Search for: All records

Herein, this work aims to demonstrate the topological effect on the mechanicalx characteristics of selfassembled block copolymers (BCPs). The lamellae-forming polystyrene- block -polydimethylsiloxane (PSb -PDMS) can be self-assembled into various nanostructured monoliths with the use of PS-selective solvent for solvent annealing, giving diamond, gyroid, and cylinder structures with increasing the swelling degree of PS domain (the effective volume fraction of the PS segment after solvent annealing followed by evaporation). The stiffness of the self-assembled monoliths is scrutinized by nanoindentation test. For intrinsic PS- b -PDMS monolith with lamellar structure, the reduced elastic modulus as calculated from the measured stiffness is 0.91 GPa. By contrast, the PS- b -PDMS monolith with cylinder structure gives a significant reduction in reduced elastic modulus with the value of 0.52 GPa due to the introduced microporosity to the PS domain from solvent annealing using PS-selective solvent, resulting in the lower confrontation for continuous layer-by-layer deformation of hard PS and soft PDMS domains. In the case of gyroid-structured PS- b -PDMS monolith, it is unexpected to exhibit a significant increase in the reduced elastic modulus with a value of 1.6 GPa: note that the effect of microporosity is still significant. Accordingly, the enhancement of the reduced elastic modulus is attributed to the effect of deliberate structuring with network topology ( i.e., three-dimensional co-continuous hard PS and soft PDMS domains) that is able to hold the occurrence of large-scale deformation. In contrast to the gyroid with a three-strut texture, the diamond-structured PS- b -PDMS monolith with a four-strut texture is superior to the gyroid with a reduced elastic modulus of 2.2 GPa, further confirming the suggested topology effect. 

A nanoporous Ni/NiO/C nanocomposite with a gyroid nanostructure was fabricated by using a nanoporous polymer with gyroid nanochannels as a template. The polymer template was obtained from the self-assembly of a degradable block copolymer, polystyrene- b -poly( l -lactide) (PS-PLLA), followed by the hydrolysis of PLLA blocks. Templated electroless plating followed by calcination was performed to create a precisely controlled Ni/NiO gyroid nanostructure. After carbon coating, a well-interconnected nanoporous gyroid Ni/NiO/C nanocomposite can be successfully fabricated. Benefiting from the well-interconnected nanoporous structure with ultrafine transition metal oxide and uniform carbon coating, the gyroid nanoporous Ni/NiO/C nanocomposite electrodes exhibited high specific capacities at various rates (1240 mA h g −1 at 0.2 A g −1 , 902 mA h g −1 at 2 A g −1 and 424 mA h g −1 at 10 A g −1 ) and excellent cyclability (809 mA h g −1 at 1 A g −1 after 1000 cycles, average coulombic efficiency 99.86%). This research demonstrates a universal approach for constructing a nanostructured electrode with explicitly controlled block copolymer phase separation.