Phase Behavior of Poly(2-vinylpyridine)-block-Poly(4-vinylpyridine) Copolymers Containing Gold Nanoparticles

Abstract

We studied the phase behavior of the poly(2-vinylpyridine)-blockpoly(4-vinylpyridine) copolymer (P24VP) containing gold nanoparticles, by rheometry, small-angle X-ray scattering, transmission electron microscopy (TEM), and differential scanning calorimetry (DSC). Although both blocks of P24VP exhibited attractive interaction to gold precursors, unusual phase behavior was observed depending on the amount of gold nanoparticles. As the amount of gold nanoparticles increased, the order-to-disorder transition temperature (T ODT ) of P24VP with gold nanoparticles decreased first, then increased, and finally decreased again. To explain this phenomenon, we prepared two block copolymers: polystyrene-block-poly(2vinylpyridine) copolymer (PS2VP) and polystyrene-block-poly(4-vinylpyridine) copolymer (PS4VP) containing gold nanoparticles. With increasing the amount of gold particles, the T ODT of PS2VP increased continuously, whereas that of PS4VP gradually decreased. For PS4VP containing gold nanoparticles, because P4VP chains can interact with the gold nanoparticle surface, density fluctuations exist near the gold nanoparticle surfaces, which causes the T ODT to decrease. On the other hand, although the pyridine ring in P2VP could be associated with the gold surface, P2VP chains become stretched due to steric hindrance arising from the ortho position of nitrogen in P2VP. The chain stretching increases the T ODT. Thus, the decrease of T ODT for P24VP originates from P4VP microdomains containing gold nanoparticles, while the increase of T ODT is attributed to the P2VP microdomains containing gold nanoparticles. With increasing the amounts of gold nanoparticles, the contribution of P4VP microdomains containing gold nanoparticles on the T ODT becomes dominant, causing the T ODT to redecrease. To verify the gold nanoparticle position in both P2VP and P4VP microdomains, we performed TEM and scanning transmission electron microscopy (STEM) experiments. At lower amounts of gold nanoparticles, they are mainly located inside P4VP microdomains. With increasing the amount of the gold nanoparticles, they are distributed in both P2VP and P4VP microdomains, though the amount of gold nanoparticles in P4VP microdomains is larger than that in P2VP microdomains.

Poly(vinylpyridine) Segments in Block Copolymers: Synthesis, Self-Assembly, and Versatility

“…In a pertinent example, Kim and coworkers showed that microphase-separated domains of P2VPb-P4VP preferentially absorb gold nanoparticles into the P4VP matrix at lower concentrations and then eventually populated both domains, albeit to a much lesser extent in P2VP domains, at increasing nanoparticle concentration (Figure 3). 84 The same concept extends to large organic guests as well. Hadjichristidis, Ruokolainen, and co-workers showed through infrared (IR) spectroscopy that bulky cholesteryl hemisuccinate (CholHS) can only partially hydrogen bond to P2VP segments (∼30%) regardless of excess CholHS loading.…”

Solvent effects leading to a variety of different 2D structures in the self-assembly of a crystalline-coil block copolymer with an amphiphilic corona-forming block

“…Generally, solvents employed for self-assembly should be poor solvents for the core-forming block and effective or good solvents for the corona-forming block. Typically, one studies the self-assembly in non-polar solvents of BCPs with a non-polar corona-forming chains such as polydimethylsiloxane (PDMS), 25,26 polystyrene (PS) [2][3][4][5]27 or polyisoprene, 9,26,[28][29][30] and in polar solvents for BCPs with a polar corona-forming chain such as poly(acrylic acid), [31][32][33] or PEO, 17,[34][35][36][37][38] or polyvinylpyridine (P2VP), [39][40][41][42][43][44][45] or poly(N-isopropyl acrylamide). [46][47][48][49] Some authors have looked at two-component solvent mixtures, for example tetrahydrofuran/isopropanol (THF/iPrOH) to enhance the solubility of the core-forming block to promote self-assembly, 50 or hexane-iPrOH mixture to create a solvent in which micelles with both PDMS and P2VP corona chains are colloidally stable.…”

Flexible conductive poly(styrene‐butadiene‐styrene)/carbon nanotubes nanocomposites: Self‐assembly and broadband electrical behavior

“…These morphologies include body centered cubic packed spheres, hexagonally packed cylinders (HEX), continuous gyroids, and alternating lamellae . Accordingly, the self‐assembly of the block copolymers can be a powerful tool to create functional materials and CPNs with tailored structures and, thereby fine‐tuning properties …”