Unraveling a chemical-bond-driven root of topology in three-dimensional chiral crystals
Shungo Aoyagi, Shunsuke Kitou, Yuiga Nakamura, Motoaki Hirayama, Hideki Matsuoka, Ryotaro Arita, Shuichi Murakami, Taka-hisa Arima, Naoya Kanazawa

TL;DR
This paper uncovers how chemical bonding in three-dimensional chiral crystals leads to topological electronic states, providing a new framework for designing quantum properties in chiral materials.
Contribution
It introduces a real-space bonding network model linking chemical bonds to topological fermions in chiral crystals, advancing understanding of topological phases without relying solely on spin-orbit coupling.
Findings
Identification of chiral bonding networks responsible for multifold topological fermions
Development of a 3D Su-Schrieffer-Heeger model explaining topological features
Topological states can be controlled by reversing chirality or tuning electron filling
Abstract
Chirality manifests across multiple scales, yielding unique phenomena that break mirror symmetry. In chiral materials, unexpectedly large spin-filtering or photogalvanic effects have been observed even in materials composed of light elements, implying crucial influence of their topological electronic states. However, an underlying framework that links chemical bonding and electronic topology remains elusive, preventing the rational design of quantum chiral properties. Here we identify the chiral bonding network responsible for multifold topological fermions by combining synchrotron X-ray diffraction and first-principles calculations on cubic chiral crystals, CoSi and FeSi. Based on the observations of asymmetric valence electron distributions around the transition metals, together with analyses of their bonding to sevenfold-coordinated silicon atoms, we develop a three-dimensional…
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