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Ti3C2 MXene co-catalyst on metal sulfide photo-absorbers for enhanced visible-light photocatalytic hydrogen production.


ABSTRACT: Scalable and sustainable solar hydrogen production through photocatalytic water splitting requires highly active and stable earth-abundant co-catalysts to replace expensive and rare platinum. Here we employ density functional theory calculations to direct atomic-level exploration, design and fabrication of a MXene material, Ti3C2 nanoparticles, as a highly efficient co-catalyst. Ti3C2 nanoparticles are rationally integrated with cadmium sulfide via a hydrothermal strategy to induce a super high visible-light photocatalytic hydrogen production activity of 14,342??mol?h-1?g-1 and an apparent quantum efficiency of 40.1% at 420?nm. This high performance arises from the favourable Fermi level position, electrical conductivity and hydrogen evolution capacity of Ti3C2 nanoparticles. Furthermore, Ti3C2 nanoparticles also serve as an efficient co-catalyst on ZnS or ZnxCd1-xS. This work demonstrates the potential of earth-abundant MXene family materials to construct numerous high performance and low-cost photocatalysts/photoelectrodes.

SUBMITTER: Ran J 

PROVIDER: S-EPMC5512649 | biostudies-literature | 2017 Jan

REPOSITORIES: biostudies-literature

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Ti<sub>3</sub>C<sub>2</sub> MXene co-catalyst on metal sulfide photo-absorbers for enhanced visible-light photocatalytic hydrogen production.

Ran Jingrun J   Gao Guoping G   Li Fa-Tang FT   Ma Tian-Yi TY   Du Aijun A   Qiao Shi-Zhang SZ  

Nature communications 20170103


Scalable and sustainable solar hydrogen production through photocatalytic water splitting requires highly active and stable earth-abundant co-catalysts to replace expensive and rare platinum. Here we employ density functional theory calculations to direct atomic-level exploration, design and fabrication of a MXene material, Ti<sub>3</sub>C<sub>2</sub> nanoparticles, as a highly efficient co-catalyst. Ti<sub>3</sub>C<sub>2</sub> nanoparticles are rationally integrated with cadmium sulfide via a h  ...[more]

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