PKNU DEPARTMENT OF PHYSICS

S. C. Jung, Y.-J. Kang, and Y.-K. Han*, “Origin of excellent rate and cycle performance of Na+-solvent cointercalated graphite vs. poor performance of Li+-solvent case”, Nano Energy, 34, 456 (2017).

Y.-J. Kang†, S. C. Jung†, H.-J. Kim, Y.-K. Han*, and S. H. Oh, “Maximum catalytic activity of Pt3M in Li-O2 batteries, M = transition metals”, Nano Energy 27, 1 (2016). (†equal contribution)

Y.-J. Kang†, S. C. Jung†, J. W. Choi*, and Y.-K. Han*, “Important role of functional groups for sodium ion intercalation in expanded graphite”, Chem. Mater. 27, 5402 (2015). (†equal contribution)

H. J. Kim†, S. C. Jung†, Y.-K. Han*, and S. H. Oh, “An atomic-level strategy for the design of a low-overpotntial catalyst for Li-O2 battery”, Nano Energy 13, 679 (2015). (†equal contribution)

S. C. Jung, H.-J. Kim, J. W. Choi, and Y.-K. Han*, “Sodium ion diffusion in Al2O3: a distinct perspective compared with lithium ion diffusion”, Nano Lett. 14, 6559 (2014).

S. C. Jung, D. S. Jung, J. W. Choi, and Y.-K. Han*, “Atom-level understanding of the sodiation process in silicon anode material”, J. Phys. Chem. Lett. 5, 1283 (2014).

S. C. Jung and Y.-K. Han*, “How do Li atoms pass through the Al2O3 coating layer during lithiation in Li-ion batteries?”, J. Phys. Chem. Lett. 4, 2681 (2013).

S. C. Jung, J. W. Choi*, and Y.-K. Han*, “Anisotropic volume expansion of crystalline silicon during electrochemical lithium insertion: an atomic level rationale”, Nano Lett. 12, 5342 (2012).