Self-assembly of 1D FeSe2 chains and Fe(dien)(2) complexes for ferrimagnetic inorganic-organic hybrid cuboids
文献类型:期刊论文
作者 | Pan, Desheng2; Kuang, Qifeng2; Tong, Peng3; Tong, Wei4; Fan, Liubing1; Zhao, Jing1; Li, Da2; Choi, Chuljin5; Zhang, Zhidong2 |
刊名 | JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS |
出版日期 | 2022-01-15 |
卷号 | 542页码:9 |
ISSN号 | 0304-8853 |
关键词 | Inorganic-organic hybrids Self-assembly Magnetic property Electron spin resonance |
DOI | 10.1016/j.jmmm.2021.168585 |
通讯作者 | Li, Da(dali@imr.ac.cn) |
英文摘要 | Challenges still remain in producing room-temperature ferromagnetism/ferrimagnetism in inorganic-organic hybrid compounds. Here, we report the Fe vacancy-doped inorganic-organic (FexSe(2))(2)Fe(dien)(2) (dien = diethylenetriamine, x = 0.86) hybrid cuboids by self-assemble of finite one-dimensional (1D) FeSe2 chains and Fe (dien)(2) complexes. A growth model is proposed by kinetically controllable syntheses of novel Fe2x+1Se4(dien)(2) hybrids. The Rietveld refinement reveals that Fe vacancies in the Fe2.71Se4(dien)(2) hybrid cuboids induce large distortions of the FeSe2 chains and the room-temperature lattice parameters are a = 9.225(4) angstrom, b = 18.021(8) angstrom and c = 11.609(6) angstrom. Magnetic measurements and electron spin resonance spectra of the Fe2.71Se4(dien)(2) hybrid cuboids show the ferrimagnetism with the Curie temperature (T-C) of 600 K and the spin glass state with the freezing temperature (T-f) of 108 K. Impressive room-temperature ferrimagnetic properties of the Fe2.71Se4(dien)(2) hybrid cuboids were ascribed to the high concentration of Fe3+ vacancies (0.29 per cell) in the hybrid cuboids, which is supported by the Fe-57 Mossbauer spectrum fitting based on the ferrimagnetic model. |
资助项目 | National Natural Science Foundation of China[51971221] ; National Natural Science Foundation of China[52031014] ; National Natural Science Foundation of China[U1732275] ; Beijing Natural Science Foundation[2182080] ; National Key R&D Program of China[2017YFA0206302] ; National Key R&D Program of China[2017YFA0700702] ; National Key R&D Program of China[2017YFA0403502] ; Ministry of Science and Technology of China ; Future Materials Discovery Program through the National Research Foundation of Korea (NRF) - Ministry of Science and technology and ICT[2016M3D1A1027835] |
WOS研究方向 | Materials Science ; Physics |
语种 | 英语 |
出版者 | ELSEVIER |
WOS记录号 | WOS:000705023900012 |
资助机构 | National Natural Science Foundation of China ; Beijing Natural Science Foundation ; National Key R&D Program of China ; Ministry of Science and Technology of China ; Future Materials Discovery Program through the National Research Foundation of Korea (NRF) - Ministry of Science and technology and ICT |
源URL | [http://ir.imr.ac.cn/handle/321006/166577] |
专题 | 金属研究所_中国科学院金属研究所 |
通讯作者 | Li, Da |
作者单位 | 1.Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, Peoples R China 2.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, 72 Wenhua Rd, Shenyang 110016, Peoples R China 3.Chinese Acad Sci, Inst Solid State Phys, Key Lab Mat Phys, Hefei 230031, Peoples R China 4.Chinese Acad Sci, Anhui Prov Key Lab Condensed Matter Phys Extreme, High Magnet Field Lab, Hefei 230031, Anhui, Peoples R China 5.Korea Inst Mat Sci, 797 Changwondaero, Chang Won 51508, Gyeongnam, South Korea |
推荐引用方式 GB/T 7714 | Pan, Desheng,Kuang, Qifeng,Tong, Peng,et al. Self-assembly of 1D FeSe2 chains and Fe(dien)(2) complexes for ferrimagnetic inorganic-organic hybrid cuboids[J]. JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS,2022,542:9. |
APA | Pan, Desheng.,Kuang, Qifeng.,Tong, Peng.,Tong, Wei.,Fan, Liubing.,...&Zhang, Zhidong.(2022).Self-assembly of 1D FeSe2 chains and Fe(dien)(2) complexes for ferrimagnetic inorganic-organic hybrid cuboids.JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS,542,9. |
MLA | Pan, Desheng,et al."Self-assembly of 1D FeSe2 chains and Fe(dien)(2) complexes for ferrimagnetic inorganic-organic hybrid cuboids".JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS 542(2022):9. |
入库方式: OAI收割
来源:金属研究所
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