journal article·2016-02-03

Organometallically Anisotropic Growth of Ultralong Sb2Se3 Nanowires with Highly Enhanced Photothermal Response

Guihuan Chen, Jun Zhou, Jian Zuo, Qing Yang

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Abstract

Ultralong orthorhombic Sb2Se3 nanowires have been successfully fabricated via an alternative facile organometallic synthetic route from the reaction of triphenylantimony(III) with dibenzyldiselenide in oleylamine at 180-240 °C without any other additives. The formation and growth mechanism of the Sb2Se3 nanowires is intensively investigated, and it is found that the anisotropic growth of the nanowires with almost constant diameters is resulted from the synergistic effects of the intrinsic property of the orthorhombic crystal structure and the weak binding assistance of oleylamine, and the length of the nanowires can be elongated easily by increasing reaction time in the synthetic route. Moreover, the photothermal response of the Sb2Se3 nanowires is first evaluated under illumination of UV light (320-390 nm), and it is especially noted that the Sb2Se3 nanowires exhibit highly enhanced photothermal responses (more than two times the intensity) as compared to the bulk Sb2Se3. In addition, the Sb2Se3 nanowires show excellent light-to-heat performance, which is superior to that of the nanostructured titanium dioxide and silicon powder under the same conditions.
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Research context

OpenAlex topics: Chalcogenide Semiconductor Thin Films · Advanced Thermoelectric Materials and Devices · Quantum Dots Synthesis And Properties

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Hefei National Laboratory of Physical Sciences at the Microscale, ‡Department of Chemistry, §Laboratory of Nanomaterials for Energy Conversion, and ∥Synergetic Innovation Center of Quantum Information & Quantum Physics, University of Science and Technology of China, Hefei 230026, Anhui, P. R. China

Funding

Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China

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