Correlated electron materials with molecular orbital states extending over transition metal clusters can host multiferroicity, spin frustration, and unconventional insulating phases. However, the fundamental criteria that govern cluster formation and stability remain unclear. Here, we identify a symmetry, correlation, and electron filling driven criteria that stabilize triangular metal trimers in materials displaying transition metal kagome patterns. Using density functional theory and chemical bonding analysis, we show that trimer formation emerges when 6 to 8 electrons occupy molecular orbitals derived from transition metal d-states, achieving near complete filling of bonding states while avoiding antibonding occupation, and correlations are of intermediate strength. This principle explains the stability of Nb3X8 (X = Cl, Br, I), and more broadly, our findings offer a general design rule to obtain quantum materials with quantum states extended across transition metal clusters.
@article{arxiv.2505.13659,
title = {Symmetry-Driven Trimer Formation in Kagome Correlated Electron Materials},
author = {Varsha Kumari and Julia Bauer and Alexandru B. Georgescu},
journal= {arXiv preprint arXiv:2505.13659},
year = {2025}
}