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, Ti 3 C 2 nanoparticles, as a highly efficient co-catalyst. Ti 3 C 2 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 μmol 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 Ti 3 C 2 nanoparticles. Furthermore, Ti 3 C 2 nanoparticles also serve as an efficient co-catalyst on ZnS or Zn x Cd 1-x S. This work demonstrates the potential of earth-abundant MXene family materials to construct numerous high performance and low-cost photocatalysts/photoelectrodes.
| Original language | English |
|---|---|
| Article number | 13907 |
| Journal | Nature Communications |
| Volume | 8 |
| DOIs | |
| State | Published - 3 Jan 2017 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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