Vibrational response of nanorods to ultrafast laser induced heating: theoretical and experimental analysis

In this paper, we elucidate the vibrational response of cylindrical nanorods to ultrafast laser-induced heating. A theoretical analysis of the expected behavior is first presented. This analysis predicts that both extensional and breathing vibrational modes of the rods should be excited by laser-induced heating. Analytical formulas are derived assuming that the heating/expansion process is instantaneous, and that the lengths of the rods are much greater than their radii. These results show that the breathing mode dominates the mechanical deformation of the rod. However, because the frequency of the extensional mode is much lower than that of the breathing mode, the extensional mode will dominate the response for a real experiment (a finite-time heating/expansion process). The results of this model are compared to data from transient absorption experiments performed on gold nanorods with average lengths between 30 and 110 nm. The transient absorption traces show pronounced modulations with periods between 40 and 120 ps, which are only observed when the probe laser is tuned to the longitudinal plasmon band. The measured periods are in good agreement with the expected values for the extensional modes of the rods. For rods wider than 20 nm, the breathing mode can also be observed and, again, the measured periods are in good agreement with the theoretical calculations. The breathing mode is not observed for thinner rods (<20 nm width) because, in this case, the period is comparable to the time scale for lattice heating.     

Rotating frame proton spin-lattice relaxation measurements of poly(ethylene oxides)

Measurements of T_1ρ as a function of temperature have been made on three polyethylene oxides (PEO) with molecular weights of 550, 6000, and 2.8 × 10⁶ in order to try to elucidate various problems arising in the interpretation of previous T₁ measurements on PEO. In contrast to the T₁ measurements, the T_1ρ measurements show discontinuities at the melting or softening points of the respective polymers concerned, and also show nonexponential magnetization decay in the case of PEO 6000 and 2.8 × 10⁶, which is presumbly due to the existence of “mobile” and “crystalline” regions, in qualitative agreement with NMR studies and x-ray measurements. Motional correlation frequencies and activation energies have been derived where possible by using the BPP theory adapted to the rotating frame and also the strong collision Slichter-Ailion theory. There is reasonable correlation with other data on motional frequencies where it is available, although the overall situation for the so-called α transition in PEO 6000 and 2.8 × 10⁶ is still not clear. It is suggested that spin-diffusion is an important mechanism for all three polymers; for PEO 550 because it contains CH₃ endgroups which act as sinks, and for the other two polymers where the mobile fraction performs the same function.     

Near‐Infrared Croconaine Rotaxanes and Doped Nanoparticles for Enhanced Aqueous Photothermal Heating

The photothermal effect is the generation of heat by molecules or particles upon high‐energy laser irradiation, and near‐infrared absorbers such as gold nanoparticles and organic dyes have a range of potential photothermal applications. The favourable photothermal properties of thiophene‐functionalised croconaine dyes were recently discovered. The synthesis and properties of novel croconaine rotaxane and pseudorotaxane architectures capable of efficient photothermal performance in both organic and aqueous environments are reported. The versatility of this dye‐encapsulation strategy was demonstrated by the preparation of two organic croconaine rotaxanes using different synthetic methods: the formation of an aqueous pseudorotaxane association complex, and the synthesis of water‐soluble, croconaine‐doped silicated micelle nanoparticles. All of these near‐infrared‐absorbing systems exhibit excellent photothermal behaviour, with pseudorotaxane and rotaxane formation vital for effective aqueous heat generation. Dye encapsulation provides steric protection to enhance the stability of a water‐sensitive croconaine dye, while rotaxane‐doped nanoparticles avoid detrimental band broadening caused by chromophore coupling.     

Gold nanostructures: engineering their plasmonic properties for biomedical applications

The surface plasmon resonance peaks of gold nanostructures can be tuned from the visible to the near infrared region by controlling the shape and structure (solid vs. hollow). In this tutorial review we highlight this concept by comparing four typical examples: nanospheres, nanorods, nanoshells, and nanocages. A combination of this optical tunability with the inertness of gold makes gold nanostructures well suited for various biomedical applications.     

On the temperature stability of gold nanorods: comparison between thermal and ultrafast laser-induced heating

The response of gold nanorods to both thermal and ultrafast laser-induced heating has been examined. The thermal heating experiments show structural changes that occur on timescales ranging from hours to days. At the highest temperature examined (250 degrees C) the nanorods are transformed into spheres within an hour. On the other hand, no structural changes are observed in the laser-induced heating experiments up to temperatures of 700 +/- 50 degrees C. This is attributed to thermal diffusion in the laser experiments. Measurements of the period of the extensional mode of the nanorods using time-resolved spectroscopy show a significant softening at high pump laser powers. However, the decrease in the period is less than expected from bulk Young's modulus vs. temperature data.