Fig. 3 Extension of our proposed programmable synthesis to the selective synthesis of a wide variety of liposome/metal hybrids. Extension of our proposed.

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Fig. 3 Extension of our proposed programmable synthesis to the selective synthesis of a wide variety of liposome/metal hybrids. Extension of our proposed programmable synthesis to the selective synthesis of a wide variety of liposome/metal hybrids. (A to C) Representative TEM images of liposome/monometallic hybrids [Ag (A), Pd (B), and Pt (C)]. (D to F) Representative TEM images of liposome/bimetallic hybrids [Au-Ag (D), Au-Pd (E), and Au-Pt (F)]. (G to I) Representative TEM images and corresponding EDS element maps of the liposome/bimetallic hybrids [Au-Ag (G), Au-Pd (H), and Au-Pt (I)]. (J to L) Representative CS-TEM images, lattice-resolved images (numbered boxes), and electron diffraction patterns (the insets of the numbered boxes) of liposome/bimetallic hybrids [Au-Ag (J), Au-Pd (K), and Au-Pt (L)]. (M and N) Atomic percentages (M) and absorbance spectra (N) of liposome/Au-Pt hybrids synthesized from the precursor molar ratios of 2:1 (Au/Pt), 1:1, and 1:2. Scale bars, 50 nm (A to F and J to L), 20 nm (A′ to F′, and G to I), and 2 nm [numbered boxes in (J), (K), and (L)]. Jin-Ho Lee et al. Sci Adv 2016;2:e1601838 Copyright © 2016, The Authors