TY - JOUR
T1 - Large-Scale Sub-1-nm Random Gaps Approaching the Quantum Upper Limit for Quantitative Chemical Sensing
AU - Zhang, Nan
AU - Hu, Haifeng
AU - Singer, Matthew
AU - Li, Kuang-hui
AU - Zhou, Lyu
AU - Ooi, Boon S.
AU - Gan, Qiaoqiang
N1 - KAUST Repository Item: Exported on 2020-11-02
Acknowledgements: This work was partially supported by NSF CMMI-1562057 and ECCS-1807463. The authors appreciate Dr. Lingmei Liu and Prof. Yu Han at KAUST for helpful suggestions on TEM characterization.
PY - 2020/10/28
Y1 - 2020/10/28
N2 - Metallic nanostructures with nanogap features can confine electromagnetic fields into extremely small volumes. In particular, as the gap size is scaled down to sub-nanometer regime, the quantum effects for localized field enhancement reveal the ultimate capability for light–matter interaction. Although the enhancement factor approaching the quantum upper limit has been reported, the grand challenge for surface-enhanced vibrational spectroscopic sensing remains in the inherent randomness, preventing uniformly distributed localized fields over large areas. Herein, a strategy to fabricate high-density random metallic nanopatterns with accurately controlled nanogaps, defined by atomic-layer-deposition and self-assembled-monolayer processes, is reported. As the gap size approaches the quantum regime of ≈0.78 nm, its potential for quantitative sensing, based on a record-high uniformity with the relative standard deviation of 4.3% over a large area of 22 mm × 60 mm, is demonstrated. This superior feature paves the way towards more affordable and quantitative sensing using quantum-limit-approaching nanogap structures.
AB - Metallic nanostructures with nanogap features can confine electromagnetic fields into extremely small volumes. In particular, as the gap size is scaled down to sub-nanometer regime, the quantum effects for localized field enhancement reveal the ultimate capability for light–matter interaction. Although the enhancement factor approaching the quantum upper limit has been reported, the grand challenge for surface-enhanced vibrational spectroscopic sensing remains in the inherent randomness, preventing uniformly distributed localized fields over large areas. Herein, a strategy to fabricate high-density random metallic nanopatterns with accurately controlled nanogaps, defined by atomic-layer-deposition and self-assembled-monolayer processes, is reported. As the gap size approaches the quantum regime of ≈0.78 nm, its potential for quantitative sensing, based on a record-high uniformity with the relative standard deviation of 4.3% over a large area of 22 mm × 60 mm, is demonstrated. This superior feature paves the way towards more affordable and quantitative sensing using quantum-limit-approaching nanogap structures.
UR - http://hdl.handle.net/10754/665736
UR - https://onlinelibrary.wiley.com/doi/10.1002/adom.202001634
UR - http://www.scopus.com/inward/record.url?scp=85093966662&partnerID=8YFLogxK
U2 - 10.1002/adom.202001634
DO - 10.1002/adom.202001634
M3 - Article
SN - 2195-1071
SP - 2001634
JO - Advanced Optical Materials
JF - Advanced Optical Materials
ER -