We report a strongly amplified photoacoustic (PA) performance of the new functional hybrid material composed of reduced graphene oxide and gold nanorods. Due to the excellent NIR light absorption properties of the reduced graphene oxide coated gold nanorods (r-GO-AuNRs) and highly efficient heat transfer process through the reduced graphene oxide layer, r-GO-AuNRs exhibit excellent photothermal stability and significantly higher photoacoustic amplitudes than those of bare-AuNRs, nonreduced graphene oxide coated AuNRs (GO-AuNRs), or silica-coated AuNR, as demonstrated in both in vitro and in vivo systems. The linear response of PA amplitude from reduced state controlled GO on AuNR indicates the critical role of GO for a strong photothermal effect of r-GO-AuNRs. Theoretical studies with finite-element-method lab-based simulation reveal that a 4 times higher magnitude of the enhanced electromagnetic field around r-GO-AuNRs can be generated compared with bare AuNRs or GO-AuNRs. Furthermore, the r-GO-AuNRs are expected to be a promising deep-tissue imaging probe because of extraordinarily high PA amplitudes in the 4-11 MHz operating frequency of an ultrasound transducer. Therefore, the r-GO-AuNRs can be a useful imaging probe for highly sensitive photoacoustic images and NIR sensitive therapeutics based on a strong photothermal effect.
The design, synthesis and control of plasmonic nanostructures, especially with ultrasmall plasmonically coupled nanogap (∼1 nm or smaller), are of significant interest and importance in chemistry, nanoscience, materials science, optics and nanobiotechnology. Here, we studied and established the thiolated DNA-based synthetic principles and methods in forming and controlling Au core-nanogap-Au shell structures [Au-nanobridged nanogap particles (Au-NNPs)] with various interior nanogap and Au shell structures. We found that differences in the binding affinities and modes among four different bases to Au core, DNA sequence, DNA grafting density and chemical reagents alter Au shell growth mechanism and interior nanogap-forming process on thiolated DNA-modified Au core. Importantly, poly A or poly C sequence creates a wider interior nanogap with a smoother Au shell, while poly T sequence results in a narrower interstitial interior gap with rougher Au shell, and on the basis of the electromagnetic field calculation and experimental results, we unraveled the relationships between the width of the interior plasmonic nanogap, Au shell structure, electromagnetic field and surface-enhanced Raman scattering. These principles and findings shown in this paper offer the fundamental basis for the thiolated DNA-based chemistry in forming and controlling metal nanostructures with ∼1 nm plasmonic gap and insight in the optical properties of the plasmonic NNPs, and these plasmonic nanogap structures are useful as strong and controllable optical signal-generating nanoprobes.
The graphene oxide (GO) was prepared by sonication-induced exfoliation from graphite oxide, which was produced by oxidation from graphite flakes with a modified Hummer's method. The GO was then treated by hydrazine to obtain reduced graphene oxide (rGO). On the basis of the characterization results, the GO was successfully reduced to rGO. Acrylonitrile-butadiene rubber (NBR)-GO and NBR-rGO composites were prepared via a solution-mixing method, and their various physical properties were investigated. The NBR-rGO nanocomposite demonstrated a higher curing efficiency and a change in torque compared to the gum and NBR-GO compounds. This agreed well with the crosslinking density measured by swelling. The results manifested in the high hardness (Shore A) and high tensile modulus of the NBR-rGO compounds. For instance, the tensile modulus at a 0.1-phr rGO loading greatly increased above 83, 114, and 116% at strain levels of 50, 100, and 200%, respectively, compared to the 0.1-phr GO loaded sample. The observed enhancement was highly attributed to a homogeneous dispersion of rGO within the NBR matrix; this was confirmed by scanning electron microscopy and transmission electron microscopy analysis. However, in view of the high ultimate tensile strength, the NBR-GO compounds exhibited an advantage; this was presumably due to strong hydrogen bonding or polar-polar interactions between the NBR and GO sheets. This interfacial interaction between GO and NBR was supported by the marginal increase in the glass-transition temperatures of the NBR compounds containing fillers.
Herein, a novel strategy is presented for enhancing light absorption by incorporating gold nanostars (Au NSs) into both the active layer of organic solar cells (OSCs) and the rear-contact hole transport layer of perovskite solar cells (PSCs). We demonstrate that the power conversion efficiencies of OSCs and PSCs with embedded Au NSs are improved by 6 and 14%, respectively. We find that pegylated Au NSs are greatly dispersable in a chlorobenzene solvent, which enabled complete blending of Au NSs with the active layer. The plasmonic contributions and accelerated charge transfer are believed to improve the short-circuit current density and the fill factor. This study demonstrates the roles of plasmonic nanoparticles in the improved optical absorption, where the improvement in OSCs was attributed to surface plasmon resonance (SPR) and in PSCs was attributed to both SPR and the backscattering effect. Additionally, devices including Au NSs exhibited a better charge separation/transfer, reduced charge recombination rate, and efficient charge transport. This work provides a comprehensive understanding of the roles of plasmonic Au NS particles in OSCs and PSCs, including an insightful approach for the further development of high-performance optoelectronic devices.
Plasmonic nanoparticle based nanotechnology plays a pivotal role in the recent advances in biomedical applications. Along with biocompatibility and robust surface chemistry, the tunable optical properties of the visible and near-infrared regions of gold nanoparticles have attracted significant attention for a wide range of biomedical applications such as in-vitro biosensing, in-vivo imaging, drug delivery, and tissue engineering. In this review we focus on the the recent advances in biomedical applications based on the use of plasmonic nanoparticles, which have been developed to solve the limitations of current technologies in biosensing, bioimaging, therapeutic drug delivery, and tissue engineering applications.
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