Solid State Sciences最新文献

{"title":"Zirconium and copper dual-doping strategy in NaNiFeMnO2: Advancing the electrochemical stability and capacity for sodium-ion batteries","authors":"Safia Bibi,&nbsp;Tao Chen,&nbsp;Dan Sun,&nbsp;Kaiyu Liu","doi":"10.1016/j.solidstatesciences.2024.107822","DOIUrl":"10.1016/j.solidstatesciences.2024.107822","url":null,"abstract":"<div><div>O3-type layered transition-metal oxide cathode materials are considered one of the most promising cathode materials for sodium ion batteries due to their high theoretical capacity and optimal operating potential. However, it encounters significant challenges, such as poor cycling stability and limited reversible capacity, primarily due to structural instability. Herein, we have successfully synthesized dual cation doped O3-type Na(Ni_0.3Fe_0.3Mn_0.3)_0.87Cu_0.12Zr_0.01O₂ (NaCuZrFNM). The co-doping of Zr/Cu into NaFNM layered structure led to an expansion of the sodium layer, enabling enhanced sodium ion mobility during charge/discharge processes compared to NaFNM. Therefore, sodium ions demonstrated faster diffusion in NaCuZrFNM than NaFNM. It was found that the Zr/Cu dual-doped NaFNM electrode deliverers a reversible capacity of 135.2 mA h/g at 0.1C as well as 121.5 mA h/g initial discharge capacity with remarkable capacity retention of 81.8 % at 1C after 250 cycles. Furthermore, it also exhibits the good rate performance of 82 mA h/g at high current density of 10C with 74.4 % capacity retention after 1000 cycles, indicating excellent structural stability. Our results demonstrate that Cu/Zr dual-doping in O3-type cathode materials is viable strategy for improving the long-term performance of sodium-ion batteries.</div></div>","PeriodicalId":432,"journal":{"name":"Solid State Sciences","volume":"160 ","pages":"Article 107822"},"PeriodicalIF":3.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143149348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Thermal expansion and ionic conductivity of K5A0.5Hf1.5(MoO4)6 (A = Sr, Pb)","authors":"Evgeniy Kovtunets ,&nbsp;Yunna Tushinova ,&nbsp;Tatyana Spiridonova ,&nbsp;Tsyrendyzhit Bazarova ,&nbsp;Alexandra Logvinova ,&nbsp;Alexandr Bogdanov ,&nbsp;Bair Bazarov","doi":"10.1016/j.solidstatesciences.2024.107816","DOIUrl":"10.1016/j.solidstatesciences.2024.107816","url":null,"abstract":"<div><div>Compounds K₅<em>A</em>_0.5Hf_1.5(MoO₄)₆ (<em>A</em> = Sr, Pb) were synthesized using solid-state ceramic method. The sequence of chemical reactions that occur during the formation of these compounds has been elucidated. It was determined that the compounds melt incongruently at 628 °C, and their crystal structures were refined using the Rietveld method. Theoretical IR spectra were calculated using the obtained structural data and DFT modeling results. These spectra exhibited a high degree of correlation with the experimental data, thereby confirming the presence of isolated MoO₄ groups within the structure. It has been shown that the electrical conductivity of K₅<em>A</em>_0.5Hf_1.5(MoO₄)₆ (<em>A</em> = Sr, Pb) reached about 10⁻⁴ S/cm, which exceeds the conductivity of previously studied similar ternary molybdates. BVSE calculations indicated a high probability of oxygen transport in the studied compounds. Thermal deformations were studied by high temperature powder X-ray diffraction in the temperature range of 30–500 °C. The results showed that the ternary molybdates K₅<em>A</em>_0.5Hf_1.5(MoO₄)₆ (<em>A</em> = Sr, Pb) are materials with high thermal expansion (α_<em>V</em> = 40–56 x10⁻⁶ °C^–1) and exhibit anisotropy along the crystallographic <em>c</em>-axis.</div></div>","PeriodicalId":432,"journal":{"name":"Solid State Sciences","volume":"160 ","pages":"Article 107816"},"PeriodicalIF":3.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143097742","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Ce(III) complex with o-phenylenediacetato ligand: Synthesis, structure and magnetic properties","authors":"Lenka Krešáková ,&nbsp;Miroslava Litecká ,&nbsp;Itziar Oyarzabal ,&nbsp;Róbert Tarasenko ,&nbsp;Hryhorii Titikov ,&nbsp;Martin Orendáč ,&nbsp;Juraj Černák","doi":"10.1016/j.solidstatesciences.2024.107798","DOIUrl":"10.1016/j.solidstatesciences.2024.107798","url":null,"abstract":"<div><div>Single crystals of Ce(III) complex {[Ce₂(<em>o</em>PDA)₃(H₂O)₂]·2H₂O}_<em>n</em> (<strong>1</strong>) with O-donor ligand H₂<em>o</em>PDA (<em>o</em>-phenylenediacetic acid) were formed under solvothermal conditions. The crystal structure of <strong>1</strong> is one-dimensional and formed by chains of the Ce(III) ions linked via <em>o</em>PDA²⁻ dianions acting as pentadentate ligands with bridging and chelating functions. The Ce(III) central atom in <strong>1</strong> is nonacoordinated by eight oxygen atoms from four different <em>o</em>PDA²⁻ ligands and one oxygen atom of the aqua ligand yielding O₈O donor set. The investigation of the static susceptibility and magnetization suggested <em>Δ/k</em>_<em>B</em> = 317 K energy difference between the ground and the first excited doublet. Field induced slow magnetic relaxation was revealed in the investigation of alternating susceptibility. The alternation of the relaxation time with temperature confirmed the coexistence of quantum tunneling and Raman relaxation processes with anomalous coefficients for Raman relaxation.</div></div>","PeriodicalId":432,"journal":{"name":"Solid State Sciences","volume":"160 ","pages":"Article 107798"},"PeriodicalIF":3.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143098233","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Second-order anisotropy due to magnetostriction for L10-FePt","authors":"D. Legut ,&nbsp;P. Nieves","doi":"10.1016/j.solidstatesciences.2024.107782","DOIUrl":"10.1016/j.solidstatesciences.2024.107782","url":null,"abstract":"<div><div>The effective magnetocrystalline anisotropy energy associated with magnetostriction is studied for tetragonal L1<span><math><msub><mrow></mrow><mrow><mn>0</mn></mrow></msub></math></span>-FePt by means of first-principles calculations, which is expressed in terms of the intrinsic anisotropy for an undeformed crystal, the magnetostrictive coefficients, and the elastic tensor. A very small correction is found for the first anisotropy constant <span><math><mrow><mi>Δ</mi><msub><mrow><mi>K</mi></mrow><mrow><mn>1</mn></mrow></msub><mo>/</mo><msub><mrow><mi>K</mi></mrow><mrow><mn>1</mn></mrow></msub><mo>=</mo><mn>0</mn><mo>.</mo><mn>07</mn></mrow></math></span>%, while a much more significant contribution is obtained for the second one <span><math><mrow><mi>Δ</mi><msub><mrow><mi>K</mi></mrow><mrow><mn>2</mn></mrow></msub><mo>/</mo><msub><mrow><mi>K</mi></mrow><mrow><mn>2</mn></mrow></msub><mo>=</mo><mn>21</mn><mo>.</mo><mn>86</mn></mrow></math></span>%. General analysis of this effect for tetragonal crystals is provided, finding that <span><math><mrow><mi>Δ</mi><msub><mrow><mi>K</mi></mrow><mrow><mn>1</mn></mrow></msub></mrow></math></span> will be always positive for any stable phase with this symmetry. The potential implications and applications of these results are discussed.</div></div>","PeriodicalId":432,"journal":{"name":"Solid State Sciences","volume":"160 ","pages":"Article 107782"},"PeriodicalIF":3.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143098239","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Sustainable thermoelectric materials for solar energy applications: A review","authors":"Neelam Baghel ,&nbsp;Anil Kumar","doi":"10.1016/j.solidstatesciences.2024.107784","DOIUrl":"10.1016/j.solidstatesciences.2024.107784","url":null,"abstract":"<div><div>The growth and implementation of sustainable thermoelectric materials for solar energy applications are investigated in this review article. Subsequently, thermoelectric materials provide a viable means of directly transforming solar heat into electricity, they are essential to improving the sustainability and efficiency of solar energy systems. This paper examines the principles of thermoelectricity, significant material properties, and the most recent developments in thermoelectric materials, such as lead telluride, bismuth telluride, organic, hybrid, and earth-abundant inorganic compounds. Special attention is given to material performance, environmental impact, scalability, and its integration into solar energy systems. Additionally, issues including stability, low efficiency, and a balance between performance and material sustainability are explored. The assessment concludes by outlining potential research approaches and technological advances that will be required to turn thermoelectric materials into an achievable and future solution to the world's energy problems.</div></div>","PeriodicalId":432,"journal":{"name":"Solid State Sciences","volume":"160 ","pages":"Article 107784"},"PeriodicalIF":3.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143098242","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Improved catalytic performance of (Fe, Cr)-ZnO/g-C3N4 nanocomposite towards electrocatalytic water splitting for clean energy","authors":"Dalal Alhashmialameer ,&nbsp;Mohammad Shariq ,&nbsp;Muhammad Azam Qamar ,&nbsp;Hanan A. Althikrallah ,&nbsp;Noha Al-Qasmi ,&nbsp;F.H. Al-abdali ,&nbsp;Leena S. Mohamed ,&nbsp;Hala I. Elzubir ,&nbsp;Zeyad M. Ahmed","doi":"10.1016/j.solidstatesciences.2025.107823","DOIUrl":"10.1016/j.solidstatesciences.2025.107823","url":null,"abstract":"<div><div>The declining quantity of nonrenewable energy sources and rising in temperatures globally pose serious concerns. Therefore, electrochemical water splitting emerges as a highly efficient and cost-effective method of preparing hydrogen and oxygen, utilizing materials such as metals and their oxides. Beyond precious metals, carbon-based materials have been realized to be efficient in facilitating these reactions. To improve efficiency and optimize potential applications, it has also been established that incorporating metal oxides into the layers of the graphite can significantly improve the activity of HER and OER. In this study, we introduce a newly designed composite electrocatalyst, (Fe, Cr)-ZnO/g-C₃N₄ ((Fe, Cr)-GZN), which demonstrates enhanced electrocatalytic performance. The composite material was synthesized through the coprecipitation of (Fe, Cr)-ZnO with g-C₃N₄. The electrocatalyst's structure was fully analyzed using the important characterization techniques. FTO glass was employed to electrodeposit catalysts to facilitate water splitting investigations. The (Fe, Cr)-GZN composite demonstrated excellent electrochemical water splitting performance, with low overpotentials of 304 mV and a Tafel slope of 89 mV dec⁻¹ for OER, resulting in 10 mA cm⁻² (current density). This performance outperforms Cr-GZN and Fe-GZN composites, demonstrating the (Fe, Cr)-GZN composite's potential as an extremely efficient electrocatalyst for water splitting.</div></div>","PeriodicalId":432,"journal":{"name":"Solid State Sciences","volume":"160 ","pages":"Article 107823"},"PeriodicalIF":3.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143149347","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"GAM-8: An organic-inorganic hybrid layered aluminium phosphate obtained by the transformation of AlPO4-5 with cyclohexylamine","authors":"Takuji Ikeda ,&nbsp;Masaki Kumada ,&nbsp;Edo Imai ,&nbsp;Kenichi Komura","doi":"10.1016/j.solidstatesciences.2024.107788","DOIUrl":"10.1016/j.solidstatesciences.2024.107788","url":null,"abstract":"<div><div>A hybrid layered aluminium phosphate material GAM-8 was synthesized by a structural change using the aluminophosphate AlPO₄-5 having an <strong>AFI</strong>-type zeolite structure. This synthesis condition is based on the interzeolite conversion of AlPO₄-5. Cyclohexylamine was used as the organic structure-directing agent (OSDA). It was found that a highly crystalline GAM-8 obtained was isostructural to Co(APSO)_N and its related compounds and UHM-5, whose structures are still unknown. The <em>ab-initio</em> crystal structure analysis by powder X-ray diffraction revealed that a 2D framework structure with a space group of <em>C</em>2/<em>c</em> and lattice constants of <em>a</em> = 37.46 Å, <em>b</em> = 5.32 Å, <em>c</em> = 9.70 Å, and <em>β</em> = 103.41°. Two aluminiumphosphate layers was included in a unit cell. A structural composition per unit cell was determined to be |(C₆H₁₁NH₂)₈|·[Al₈P₈O₂₄(OH)₁₆]. The layered framework was composed of one PO₄ tetrahedral site and two AlO₆ octahedral sites. All the AlO₆ octahedra were edge-shared and connected in a zigzag pattern along the <em>c</em>-axis. The ²⁷Al MAS NMR showed a large quadrupolar interaction of ²⁷Al nuclei. The cyclohexylamine molecules were orderly arranged between the layers, forming a bilayer, and its interlayer distance between the terminal oxygen atoms of the aluminium phosphate layers was considerable, ca. 11.7 Å. The NH₂ group of the OSDA was located close to O atoms of the layer surface with the interatomic distance <em>d</em>(N–O) of ca. 2.7–2.9 Å, suggesting the position of cyclohexylamine was stabilized by the hydrogen bonding of O···H–N.</div></div>","PeriodicalId":432,"journal":{"name":"Solid State Sciences","volume":"160 ","pages":"Article 107788"},"PeriodicalIF":3.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143149427","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Synthesis and characterization of graphitic carbon Nitride/Cd2SnO4 nanostructures for high-performance flexible supercapacitors","authors":"Waris ,&nbsp;Sayfa Bano ,&nbsp;Moha Suhail Chaudhary ,&nbsp;Saima Sultana ,&nbsp;Mahendra Yadav ,&nbsp;Mohammad Zain Khan","doi":"10.1016/j.solidstatesciences.2024.107817","DOIUrl":"10.1016/j.solidstatesciences.2024.107817","url":null,"abstract":"<div><div>The development of electrode materials based on heterojunctions shows a promising approach for enhancing electrochemical performance, offering the potential for future advancements in energy storage applications. This investigation, a graphitic carbon nitride (g-C₃N₄) matrix functioned as a supportive network, regulating the aggregation of cadmium stannate (Cd₂SnO₄) nanoparticles (NPs) thereby giving promising stability during electrochemical cycling. The optimized g-C₃N₄/Cd₂SnO₄ composite demonstrated excellent electrochemical performance, characterized by a high specific capacitance and improved cycling stability. X-ray diffraction (XRD) patterns of the composite revealed distinct crystalline phases of individual components, confirming the orthorhombic structure of the composite. The electrochemical charge storage performance of the synthesized electrode material has been evaluated in an aqueous acidic and gel-electrolyte (PVA/H₂SO₄) medium. The results indicate that among the prepared electrode materials, the g-C₃N₄/Cd₂SnO₄ sample exhibits the highest electrochemical capacitance of 601.20 Fg^-1 at 0.5 Ag^-1. Even after 5000 charge-discharge cycles, the electrode maintained its cycling stability with 94.69 % capacitance retention. The performance of the g-C₃N₄/Cd₂SnO₄ electrode was further evaluated in a gel polymer electrolyte by assembling a symmetric capacitor for real-world application using a two-electrode system. The use of a gel electrolyte allowed the device to achieve an energy density of 48.81 Wh kg⁻¹ and a power density of 250 W kg⁻¹ within a voltage window of 1.0 V at an operating current density of 0.5 A g⁻¹. Notably, the g-C₃N₄/Cd₂SnO₄ electrode demonstrated strong cycling stability in the gel electrolyte, maintaining performance for up to 5000 cycles. Furthermore, the symmetric device in the gel electrolyte exhibited excellent electrochemical stability across various bending angles, highlighting its potential for use as a flexible electrode in supercapacitors.</div></div>","PeriodicalId":432,"journal":{"name":"Solid State Sciences","volume":"160 ","pages":"Article 107817"},"PeriodicalIF":3.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143097796","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Fabrication of Cd-modified Zn-Pb-W-borate glass for enhanced optical, thermal, and radiation attenuation","authors":"Usman Iliyasu ,&nbsp;Mohamad Syazwan Mohd Sanusi ,&nbsp;Nor Ezzaty Ahmad ,&nbsp;M.S. Al-Buriahi ,&nbsp;Hammam Abdurabu Thabit ,&nbsp;M. Bature ,&nbsp;Ngaram Suleman Modu","doi":"10.1016/j.solidstatesciences.2024.107797","DOIUrl":"10.1016/j.solidstatesciences.2024.107797","url":null,"abstract":"<div><div>Fabrication of glass composition (60-<em>x</em>)B₂O₃+10WO₃+15ZnO+15Pb₃O₄+<em>x</em>CdCO₃, where <em>x</em> varied from 10, 20–30 mol%, have been synthesized via melt-quenching techniques. The effect of CdO was investigated on the optical, thermal, and radiation shielding properties using the Phy-X/PSD. The refractive index varied from 2.04 to 2.13 and the molar refractivity increased from 15.00 cm³/mol to 15.28 cm³/mol. The Fermi energy level decreased from 3.31 eV to 3.19 eV suggesting a p-type semiconductor behavior, with holes serving as the primary charge carriers. The Glass transition temperature (<span><math><mrow><msub><mi>T</mi><mi>g</mi></msub></mrow></math></span>), crystallization temperature (<span><math><mrow><msub><mi>T</mi><mi>c</mi></msub></mrow></math></span>), and melting temperature (<span><math><mrow><msub><mi>T</mi><mi>m</mi></msub></mrow></math></span>) improved with higher CdO levels. The photon shielding properties of the synthesized glasses were improved, as evidenced by an increase in the linear attenuation coefficient from 34.17 cm⁻¹–43.42 cm⁻¹, while the half-value thickness reduced from 0.020 cm to 0.016 cm at 0.05 MeV, upon incorporating 10 and 30 mol% of CdO. The radiation protection efficiency of all the studied glasses were approximately 100 % at energy between 0.05 and 0.1 MeV. The fast neutron removal cross-section has a maximum value of 0.130 cm⁻¹ for sample containing 20 mol% CdO outperforming some standard neutron shielding materials. The combined optical, photon, and neutron shielding properties of these glasses highlight their potential as promising candidates for applications in optoelectronics and radiation shielding.</div></div>","PeriodicalId":432,"journal":{"name":"Solid State Sciences","volume":"160 ","pages":"Article 107797"},"PeriodicalIF":3.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143098234","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Systematic study on the quality of flux-grown Al2O3 single crystals for dosimetry applications","authors":"C. Rodrigues ,&nbsp;J.G.M. Saraiva ,&nbsp;A.P. Gonçalves ,&nbsp;L. Peralta","doi":"10.1016/j.solidstatesciences.2025.107835","DOIUrl":"10.1016/j.solidstatesciences.2025.107835","url":null,"abstract":"<div><div>Understanding the intricate effects of radiation at the microscale is pivotal for advancing cancer treatment strategies. This study focuses on the development of cutting-edge Al₂O₃-based passive dosimeters that are able to achieve microscale sensitivity and improve such description. Corundum (Al₂O₃) single crystals were grown isothermally with a Li₂O–MoO₃ flux system. Herein, we report the effects of flux composition, solute concentration, holding time and temperature on crystal quality, which directly impacts the detector's performance. Higher Li₂O concentration and higher holding temperature improved crystal transparency. Lower solute concentration led to larger crystals. Holding time did not appear to have a significant impact on crystal size or quality. Using a 15 % mol Li₂O – 85 % mol MoO₃ flux system with 6 % mol of Al₂O₃ and a holding temperature of 1180 °C, highly transparent Al₂O₃ single crystals up to 5 mm in size can be grown. The grown crystals show promising features for future radiation detection applications.</div></div>","PeriodicalId":432,"journal":{"name":"Solid State Sciences","volume":"160 ","pages":"Article 107835"},"PeriodicalIF":3.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143098241","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}