Effect of precipitation temperature and organic additives on size and morphology of ZnO nanoparticles
Source abstract
Abstract
Low temperature (25 °C–80 °C) synthesis of zinc oxide (ZnO) nanoparticles (,20 nm) at short synthesis periods (;30 min) was achieved by precipitation. The precipitation system was formed using zinc acetate dihydrate as zinc source, ethylene glycol (EG) as solvent and polyvinyl pyrrolidone (PVP) as chelating agent. The size of spherical ZnO nanoparticles was manipulated by the choice of precipitation temperature (13.0 6 1.9 nm at 25 °C and 9.0 6 1.3 nm at 80 °C), which essentially changes the nature of adsorption events between ZnO crystals and organic molecules. The particle size can also be regulated by the amount of chelating agent as a result of further enhancement in adsorption between ZnO crystals and organic additives. The spherical ZnO nanoparticles were agglomerated into triangular form when different solvent was used–by substituting water for EG, which has different adsorption ability. Accordingly, formation and growth mechanisms controlling the size and morphology of ZnO nanoparticles have been proposed.
Source: expertdata · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: ZnO doping and properties · Gas Sensing Nanomaterials and Sensors · Copper-based nanomaterials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (44)
Show source-provided references
1. 10.1016/j.materresbull.2006.11.03510.1016/j.materresbull.2006.11.035 ↗
2. 10.1016/0022-2313(92)90047-D10.1016/0022-2313(92)90047-D ↗
3. 10.3390/ma304264310.3390/ma3042643 ↗
4. 10.1016/j.colsurfa.2008.07.01010.1016/j.colsurfa.2008.07.010 ↗
5. 10.1016/j.jcrysgro.2008.02.01410.1016/j.jcrysgro.2008.02.014 ↗
6. 10.1016/j.apsusc.2009.03.02310.1016/j.apsusc.2009.03.023 ↗
7. 10.1021/cg060289h10.1021/cg060289h ↗
8. 10.1007/s00339-009-5335-710.1007/s00339-009-5335-7 ↗
9. 10.1088/0953-8984/16/25/R0110.1088/0953-8984/16/25/R01 ↗
10. 10.1063/1.140697310.1063/1.1406973 ↗
11. 10.1016/S0927-7757(01)00959-110.1016/S0927-7757(01)00959-1 ↗
12. 10.1016/j.matlet.2005.04.03110.1016/j.matlet.2005.04.031 ↗
13. 10.1016/j.jcrysgro.2004.07.07510.1016/j.jcrysgro.2004.07.075 ↗
14. 10.1016/j.jallcom.2005.01.04510.1016/j.jallcom.2005.01.045 ↗
15. 10.1021/ja029945210.1021/ja0299452 ↗
16. 10.1016/S0022-0248(01)01393-810.1016/S0022-0248(01)01393-8 ↗
17. 10.1002/1521-3773(20020402)41:7<1188::AID-ANIE1188>3.0.CO;2-510.1002/1521-3773(20020402)41:7<1188::AID-ANIE1188>3.0.CO;2-5 ↗
18. 10.1063/1.36829510.1063/1.368295 ↗
19. 10.1016/S0022-2860(99)00161-110.1016/S0022-2860(99)00161-1 ↗
20. 10.1021/jp065963k10.1021/jp065963k ↗
21. 10.1016/j.jcrysgro.2009.08.00810.1016/j.jcrysgro.2009.08.008 ↗
22. 10.1007/s10853-010-4294-x10.1007/s10853-010-4294-x ↗
23. 10.1063/1.163334310.1063/1.1633343 ↗
24. 10.1016/j.jlumin.2008.11.02110.1016/j.jlumin.2008.11.021 ↗
25. 10.1111/j.1151-2916.1990.tb05232.x10.1111/j.1151-2916.1990.tb05232.x ↗
26. 10.1016/j.cplett.2006.04.05310.1016/j.cplett.2006.04.053 ↗
27. 10.1016/j.jcrysgro.2009.07.03510.1016/j.jcrysgro.2009.07.035 ↗
28. 10.1016/j.matlet.2006.11.09410.1016/j.matlet.2006.11.094 ↗
29. 10.1016/j.jcrysgro.2007.11.05410.1016/j.jcrysgro.2007.11.054 ↗
30. 10.1016/S0032-3861(01)00611-510.1016/S0032-3861(01)00611-5 ↗
31. 10.1016/j.jallcom.2010.07.12510.1016/j.jallcom.2010.07.125 ↗
32. 10.1088/0957-4484/17/5/01210.1088/0957-4484/17/5/012 ↗
33. 10.1007/s00339-004-3075-210.1007/s00339-004-3075-2 ↗
34. 10.1016/j.jcis.2010.03.05210.1016/j.jcis.2010.03.052 ↗
35. 10.1016/j.jcis.2009.07.01110.1016/j.jcis.2009.07.011 ↗
36. 10.1021/j100313a04710.1021/j100313a047 ↗
37. 10.1021/jp060544910.1021/jp0605449 ↗
38. 10.1021/jp052496i10.1021/jp052496i ↗
39. 10.1039/b307565f10.1039/b307565f ↗
40. 10.1016/S0025-5408(96)00175-410.1016/S0025-5408(96)00175-4 ↗
41. 10.1016/j.apsusc.2009.05.13910.1016/j.apsusc.2009.05.139 ↗
42. 10.1016/S0022-0248(02)01917-610.1016/S0022-0248(02)01917-6 ↗
43. 10.1021/jp049657n10.1021/jp049657n ↗
44. 10.1063/1.173817410.1063/1.1738174 ↗