Stable 1T″ HfCl2monolayer with strong excitonic effects and promising solar harvesting efficiency

Palheta J.M.T.; Batista A.L.O.; Flores E.M.; Rêgo C.R.C.; Santos A.S.; Guedes-Sobrinho D.; Cavalheiro Dias A.; Piotrowski M.J. · Nanoscale (2026) · DOI: 10.1039/d5nr04047g

Resumen

In this work, we performed a computational screening of group IV transition-metal dihalide monolayers in the recently proposed 1T″ phase. We have thoroughly examined their structural, electronic, optical, and excitonic characteristics, using density functional theory with both the generalized gradient approximation (PBE) and hybrid (HSE06) exchange–correlation approaches including spin–orbit coupling, complemented by Wannier-function-based tight-binding and Bethe–Salpeter equation analyses; as well as phonon dispersion calculations and ab initio molecular dynamics to shed light on the material stability. Out of the nine candidate systems, only 1T″ ZrCl2, HfCl2, and HfBr2 were found to be dynamically and thermally stable, with semiconducting behavior observed exclusively for HfCl2. From a detailed analysis of this compound, we have revealed pronounced excitonic effects, with a binding energy of 275 meV, strong optical anisotropy, and broadband absorption covering the infrared, visible, and ultraviolet ranges. Moreover, efficiencies of up to 20% were obtained by evaluating the 1T″-HfCl2 photovoltaic performance using the spectroscopic limited maximum efficiency and the Shockley–Queisser limit. These results highlight 1T″-HfCl2 as a promising two-dimensional semiconductor for optoelectronic and solar energy applications. This journal is © The Royal Society of Chemistry, 2026

Instituciones: Universidad Nacional Jorge Basadre Grohmann