Magnetochemistry最新文献

{"title":"Process-Gas-Influenced Anti-Site Disorder and Its Effects on Magnetic and Electronic Properties of Half-Metallic Sr2FeMoO6 Thin Films","authors":"Ekta Yadav, Ketan S. Navale, G. L. Prajapati, K. Mavani","doi":"10.3390/magnetochemistry9070167","DOIUrl":"https://doi.org/10.3390/magnetochemistry9070167","url":null,"abstract":"Anti-site disorder, arising due to the similar size of Fe and Mo ions in Sr2FeMoO6 (SFMO) double perovskites, hampers spintronic applicability by deteriorating the magnetic response of this double perovskite system. A higher degree of anti-site disorder can also completely destroy the half-metallicity of the SFMO system. To study the effects of different process gas conditions on the anti-site disorder, we have prepared a series of SFMO thin films on SrTiO3 (001) single-crystal substrate using a pulsed laser deposition (PLD) technique. The films are grown either under vacuum or under N2/O2 partial gas pressures. The vacuum-grown SFMO film shows the maximum value of saturation magnetization (MS) and Curie temperature (TC), signaling the lowest anti-site disorder in this series. In other words, there is a long-range Fe/Mo-O-Mo/Fe ferrimagnetic exchange in the vacuum-grown thin film, thereby enhancing the magnetization. Further, all the SFMO films show a semiconducting state with a systematic increase in overall resistivity with the increased anti-site disorder. The electrical conduction mechanism is defined by the variable-range hopping model at low temperatures. Raman spectra show a weak Fano peak, suggesting the presence of electron–phonon coupling in SFMO thin films. These results show the significance of the process gas in causing anti-site disorder, tuning the degree of this disorder and therefore its influence on the structural, magnetic, electrical, and vibrational properties of SFMO thin films.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49347897","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"NMR Magnetic Shielding in Transition Metal Compounds Containing Cadmium, Platinum, and Mercury","authors":"Andy D. Zapata-Escobar, Alejandro F. Maldonado, Jose L. Mendoza-Cortes, G. Aucar","doi":"10.3390/magnetochemistry9070165","DOIUrl":"https://doi.org/10.3390/magnetochemistry9070165","url":null,"abstract":"In this article, we delve into the intricate behavior of electronic mechanisms underlying NMR magnetic shieldings σ in molecules containing heavy atoms, such as cadmium, platinum, and mercury. Specifically, we explore PtXn−2 (X = F, Cl, Br, I; n = 4, 6) and XCl2Te2Y2H6 (X = Cd, Hg; Y = N, P) molecular systems. It is known that the leading electronic mechanisms responsible for the relativistic effects on σ are well characterized by the linear response with elimination of small components model (LRESC). In this study, we present the results obtained from the innovative LRESC-Loc model, which offers the same outcomes as the LRESC model but employs localized molecular orbitals (LMOs) instead of canonical MOs. These LMOs provide a chemist’s representation of atomic core, lone pairs, and bonds. The whole set of electronic mechanisms responsible of the relativistic effects can be expressed in terms of both non-ligand-dependent and ligand-dependent contributions. We elucidate the electronic origins of trends and behaviors exhibited by these diverse mechanisms in the aforementioned molecular systems. In PtX4−2 molecules, the predominant relativistic mechanism is the well-established one-body spin–orbit (σSO(1)) mechanism, while the paramagnetic mass–velocity (σMv) and Darwin (σDw) contributing mechanisms also demand consideration. However, in PtX6−2 molecules, the σ(Mv/Dw) contribution surpasses that of the SO(1) mechanism, thus influencing the overall ligand-dependent contributions. As for complexes containing Cd and Hg, the ligand-dependent contributions exhibit similar magnitudes when nitrogen is substituted with phosphorus. The only discrepancy arises from the σSO(1) contribution, which changes sign between the two molecules due to the contribution of bond orbitals between the metal and tellurium atoms.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47301425","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Interplay of Magnetic Interaction and Electronic Structure in New Structure RE-12442 Type Hybrid Fe-Based Superconductors","authors":"Amit Pokhriyal, Abyay Ghosh, Smritijit Sen, H. Ghosh","doi":"10.3390/magnetochemistry9070164","DOIUrl":"https://doi.org/10.3390/magnetochemistry9070164","url":null,"abstract":"We present detailed first-principles density functional theory-based studies on RbRE2Fe4As4O2 (RE = Sm, Tb, Dy, Ho) hybrid 12442-type iron-based superconducting compounds with particular emphasis on competing magnetic interactions and their effect on possible magneto-structural coupling and electronic structure. The stripe antiferromagnetic (sAFM) pattern across the xy plane emerges as the most favorable spin configuration for all the four compounds, with close competition among the different magnetic orders along the z-axis. The structural parameters, including arsenic heights, Fe-As-Fe angle, and other relevant factors that influence superconducting Tc and properties, closely match the experimental values in stripe antiferromagnetic arrangement of Fe spins. Geometry optimization with inclusion of explicit magnetic ordering predicts a spin–lattice coupling for all the four compounds, where a weak magneto–structural transition, a tetragonal-to-orthorhombic structural transition, takes place in the relaxed stripe antiferromagnetic spin configuration. Absence of any experimental evidence of such structural transition is possibly an indication of nematic transition in RE-12442 compounds. As a result of structural distortion, the lattice contracts (expands) along the direction with parallel (anti-parallel) alignment of Fe spins. Introduction of stripe antiferromagnetic order in Fe sub-lattice reconstructs the low-energy band structure, which results in significantly reduced number of bands crossing the Fermi level. Moreover, the dispersion of bands and their orbital characteristics also are severely modified in the stripe antiferromagnetic phase similar to BaFe2As2. Calculations of exchange parameters were performed for all the four compounds. Exchange coupling along the anti-parallel alignment of Fe spins J1a is larger than that for the parallel aligned spins J1b. A crossover between the super-exchange-driven in-plane next-nearest-neighbor exchange coupling J2 and in-plane exchange coupling J1a due to lanthanide substitution was found. A large super-exchange-driven next-nearest-neighbor exchange interaction is justified using the construction of 32 maximally localized Wannier functions, where the nearest-neighbor Fe-As hopping amplitudes were found to be larger than the nearest- and the next-nearest-neighbor Fe-Fe hopping amplitudes. We compare the hopping parameters in the stripe antiferromagnetic pattern with non-magnetic configuration, and increased hopping amplitude was found along the anti-parallel spin alignment with more majority-spin electrons in Fe dxz and dxy but not in Fe dyz. On the other hand, the hopping amplitudes are increased in stripe antiferromagnetic phase along the parallel spin alignment with more majority-spin electrons in only Fe dyz. This difference in hopping amplitudes in the stripe antiferromagnetic order enables more isotropic hopping.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42180795","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Structural and Magnetic Investigations of the Novel Pyrophosphate Na7Ni3Fe(P2O7)4","authors":"Sirine El Arni, Mohammed Hadouchi, A. Assani, M. Saadi, M. El Marssi, A. Lahmar, Lahcen El Ammari","doi":"10.3390/magnetochemistry9070162","DOIUrl":"https://doi.org/10.3390/magnetochemistry9070162","url":null,"abstract":"A novel pyrophosphate Na7Ni3Fe(P2O7)4 was synthesized in two distinct forms, single-crystal and powder. Single-crystal X-ray diffraction was used to determine the crystal structure, and powder X-ray diffraction and scanning electron microscopy were used to examine the purity and morphology of the elaborated powder. This phosphate crystallizes in the P1¯ space group of the triclinic system with a = 6.3677 (2) Å, b = 9.3316 (4) Å, c = 10.8478 (4) Å, α = 65.191 (1)°, β = 80.533 (1)° and γ = 73.042 (1)°. The crystal framework is assembled from the linkage of centro-symmetrical clusters Ni2(Ni/Fe)2P4O28. Each cluster consists of two (Fe1/Ni1)O6 octahedra, two Ni2O6 octahedra and two P2O7 units. The linkage of these clusters is provided by two other P2O7 units to generate a three-dimensional structure with distinct tunnels in the [100], [010] and [001] directions, housing the Na+ cations. The infrared and Raman analyses show the characteristic bands of the pyrophosphate anion P2O74−. Remarkably, the magnetic investigations revealed the coexistence of two magnetic transitions at ~29 K and ~4.5 K with dominating antiferromagnetic interactions.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49402911","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Removal of Metal Ions via Adsorption Using Carbon Magnetic Nanocomposites: Optimization through Response Surface Methodology, Kinetic and Thermodynamic Studies","authors":"S. Muntean, L. Halip, M. Nistor, C. Păcurariu","doi":"10.3390/magnetochemistry9070163","DOIUrl":"https://doi.org/10.3390/magnetochemistry9070163","url":null,"abstract":"The toxicity of metal ions on ecosystems has led to increasing amounts of research on their removal from wastewater. This paper presents the efficient application of a carbon magnetic nanocomposite as an adsorbent for the elimination of metal ions (copper, lead and zinc) from aqueous solutions. A Box–Behnken factorial design combined with the response surface methodology was conducted to investigate the effect and interactions of three variables on the pollutant removal process. Highly significant (p < 0.001) polynomial models were developed for each metal ion: the correlation coefficient was 0.99 for Cu(II) and Pb(II), and 0.96 for Zn(II) ion removal. The experimental data were in agreement and close to the theoretical results, which supports the applicability of the method. Working at the natural pH of the solutions, with a quantity of carbon magnetic nanocomposite of 1 g/L and a metal ions’ concentration of 10 mg/L, for 240 min, removal efficiencies greater than 75% were obtained. The kinetic study indicated that a combination of kinetic models pseudo-second order and intraparticle diffusion were applied appropriately for copper, lead and zinc ion adsorption on carbon magnetic nanocomposite. The maximum adsorption capacities determined from the Langmuir isotherm model were 81.36, 83.54 and 57.11 mg/g for copper, lead and zinc ions. The average removal efficiency for five adsorption–desorption cycles was 82.21% for Cu(II), 84.50% for Pb(II) and 72.68% for Zn(II). The high adsorption capacities of metal ions, in a short time, as well as the easy separation of the nanocomposite from the solution, support the applicability of the magnetic carbon nanocomposite for wastewater treatment.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42935237","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Tunable Iron–Cobalt Thin Films Grown by Electrodeposition","authors":"Sofia Gonçalves, V. Andrade, C. Sousa, J. P. Araújo, J. Belo, A. Apolinário","doi":"10.3390/magnetochemistry9070161","DOIUrl":"https://doi.org/10.3390/magnetochemistry9070161","url":null,"abstract":"Iron–cobalt (FeCo) alloys are highly desirable for their exceptional and adjustable physicochemical properties, particularly in the form of thin films. This study focuses on the growth of iron–cobalt (FeCo) alloy thin films using potentiostatic electrodeposition. The effects of applied voltage and FeCo stoichiometry on the morphology, structure, and magnetic properties of the films are investigated. The results indicate that the electrodeposition potential does not affect the overall stoichiometry or the structural and magnetic properties. However, it does impact film thickness and grain sizes. Higher applied potentials lead to thicker films with faster growth rates, as well as smoother and more homogeneous films with smaller grains. Films with different Fe:Co ratios (Fe90Co10, Fe50Co50, and Fe10Co90) are obtained, and their compositions have a direct impact on morphology, with the amount of Fe influencing film thickness, growth rates, and grain sizes. Increasing Fe content (50, 90%) leads to thicker films and smaller grains. Films with low Fe content (10%) exhibit a face-centered cubic (fcc) structural phase instead of the typical body-centered cubic (bcc) structure. All FeCo alloys display soft magnetic properties with characteristic coercivities, and the low Fe (10%) sample with the fcc structure exhibits the highest coercivity among all the samples. The nucleation and growth mechanisms are investigated using electrodeposition curves and the Scharifker and Hills model. Increasing the applied potential leads to thicker films and higher growth rates, with the nucleation mechanism identified as instantaneous nucleation in the diffusion-controlled regime.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42123486","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Nonlinear Electromagnetic Properties of Thinfilm Nanocomposites (CoFeZr)x(MgF2)100−x","authors":"E. Domashevskaya, S. Ivkov, P. Seredin, Dmitry L. Goloshchapov, K. Barkov, S. Ryabtsev, Yrii G. Segal, A. Sitnikov, E. Ganshina","doi":"10.3390/magnetochemistry9060160","DOIUrl":"https://doi.org/10.3390/magnetochemistry9060160","url":null,"abstract":"The aim of this work is a comprehensive study of the effect of variable atomic composition and structural-phase state of (CoFeZr)x(MgF2)100−x nanocomposites (NCs) on their nonlinear electronic and magnetic/magneto-optical properties. Micrometer-thick nanocomposite layers on the glass substrates were obtained by ion-beam sputtering of a composite target in the argon atmosphere in a wide range of compositions x = 9–51 at·%. The value of the resistive percolation threshold, xper = 34 at·%, determined from the concentration dependencies of the electrical resistance of NCs, coincides with the beginning of nucleation of metallic nanocrystals CoFeZr in MgF2 dielectric matrix. The absolute value of maximum magnetoresistance of NCs is 2.4% in a magnetic field of 5.5 kG at x = 25 at·%, up to the percolation threshold. Two maxima appear in the concentration dependencies of magneto-optical transversal Kerr effect, one of which, at x = 34 at·%, corresponds to the formation of CoFeZr alloy nanocrystals of a hexagonal structure, and the second one at x = 45 at·% corresponds to the phase transition of nanocrystals from a hexagonal to a cubic body-centered structure. The magnetic percolation threshold in (CoFeZr)x(MgF2)100−x system at xfm = 34 at·%, with the appearance of a hysteresis loop and a coercive force of Hc ≈ 8 Oe, coincides with the resistive percolation threshold xper = 34 at·%. Concentration dependence of the coercive force showed that at low contents of metallic alloy x < 30 at·%, NCs are superparamagnetic (Hc = 0). With an increase of the alloy content, in the region of magnetic and resistive percolation thresholds, NCs exhibit a magnetically soft ferromagnetic character and do not change it far beyond the percolation threshold, with the maximum value of the coercive force Hc < 30 Oe.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48201578","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The Organic Ammonium Counterion Effect on Slow Magnetic Relaxation of the [Er(hfac)4]− Complexes","authors":"T. Prokhorova, D. Korchagin, G. Shilov, A. Dmitriev, M. Zhidkov, E. Yagubskii","doi":"10.3390/magnetochemistry9060159","DOIUrl":"https://doi.org/10.3390/magnetochemistry9060159","url":null,"abstract":"The first mononuclear anionic erbium complex [Er(hfac)4]− (hfac = hexafluoroacetylacetone) with an organic ammonium cation [(CH3)4N+] as the counterion was synthesized and structurally and magnetically characterized. The coordination geometries around the Er ions are square antiprisms with pseudo-D4d symmetry. The complex shows distinct field-induced slow magnetization relaxation, which is described by a combination of Orbach (Ueff/kB~28.54(8) K.) and direct mechanisms. Quantum chemical calculations were performed to analyze the magnetic properties of the complex under consideration.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45046647","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Dynamic Footprints of the Specific Artificial Spin Ice Microstate on Its Spin Waves","authors":"Pietro Micaletti, F. Montoncello","doi":"10.3390/magnetochemistry9060158","DOIUrl":"https://doi.org/10.3390/magnetochemistry9060158","url":null,"abstract":"We present a micromagnetic investigation of the spin dynamics at remanence (zero applied field) in a periodic square artificial spin ice (ASI) prepared four different microstates (i.e., with zero, two or four magnetic charges at the vertex). The ASI elements consist of permalloy elliptical dots with a fixed long axis, and a variable width and interdot separation. For each vertex configuration, we compute the equilibrium ground state at zero applied field by relaxing a previously set magnetic configuration (microstate). After the excitation of such ground state, we perform a Fourier analysis obtaining frequency spectra and space phase profiles. We discuss the behavior of the spectra in changing the system’s microstate and geometry, with reference to the spin mode space profiles, magnetization configuration, and effective internal field. Our results draw a correlation between ASI macrospin orientation at vertex and a few important dynamic properties like a phase-shift in the mode profiles or the frequency gap between the edge and fundamental modes. We suggest a few specific experiments to validate of our predictions, as well as applications in the field of interferometric magnonic devices. We believe that our results can help, from the fabrication stage, in tailoring the appropriate ASI geometry for specific application purposes.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42015579","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Ferrite Nanoparticles as Catalysts in Organic Reactions: A Mini Review","authors":"Nilima Maji, H. S. Dosanjh","doi":"10.3390/magnetochemistry9060156","DOIUrl":"https://doi.org/10.3390/magnetochemistry9060156","url":null,"abstract":"Ferrites have excellent magnetic, electric, and optical properties that make them an indispensable choice of material for a plethora of applications, such as in various biomedical fields, magneto–optical displays, rechargeable lithium batteries, microwave devices, internet technology, transformer cores, humidity sensors, high-frequency media, magnetic recordings, solar energy devices, and magnetic fluids. Recently, magnetically recoverable nanocatalysts are one of the most prominent fields of research as they can act both as homogeneous and heterogenous catalysts. Nano-ferrites provide a large surface area for organic groups to anchor, increase the product and decrease reaction time, providing a cost-effective method of transformation. Various organic reactions were reported, such as the photocatalytic decomposition of a different dye, alkylation, dehydrogenation, oxidation, C–C coupling, etc., with nano-ferrites as a catalyst. Metal-doped ferrites with Co, Ni, Mn, Cu, and Zn, along with the metal ferrites doped with Mn, Cr, Cd, Ag, Au, Pt, Pd, or lanthanides and surface modified with silica and titania, are used as catalysts in various organic reactions. Metal ferrites (MFe2O4) act as a Lewis acid and increase the electrophilicity of specific groups of the reactants by accepting electrons in order to form covalent bonds. Ferrite nanocatalysts are easily recoverable by applying an external magnetic field for their reuse without significantly losing their catalytic activities. The use of different metal ferrites in different organic transformations reduces the catalyst overloading and, at the same time, reduces the use of harmful solvents and the production of poisonous byproducts, hence, serving as a green method of chemical synthesis. This review provides insight into the application of different ferrites as magnetically recoverable nanocatalysts in different organic reactions and transformations.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49124418","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}