 672 mAh g(-1)after 1000 cycles at 200 mA g(-1)which has shown best performance.</p>
10aBatteries10achalcogenides10aDiffusion coefficient10alithium10aTernary sulfides1 aYadav, Poonam1 aSharma, Neha1 aPatrike, Apurva1 aSabri, Ylias, M.1 aJones, Lathe, A.1 aShelke, Manjusha  uhttps://library.ncl.res.in/content/electrochemical-evaluation-stability-and-capacity-r-go-wrapped-copper-antimony-chalcogenide02271nas a2200217   4500008004100000022001400041245011600055210006900171260000900240300001100249490000800260520150600268653003301774653002101807653002101828653003001849100002101879700002001900700000501920856012801925       2025                        eng d  a0013-468600aExploring FeSe2 and porous carbon composite as a cost-effective host for Al3+ in aqueous Aluminum ion batteries0 aExploring FeSe2 and porous carbon composite as a costeffective h  cOCT   a1468230 v5373 a<p>
	Aluminum is a high-energy-density material with low cost, making rechargeable aluminum ion batteries (AIBs) a attractive alternative to alkali metal ion batteries. However, the practical development of aqueous AIBs is hindered by limited electrode. Herein, we report FeSe2-decorated porous nitrogen and sulfur-doped carbon spheres (FSPNSCS) as a cathode material for aqueous AIBs, with an emphasis on the reaction kinetics and electrochemical performance. FSPNSCS is synthesized through a hydrothermal approach, confirmed by comprehensive characterizations using X-ray Diffraction for crystalline structure validation and Scanning Electron Microscopy for analyzing composite morphology. Electrochemical properties and kinetics are probed using cyclic voltammetry and galvanostatic charge-discharge tests. Ex-situ XRD reveals a notable peak shift towards higher 2 theta values during discharge, indicating lattice contraction due to Al3+ insertion. Sulfur and nitrogen doping impart elasticity to the lattice structure, enhancing stability during cycling. Ex-situ XPS confirms Al3+ storage and minimal oxide formation, as further supported by microscopic elemental mapping with HRTEM. The FSPNSCS cathode achieves a reversible capacity of 60 mAh g- 1 at a current density of 200 mA g- 1. The system exhibits outstanding cycling stability, retaining over 90 % of its capacity at 500 mA g- 1 over 1000 cycles, highlighting its potential to advance aqueous AIBs for sustainable energy storage.</p>
10aAqueous aluminum ion battery10acathode material10aElectrochemistry10aTransition metal selenide1 aMirzapure, Vinay1 aPatrike, Apurva1 a  uhttps://library.ncl.res.in/content/exploring-fese2-and-porous-carbon-composite-cost-effective-host-al3-aqueous-aluminum-ion