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Joonwon Lim

Publications and source records attributed to Joonwon Lim.

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TBA-enabled spin-coating of a percolatively connected GO nanosieve for thru-hole epitaxy: tuning GO flake stacking and coverage to control GaN nucleation

We report a spin-coating-based approach for forming a percolatively connected graphene oxide (GO) nanosieve on SiO$_2$-patterned sapphire substrates, where the addition of tetrabutylammonium (TBA) to the GO solution significantly improves the uniformity of flake coverage and modulates GaN nucleation behavior. Upon thermal annealing of GO, the resulting reduced graphene oxide (rGO) films exhibit spatially varying coverage, leading to three distinct GaN nucleation outcomes: (i) ELOG-like nucleation on exposed substrate regions, (ii) thru-hole epitaxy (THE)-like nucleation through appropriately thin areas, and (iii) complete nucleation suppression on thickly stacked zones. On spin-coated GO films without TBA, all three behaviors coexist, and undesired ELOG- and no-nucleation modes persist due to uneven coverage. Importantly, these issues cannot be resolved by simply adjusting GO flake concentration, as concentration tuning alone fails to eliminate the formation of locally bare and overly thick regions. In contrast, the addition of TBA results in a more uniform, moderately stacked rGO morphology that suppresses both ELOG- and no-nucleation modes while expanding THE-like nucleation regions. This reshaped nucleation landscape confines GaN growth to areas with engineered percolative transport. The approach offers a scalable, lithography-free route for controlling GaN epitaxy using solution-processable 2D material masks.

cond-mat.mtrl-sci

Orientation disparity in GaN/graphene/$m$-sapphire: control-based re-examination of thru-hole epitaxy

The crystallographic orientation of films grown on 2D-masked substrates is often used to infer the pathway among remote, van der Waals, and thru-hole (pinhole-seeded) epitaxy. However, attribution of a specific growth mechanism based on orientation can be ambiguous unless mask continuity and substrate pre-treatment are evaluated within a single process window. We compare GaN grown under identical conditions on four m-plane sapphire templates: (i) bare, (ii) "graphene-grown" (high-temperature Ar/H2 with CH4 on), (iii) "anneal-only" (high-temperature Ar/H2 with CH4 off), and (iv) graphene oxide spin-coated and reduced on pristine sapphire. GaN selects (103) on graphene-grown and anneal-only m-plane sapphire, selects (100) on bare m-plane sapphire, and is predominantly (100) with a minority (103) on graphene oxide spin-coated and reduced/pristine m-plane sapphire. High-resolution TEM shows that, on partly graphene-covered samples, nucleation occurs on exposed sapphire (thru-hole), not on graphene, providing mechanism evidence independent of orientation. Within this window, the substrate surface state set by high-temperature Ar/H2 pre-treatment (rather than mask continuity) primarily governs orientation, while open-area effects can play a secondary role. Thus, preferred orientation alone may not determine the growth mechanism; mask continuity and substrate pre-treatment must be explicitly controlled when using orientation as evidence for mechanism assignment.

cond-mat.mtrl-sci