Semiconductor-Semimetal Transition in van der Waals Carbyne Crystals

TL;DR

This study combines experimental spectroscopy and theoretical modeling to reveal a semimetal-semiconductor transition in van der Waals carbyne crystals, highlighting the role of chain length and hyperbolic excitons in their electronic properties.

Contribution

It provides a comprehensive framework for understanding the electronic transition in van der Waals carbyne crystals through combined experimental and theoretical approaches.

Findings

Semiconductor phase characterized by hyperbolic van Hove singularity.

Hyperbolic exciton oscillator strength decreases with chain length.

Predicted transition occurs in chains of about 42 atoms long.

Abstract

Freestanding van der Waals crystals made of single-atom carbon chains (carbynes) have been recently realized technologically. Here we investigate their electronic and optical properties experimentally, by continuous-wave and time-resolved photoluminescence spectroscopy, and theoretically. Employing a fully three-dimensional tight-binding formalism benchmarked against density functional theory calculations we predict the semimetal-semiconductor transition to occur in van der Waals carbyne crystals composed by the chains of about 42 atoms long. The semiconductor phase is characterized by a hyperbolic van Hove singularity which gives rise to unconventional hyperbolic exciton states. Experimentally, we access the semiconductor phase, where resonant features associated with hyperbolic excitons are clearly visible. The exciton oscillator strength is found to be strongly sensitive to the length of carbon chains: our experiments show that it decreases with the increasing chain length. This tendency, confirmed by the theoretical modeling, manifests the evolution of the hyperbolic exciton state on the way to the semiconductor-semimetal crossover. Our approach accounts for the actual crystalline geometry, including alternating intra-chain hoppings and inter-chain couplings. By fitting tight-binding dispersions to density functional theory data we extract consistent parameters and establish a comprehensive framework for the physics of carbyne crystals. This study paves the way towards efficient band-gap engineering in ultimate one-dimensional carbon crystals.