High Photoluminescence Quantum Yield Perovskite/Polymer Nanocomposites for High Contrast X-ray Imaging
Source abstract
Abstract
A surface modified-CsPbBr3/polybutylmethacrylate (PBMA) nanocomposite is reported to be a scintillator that enables us to provide a high contrast X-ray image using a common charge-coupled device (CCD) camera. Bis(2-(methacryloyloxy)ethyl) phosphate (BMEP) was employed to alter the ratio of the original ligands on the CsPbBr3 nanocrystal (NC) surface for optimizing the optical performance of the CsPbBr3/PBMA nanocomposites. The nanocomposites with a concentration of 0.02 wt % NCs exhibit more than 70% transmittance in the visible region and show a green emission at 515 nm, the fast decay time is 13 ns, while the photoluminescence quantum yield value is 99.2%. Under X-ray excitation, the emission peak wavelength is centered at 524 nm and shows a narrow full width at half-maximum of 26.6 nm; the result nicely matches with the peak quantum efficiency of most commercial CCD/complementary metal oxide semiconductor cameras. The high contrast X-ray image is recorded at a low dose rate of 4.6 μGyair/s, which enables read out with software. Our results demonstrate that these CsPbBr3/PBMA nanocomposites have promising application prospects for ionizing radiation detection, especially for X-ray imaging.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Luminescence Properties of Advanced Materials · Solid-state spectroscopy and crystallography
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Nuclear Science and Engineering, Nanjing University of Aeronautics and Astronautics, Nanjing 211106, China
Shaanxi Engineering Research Center of Controllable Neutron Source, School of Science, Xijing University, Xi’an 710123, China
Northwest Institute of Nuclear Technology, Xi’an 710024, China
Funding
National Natural Science Foundation of China
References (32)
Show source-provided references
1. 10.1002/ADMA.20170695610.1002/ADMA.201706956 ↗
2. Knoll G. F. · 2010
3. 10.1209/0295-5075/97/2200210.1209/0295-5075/97/22002 ↗
4. 10.1039/C4TC00815D10.1039/C4TC00815D ↗
5. 10.1038/S41565-020-0683-810.1038/S41565-020-0683-8 ↗
6. 10.1016/S0168-9002(99)00595-110.1016/S0168-9002(99)00595-1 ↗
7. 10.1021/NL504877910.1021/NL5048779 ↗
8. 10.1038/S41586-018-0451-110.1038/S41586-018-0451-1 ↗
9. 10.1038/NCOMMS640410.1038/NCOMMS6404 ↗
10. 10.1126/science.aaa576010.1126/science.aaa5760 ↗
11. 10.1063/1.509887110.1063/1.5098871 ↗
12. 10.1021/ACSNANO.5B0499510.1021/ACSNANO.5B04995 ↗
13. 10.1039/C6RA17008K10.1039/C6RA17008K ↗
14. 10.1021/ACS.NANOLETT.5B0240410.1021/ACS.NANOLETT.5B02404 ↗
15. 10.1002/ADFM.20160010910.1002/ADFM.201600109 ↗
16. 10.1021/JACS.7B0281710.1021/JACS.7B02817 ↗
17. 10.1002/ANIE.20170326410.1002/ANIE.201703264 ↗
18. 10.1007/S40820-019-0283-Z10.1007/S40820-019-0283-Z ↗
19. 10.1016/J.PROGPOLYMSCI.2018.10.00310.1016/J.PROGPOLYMSCI.2018.10.003 ↗
20. 10.1021/MA400138510.1021/MA4001385 ↗
21. 10.1016/J.PROGPOLYMSCI.2013.02.00310.1016/J.PROGPOLYMSCI.2013.02.003 ↗
22. 10.1021/AM200983H10.1021/AM200983H ↗
23. 10.1039/C6TC00447D10.1039/C6TC00447D ↗
24. 10.1002/ADFM.20150143910.1002/ADFM.201501439 ↗
25. 10.1021/ACSNANO.7B0292310.1021/ACSNANO.7B02923 ↗
26. 10.1021/ACS.CHEMMATER.7B0283410.1021/ACS.CHEMMATER.7B02834 ↗
27. 10.1021/ACS.CHEMREV.8B0064410.1021/ACS.CHEMREV.8B00644 ↗
28. 10.1039/C6RA27665B10.1039/C6RA27665B ↗
29. 10.1002/ADMA.20160078410.1002/ADMA.201600784 ↗
30. 10.1016/J.APMT.2019.04.00210.1016/J.APMT.2019.04.002 ↗
31. 10.1103/PhysRevLett.82.178010.1103/PhysRevLett.82.1780 ↗
32. 10.1016/J.MTPHYS.2021.10039010.1016/J.MTPHYS.2021.100390 ↗