Polydopamine and Its Derivative Surface Chemistry in Material Science: A Focused Review for Studies at KAIST

Polydopamine coating, the first material-independent surface chemistry, and its related methods significantly influence virtually all areas of material science and engineering. Functionalized surfaces of metal oxides, synthetic polymers, noble metals, and carbon materials by polydopamine and its related derivatives exhibit a variety of properties for cell culture, microfluidics, energy storage devices, superwettability, artificial photosynthesis, encapsulation, drug delivery, and numerous others. Unlike other articles, this review particularly focuses on the development of material science utilizing polydopamine and its derivatives coatings at the Korea Advanced Institute of Science and Technology for a decade. Herein, it is demonstrated how material-independent coating methods provide solutions for challenging problems existed in many interdisciplinary areas in bio-, energy-, and nanomaterial science by collaborations and independent research.     

Effects of microporous layer penetration ratio and substrate carbonization temperature on the performance of proton exchange membrane fuel cells

The gas diffusion layer (GDL) is composed of a microporous layer (MPL) and a substrate; this substrate is generally fabricated from carbon fiber, carbonized resin, and polytetrafluoroethylene. When the MPL penetrates deeper into the substrate, the porosity and pore size of the GDL decrease, and the tortuosity increases; this leads to a reduction in the water discharge capability of the GDL. In this study, the MPL penetration ratio over the total GDL thickness was controlled using three different substrate manufacturing methods. These manufacturing methods for preventing the MPL from penetrating deeper into the substrate were based on the carbon fiber content within the substrate, the amount of carbonized resin coating on the substrate, and the approach used for loading the MPL. Furthermore, the GDLs were manufactured at different carbonization temperatures to investigate the effects of the carbonization temperature of the substrate on the performance of the proton-exchange membrane fuel cell.