ABSTRACT
Plasmon-enhanced second-harmonic generation (PESHG) based on hybrid metal-dielectric nanostructures have extraordinary importance for developing efficient nanoscale nonlinear sources, which pave the way for new applications in photonic circuitry, quantum optics, and biosensors. However, the relatively high loss of excitation energies and the low spatial overlapping between the locally enhanced electromagnetic field and nonlinear materials still limit the promotion of nonlinear conversion performances in such hybrid systems. Here, we design and fabricate an array of silver nanoparticle-ZnO (AgNP-ZnO) nanocavities to serve as an efficient PESHG platform. The geometry of AgNP-ZnO nanocavity arrays provides a way to flexibly modulate hot spots in three-dimensional space, and to achieve a good mutual overlap of hot spots and ZnO material layers for realizing efficient SH photon generation originating from ZnO nanocavities. Compared to bare ZnO nanocavity arrays, the resulting hybrid AgNP-ZnO design of nanocavities reaches the maximum PESHG enhancement by a factor of approximately 31. Validated by simulations, we can further interpret the relative contribution of fundamental and harmonic modes to Ag-NP dependent PESHG performances, and reveal that the enhancement stems from the co-cooperation effect of plasmon-resonant enhancements both for fundamental and harmonic frequencies. Our findings offer a previously unreported method for designing efficient PESHG systems and pave a way for further understanding of a surface plasmon-coupled second-order emission mechanism for the enhancement of hybrid systems.
ABSTRACT
Ni catalyst is a low-cost catalyst for oxygen evolution reaction (OER) on silicon metal-insulator-semiconductor photoanode. We found that Au nanoparticles incorporated with Ni nanoparticles can enhance the OER activity and stability of Ni nanoparticles due to the local surface plasmon resonance (LSPR) effect of the Au nanoparticles. The efficiency of NiAu/TiO2/n-Si photoanode can be boosted at least three times under the illumination (100 mW/cm2) by LSPR effect of the Au nanoparticles. A small onset potential of 1.03 V versus reversible hydrogen electrode (overpotential, η0 = -0.20 V) and a current density of 18.80 mA/cm2 at 1.23 V versus reversible hydrogen electrode can be obtained. The NiAu/TiO2/n-Si photoanode exhibits a high saturation current density of 35 mA/cm2, which is greater than that of most of the state-of-the-art silicon photoanodes.
ABSTRACT
Because of either thermal/chemical instability or high optical loss in noble metal nanostructures, searching for alternative plasmonic materials is becoming more and more urgent, considering the practical biosensing applications under various extreme conditions. In this work, titanium nitride (TiN), a low-loss metal-like material with both excellent thermal and excellent chemical stabilities, was proposed to composite with Ag hollow nanosphere (HNS) nanostructures as an effective surface-enhanced Raman scattering (SERS) substrate to realize both highly sensitive and highly stable molecular detection. Because of the multiple-mode local surface plasmon resonance around the spherical composite nanospheres and the "gap effect" derived from the ultrasmall nanogaps within the precisely controlled plasmonic arrays, an intensively enhanced local field was successfully induced on this SERS substrate. Combined with the unique charge transferring process between Ag and TiN, a synergistically enhanced SERS sensitivity involving both physical and chemical mechanisms was achieved. Especially, with the isolation of TiN, a time-durable Raman detection on these TiN-Ag HNS arrays was accomplished, showing great potential for practical applications.
