Ultrafast Electrochemical Synthesis of Defect-Free In<sub>2</sub> Se<sub>3</sub> Flakes for Large-Area Optoelectronics.

Shi, Huanhuan; Li, Mengmeng; Shaygan Nia, Ali; Wang, Mingchao; Park, SangWook; Zhang, Zhen; Lohe, Martin R; Yang, Sheng et al. · Adv Mater · 2020

basic_science · Level V

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Abstract

Because of its thickness-dependent direct bandgap and exceptional optoelectronic properties, indium(III) selenide (In<sub>2</sub> Se<sub>3</sub> ) has emerged as an important semiconductor for electronics and optoelectronics. However, the scalable synthesis of defect-free In<sub>2</sub> Se<sub>3</sub> flakes remains a significant barrier for its practical applications. Here, a facile electrochemical strategy is presented for the ultrafast delamination of bulk layered In<sub>2</sub> Se<sub>3</sub> crystals in nonaqueous media, resulting in high-yield (83%) production of defect-free In<sub>2</sub> Se<sub>3</sub> flakes with large lateral size (up to 26 µm). The intercalation of tetrahexylammonium (THA<sup>+</sup> ) ions mainly creates stage-3 intercalated compounds in which every three layers of In<sub>2</sub> Se<sub>3</sub> are occupied by one layer of THA molecules. The subsequent exfoliation leads to a majority of trilayer In<sub>2</sub> Se<sub>3</sub> nanosheets. As a proof of concept, solution-processed, large-area (400 µm × 20 µm) thin-film photodetectors embedded with the exfoliated In<sub>2</sub> Se<sub>3</sub> flakes reveal ultrafast response time with a rise and decay of 41 and 39 ms, respectively, and efficient responsivity (1 mA W<sup>-1</sup> ). Such performance surpasses most of the state-of-the-art thin-film photodetectors based on transition metal dichalcogenides.