TY - JOUR
T1 - Vector Beam-Enhanced Raman Decodes DNA Nucleobases
AU - Wang, Yueweiying
AU - Lu, Fanfan
AU - Mei, Ting
AU - Zhang, Wending
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/8/6
Y1 - 2026/8/6
N2 - To overcome challenges in DNA nucleobase Raman analysis, such as strong backbone signals, spectral overlap, and background noise, we propose a surface-enhanced Raman scattering (SERS) method employing a k-space filter-assisted radial vector beam (RVB) coupled with gold nanospheres (AuNPs). A spatial frequency-modulated RVB is tightly focused to excite AuNPs, producing a localized plasmonic field with a strong longitudinal component that spatially overlaps with DNA segments located in the AuNP near-field region. This configuration achieves strong near-field enhancement while suppressing background noise. The orientation-dependent near-field selection is interpreted through the projection between the local plasmonic field and the vibrational polarizability derivatives of DNA modes. Under orientation-favorable configurations, backbone-related modes with weak field projection are relatively suppressed, whereas nucleobase-related modes with larger projection are preferentially enhanced. Experimental results show effective suppression of backbone signals (900–1250 cm–1) and clearer DFT-assisted assignment of nucleobase-related Raman bands (1350–1500 cm–1). Combined with density functional theory (DFT), overlapping peaks were accurately identified and decoupled. This approach provides a physical mechanism for selective enhancement and noise suppression, offering a label-free optical method for specific DNA nucleobase identification.
AB - To overcome challenges in DNA nucleobase Raman analysis, such as strong backbone signals, spectral overlap, and background noise, we propose a surface-enhanced Raman scattering (SERS) method employing a k-space filter-assisted radial vector beam (RVB) coupled with gold nanospheres (AuNPs). A spatial frequency-modulated RVB is tightly focused to excite AuNPs, producing a localized plasmonic field with a strong longitudinal component that spatially overlaps with DNA segments located in the AuNP near-field region. This configuration achieves strong near-field enhancement while suppressing background noise. The orientation-dependent near-field selection is interpreted through the projection between the local plasmonic field and the vibrational polarizability derivatives of DNA modes. Under orientation-favorable configurations, backbone-related modes with weak field projection are relatively suppressed, whereas nucleobase-related modes with larger projection are preferentially enhanced. Experimental results show effective suppression of backbone signals (900–1250 cm–1) and clearer DFT-assisted assignment of nucleobase-related Raman bands (1350–1500 cm–1). Combined with density functional theory (DFT), overlapping peaks were accurately identified and decoupled. This approach provides a physical mechanism for selective enhancement and noise suppression, offering a label-free optical method for specific DNA nucleobase identification.
UR - https://www.scopus.com/pages/publications/105046693907
U2 - 10.1021/acs.jpcb.6c02526
DO - 10.1021/acs.jpcb.6c02526
M3 - 文章
C2 - 42489023
AN - SCOPUS:105046693907
SN - 1520-6106
VL - 130
SP - 7819
EP - 7826
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 31
ER -