Magnetic properties of electrochemically prepared crystalline films of Prussian blue-based molecular magnets KjCrIIk[CrIII(CN)6]l · mH2O
Magnetic properties of electrochemically prepared crystalline films of Prussian blue-based molecular magnets KjCrIIk[CrIII(CN)6]l · mH2O
复制标题
电化学制备普鲁士蓝基分子磁体KjCrIIk[CrIII(CN)6]l·mH2O晶体薄膜的磁性能
DOI:
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发表时间:
2013
影响因子:
2.5
通讯作者:
Gisela Schütz
中科院分区:
文献类型:
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作者:
P. Bhatt;S. Yusuf;R. Bhatt;Gisela Schütz
Crystalline films (thickness ∼1 μm) of Prussian blue-based molecular magnets, synthesized using electrochemical method at two different reduction potentials −0.5 and −0.9 V, result into K0.1CrII1.45[CrIII(CN)6] · mH2O (film 1) and K0.8CrII1.1[CrIII(CN)6] · mH2O (film 2), respectively. The structural and magnetic properties of such films are investigated using atomic force microscopy (AFM), X-ray diffraction (XRD), infrared (IR) spectroscopy, and dc magnetization measurements. The film morphology, examined using AFM, shows uniformly distributed triangular crystallites over the substrate surface. The presence of CrIII–C≡N–CrII sequence, in the range of 1,900 to 2,300 cm−1 in IR spectra, confirms formation of Prussian blue analogues. The XRD results reveal information about the crystalline nature of the films and the relative intensities of the Bragg peaks change with the K+ ions. The exchange interaction between Cr ions through C≡N ligand confirms that the electron transfer from C≡N molecule to Cr ions is ferrimagnetic in nature. The high Curie temperatures (TC) are found to be ∼195 and ∼215 K for film 1 and film 2, respectively. The higher value of TC is attributed to the inclusion of more K+ ions for film 2, resulting decreases in the CrIII(C≡N)6 vacancies and increases in the number of nearest neighbors of CrII ions. The branching in the zero field-cooled and field-cooled magnetization data below Curie temperature is explained in terms of kinetic behavior of magnetic domains with different cooling conditions and the presence of water molecule vacancies in the lattice.