Solid-State Displacement Synthesis of Alkaline-Earth Selenide for White Emission through Alternating Current Electroluminescence
Source abstract
Abstract
Alkaline-earth selenides (AESe) are functional materials of both fundamental and technological importance, but their chemical synthesis has met with limited success. Herein, a solid-state displacement reaction is described for the rapid synthesis of various AESe crystals without the need for hazardous chemicals. The reaction mechanism is studied by careful control of the experimental variables such as the reaction temperature (800–1400 °C), atmospheres (air, N2, and N2/H2 mixture), and Se precursors (ZnSe and Se). Using AECO3 and ZnSe (ZnS) as precursor materials under N2/H2 mixture atmosphere, we synthesized a series of AESe, AES, and AE(S,Se) crystals with high crystallinities. Doping of luminescent lanthanide ions such as Eu2+ is concomitantly achieved during the synthesis, yielding tunable photoluminescence that is useful for constructing white light-emitting devices in combination with electroluminescent ZnS:Cu.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Quantum Dots Synthesis And Properties · Luminescence Properties of Advanced Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon999077, Hong Kong SAR, China
City University of Hong Kong Shenzhen Research Institute, Shenzhen518057, China
Funding
Research Grants Council, University Grants Committee
References (44)
Show source-provided references
1. 10.1021/ja01186a01810.1021/ja01186a018 ↗
2. 10.1021/acs.inorgchem.1c0317110.1021/acs.inorgchem.1c03171 ↗
3. 10.1039/D1TC01806J10.1039/D1TC01806J ↗
4. 10.1039/C9CC07112A10.1039/C9CC07112A ↗
5. 10.1021/ja01199a04510.1021/ja01199a045 ↗
6. 10.3938/jkps.68.22710.3938/jkps.68.227 ↗
7. 10.1016/j.matlet.2015.01.15010.1016/j.matlet.2015.01.150 ↗
8. 10.1039/C9NR03421H10.1039/C9NR03421H ↗
9. 10.1002/pssb.222118011110.1002/pssb.2221180111 ↗
10. 10.1088/0022-3727/42/10/10510310.1088/0022-3727/42/10/105103 ↗
11. 10.1143/JPSJ.53.41910.1143/JPSJ.53.419 ↗
12. 10.1143/JJAP.34.553910.1143/JJAP.34.5539 ↗
13. 10.1002/anie.20210048610.1002/anie.202100486 ↗
14. 10.1002/adom.20210243010.1002/adom.202102430 ↗
15. 10.3390/molecules1705502110.3390/molecules17055021 ↗
16. 10.1016/j.materresbull.2008.10.01010.1016/j.materresbull.2008.10.010 ↗
17. 10.1021/ja400069s10.1021/ja400069s ↗
18. 10.1021/ja300064t10.1021/ja300064t ↗
19. 10.1016/j.jpcs.2010.08.01210.1016/j.jpcs.2010.08.012 ↗
20. 10.1023/A:102268571564410.1023/A:1022685715644 ↗
21. 10.1007/s10812-017-0460-010.1007/s10812-017-0460-0 ↗
22. 10.3390/ma304283410.3390/ma3042834 ↗
23. 10.1016/0022-2313(94)00059-L10.1016/0022-2313(94)00059-L ↗
24. 10.1016/j.matchemphys.2011.01.01610.1016/j.matchemphys.2011.01.016 ↗
25. 10.1016/j.jssc.2006.04.03210.1016/j.jssc.2006.04.032 ↗
26. 10.1016/j.matlet.2004.11.01410.1016/j.matlet.2004.11.014 ↗
27. 10.1007/s10854-016-5607-x10.1007/s10854-016-5607-x ↗
28. 10.1016/j.optmat.2006.11.06110.1016/j.optmat.2006.11.061 ↗
29. 10.1016/j.mseb.2006.03.00810.1016/j.mseb.2006.03.008 ↗
30. 10.1038/s41467-020-17469-x10.1038/s41467-020-17469-x ↗
31. 10.1149/1.220600610.1149/1.2206006 ↗
32. 10.1021/acsnano.6b0318810.1021/acsnano.6b03188 ↗
33. 10.1021/nn301531b10.1021/nn301531b ↗
34. 10.3390/s1921460710.3390/s19214607 ↗
35. 10.1021/nl060392t10.1021/nl060392t ↗
36. 10.1364/OE.24.01997810.1364/OE.24.019978 ↗
37. 10.1016/j.nanoen.2019.01.05810.1016/j.nanoen.2019.01.058 ↗
38. 10.1021/acs.jpcc.5b0693110.1021/acs.jpcc.5b06931 ↗
39. 10.1039/D2TC01871C10.1039/D2TC01871C ↗
40. 10.1002/adfm.20200520010.1002/adfm.202005200 ↗
41. 10.1002/adma.20200884910.1002/adma.202008849 ↗
42. 10.1002/admt.20210144010.1002/admt.202101440 ↗
43. 10.1038/s41598-022-13167-410.1038/s41598-022-13167-4 ↗
44. 10.1002/adom.20210191810.1002/adom.202101918 ↗