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Seung Soon Jang

Publications and source records attributed to Seung Soon Jang.

2 recordsLinked to original sources

Proton-electron coupled catalyst for ionomer-free electrochemical energy conversion

Efficient electrochemical energy devices are vital to renewable energy technology, yet coordinating the effective flow of electrons, ions, and chemical species continues to be a major challenge. In conventional proton-exchange membrane fuel cell (PEMFC) catalyst layers, proton and electron transport are supplied separately through percolating carbon networks and ionomer binders, rendering the catalyst largely passive and imposing fundamental trade-offs between reactant accessibility, ionic conductivity, and catalyst activity. Here, we introduce a one-dimensional proton-electron coupled catalyst (PECC) design, a transport-integrated electrocatalyst architecture in which the catalyst itself simultaneously supplies electronic and protonic transport to catalyst active sites. Using this PECC, PEMFCs can have an ionomer-free cathode catalyst layer (CCL), resulting in a dramatic 95% reduction in non-Fickian oxygen transport and boosting power density by 34% and 85% compared to traditional CCLs, with cathode Pt loadings of approximately 0.090 mg/cm^2 and 0.037 mg/cm^2, respectively. Meanwhile, PECC retains 65% of its mass activity and exhibits 32% higher power density than its ionomer-based CCL counterpart after 30k accelerated stressed test. Similar mass transport improvements have been observed in the electrochemical hydrogen pump (EHP) using PECC in the catalyst layers. Molecular dynamics simulations show the PECC's proton conductivity is 249% higher than Nafion. This PECC catalyst structure addresses core transport problems in PEMFCs, leading to almost 20% improvement in fuel efficiency and opens up new possibilities for designing high-performance, cost-effective electrochemical devices.

cond-mat.mtrl-sci↗

Origin and Control of Polyacrylonitrile Alignments on Carbon Nanotube and Graphene Nanoribbon

While one of the most promising applications of carbon nanotubes (CNTs) is to enhance polymer orientation and crystallization to achieve advanced carbon fibers, the successful realization of this goal has been hindered by the insufficient atomistic understanding of polymer-CNT interfaces. We herein theoretically study polyacrylonitrile (PAN)-CNT hybrid structures as a representative example of polymer-CNT composites. Based on density-functional theory calculations, we first find that the relative orientation of polar PAN nitrile groups with respect to the CNT surface is the key factor that determines the PAN-CNT interface energetics and the lying-down PAN configurations are much more preferable than their standing-up counterparts. The CNT curvature is identified as another important factor, giving the largest binding energy in the zero-curvature graphene limit. Charge transfer analysis explains the unique tendency of linear PAN alignments on the CNT surface and the possibility of ordered PAN-PAN assembly. Next, performing large-scale molecular dynamics simulations, we show that the desirable linear PAN-CNT alignment can be achieved even for relatively large initial misorientations and further demonstrate that graphene nanoribbons are a promising carbon nano-reinforcement candidate. The microscopic understanding accumulated in this study will provide design guidelines for the development of next-generation carbon nanofibers.

cond-mat.mtrl-sci↗