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First, lanthanide oleate (Ln(oleate)3,Ln=Y, Yb, and Er/Tm) complexes were prepared by adapting the synthesis method for preparing the iron oleate complex to synthesize UCNPs. For the green-emitting UCNPs, 0.8mmol YCl3.6H2O, 0.18mmol YbCl3.6H2O, 0.02mmol ErCl3.6H2O, and 3.1mmol sodium oleate were loaded into a three-necked flask containing a solvent mixture of deionized (DI) water (3ml), ethanol (3.5ml) and hexane (7ml). The reaction solution was heated to 70¡æ heating for 4h, the synthesized Ln(oleate)3 complexes (Ln=Y, Yb, and Er) were washed three times with DI water. These complexes were then mixed with OA and ODE in which the ratio of OA to ODE varied from 0:21 to 21:0 to investigate the effect of OA on the size and morphology of the UCNPs. The mixture was heated to 150¡æ to form a transparent solution. After cooling to 50¡æ, 10ml of a methanol (MeOH) solution containing NaOH (2.5mmol) and NH4F (4mmol) was added to the reaction flask. The mixture was stirred for 40 min and then the MeOH was removed. Finally, the reaction mixture was heated to 320¡æ at a rate of 15¡æ/min and maintained for 90 min under a protective Ar atmosphere. The synthesized NCs were washed several times with ethanol and then dispersed in hexane.
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