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Weixuan Zeng

Publications and source records attributed to Weixuan Zeng.

2 recordsLinked to original sources

OmniDiT: Extending Diffusion Transformer to Omni-VTON Framework

Despite the rapid advancement of Virtual Try-On (VTON) and Try-Off (VTOFF) technologies, existing VTON methods face challenges with fine-grained detail preservation, generalization to complex scenes, complicated pipeline, and efficient inference. To tackle these problems, we propose OmniDiT, an omni Virtual Try-On framework based on the Diffusion Transformer, which combines try-on and try-off tasks into one unified model. Specifically, we first establish a self-evolving data curation pipeline to continuously produce data, and construct a large VTON dataset Omni-TryOn, which contains over 380k diverse and high-quality garment-model-tryon image pairs and detailed text prompts. Then, we employ the token concatenation and design an adaptive position encoding to effectively incorporate multiple reference conditions. To relieve the bottleneck of long sequence computation, we are the first to introduce Shifted Window Attention into the diffusion model, thus achieving a linear complexity. To remedy the performance degradation caused by local window attention, we utilize multiple timestep prediction and an alignment loss to improve generation fidelity. Experiments reveal that, under various complex scenes, our method achieves the best performance in both the model-free VTON and VTOFF tasks and a performance comparable to current SOTA methods in the model-based VTON task.

cs.CV

Coulombic control of charge transfer in luminescent radicals with long-lived quartet states

Excitons in organic materials are emerging as an attractive platform for tunable quantum technologies. Structures with near-degenerate doublet and triplet excitations in linked trityl radical, acene and carbazole units can host quartet states. These high spin states can be coherently manipulated, and later decay radiatively via the radical doublet transition. However, this requires controlling the deexcitation pathways of all metastable states. Here we establish design rules for efficient quartet generation in luminescent radicals, using different connection arrangements of the molecular units. We discover that electronic coupling strength between these units dictates luminescence and quartet formation yields, particularly through the energetics of an acene-radical charge transfer state, which we tune Coulombically. This state acts as a source of non-radiative decay when acene-radical separation is small, but facilitates doublet-quartet spin interconversion when acene-radical separation is large. Using these rules we report a radical-carbazole-acene material with 55% luminescence yield, where 94% of emitting excitons originate from the quartet at microsecond times. This reveals the central role of molecular topology in luminescent quantum materials.

cond-mat.mtrl-sci