TY - JOUR

T1 - Atomic Structure, Dynamics, Changes in Chemical Bonding and Semiconductor-Metal Transition in Sb2Se3: A Remarkable Material for Quantum Networks and Energy Applications

AU - Kassem, Mohammad

AU - Benmore, Chris J.

AU - Tverjanovich, Andrey

AU - Bokova, Maria

AU - Khomenko, Maxim

AU - Usuki, Takeshi

AU - Sokolov, Anton

AU - Fontanari, Daniele

AU - Bereznev, Sergei

AU - Ohara, Koji

AU - Fourmentin, Marc

AU - Masselin, Pascal

AU - Bychkov, Eugene

PY - 2025/3/10

Y1 - 2025/3/10

N2 - Antimony sesquiselenide has become an outstanding functional material for photovoltaics, energy storage and transformation, memory and photonic applications. Sb2Se3 is one of the most successful emerging solar light absorbers and has also been identified as a highly promising ultralow-loss phase-change material (PCM) for next-generation coherent nanophotonic processors, photonic tensor cores, quantum and neuromorphic networks. Unlike benchmark telluride PCMs, Sb2Se3 features a quasi-one-dimensional (1D) crystalline structure consisting of (Sb4 Se6)∞ ribbons, lacks the typical PCM chemical bonding, and undergoes an extended semiconductor-metal transition above the melting point. Consequently, the origin of high optical contrast between crystalline (SET) and amorphous (RESET) logic states remains elusive and presents a significant challenge. Using high-energy X-ray diffraction and Raman spectroscopy over a wide temperature range, supported by first-principles simulations and complemented by thermal, optical and electrical measurements, as well as by 121Sb-Mössbauer spectroscopy, the quasi-1D network of orthorhombic antimony sesquiselenide was found to undergo significant evolution in amorphous and supercooled Sb2Se3, leading to lower coordination, shorter interatomic distances and a higher p-electron density on antimony, indicating changes in chemical bonding. The observed novel Sb2Se3 nanocrystalline polymorph, characterized by trigonal antimony coordination and more isolated Sb-Se ribbons, could help reduce multiple trapping defect states in the bandgap, which are typical of orthorhombic Sb2Se3, thereby enhancing the power-conversion efficiency of photovoltaic devices. Semimetallic and metallic liquid Sb2Se3 exhibit a gradual transformation into a denser 2D and/or 3D network with higher antimony coordination. Localized electron states in the pseudogap are becoming extended, leading to an increase in electronic conductivity σ following the relationship σ ∝ N(EF)2. Liquid Sb2Se3 also appears to be strongly fragile, with a nonmonotonic change in viscosity and higher atomic mobility in the metallic liquid. These results explain extraordinary functionalities of Sb2Se3 for photonic and energy applications.

AB - Antimony sesquiselenide has become an outstanding functional material for photovoltaics, energy storage and transformation, memory and photonic applications. Sb2Se3 is one of the most successful emerging solar light absorbers and has also been identified as a highly promising ultralow-loss phase-change material (PCM) for next-generation coherent nanophotonic processors, photonic tensor cores, quantum and neuromorphic networks. Unlike benchmark telluride PCMs, Sb2Se3 features a quasi-one-dimensional (1D) crystalline structure consisting of (Sb4 Se6)∞ ribbons, lacks the typical PCM chemical bonding, and undergoes an extended semiconductor-metal transition above the melting point. Consequently, the origin of high optical contrast between crystalline (SET) and amorphous (RESET) logic states remains elusive and presents a significant challenge. Using high-energy X-ray diffraction and Raman spectroscopy over a wide temperature range, supported by first-principles simulations and complemented by thermal, optical and electrical measurements, as well as by 121Sb-Mössbauer spectroscopy, the quasi-1D network of orthorhombic antimony sesquiselenide was found to undergo significant evolution in amorphous and supercooled Sb2Se3, leading to lower coordination, shorter interatomic distances and a higher p-electron density on antimony, indicating changes in chemical bonding. The observed novel Sb2Se3 nanocrystalline polymorph, characterized by trigonal antimony coordination and more isolated Sb-Se ribbons, could help reduce multiple trapping defect states in the bandgap, which are typical of orthorhombic Sb2Se3, thereby enhancing the power-conversion efficiency of photovoltaic devices. Semimetallic and metallic liquid Sb2Se3 exhibit a gradual transformation into a denser 2D and/or 3D network with higher antimony coordination. Localized electron states in the pseudogap are becoming extended, leading to an increase in electronic conductivity σ following the relationship σ ∝ N(EF)2. Liquid Sb2Se3 also appears to be strongly fragile, with a nonmonotonic change in viscosity and higher atomic mobility in the metallic liquid. These results explain extraordinary functionalities of Sb2Se3 for photonic and energy applications.

KW - atomic structure

KW - chemical bonding

KW - electronic properties

KW - first-principles simulations

KW - phase-change materials

KW - semiconductor-metal transition

KW - viscosity

UR - https://www.mendeley.com/catalogue/4390f3e4-d779-3014-bf30-d61502f64e84/

U2 - 10.1021/acsami.5c00008

DO - 10.1021/acsami.5c00008

M3 - Article

VL - 17

SP - 17075

EP - 17095

JO - ACS applied materials & interfaces

JF - ACS applied materials & interfaces

SN - 1944-8244

IS - 11

ER -