Solid State Research Articles

Bridging Titanium Nitrido Complexes Containing A Linear Ti-N-Ti Core with A Two-Coordinate Nitrido Ligand.

A series of titanium m2-nitrido complexes supported by the triamidoamine ligand Xy-N3N (Xy-N3N = {(3,5-Me2C6H3)NCH2CH2}3N3-) is reported. The titanium azido complex [(Xy-N3N)TiN3] (1-N3), prepared by salt metathesis of the chloride complex [(Xy-N3N)TiCl] (1-Cl) with NaN3, reacted with lithium metal or with alkali metal naphthalenides (alkali metal M = Na, K, and Rb) in THF to give the corresponding dinuclear m2-nitrido complexes M[(Xy-N3N)Ti=N-Ti(Xy-N3N)] (2-M; M = Li, Na, K, Rb). Single crystal X-ray diffraction studies of 2-Li, 2-Na, and 2-K revealed alkali metal dependent structures in the solid state. While 2-Li and 2-K contain a m2-nitrido ligand with a linear Ti-N-Ti core, 2-Na includes a m3-nitrido ligand as part of a T-shape Ti2NaN fragment with the sodium cation weekly coordinated to the nitrido nitrogen atom. When the synthesis of the nitrido complexes was carried out in the presence of excess alkali metals, selective decomposition of the nitrido complexes was observed affording some intractable titanium species along with the trialkali metal salts [M3(Xy-N3N)] (3-M) (M = Li, Na, K, and Rb). These salts were also prepared by deprotonation of (Xy-N3N)H3 with the corresponding alkali metal hexamethyldisilazide and characterized by multinuclear NMR spectroscopy as well as single crystal X-ray diffraction.

Investigation on Luminescence Properties of Dy3+ Ions Doped NaBaB9O15 Phosphors for Optoelectronic Applications.

A series of Dy3+ ions doped NaBaB9O15 phosphors with different dopant concentration was synthesized by solid state reaction. The phase purity was checked by X-ray diffraction analysis and the functional groups present in as prepared phosphors was investigated with the help of FTIR spectral analysis. Under 386nm excitation, the photoluminescence spectra exhibit three emission bands around 482nm, 574nm and 664nm due to 4F9/2→6HJ/2 (J = 15, 13, 11) transions respectively. The optimum doping concentration of Dy3+ ions was found to be 5mol%. The color coordinates are estimated from the emission spectra to check the dominant emission color and the color coordinates of the studied phosphors are fall on white region of CIE 1931 diagram. The decay curve analysis was made to determine the lifetime of excited state of Dy3+ ions and the decay curves are exhibited bi-exponential behavior irrespective of Dy3+ ion concentration. All these measurents are done in room temperature and the results obtained from these studies are discussed in detail to claim their usage in light emitting devices.

Aggregation-Induced Emission Phosphorescence Featured Au-Ag Coordination Polymer with a Diphosphine N-Heterocyclic Carbene Ligand for Highly Sensitive Detection of Cr(VI).

Luminescent materials with aggregation-induced emission (AIE) characteristics have been recognized as highly selective and sensitive probes for the detection of toxic metal ions in recent years. In this paper, a Au-Ag cluster-based coordination polymer [Au3Ag3(L)2(CN)6(H2O)2]n [1, L = 1,3-bis((diphenylphosphanyl)methyl)-4,5-dihydro-imidazolylidene] was prepared by in situ generation of the diphosphine N-heterocyclic carbene (PCNHCP)-type ligand L in the presence of the corresponding metal salts. Compound 1 exhibited 530 nm phosphorescence under 380 nm excitation with a QY of 6.30% and a lifetime (τ) of 7.14 μs in the solid state. 1 showed good AIE behavior in the mixture of MeOH/H2O while the best aggregation state (fwater = 90%, QY = 6.79%, τ = 6.70 μs) exhibited selective and sensitive emission quenching toward Cr(VI) ions. Ultralow detection limits of 9.7 ppb (w/w) for Cr2O72- and 17.9 ppb (w/w) for CrO42- were achieved.

Low molar mass cyclic poly(L-lactide)s: separate transesterification reactions of cycles and linear chains in the solid state.

L-Lactide (LA) was polymerized with neat tin(II) 2-ethylhexanoate (SnOct2) in toluene at 115 °C at low concentration with variation of the LA/Cat ratio. Cyclic polylactides (cPLAs) with number average molecular weights (Mn) between 7000 and 17 000 were obtained. MALDI-TOF mass spectrometry also revealed the formation of a few percent of linear chains. Crystalline cPLAs with Mn around 9000 and 14 000 were annealed at 140 °C in the presence of ScOct2 or dibutyl-2-stanna-1,3-dithiolane (DSTL). Simultaneously, crystallites of extended linear chains and crystallites of extended cycles were formed regardless of the catalyst, indicating that transesterification reaction proceeded different for linear chains and for cycles, governed by thermodynamic control. The formation of extended chain crystallites with low dispersity indicates the existence of symproportionation of short and long chains. A complementary experiment was carried out with a PLA ethyl ester composed mainly of linear chains with a small fraction of cycles.

Photophysical and redox properties of new donor-acceptor-donor (DAD) compounds containing benzothiadiazole (A) and dimethyldihydroacridine (D) units: a combined experimental and theoretical study.

Four donor-acceptor-donor compounds consisting of 9,9-dimethyl-9,10-dihydroacridine donors differently linked to a benzothiadiazole acceptor were designed using DFT calculations and synthesized, namely 4,7-bis(4-(9,9-dimethyl-9,10-dihydroacridine)phenyl)benzo[c][1,2,5]thiadiazole (1), 4,7-bis(2,5-dimethyl-4-(9,9-dimethyl-9,10-dihydroacridine)phenyl)benzo[c][1,2,5]thiadiazole (2), 4,7-bis(3,5-di(9,9-dimethyl-9,10-dihydroacridine)phenyl)benzo[c][1,2,5]thiadiazole (3), and 4-(3,5-di(9,9-dimethyl-9,10-dihydroacridine)phenyl)-7-(thiophen-2-yl)benzo[c][1,2,5]thiadiazole (4). As predicted theoretically, all studied compounds were electrochemically active both in the reduction as well as in the oxidation modes. They underwent one electron quasi-reversible reduction. Oxidation of 1 and 2 involved a two electron process transforming them into dications and carrying out, in parallel, their dimerization. Oxidation of 3 and 4 resulted in their oligomerization (polymerization). The electrochemically determined ionisation potentials (IP) of 1-4 were similar, covering a narrow range of 5.28-5.33 eV and were consistent with DFT calculations. Larger differences were found for experimentally determined electron affinity (EA) values, being significantly lower for 2 (|EA| = 2.59 eV) as compared to 1, 3 and 4 whose |EA| values were higher by 0.15-0.25 eV, again consistent with DFT calculations. DFT calculations predict positive values of ΔE(S1-T1) for all compounds i.e. in the range of 0.18 eV to 0.43 eV for 1, 3 and 4 and a significantly lower value for 2 (0.06 eV), indicating a possible RISC process in this case. DFT calculations of ΔE(S1-T2) lead to negative and very small values for 2-4 implying a possible involvement of higher lying triplets in the generation of singlet excitons. The investigated derivatives exhibited fluorescence in the orange-red spectral range (550-770 nm) and were strongly dependent on the solvent polarity. The highest PLQY value of 37% was measured for 1 in toluene. The PLQY values significantly improved upon deoxygenation of the studied solutions. Solid state samples also exhibited higher PLQY values as compared to those determined for DCM solutions. These findings were rationalized by partial suppression of the vibrationally induced emission quenching in the solid state due to the intermolecular interaction confinement.

Contemporary roof pattern for energy efficient buildings: Air conditioning cost alleviation, CO2 emission mitigation potential and acceptable payback period

Buildings account for a significant portion of global energy use and consumption. Buildings have substantial energy consumption due to the use of heating, ventilation, and cooling systems. It is evident that the use of insulation materials and phase change materials (PCMs) in the design of buildings can effectively reduce the cost of air conditioning by reducing external heat gains and losses. Additionally, the use of environmentally friendly, cost-effective, and natural materials can be beneficial from an environmental standpoint. This paper aims to evaluate the potential for cost savings in the air conditioning of various PCMs and insulation-stuffed building roof configurations. In that respect, four types of phase change materials (HS29, HS36, FS42, and FS30) and four insulation materials (Therma cork, sawdust, aerogel, and sheep wool) were selected. The thermophysical properties of PCMs (solid and liquid state), insulation materials, and building elements were determined experimentally as per ASTM D 5334 standards. Ten various building roof models (contemporary roof pattern) are studied with four various PCMs and four various insulations. In addition, novel building roof design integrated with PCM/insulation were analysed numerically, related to environmental conditions that refer to two different scenarios in India (hot dry and composite climates). It further analyses the reduction in greenhouse gas emissions associated with different roof configurations. The aforementioned PCM/insulation materials were stuffed in the void spaces of the contemporary roof pattern. Thermo-economic analysis of novel roof design with PCM/insulation materials on air-conditioning costs, carbon dioxide emissions and payback time are compared with conventional roofs (CR) and contemporary roof patterns (CRP). The thermo-economic analysis was carried out based on the number of degree-hours of heating and cooling to determine the building's annual energy usage. HS29 PCM stuffed roof pattern (HS29RP) saved the highest total energy cost savings of 11.89/14.71 $/m2/year when compared with conventional roof and 11.35/13.89 $/m2/year compared with contemporary roof pattern for Jabalpur/Kota climatic conditions. HS29 PCM stuffed roof pattern (HS29RP) exhibits the maximum carbon emission mitigation of 215.32/275.37 kg/kWh when compared with conventional roof and 204.95/259.57 kg/kWh for climatic conditions of Jabalpur/Kota. While considering shortest payback span, sawdust stuffed roof pattern shows the minimum payback period of 0.69 and 2.15 years when compared with conventional roof and contemporary roof pattern. The findings of this research offer significant contributions to the development of energy-efficient building envelopes applicable to a wider range of buildings, including those with and without air conditioning systems.

Detection of diheptacendiyl diradical intermediate in the cycloreversion of diheptacene to heptacene.

Cycloreversion of diheptacenes, the covalently bound dimers of heptacene, in the solid state produces heptacene. In addition, diheptacendiyl diradical can be detected by ESR spectroscopy. The diradical has a small singlet-triplet energy gap of -0.02 kJ mol-1 (-4.8 × 10-3 kcal mol-1) in favor of the singlet state and is persistent in solid heptacene.

Infrared Spectroscopic and Physical Properties of Methanol Ices—Reconciling the Conflicting Published Band Strengths of an Important Interstellar Solid

Infrared spectroscopic observations have established the presence of solid methanol (CH3OH) in the interstellar medium and in solar system ices, but the abundance of frozen CH3OH cannot be deduced without accurate band strengths, optical constants, and reference spectra. In this paper we identify disagreements, omissions, and gaps in the literature on infrared (IR) intensities of methanol ices, including unaddressed concerns that reach back several decades. New spectra are presented with intensity measurements aided by new data on the index of refraction and density of solid CH3OH. The result is that the large discordant results from different laboratory groups can now be reconciled. Multiple ices have been used to determine, apparently for the first time, IR intensities of H2O + CH3OH mixtures of accurately known composition for use with observations of interstellar ices. Also for the first time, measurements on CH3OH ices with different thicknesses have allowed us to report both near-IR band strengths and optical constants for two near-IR features used by planetary scientists. We have used our new IR results to determine vapor pressures of solid CH3OH and have compared them to measurements made with a quartz-crystal microbalance. Thermal annealings of methanol ices have been carried out and phase changes in the solid state examined. Comparisons of our results to earlier work are presented where possible, and electronic versions of our new results are made available.

Synthesis of 2,4,6‐Triaryl‐1,3,5‐triazines via the Cyclotrimerization of Benzonitriles with Catalytic Systems Composed of Titanium Chlorido Complexes and Magnesium

The catalytic activity of low‐valent transition metals for the cyclotrimerization of nitriles has rarely been investigated to date. Here, we report on the cyclotrimerization of benzonitrile (PhCN) and its derivatives using catalytic systems composed of magnesium and bis(indolyl)TiCl2 (bis(indolyl) = di(3‐methylindol‐2‐yl)phenylmethane), Cp2TiCl2 (Cp = η5‐C5H5), (CGC)TiCl2 (CGC = Me2Si(Me4C5)(tBuN)), TiCl4(thf)2 (thf = tetrahydrofuran), Cp*TiCl3 (Cp* = η5‐Me5C5), or CpTiCl3, which can be expected to generate coordinatively unsaturated Ti(II) complexes as the catalytically active species. All the investigated catalytic systems were active for the cyclotrimerization of PhCN. Notably, even the simple catalytic precursor (TiCl4(thf)2) mediated the cyclotrimerization of PhCN as well as p‐ and m‐tolunitriles. Moreover, these reactions can be carried out on the gram scale and the cyclotrimerized products can be isolated via recrystallization of the reaction mixture from hot toluene. The findings of this study suggest that low‐valent titanium species have the potential to serve as catalysts for the cyclotrimerization of PhCN and its derivatives. During this study, we also found that 2,4,6‐tri(p‐tolyl)‐1,3,5‐triazine, which is obtained from the cyclotrimerization of p‐tolunitrile, exhibits fluorescent properties in both the solid state and in solution.

Stimuli‐Responsive Interconversion between Poly‐NHC‐Based Organometallic Assemblies and Their Self‐Aggregated Dimers

Comprehensive SummaryPoly‐NHC‐based organometallic assemblies 3‐PF6, 3‐SbF6 and 3‐OTf were obtained and verified by NMR spectroscopy, ESI mass spectrometry and single‐crystal X‐ray diffraction analyses. Controllable structural interconversion was observed between the poly‐NHC‐based organometallic assemblies and their self‐aggregated dimers in solution affected by concentration, solvent and metal ion. 1H NMR spectra of assembly 3‐PF6 in CD3CN at different concentrations demonstrated controllable structural interconversion, and 19F NMR spectrum of assembly 3‐PF6 at high concentration further evidenced the presence of the free hexafluorophosphate anion and encapsulated hexafluorophosphate anion for its two sets of signals. In addition, single‐crystal X‐ray diffraction analysis provided clear evidence that in the solid state, two assemblies 3‐PF6 were vertically stuck, forming a self‐aggregated dimer with an encapsulated hexafluorophosphate anion. Investigating the reversible structural interconversion is beneficial for revealing the intrinsic nature on the atom level and paving the way to design the stimuli‐responsive functional system.

A Series of Lanthanide Coordination Polymers as Luminescent Sensors for Selective Detection of Inorganic Ions and Nitrobenzene

Seven new lanthanide coordination polymers, namely [Ln(cpt)3H2O)]n(Ln = La (1), Pr (2), Sm (3), Eu (4), Gd (5), Dy (6), and Er (7)), which were synthesized under hydrothermal conditions using 4′-(4-(4-carboxyphenyloxy)phenyl)-4,2′:6′,4′-tripyridine (Hcpt) as the ligand. The crystal structures of these seven complexes were determined using single-crystal X-ray diffraction, and they were found to be isostructural, crystallizing in the triclinic P1¯ space group. The Ln(Ⅲ) ions were nine-coordinated with tricapped trigonal prism coordination geometry. The Ln(Ⅲ) cations were coordinated by carboxylic and pyridine groups from (cpt)− ligands, forming one-dimensional ring-chain structures. Furthermore, the luminescent properties of complexes 1–7 were investigated using fluorescent spectra in the solid state. The fluorescence sensing experiments demonstrated that complex 4 exhibits high selectivity and sensitivity for detecting Co2+, Cu2+ ions, and nitrobenzene. Moreover, complex 3 shows good capability for detecting Cu2+ ions and nitrobenzene. Additionally, the sensing mechanism was also thoroughly examined through theoretical calculations.

Fabrication, structural, morphological, and mechanical behaviour of fly ash doped clay ceramics based CO2 gas sensor

Abstract Various attempts have been made to fabricate fly ash-doped clay composites via solid state reaction method. Additionally, to investigate the structural, mechanical, surface morphology, and CO2 gas sensing behavior, the fabricated clay composites were sintered at three different temperatures 1000, 1100, and 1200 °C (COF1, COF2, COF3) for 4 h. The green and sintered densities of the fabricated composites were found to be in the range of 2.17-2.13 g/cm3 and 1.38 to 1.30 g/cm3. Further, various characterization techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, universal testing machine (UTM) and scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDAX) were carried out. Moreover, to determine the compressive strength and Young’s modulus values, a universal testing machine (UTM) was used. The fracture toughness of the fabricated composites, COF2 and COF3 were found to be 7.84 MPa-m1/2 and 2.22 MPa-m1/2. The COF3 composite exhibited a sensing response, response time, recovery time of 3.39 at 1200 ppm CO2, 16.95 s and 18.05 s respectively. Consequently, this porous clay composite can be fabricated in a cost-effective and eco-friendly manner, hence beneficial for CO2 gas sensing applications.

Cold Moves: Cryogenics in Indo-German Research Networks.

By unravelling the complexities and dynamics of a collaboration between scientists in India and West Germany to establish a cryogenic network, this paper intends to contribute to our understanding of the transnational movement of research technologies during the Cold War. In 1971, a cryogenic laboratory including a helium and a nitrogen liquefier was set up at the physics department of the Indian Institute of Technology (IIT) Madras as part of the Indo-German partnership at IIT Madras between 1959 and 1974. As a generic research technology with many applications, cryogenics became crucial for a solid state research agenda for semiconductor development. After initial difficulties, Ramaswami Srinivasan at IIT Madras and Gustav Klipping of the Fritz Haber Institute in Berlin built a successful collaboration based on mutual trust and on Indian and German scientists travelling and working in each other's laboratories. If the initial motivation of the Indo-German partnership was informed by the logic of Cold War development policy, Klipping and Srinivasan developed their collaboration into a vibrant cryogenic research network around different actors, instruments, and skills moving between India and the Federal Republic of Germany.

Leveraging Insulator's Tacticity in Semiconducting Polymer Blends.

Blending conjugated polymers with insulating matrices is often utilized for engineering extrinsic properties in organic electronics. Semiconductor/insulator blends are typically processed to form a uniformly distributed network of conductive domains within the insulating matrix, marrying electronic and physical properties from individual components. Understanding of polymer-polymer interactions in such systems is thus crucial for property co-optimization. One of the commonly overlooked parameters is the structural configuration of the insulator on the resulting properties, especially the electronic properties. This study investigated how the tacticity of the matrix polymer, among other relevant parameters in play, impacts solid state crystallization in semiconductor/matrix blends and hence the resulting charge transport properties. We found an intricate dependence of the film morphology, aggregation behavior, electronic charge transport, and mixed ionic-electronic coupling properties on the insulator's tacticity. Our experimentally iterative approach shows that for a given application, when selecting semiconductor/insulator combinations, the tacticity of the matrix can be leveraged to optimize performance and vary solid-state structure.

New Calamitic Mesogens Exhibiting Aggregation-Induced Emission (AIE)

Aggregation-induced emitters or AIEgens are generally signified by their stronger photoluminescence in aggregation than in the solution state. Due to high emission efficiency in aggregate and solid states and good processability, organic AIEgens drew attention to the development of advanced luminescent materials. However, as mesogenic materials self-assemble to a different molecular arrangement in different phases, achieving liquid crystallinity and AIE properties in the same molecule would provide a valuable tool to develop solvent-independent AIEgenic materials. With this goal, the present work reports the synthesis of new organic thermotropic liquid crystalline compounds exhibiting aggregation-induced emission (AIE). The synthesized compounds exhibit strong green luminescence in a solid state which sharply quenches upon entering smectic mesophase by heating. This is in addition to the exhibition of dispersion medium (solvent)-dependent emission, thus providing a dual mode of AIE. The mesogenic property of the synthesized compounds was studied by XRD, POM, and DSC. The AIE was studied by fluorescence spectroscopy and variable temperature fluorescence microscopy. A DFT study was carried out to gain an insight into the AIEgenic behavior of the material.

Emerging Solid–State Thermal Switching Materials

Emerging Solid–State Thermal Switching Materials

A supramolecular host matrix for preserving fluorescence in the solid-state.

Fluorescent materials find numerous applications in light-based devices, but their utilization is severely affected by concentration caused quenching of fluorescence, the extreme form of which is the total loss of fluorescence in the solid state. Introduction of bulky substituents remains the most frequently applied fluorescence revival strategy, but requires multi-step synthetic modifications. We have demonstrated a simple one step supramolecular gel-based strategy to preserve the fluorescence in the solid state.

Phosphorescent PdII-PdII Emitter-Based Red OLEDs with an EQEmax of 20.52.

Three dinuclear Pd(II) complexes (1, 2, and 3) with intense red phosphorescence at room temperature are here synthesized using strong ligand field strength compounds. All three complexes are characterized by nuclear magnetic resonance, high-resolution mass spectrometry, and elemental analyses. Complexes 2 and 3 are characterized by single-crystal X-ray diffraction. The crystalline data of 2 and 3 reveal complex double-layer structures, with Pd-Pd distances of 2.8690(9) Å and 2.8584(17) Å, respectively. Furthermore, complexes 1, 2, and 3 show phosphorescence at room temperature in their solid states at the wavelengths of 678, 601, and 672nm, respectively. In addition, they show phosphorescence at 634, 635, and 582nm, respectively, in the 2wt.% (PMMA) films, and phosphorescence at 670, 675, and 589nm, respectively, in the deoxygenated CH2Cl2 solutions. Among three complexes, complex 1 shows red emission at 634nm with phosphorescent quantum yield Ф = 67% in the 2wt.% PMMA film. Furthermore, complex 1-based organic light-emitting diode is fabricated using a vapor-phase deposition process, and their maximum external quantum efficiency reaches 20.52%, which is the highest percentage obtained by using the dinuclear Pd(II) complex triplet emitters with the CIE coordinates of (0.62, 0.38).

Structural and photoluminescence properties of SrNb2O6: RE3+ (RE = Sm, Tb) phosphors for solid state lighting

The phosphors for pc-LEDs have high thermal stability requirements due to the high operating temperature of LEDs. In addition, there are many phosphors based on SrNb2O6, but no one has studied Sm3+ or Tb3+ as the luminescent center of SrNb2O6 host. Therefore, two new phosphors based on SrNb2O6 host are proposed in this work. One is an orange phosphor with negative thermal quenching phenomenon using Sm3+ as the luminescent center, and the other is a green phosphor with Tb3+ as the luminescent center. In this work, a series of SrNb2O6:Sm3+ and SrNb2O6:Tb3+ phosphors were prepared by the solid-state reaction method. The structure, morphology, chemical composition, absorption properties and luminescence properties of Sm3+ and Tb3+ doped SrNb2O6 samples were studied. Under 405 nm excitation, the SrNb2O6:Sm3+ samples exhibit the 4f-4f transition of Sm3+ with the strongest emission intensity at 607 nm, the emission intensity of SrNb2O6:0.03Sm3+ phosphor at 150 °C remains at 100.56% of its room temperature value and the chromaticity coordinates are located in the orange region, with a color purity of 88.19%. Under 307 nm excitation, the SrNb2O6:Tb3+ samples exhibit the 4f-4f transition of Tb3+ with the strongest emission intensity at 544 nm, the emission intensity of SrNb2O6:0.09Tb3+ phosphor at 150 °C remains at 7.68% of its room temperature value and the chromaticity coordinates are located in the green region with a color purity of 74.29%. Additionally, Na+ is introduced as a charge compensator in the Sm3+ or Tb3+ doped phosphors, which enhances their luminescence intensity. These results indicate that the two phosphors synthesized in this work have the prospect of application in the field of solid-state lighting.

Recycle of spent LiFePO4 batteries: An eco-friendly closed-loop technique based on less solvent solid state reaction

Lithium iron phosphate (LFP) batteries have become one of the most popular batteries due to their high safety and low cost. However, the lifespan of LFP batteries is limited, making effective recycling processes crucial for environmental protection, resource conservation, and economic benefits. Less solvent solid state reaction (LSR) is reactions of solids with the help of a little solvent, which has advantage of almost 100% conversion of reactants and no waste generation. Herein, LFP (S-LFP) from spent batteries was first entirely decomposed to produce FePO4 and LiH2PO4 in H3PO4-H2O2 leaching systems using the LSR method. Then, battery-grade Li2CO3 was prepared by adding CaCl2 and Na2CO3 to LiH2PO4. As a result, the battery of regenerated LiFePO4 (R-LFP) using recycled FePO4 and Li2CO3 exhibits superior electrochemical performance compared to those with unused LiFePO4, including a higher discharge specific capacity (140.7 mAhg−1 at 0.1C) and excellent cycle life, with a capacity retention of 98.6% over 500cycles at 1.0C. The LSR method provides a green and sustainable closed-loop recovery strategy for S-LFP cathode materials, which reduces the number of processing steps and chemical consumption, promotes resource conservation and environmental protection, and facilitates the sustainable industrial development of S-LFP batteries.