Onnuri Kim

Synthesis of three-dimensionally interconnected sulfur-rich polymers for cathode materials of high-rate lithium–sulfur batteries

Elemental sulfur is one of the most attractive cathode active materials in lithium batteries because of its high theoretical specific capacity. Despite the positive aspect, lithium–sulfur batteries have suffered from severe capacity fading and limited rate capability. Here we report facile large-scale synthesis of a class of organosulfur compounds that could open a new chapter in designing cathode materials to advance lithium–sulfur battery technologies. Porous trithiocyanuric acid crystals are synthesized for use as a soft template, where the ring-opening polymerization of elemental sulfur takes place along the thiol surfaces to create three-dimensionally interconnected sulfur-rich phases. Our lithium–sulfur cells display discharge capacity of 945 mAh g−1 after 100 cycles at 0.2 C with high-capacity retention of 92%, as well as lifetimes of 450 cycles. Particularly, the organized amine groups in the crystals increase Li+-ion transfer rate, affording a rate performance of 1210, mAh g−1 at 0.1 C and 730 mAh g−1 at 5 C.

Fast low-voltage electroactive actuators using nanostructured polymer electrolytes

Electroactive actuators have received enormous interest for a variety of biomimetic technologies ranging from robotics and microsensors to artificial muscles. Major challenges towards practically viable actuators are the achievement of large electromechanical deformation, fast switching response, low operating voltage and durable operation. Here we report a new electroactive actuator composed of self-assembled sulphonated block copolymers and ionic liquids. The new actuator demonstrated improvements in actuation properties over other polymer actuators reported earlier, large generated strain (up to 4%) without any signs of back relaxation. In particular, the millimetre-scale displacements obtained for the actuators, with rapid response (<1 s) at sub-1-V conditions over 13,500 cycles in air, have not been previously reported in the literature. The key to success stems from the evolution of the unique hexagonal structure of the polymer layer with domain size gradients beneath the cathode during actuation, which promotes the bending motion of the actuators.

Blue-emitting self-assembled polymer electrolytes for fast, sensitive, label-free detection of Cu(II) ions in aqueous media.

We have developed a light-emitting material based on nonconjugated block copolymers that contain polystyrene sulfonate (PSS) chains. The confinement of the PSS chains within nanosized domains appeared to be a powerful means of achieving enhanced fluorescence signals. High fluorescence quantum yield, with a maximum value of 37%, was obtained by adjusting the types of self-assembled morphologies of PSS-containing block copolymers; in contrast, the fluorescence quantum yield was merely 5% for the PSS homopolymer lacking organization. The wavelength of fluorescence emission was tunable by rational molecular design. In addition, significant self-quenching behavior was not noticed in diverse forms of this material such as solutions, thin films, and free-standing membranes. Notably, the light-emitting self-assembled block copolymer electrolytes exhibited high sensitivity toward Cu(2+) ions, with a detection limit of parts per billion levels, rapid response time of ≤1 min, and insignificant interference of other competitive metal ions.

One-volt-driven superfast polymer actuators based on single-ion conductors

The key challenges in the advancement of actuator technologies related to artificial muscles include fast-response time, low operation voltages and durability. Although several researchers have tackled these challenges over the last few decades, no breakthrough has been made. Here we describe a platform for the development of soft actuators that moves a few millimetres under 1 V in air, with a superfast response time of tens of milliseconds. An essential component of this actuator is the single-ion-conducting polymers that contain well-defined ionic domains through the introduction of zwitterions; this achieved an exceptionally high dielectric constant of 76 and a 300-fold enhancement in ionic conductivity. Moreover, the actuator demonstrated long-term durability, with negligible changes in the actuator stroke over 20,000 cycles in air. Owing to its low-power consumption (only 4 mW), we believe that this actuator could pave the way for cutting-edge biomimetic technologies in the future.

Ion Transport in Nanostructured Phosphonated Block Copolymers Containing Ionic Liquids

The morphology and conductivity of poly(styrenephosphonate-b-methylbutylene) block copolymers containing ionic liquids are investigated. The block copolymers display a series of well-defined self-assembled morphologies, i.e., lamellae, gyroid, hexagonal cylinder (HEX), body-centered cubic, and A15 lattice, in the absence and presence of ionic liquids. The observation of an equilibrium A15 lattice for linear diblock copolymers, in contrast to a number of theoretical studies, is ascribed to the packing frustration accompanied by prevailing electrostatic interactions. The samples having the A15 lattice show a substantially higher morphology factors (0.83-0.96) than those with the HEX phases (0.42-0.69). This indicates the structural advantage of the A15 lattice with a well-defined 3D symmetry over the 2D HEX structure for constructing less tortuous ion-conduction pathways. This unprecedented study portends the rational design of nanostructured phosphonated polymer membranes with improved conductivity.