Pressure engineered Antimonite for better semiconductors

Antimonite has potential applications for solar energy, but how its layered structure changes under pressure is incompletely understood. Here diamond anvil cell experiments supported by first principles calculations offer a structural explanation for experimentally observed phase transitions.
Published in Chemistry
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Semiconductors were widely used in manufacturing chops, solar cells, photovoltaic devices and so on, which have defined the third industrial revolution since the late 1900s. Although a large number of semiconductor materials are in production, people are still seeking new semiconductor materials with higher energy conversion efficiency. Choices for environmentally friendly and affordable semiconductors are limited. However, it is possible to optimize the properties of semiconductor materials through doping, preparing thin films, and high-temperature annealing. Here, we introduce an effective, energy-efficient and pollution-free approach to continuously modulate the band gap of Sb2S3 at gigapascal pressures by means of hydrostatic pressure compression.

 

One of the most important parameters for semiconductor is its band-gap energy, which will determine its field of implication. Sb2S3 is a typical transition metal sulfide, with a favorable band-gap energy of 1.5eV~2.2eV for solar energy conversion. It features a wide response range to the solar spectrum and has higher conversion efficiency than single-crystal silicon in absorbing near infrared light. With good Earth abundance and tolerance to high temperature, Sb2S3, or the mineral stibnite, makes a promising material for photoelectric and potentially a thermoelectric material which converts heat to controllable energy. The only drawback of Sb2S3 is its band-gap energy is slightly higher than the optimal band gap value of 1.5 eV for the absorber layer of solar cells, which reduces the efficiency of its absorption of sunlight.

 

Our group reported a novel form of bulk Sb2S3 samples by breaking its ambient layered structure using pressure. We applied external stress to squeeze the Sb2S3 layer supported by the weak van der Waals forces. This method is the opposite way of manufacturing graphene, which breaks van der Waals carbon layers by striping graphite. Instead, we attached those layers together and enforced them to form stronger covalent bonds. This 3D structure of Sb2S3 features lower bandgaps upon the structural transformation at gigapascal pressures.

 

Applying external stress has renovated both the crystal and electronic structure of Sb2S3. Raman spectroscopy is sensitive to the chemical bonds and the evolution of Raman under compression suggest a large number of soft interlayer bonds disappear and was replaced by rigid interatomic bonds near the transition pressure. This is also consistent with other structural probes like x-ray diffraction and computational simulations. Moreover, during the pressurization process, the band gap of Sb2S3 transforms from  the indirect band gap type to the direct band gap type, which will shorten the recombination lifetime and improve photovoltaic properties. We found the phase transition is irreversible if pressure was removed. This means that even Sb2S3 returned to atmospheric pressure, it still maintains the compact 3D structure. This property opens up the possibility of designing semiconductor devices using 3D-Sb2S3.

 

Our experiment is among the many examples of showing pressure as an effective means of modulating material properties. Compressed structure can engineer electronic structures and design better materials for industrial implications.

 

Caption. Band gap engineering of Sb2S3 by pressure

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