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Akihiro Otsuka

Publications and source records attributed to Akihiro Otsuka.

4 recordsLinked to original sources

Algebraic Quantum Intelligence: A New Framework for Reproducible Machine Creativity

Large language models (LLMs) have achieved remarkable success in generating fluent and contextually appropriate text; however, their capacity to produce genuinely creative outputs remains limited. This paper posits that this limitation arises from a structural property of contemporary LLMs: when provided with rich context, the space of future generations becomes strongly constrained, and the generation process is effectively governed by near-deterministic dynamics. Recent approaches such as test-time scaling and context adaptation improve performance but do not fundamentally alter this constraint. To address this issue, we propose Algebraic Quantum Intelligence (AQI) as a computational framework that enables systematic expansion of semantic space. AQI is formulated as a noncommutative algebraic structure inspired by quantum theory, allowing properties such as order dependence, interference, and uncertainty to be implemented in a controlled and designable manner. Semantic states are represented as vectors in a Hilbert space, and their evolution is governed by C-values computed from noncommutative operators, thereby ensuring the coexistence and expansion of multiple future semantic possibilities. In this study, we implement AQI by extending a transformer-based LLM with more than 600 specialized operators. We evaluate the resulting system on creative reasoning benchmarks spanning ten domains under an LLM-as-a-judge protocol. The results show that AQI consistently outperforms strong baseline models, yielding statistically significant improvements and reduced cross-domain variance. These findings demonstrate that noncommutative algebraic dynamics can serve as a practical and reproducible foundation for machine creativity. Notably, this architecture has already been deployed in real-world enterprise environments.

cs.AI↗

Magnetic field-driven transition between valence bond solid and antiferromagnetic order in distorted triangular lattice

A molecular Mott insulator $κ$-(ET)$_2$B(CN)$_4$ [ET = bis(ethylenedithio)tetrathiafulvalene] with a distorted triangular lattice exhibits a quantum disordered state with gapped spin excitation in the ground state. $^{13}$C nuclear magnetic resonance, magnetization, and magnetic torque measurements reveal that magnetic field suppresses valence bond order and induces long-range magnetic order above a critical field $\sim 8$ T. The nuclear spin-lattice relaxation rate $1/T_1$ shows persistent evolution of antiferromagnetic correlation above the transition temperature, highlighting a quantum spin liquid state with fractional excitations. The field-induced transition as observed in the spin-Peierls phase suggests that the valence bond order transition is driven through renormalized one-dimensionality and spin-lattice coupling.

cond-mat.str-el↗

A molecular diamond lattice antiferromagnet as a Dirac semimetal candidate

The ground state of a molecular diamond-lattice compound (ET)Ag$_4$(CN)$_5$ is investigated by the magnetization and nuclear magnetic resonance spectroscopy. We found that the system exhibits antiferromagnetic long-range ordering with weak ferromagnetism at a high temperature of 102 K owing to the strong electron correlation. The spin susceptibility is well fitted into the diamond-lattice Heisenberg model with a nearest neighbor exchange coupling of 230 K, indicating the less frustrated interactions. The transition temperature elevates up to $\sim$195 K by applying pressure of 2 GPa, which records the highest temperature among organic molecular magnets. The first-principles band calculation suggests that the system is accessible to a three-dimensional topological semimetal with nodal Dirac lines, which has been extensively searched for a half-filling diamond lattice.

cond-mat.str-el↗

Pressure-Tuned Exchange Coupling of a Quantum Spin Liquid in the Molecular Triangular Lattice $κ$-(ET)$_2$Ag$_2$(CN)$_3$

The effects of pressure on a quantum spin liquid are investigated in an organic Mott insulator $κ$-(ET)$_2$Ag$_2$(CN)$_3$ with a spin-1/2 triangular lattice. The application of negative chemical pressure to $κ$-(ET)$_2$Cu$_2$(CN)$_3$, which is a well-known sister Mott insulator, allows for extensive tuning of antiferromagnetic exchange coupling, with $J/k_{\rm B} = 175 - 310$ K, under hydrostatic pressure. Based on $^{13}$C nuclear magnetic resonance measurements under pressure, we uncover universal scaling in the static and dynamic spin susceptibilities down to low temperatures $\sim 0.1k_{\rm B}T/J$. The persistent fluctuations and residual specific heat coefficient are consistent with the presence of gapless low-lying excitations. Our results thus demonstrate fundamental finite-temperature properties of quantum spin liquid in a wide parameter range.

cond-mat.str-el↗