Searcharxiv⌕ Search

arXiv subjects

Jin-Sung Park

Publications and source records attributed to Jin-Sung Park.

5 recordsLinked to original sources

Multi-Persona Debate System for Automated Scientific Hypothesis Generation

Modern scientific discovery is bottlenecked not by data scarcity, but by the inability to synthesize fragmented knowledge into actionable hypotheses. This challenge is especially acute in battery materials research, where electrochemical performance, interfacial behavior, and manufacturing feasibility must be optimized simultaneously. Here, we present the Multi-Persona Debate System (MPDS), a literature-grounded framework for automated scientific hypothesis generation that combines literature retrieval, long-context large language model reasoning, corpus-driven persona induction, and structured multi-agent debate. MPDS constructs literature snapshots of up to 500 papers, grounds agents in role-specific evidence pools, and conducts a three-round citation-aware debate followed by moderator synthesis, enabling negotiation between personas while preserving evidence traceability. We evaluate MPDS using a temporally controlled protocol excluding direct access to target papers, including two held-out battery-materials case studies and a blinded comparison across 30 matched cases. In sodium-ion anode and all-solid-state battery cathode design tasks, MPDS recovered design logics aligned with experimentally validated solution spaces and generated more mechanistically explicit, process-aware proposals than simpler baselines. To assess the impact of personas and debate, we introduce Integrative Hypothesis Quality scoring. In ablation studies, MPDS achieved the highest mean score among five conditions, with its largest advantage in cross-perspective integration. A laboratory follow-up suggests utility as a diagnostic aid for identifying practical bottlenecks in workflows. These results indicate that structured debate over literature snapshots improves hypothesis formation under coupled engineering constraints and provides a reusable workflow for text-intensive scientific discovery.

cs.CL↗

1.5 million materials narratives generated by chatbots

The advent of artificial intelligence (AI) has enabled a comprehensive exploration of materials for various applications. However, AI models often prioritize frequently encountered materials in the scientific literature, limiting the selection of suitable candidates based on inherent physical and chemical properties. To address this imbalance, we have generated a dataset of 1,494,017 natural language-material paragraphs based on combined OQMD, Materials Project, JARVIS, COD and AFLOW2 databases, which are dominated by ab initio calculations and tend to be much more evenly distributed on the periodic table. The generated text narratives were then polled and scored by both human experts and ChatGPT-4, based on three rubrics: technical accuracy, language and structure, and relevance and depth of content, showing similar scores but with human-scored depth of content being the most lagging. The merger of multi-modality data sources and large language model (LLM) holds immense potential for AI frameworks to help the exploration and discovery of solid-state materials for specific applications.

cond-mat.mtrl-sci↗

Axial Profiling of Interferometric Scattering Enables an Accurate Determination of Nanoparticle Size

Interferometric scattering (iSCAT) microscopy has undergone significant development in recent years. It is a promising technique for imaging and tracking nanoscopic label-free objects with nanometer localization precision. The current iSCAT-based photometry technique allows quantitative estimation for the size of a nanoparticle by measuring iSCAT contrast and has been successfully applied to nano-objects smaller than the Rayleigh scattering limit. Here we provide an alternative method that overcomes such size limitations. We take into account the axial variation of iSCAT contrast and utilize a vectorial point spread function model to uncover the position of a scattering dipole and, consequently, the size of the scatterer, which is not limited to the Rayleigh limit. We found that our technique accurately measures the size of spherical dielectric nanoparticles in a purely optical and non-contact way. We also tested fluorescent nanodiamonds (fND) and obtained a reasonable estimate for the size of fND particles. Together with fluorescence measurement from fND, we observed a correlation between the fluorescent signal and the size of fND. Our results showed that the axial pattern of iSCAT contrast provides sufficient information for the size of spherical particles. Our method enables us to measure the size of nanoparticles from tens of nanometers and beyond the Rayleigh limit with nanometer precision, making a versatile all-optical nanometric technique.

physics.optics↗

Focusing of light energy inside a scattering medium by controlling the time-gated multiple light scattering

The efficient delivery of light energy is a prerequisite for non-invasive imaging and stimulating of target objects embedded deep within a scattering medium. However, injected waves experience random diffusion by multiple light scattering, and only a small fraction reaches the target object. Here we present a method to counteract wave diffusion and to focus multiplescattered waves to the deeply embedded target. To realize this, we experimentally inject light to the reflection eigenchannels of a specific flight time where most of the multiple-scattered waves have interacted with the target object and maximize the intensity of the returning multiple-scattered waves at the selected time. For targets that are too deep to be visible by optical imaging, we demonstrated a more than 10-fold enhancement in light energy delivery in comparison with ordinary wave diffusion cases. This work will lay a foundation for enhancing the working depth of imaging, sensing, and light stimulation.

physics.optics↗

Assembly of 3D plasmonic metamolecules by 2D AFM nanomanipulation of highly uniform and smooth gold nanospheres

Atomic force microscopy (AFM) nanomanipulation has been viewed as a deterministic method for the assembly of plasmonic metamolecules because it enables unprecedented engineering of clusters with exquisite control over particle number and geometry. Nevertheless, the dimensionality of plasmonic metamolecules via AFM nanomanipulation is limited to 2D, so as to restrict the design space of available artificial electromagnetisms. Here, we show that 2D nanomanipulation of the AFM tip can be used to assemble 3D plasmonic metamolecules in a versatile and deterministic way by dribbling highly spherical and smooth gold nanospheres (NSs) on a nanohole template rather than on a flat surface. Various 3D plasmonic clusters with controlled symmetry were successfully assembled with nanometer precision, the relevant 3D plasmonic modes (i.e., artificial magnetism and magnetic-based Fano resonance) were fully rationalized by both numerical calculation and dark-field spectroscopy. This templating strategy for advancing AFM nanomanipulation can be generalized to exploit the fundamental understanding of various electromagnetic 3D couplings and can serve as the basis for the design of metamolecules, metafluids, and metamaterials.

physics.optics↗