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Nhat Huy Tran

Publications and source records attributed to Nhat Huy Tran.

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AIMS: an AI experimentalist turns uncertainty into quantum matter discovery

Most AI agents act only after scientists have defined the task. Discovery is harder under practical uncertainties: the probe may not be where it is expected, the signal may occupy only a small region of a disordered sample, and the evidence may not distinguish among competing explanations. Here we show that an AI agent can decide what evidence an uncertain experiment needs next, and act on it. Beyond automation, AIMS, an uncertainty-aware experimentalist for cryogenic microwave impedance microscopy, quantifies uncertainty where it originates, in perception, sampling, and interpretation, and converts each into its own corrective action rather than a single confidence score. Given only an open objective, AIMS relocated a probe lost during cooldown while flagging its own unreliable estimates, mapped twist angle disorder to locate the strongest correlated states in twisted bilayer MoSe$_2$, and uncovered a paradox: the half-filled stripe that classical theory predicts should melt first survived longest. Distinguishing an incomplete model from a wrong mechanism, AIMS commissioned a beyond-mean-field calculation and an independent structural measurement as the decisive tests, revising its interpretation as each arrived: quantum motion reverses the classical hierarchy, stabilizing the half-filled stripe while destabilizing its neighbors. These uncertainty-to-action loops are generic to scanning probe experiments, and AIMS turns uncertainty from an obstacle into a driver of discovery.

cond-mat.str-el

Machine Learning Reconstruction of High-Dimensional Electronic Structure from Angle-Resolved Photoemission Spectroscopy

The emergent behavior of quantum materials is governed by their electronic structure, which can be experimentally probed by photoemission spectroscopy techniques that generate a four-dimensional dataset of energy and momentum. However, the quantitative extraction of Hamiltonian parameters from these high-dimensional spectra remains a significant challenge, currently relying on labor-intensive, expert-dependent analysis rather than standardized workflows. Here, we introduce a deep learning framework based on implicit neural representations to accelerate the retrieval of Hamiltonian parameters in two types of transition-metal oxides: perovskite nickelates and manganites. Our approach outperforms traditional analytical fitting procedures, yielding superior agreement with experimental Fermi surface topologies and energy-momentum dispersions. This work highlights the potential of deep learning tools to bridge the gap between theory and experiment, paving the way for high-throughput, autonomous discovery pipelines in quantum materials.

cond-mat.str-el