A hybrid aerogel, composed of MoS2 sheets of 1T (distorted octahedral) and 2H (trigonal prismatic) phases, finely mixed with few layers of reduced graphene oxide (rGO) and obtained by means of a facile environmentfriendly hydrothermal cosynthesis, is proposed as electrode material for supercapacitors. By electrochemical characterizations in three- and two-electrode configurations and symmetric planar devices, unique results have been obtained, with specific capacitance values up to 416 F g−1 and a highly stable capacitance behavior over 50000 charge−discharge cycles. The in-depth morphological and structural characterizations through field emission scanning electron microscopy, Raman, X-ray photoelectron spectroscopy, X-ray diffraction, Brunauer−Emmett− Teller, and transmission electron microscopy analysis provides the proofs of the unique assembly of such 3D structured matrix. The unpacked MoS2 structure exhibits an excellent distribution of 1T and 2H phase sheets that are highly exposed to interaction with the electrolyte, and so available for surface/near-surface redox reactions, notwithstanding the quite low overall content of MoS2 embedded in the reduced graphene oxide (rGO) matrix. A comparison with other “more conventional” hybrid rGO-MoX2 electrochemically active materials, synthesized in the same conditions, is provided to support the outstanding behavior of the cosynthesized rGO-MoS2.

Mixed 1T–2H Phase MoS2/Reduced Graphene Oxide as Active Electrode for Enhanced Supercapacitive Performance / Gigot, ARNAUD NICOLAS; Fontana, Marco; Serrapede, Mara; Castellino, Micaela; Bianco, Stefano; Armandi, Marco; Bonelli, Barbara; Pirri, Candido; Tresso, Elena Maria; Rivolo, Paola. - In: ACS APPLIED MATERIALS & INTERFACES. - ISSN 1944-8244. - 8:(2016), pp. 32842-32852. [10.1021/acsami.6b11290]

Mixed 1T–2H Phase MoS2/Reduced Graphene Oxide as Active Electrode for Enhanced Supercapacitive Performance

GIGOT, ARNAUD NICOLAS;FONTANA, MARCO;SERRAPEDE, MARA;Castellino, Micaela;BIANCO, STEFANO;ARMANDI, MARCO;BONELLI, BARBARA;PIRRI, Candido;TRESSO, Elena Maria;RIVOLO, PAOLA
2016

Abstract

A hybrid aerogel, composed of MoS2 sheets of 1T (distorted octahedral) and 2H (trigonal prismatic) phases, finely mixed with few layers of reduced graphene oxide (rGO) and obtained by means of a facile environmentfriendly hydrothermal cosynthesis, is proposed as electrode material for supercapacitors. By electrochemical characterizations in three- and two-electrode configurations and symmetric planar devices, unique results have been obtained, with specific capacitance values up to 416 F g−1 and a highly stable capacitance behavior over 50000 charge−discharge cycles. The in-depth morphological and structural characterizations through field emission scanning electron microscopy, Raman, X-ray photoelectron spectroscopy, X-ray diffraction, Brunauer−Emmett− Teller, and transmission electron microscopy analysis provides the proofs of the unique assembly of such 3D structured matrix. The unpacked MoS2 structure exhibits an excellent distribution of 1T and 2H phase sheets that are highly exposed to interaction with the electrolyte, and so available for surface/near-surface redox reactions, notwithstanding the quite low overall content of MoS2 embedded in the reduced graphene oxide (rGO) matrix. A comparison with other “more conventional” hybrid rGO-MoX2 electrochemically active materials, synthesized in the same conditions, is provided to support the outstanding behavior of the cosynthesized rGO-MoS2.
File in questo prodotto:
File Dimensione Formato  
1T-2H mixed phase_def_acsami.6b11290.pdf

non disponibili

Tipologia: 2a Post-print versione editoriale / Version of Record
Licenza: Non Pubblico - Accesso privato/ristretto
Dimensione 7.47 MB
Formato Adobe PDF
7.47 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11583/2659623
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo