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Elucidating Structural Disorder in Ultra-Thin Bi-Rich Bismuth Oxyhalide Photocatalysts
Melissa Marks1,2, Henrik Jeppesen3, Mads Lund Nygaard Nielsen1
1Interdisciplinary Nanoscience Centre (iNANO), Aarhus University, Gustav Wieds Vej 14, Aarhus C, 8000, Denmark.
Small (Weinheim an Der Bergstrasse, Germany)
|May 11, 2024
Summary
This study clarifies the structure of ultra-thin bismuth oxyhalide photocatalysts, revealing that larger surface area significantly boosts their performance in chemical reactions.
Area of Science:
- Materials Science
- Solid State Chemistry
- Photocatalysis
Background:
- Bismuth oxyhalides are promising photocatalysts but their complex structures hinder understanding.
- High disorder and similar compounds make structural determination challenging.
Purpose of the Study:
- To elucidate the crystal structure of layered, Bi-rich bismuth oxyhalides.
- To establish the structure-property relationship for these ultra-thin photocatalysts.
Main Methods:
- Utilized multiple scattering techniques (electron, X-ray, neutron probes).
- Determined crystal phase as layered Bi24O31X10 (X = Cl, Br).
- Employed femtosecond transient absorption spectroscopy (fs-TAS) to measure excited state lifetimes.
Main Results:
- Identified layered Bi24O31X10 with anisotropic, platelet-shaped domains.
- Observed in-plane ordering but disorder in layer stacking.
- Found increased synthesis pH led to larger domains and longer excited state lifetimes.
- Determined increased surface area provided the most significant photocatalytic improvement.
Conclusions:
- Phase allocation of complex bismuth oxyhalides achieved.
- Structure-property relationships for ultra-thin photocatalysts discussed.
- Surface area identified as a critical factor for enhanced photocatalytic activity.
Keywords:
disordered functional materialslayered materialsstructure‐activity relationshipstime‐resolved spectroscopyMore Related Videos
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