4.8 Article

3D hierarchical FeSe2 microspheres: Controlled synthesis and applications in dye-sensitized solar cells

Journal

NANO ENERGY
Volume 15, Issue -, Pages 205-215

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nanoen.2015.04.027

Keywords

FeSe2; Counter electrode; Diselenide; Hierarchical microspheres; Dye-sensitized solar cells

Funding

  1. Shanghai Nano-Project [12nm0504300]
  2. National Natural Science Foundation of China [21371121, 21331004]
  3. SDSU EE PhD program and Pakistan-US Science and Technology Cooperation Program, open funds of SKLMMC of SJTU [mmc-kf14-09]
  4. Science and Technology Commission of Shanghai Municipality [14DZ2250800]

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Mastery over the structures at nano/microscale can effectively tailor the catalytic activity and durability of materials. Herein, three dimension (3D) hierarchical iron diselenide (FeSe2) microspheres have been successfully synthesized via a hot-injection method. The morphologies of building blocks and final products can be simply controlled by the amount and/or the type of alkythiols, from irregular micro/nanoparticles to uniform 3D hierarchical microspheres made of ultrathin nanosheets or rhombus-like nanorods. A formation mechanism has been understood based on the inherent crystal structure of FeSe2 and the selective adsorption of alkythiols. The as-obtained FeSe2 samples were employed as counter electrode (CE) materials in dye-sensitized solar cells (DSSCs). Electrochemical characterizations indicated that the 3D hierarchical FeSe2 microspheres composed of ultrathin nanosheets (FeSe2 NSs) exhibited low charge transfer resistance at the electrolyte-electrode interface, high electrocatalytic activity and fast reaction kinetics for the I-/I-3(-) redox reaction. A DSSC with FeSe2 NSs CE achieved a high power conversion efficiency of 8.39% under a simulated solar illumination of 100 mW cm(-2) (AM 1.5), comparable to that of Pt based devices (8.20%). Moreover, the fast activity onset and relatively long stability demonstrated that the FeSe2 NSs is a promising alternative to Pt in DSSC. (C) 2015 Elsevier Ltd. All rights reserved.

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