Surface plasmons on silver gratings transform pyrolytic carbon into luminescent graphitized carbon dots

被引:0
|
作者
Walia, Jaspreet [1 ,2 ]
Rashid, Sabaa [1 ,5 ]
Naeini, Maryam Sadat Amiri [1 ,3 ]
Killaire, Graham [1 ,3 ]
Variola, Fabio [4 ]
Weck, Arnaud [1 ,3 ,4 ]
Berini, Pierre [1 ,2 ,3 ]
机构
[1] Univ Ottawa, Nexus Quantum Technol Inst, Ottawa, ON K1N 6N5, Canada
[2] Univ Ottawa, Sch Elect Engn & Comp Sci, Ottawa, ON K1N 6N5, Canada
[3] Univ Ottawa, Dept Phys, Ottawa, ON K1N 6N5, Canada
[4] Univ Ottawa, Dept Mech Engn, Ottawa, ON K1N 6N5, Canada
[5] McMaster Univ, Canadian Ctr Electron Microscopy, Hamilton, ON L8S 4M1, Canada
来源
JOURNAL OF CHEMICAL PHYSICS | 2024年 / 161卷 / 14期
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
GRAPHENE QUANTUM DOTS; RAMAN-SPECTROSCOPY; REDUCTION; NANODOTS; SOLAR; CO2;
D O I
10.1063/5.0222268
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Plasmonic catalysis holds the promise of opening new reaction pathways that are inaccessible thermally or via direct UV-vis electronic transitions. Here, energetic carriers produced via the decay of surface plasmons excited by visible light at 532 nm (2.33 eV, green) on a Ag-grating-bearing pyrolytic carbon residue drive its transformation into light-emitting graphitized carbon dots. The pyrolytic carbon residue is detectable via high-magnification surface-enhanced Raman scattering but cannot be directly observed using optical, electron, atomic force, or helium ion microscopy. When a Ag-grating-bearing pyrolyzed residue is introduced into a high-purity O-2-depleted gas environment (Ar, N-2, and CO2) and excited with 532 nm light, bright yellow luminescence emerges and is readily observed. Light emission is not observed without the pyrolytic carbon, without the excitation of plasmons, or in air or an Ar/O-2 gas mixture. This process, driven by visible light and a nanostructured Ag surface bearing pyrolytic carbon, will be of interest to researchers involved in plasmonic catalysis, catalytic processes involving carbon, and luminescent plasmonic surfaces.
引用
收藏
页数:13
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