ArticleNature communications2018
Pulsed axial epitaxy of colloidal quantum dots in nanowires enables facet-selective passivation.
Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Emerging flexible heterojunctions: fabrication, properties and optoelectronic applications.Chemical science · 2025Review
- A superlattice interface and S-scheme heterojunction for ultrafast charge separation and transfer in photocatalytic HNature communications · 2024Article
- Stress-induced ordering evolution of 1D segmented heteronanostructures and their chemical post-transformations.Nature communications · 2024Article
- Layer-Structured Anisotropic Metal Chalcogenides: Recent Advances in Synthesis, Modulation, and Applications.Chemical reviews · 2023Review
- On-demand synthesis of high-quality, blue-light-active ZnSe colloidal quantum wires.National science review · 2022Article
- Boosting photoelectrochemical efficiency by near-infrared-active lattice-matched morphological heterojunctions.Nature communications · 2021Article
- Single crystalline quaternary sulfide nanobelts for efficient solar-to-hydrogen conversion.Nature communications · 2020Article
- Regioselective magnetization in semiconducting nanorods.Nature nanotechnology · 2020Article
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Authors and funding
11 authors.
Funding
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Abstract
Epitaxially stacking colloidal quantum dots in nanowires offers a route to selective passivation of defective facets while simultaneously enabling charge transfer to molecular adsorbates - features that must be combined to achieve high-efficiency photocatalysts. This requires dynamical switching of precursors to grow, alternatingly, the quantum dots and nanowires - something not readily implemented in conventional flask-based solution chemistry. Here we report pulsed axial epitaxy, a growth mode that enables the stacking of multiple CdS quantum dots in ZnS nanowires. The approach relies on the energy difference of incorporating these semiconductor atoms into the host catalyst, which determines the nucleation sequence at the catalyst-nanowire interface. This flexible synthetic strategy allows precise modulation of quantum dot size, number, spacing, and crystal phase. The facet-selective passivation of quantum dots in nanowires opens a pathway to photocatalyst engineering: we report photocatalysts that exhibit an order-of-magnitude higher photocatalytic hydrogen evolution rates than do plain CdS quantum dots.
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