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Well-defined CoSe2@MoSe2 hollow heterostructured nanocubes with enhanced dissociation kinetics for overall water splitting

Chen, Zhiwen (författare)
Shanghai Univ, Peoples R China
Wang, Wenwen (författare)
Shanghai Univ, Peoples R China
Huang, Shoushuang (författare)
Shanghai Univ, Peoples R China
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Ning, Ping (författare)
Shanghai Univ, Peoples R China
Wu, Ye (författare)
Shanghai Univ, Peoples R China
Gao, Chunyan (författare)
Shanghai Univ, Peoples R China
Le, Thanh-Tung (författare)
Shanghai Univ, Peoples R China
Zai, Jiantao (författare)
Shanghai Jiao Tong Univ, Peoples R China
Jiang, Yong (författare)
Shanghai Univ, Peoples R China
Hu, Zhang-Jun (författare)
Linköpings universitet,Molekylär ytfysik och nanovetenskap,Tekniska fakulteten,Shanghai Univ, Peoples R China
Qian, Xuefeng (författare)
Shanghai Jiao Tong Univ, Peoples R China; Shanghai Jiao Tong Univ, Peoples R China
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 (creator_code:org_t)
2020
2020
Engelska.
Ingår i: Nanoscale. - : ROYAL SOC CHEMISTRY. - 2040-3364 .- 2040-3372. ; 12:1, s. 326-335
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Hollow heterostructures have tremendous advantages in electrochemical energy storage and conversion areas due to their unique structure and composition characteristics. Here, we report the controlled synthesis of hollow CoSe2 nanocubes decorated with ultrathin MoSe2 nanosheets (CoSe2@MoSe2) as an efficient and robust bifunctional electrocatalyst for overall water splitting in a wide pH range. It is found that integrating ultrathin MoS2 nanosheets with hollow CoSe2 nanocubes can provide abundant active sites, promote electron/mass transfer and bubble release and facilitate the migration of charge carriers. Additionally, the surface electron coupling in the heterostructures enables it to serve as a source of sites for H+ and/or OH- adsorption, thus reducing the activation barrier for water molecules adsorption and dissociation. As a result, the title compound, CoSe2@MoSe2 hollow heterostructures, exhibits an overpotential of 183 mV and 309 mV at a current density of 10 mA cm(-2) toward hydrogen evolution reactions and oxygen evolution reactions in 1.0 M KOH, respectively. When applied as both cathode and anode for overall water splitting, a low battery voltage of 1.524 V is achieved along with excellent stability for at least 12 h. This work provides a new idea for the design and synthesis of high-performance catalysts for electrochemical energy storage and conversion.

Ämnesord

NATURVETENSKAP  -- Kemi -- Oorganisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)

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