We report a complete investigation of the structural, electronic, vibrational, elastic and piezoelectric properties of the P2 1 2 1 2 1 orthorhombic phase in cadmium diiodate (δ-Cd(IO 3) 2) by combining experiments and first-principles based calculations. We revisited the nature of the electronic band gap and suggest an indirect band gap with a value of 4.6 eV. The infrared and Raman responses were measured and the different phonon modes assigned. To date, the δ-Cd(IO 3) 2 piezoelectric response remains unknown. We reported the different mechanisms involved in its piezoelectric response from the density functional perturbation theory. The highest value of the piezoelectric-stress and piezoelectric-strain constants in the zero Kelvin limit is predicted for e 41 =-0.27 C/m 2 and d 41 =-10.32 pC/N. These sizable values associated with the thermal stability (no phase transition up to the thermal decomposition at 550°C) and a relative large electronic band gap make δ-Cd(IO 3) 2 a potential candidate for piezoelectric applications.

Double-walled carbon nanotubes (DWNTs), often regarded as the simplest one-dimensional (1D) van der Waals moiré superlattices, are the ideal structures to explore the interlayer coupling, including mechanical and electronical coupling, at the nanoscale in 1D systems. By combining spatial modulation spectroscopy (SMS) and resonant Raman scattering (RRS) experiments on well-identified individual free-standing DWNTs with the calculations of their optical absorption by using the recursion method with non-orthogonal tight-binding (NTB) basis functions, we are able to unambiguously assign the nature, namely mirror transition or cross transition, of each optical transitions in DWNTs. Our study identifies and allows to determine the conditions of the mixing of the electronic states leading to the appearance of cross transitions in the optical absorption of DWNTs, beyond of the so-called Koshino's criteria previously derived. On the other hand, the striking behavior of the resonant excitation profile (REP) of the Raman active modes around the cross transition reveals the strong sensitivity of the modes intensity on the electronic interlayer coupling in DWNTs, emphasizing the relevance of Raman spectroscopy for studying the electronic and mechanical coupling at the nanoscale.

There is a pressing need for reliable, reproducible and accurate measurements of graphene’s properties, through international standards, to facilitate industrial growth. However, trustworthy and verified standards require rigorous metrological studies, determining, quantifying and reducing the sources of measurement uncertainty. Towards this effort, we report the procedure and the results of an international interlaboratory comparison (ILC) study, conducted under Versailles Project on Advanced Materials and Standards. This ILC focusses on the comparability of Raman spectroscopy measurements of chemical vapour deposition (CVD) grown graphene using the same measurement protocol across different institutes and laboratories. With data gathered from 17 participants across academia, industry (including instrument manufacturers) and national metrology institutes, this study investigates the measurement uncertainty contributions from both Raman spectroscopy measurements and data analysis procedures, as well as provides solutions for improved accuracy and precision. While many of the reported Raman metrics were relatively consistent, significant and meaningful outliers occurred due to differences in the instruments and data analysis. These variations resulted in inconsistent reports of peak intensity ratios, peak widths and the coverage of graphene. Due to a lack of relative intensity calibration, the relative difference reported in the 2D- and G peak intensity ratios ( I 2 D / I G ) was up to 200%. It was also shown that the standard deviation for Γ 2 D values reported by different software packages, was 15× larger for Lorentzian fit functions than for pseudo-Voigt functions. This study has shown that by adopting a relative intensity calibration and consistent peak fitting and data analysis methodologies, these large, and previously unquantified, variations can be significantly reduced, allowing more reproducible and comparable measurements for the graphene community, supporting fundamental research through to the growing graphene industry worldwide. This project and its findings directly underpin the development of the ISO/IEC standard ‘ DTS 21356-2—Nanotechnologies—Structural Characterisation of CVD-grown Graphene ’.

Surface plasmon resonance sensors (SPR) using copper for sensitive parts are a competitivealternative to gold and silver. Copper oxide is a semiconductor and has a non-toxic nature. Theunavoidable presence of copper oxide may be of interest as it is non-toxic, but it modifies thecondition of resonance and the performance of the sensor. Therefore, the characterization of theoptical properties of copper and copper oxide thin films is of interest. We propose a method torecover both the thicknesses and optical properties of copper and copper oxide from absorbancecurves over the(0.9; 3.5)eV range, and we use these results to numerically investigate the surfaceplasmon resonance of copper/copper oxide thin films. Samples of initial copper thicknesses 10, 30and 50 nm, after nine successive oxidations, are systematically studied to simulate the signal of aSurface Plasmon Resonance setup. The results obtained from the resolution of the inverse problem ofabsorbance are used to discuss the performance of a copper-oxide sensor and, therefore, to evaluatethe optimal thicknesses.

Photoluminescence of single-walled carbon nanotubes is monitored at the individual scale by molecule encapsulation into their hollow core. Depending on the electronic character (electron donor or acceptor) of the confined molecule, enhancement or quenching of the photoluminescence intensity is demonstrated. This behavior is assigned to a charge transfer, evidenced by the shift of the Raman G-band, and a correlated Fermi level shift shown by photoemission experiments. Our experimental results are supported by DFT calculations. A consistent picture of the physical interactions taking place in the hybrid systems and their effects on the optical and electronic properties is given. Our results indicate that the electron affinity or ionization potential of the encapsulated molecules and the diameter of the nanotube are relevant parameters to tune the light emission properties of the hybrid systems at the nanoscale.