Controllable Tuning Plasmonic Coupling with Nanoscale Oxidation.

The nanoparticle on mirror (NPoM) construct is ideal for the strong coupling of localized plasmons because of its simple fabrication and the nanometer-scale gaps it offers. Both of these are much harder to control in nanoparticle dimers. Even so, realizing controllable gap sizes in a NPoM remains difficult and continuous tunability is limited. Here, we use reactive metals as the mirror so that the spacing layer of resulting metal oxide can be easily and controllably created with specific thicknesses resulting in continuous tuning of the plasmonic coupling. Using Al as a case study, we contrast different approaches for oxidation including electrochemical oxidation, thermal annealing, oxygen plasma treatments, and photo-oxidation by laser irradiation. The thickness of the oxidation layer is calibrated with depth-mode X-ray photoemission spectroscopy (XPS). These all consistently show that increasing the thickness of the oxidation layer blue-shifts the plasmonic resonance peak while the transverse mode remains constant, which is well matched by simulations. Our approach provides a facile and reproducible method for scalable, local and controllable fabrication of NPoMs with tailored plasmonic coupling, suited for many applications of sensing, photochemistry, photoemission, and photovoltaics.EPSRC grant EP/G060649/1, EP/I012060/1, ERC grant LINASS 320503.This is the final version of the article. It first appeared from the American Chemical Society via http://dx.doi.org/10.1021/acsnano.5b0128

Facile Fabrication of Spherical Nanoparticle-Tipped AFM Probes for Plasmonic Applications.

We wish to acknowledge the support of grants UK EPSRC EP/G060649/1, EP/H007024/1, a Marie Curie Intra-European Fellowship (FP7-PEOPLE-2011-IEF 298012 to L.Z.), ERC LINASS 320503, and Royal Society IE120879. R.W.B. thanks Queens’ College, Cambridge for financial support.This is the final published version. It originally appeared in Particle & Particle Systems Characterization and is available in http://onlinelibrary.wiley.com/doi/10.1002/ppsc.201400104/abstract

Plasmonic enhancement in BiVO4 photonic crystals for efficient water splitting.

Photo-electrochemical water splitting is a very promising and environmentally friendly route for the conversion of solar energy into hydrogen. However, the solar-to-H2 conversion efficiency is still very low due to rapid bulk recombination of charge carriers. Here, a photonic nano-architecture is developed to improve charge carrier generation and separation by manipulating and confining light absorption in a visible-light-active photoanode constructed from BiVO4 photonic crystal and plasmonic nanostructures. Synergistic effects of photonic crystal stop bands and plasmonic absorption are observed to operate in this photonic nanostructure. Within the scaffold of an inverse opal photonic crystal, the surface plasmon resonance is significantly enhanced by the photonic Bragg resonance. Nanophotonic photoanodes show AM 1.5 photocurrent densities of 3.1 ± 0.1 mA cm(-2) at 1.23 V versus RHE, which is among the highest for oxide-based photoanodes and over 4 times higher than the unstructured planar photoanode.UK Engineering and Physical Science Research Council. Grant Numbers: EP/H00338X/2, EP/G060649/1 European Community's Seventh Framework Programme. Grant Number: FP7/2007–2013 CARINHYPH project. Grant Number: 310184 Minstry of Science and Technology of Taiwan. Grant Number: 102-2218-E-006-014-MY2 Christian Doppler Research Association OMV Group, a Marie Curie Intra-European Fellowship. Grant Number: FP7-PEOPLE-2011-IEF 298012 ERC. Grant Number: 320503This is the final published version currently under embargo. This will be updated once the publisher has granted a CC BY license

14-3-3σ Contributes to Radioresistance by Regulating DNA Repair and Cell Cycle via PARP1 and CHK2

14-3-3σ has been implicated in the development of chemo and radiation resistance and in poor prognosis of multiple human cancers. While it has been postulated that 14-3-3σ contributes to these resistances via inhibiting apoptosis and arresting cells in G2–M phase of the cell cycle, the molecular basis of this regulation is currently unknown. In this study, we tested the hypothesis that 14-3-3σ causes resistance to DNA-damaging treatments by enhancing DNA repair in cells arrested in G2–M phase following DNA-damaging treatments. We showed that 14-3-3σ contributed to ionizing radiation (IR) resistance by arresting cancer cells in G2–M phase following IR and by increasing non-homologous end joining (NHEJ) repair of the IR-induced DNA double strand breaks (DSB). The increased NHEJ repair activity was due to 14-3-3σ–mediated upregulation of PARP1 expression that promoted the recruitment of DNA-PKcs to the DNA damage sites for repair of DSBs. On the other hand, the increased G2–M arrest following IR was due to 14-3-3σ–induced Chk2 expression. Implications: These findings reveal an important molecular basis of 14-3-3σ function in cancer cell resistance to chemo/radiation therapy and in poor prognosis of human cancers

Ultrathin CdSe in Plasmonic Nanogaps for Enhanced Photocatalytic Water Splitting.

Enhanced plasmonic fields are a promising way to increase the efficiency of photocatalytic water splitting. The availability of atomically thin materials opens up completely new opportunities. We report photocatalytic water splitting on ultrathin CdSe nanoplatelets placed in plasmonic nanogaps formed by a flat gold surface and a gold nanoparticle. The extreme field intensity created in these gaps increases the electron–hole pair production in the CdSe nanoplatelets and enhances the plasmon-mediated interfacial electron transfer. Compared to individual nanoparticles commonly used to enhance photocatalytic processes, gap-plasmons produce several orders of magnitude higher field enhancement, strongly localized inside the semiconductor sheet thus utilizing the entire photocatalyst efficiently.This work was supported by the U.K. EPSRC grant EP/G060649/1 and EPSRC grant EP/L027151/1, Defence Science and Technology Laboratory (DSTL), a Marie Curie Intra-European Fellowship (FP7-PEOPLE-2011-IEF 298012 to L.Z.) and ERC grant 320503 LINASS.This is the final version of the article. It first appeared from ACS via http://dx.doi.org/10.1021/acs.jpclett.5b0027

Size Dependent Plasmonic Effect on BiVO4 Photoanodes for Solar Water Splitting.

Plasmonic nanostructures show great promise in enhancing the solar water splitting efficiency due to their ability to confine light to extremely small volumes inside semiconductors. While size plays a critical role in the plasmonic performance of Au nanoparticles (AuNPs), its influence on plasmon-assisted water splitting is still not fully understood. This holds especially true for low band gap semiconductors, for which interband excitations occur in wavelength regions that overlap with plasmonic resonances. Here, BiVO4 films are modified with AuNPs of diameters varying from 10 to 80 nm to study the size dependence of the plasmonic effect. Plasmon resonance energy transfer (PRET) is found to be the dominant effect in enhancing the water splitting efficiency of BiVO4. "Hot electron" injection effect is weak in the case of BiVO4/AuNP. This is attributed to the interband excitation of BiVO4, which is unfavourable for the hot electrons accumulation in BiVO4 conduction band. The resonant scattering effect also contributes to the enhanced water splitting efficiency for the larger diameter AuNPs. It is also for the first time found that higher PRET effect can be achieved at larger off-normal irradiation angle

Dual-functional Au-porous anodic alumina (PAA) sensors for enrichment and label-free detection of airborne virus with surface-enhanced Raman scattering

The development of a rapid and sensitive method for the enrichment and direct detection of airborne viruses has become urgently needed to prevent their spread. We have developed a dual-functional, label-free platform for the enrichment and optical identification of airborne viruses. This platform allows for the on-site enrichment and identification of airborne viruses through a virus enrichment component combined with surface-enhanced Raman scattering (SERS). In this work, we created an Au-porous anodic alumina (PAA) composite film, by ion sputtering Au nanoparticles (Au NPs) on a porous structure. The Au-PAA serves as a dual-functional sensor: it combines ultrafiltration through the vertical nanopores in the PAA for virus enrichment and constitutes a plasmonic substrate due to the surface plasmon near-field enhancements within the nanochannel structure. This sensor demonstrates an extraordinary enrichment efficiency (about 98 %) of obtained bioaerosols and enables simultaneous, sensitive detection at the single-virus level. Finite-difference time-domain (FDTD) simulations evidenced the electric field intensity and charge distribution of the Au-PAA. This Au-PAA composite film offers a powerful system for on-site, label-free viral particle enrichment and SERS detection. Contaminated air containing viruses can be collected in a few minutes and analyzed immediately by our platform, which is particularly beneficial for timely monitoring of viruses in the air of large public spaces. Additionally, this platform can be applied to evaluate the indoor air quality.</p