Scandium Molybdate Nanofibers with Negative Thermal Expansion for Fabricating Composites with Controllable Coefficients of Thermal Expansion
Source abstract
Abstract
Single-crystal Sc2Mo3O12 nanofibers, an one-dimensional negative thermal expansion (NTE) material, have been successfully synthesized by electrospinning. The crystal structure, morphology, and NTE property of Sc2Mo3O12 nanofibers were characterized using typical X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDX), and variable-temperature XRD. Results indicate that as-deposited Sc2Mo3O12 nanofibers are amorphous and display a smooth surface and uniform diameter. Single-crystal Sc2Mo3O12 nanofibers are fabricated at 500 °C for 3 h and grown along the (111) orientation with an orthorhombic structure. The average diameter of single-crystal Sc2Mo3O12 nanofibers is ∼100 nm. Sc2Mo3O12 nanofibers exhibit anisotropic NTE with an average volumetric coefficient of thermal expansion (CTE) of −6.53 × 10–6 °C–1 from 25 °C to 700 °C. The average CTEs along the a-, b-, and c-axes are −6.62 × 10–6, 5.33 × 10–6, and −5.21 × 10–6 °C–1, respectively.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Thermal Expansion and Ionic Conductivity · Layered Double Hydroxides Synthesis and Applications · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Physical Science and Technology, Yangzhou University, Yangzhou, 225002, People’s Republic of China
Department of Mechanical and Electrical Engineering, Guangling College, Yangzhou University, Yangzhou, 225000, People’s Republic of China
Funding
Yangzhou University · National Natural Science Foundation of China · Qing Lan Project of Jiangsu Province
References (27)
Show source-provided references
1. 10.1126/science.272.5258.9010.1126/science.272.5258.90 ↗
2. 10.1126/science.280.5365.88610.1126/science.280.5365.886 ↗
3. 10.1103/PhysRevLett.80.490310.1103/PhysRevLett.80.4903 ↗
4. 10.1557/JMR.1999.012210.1557/JMR.1999.0122 ↗
5. 10.1016/j.molstruc.2004.10.04910.1016/j.molstruc.2004.10.049 ↗
6. 10.1006/jssc.1998.774410.1006/jssc.1998.7744 ↗
7. 10.1016/S1466-6049(00)00012-X10.1016/S1466-6049(00)00012-X ↗
8. 10.1016/S0022-0248(00)00771-510.1016/S0022-0248(00)00771-5 ↗
9. 10.1016/S0925-8388(01)02003-510.1016/S0925-8388(01)02003-5 ↗
10. 10.1063/1.175765910.1063/1.1757659 ↗
11. 10.1007/s10971-010-2364-910.1007/s10971-010-2364-9 ↗
12. 10.1016/j.tca.2009.10.02110.1016/j.tca.2009.10.021 ↗
13. 10.1007/s10853-012-7076-910.1007/s10853-012-7076-9 ↗
14. 10.1016/j.ceramint.2015.12.04510.1016/j.ceramint.2015.12.045 ↗
15. 10.1016/j.ceramint.2016.02.12410.1016/j.ceramint.2016.02.124 ↗
16. 10.1021/acs.inorgchem.8b0305610.1021/acs.inorgchem.8b03056 ↗
17. 10.1039/C6CE01640E10.1039/C6CE01640E ↗
18. 10.1088/0953-8984/17/2/00410.1088/0953-8984/17/2/004 ↗
19. 10.1088/0953-8984/17/27/00410.1088/0953-8984/17/27/004 ↗
20. Zhu J. J. · J. Chin. Ceram. Soc. · 2011 · 39 · 1456
21. 10.1016/j.materresbull.2016.06.00410.1016/j.materresbull.2016.06.004 ↗
22. 10.1016/j.jlumin.2009.07.01210.1016/j.jlumin.2009.07.012 ↗
23. 10.1016/j.ssc.2003.08.03210.1016/j.ssc.2003.08.032 ↗
24. 10.1016/j.pmatsci.2012.01.00110.1016/j.pmatsci.2012.01.001 ↗
25. 10.1063/1.181997510.1063/1.1819975 ↗
26. 10.1103/PhysRevB.69.09411110.1103/PhysRevB.69.094111 ↗
27. 10.1016/j.ceramint.2012.05.03310.1016/j.ceramint.2012.05.033 ↗