Correction to: Foreword to the memorial issue for Professor Roberto Marassi

Journal of Solid State Electrochemistry -     

Metal Artifacts in Attenuation and Phase Contrast X-Ray Microcomputed Tomography: A Comparative Study

Experimental Mechanics - Metal artifacts arising around high-density components are a widely known problem in X-ray computed tomography (XCT) for both medical and industrial applications. Although...     

Quantitative Analysis of Al in Flour Products by Laser-Induced Breakdown Spectroscopy Combined with Partial Least Squares

Journal of Applied Spectroscopy - Based on partial least squares (PLS) analysis, the effects of different smoothing points and different preprocessing methods on the accuracy and precision of the...     

Empirical tail conditional allocation and its consistency under minimal assumptions

Annals of the Institute of Statistical Mathematics - Under minimal assumptions, we prove that an empirical estimator of the tail conditional allocation (TCA), also known as the marginal expected...     

Langevin dynamic for the 2D Yang–Mills measure

Publications mathématiques de l'IHÉS - It is well known that a real analytic symplectic diffeomorphism of the $2d$ -dimensional disk ( $d\geq 1$ ) admitting the origin as a...     

Dynamical analysis and multistability in autonomous hyperchaotic oscillator with experimental verification

Nonlinear Dynamics - In this contribution, a modified oscillator of Tamasevicius et al. (Electron Lett 33:542–544, 1997) (referred to as the mTCMNL oscillator hereafter) is introduced with...     

Supramolecular Tuning Enables Selective Oxygen Reduction Catalyzed by Cobalt Porphyrins for Direct Electrosynthesis of Hydrogen Peroxide

We report a supramolecular strategy for promoting the selective reduction of O₂ for direct electrosynthesis of H₂O₂. We utilized cobalt tetraphenylporphyrin (Co-TPP), an oxygen reduction reaction (ORR) catalyst with highly variable product selectivity, as a building block to assemble the permanently porous supramolecular cage Co-PB-1(6) bearing six Co-TPP subunits connected through twenty-four imine bonds. Reduction of these imine linkers to amines yields the more flexible cage Co-rPB-1(6). Both Co-PB-1(6) and Co-rPB-1(6) cages produce 90–100 % H₂O₂ from electrochemical ORR catalysis in neutral pH water, whereas the Co-TPP monomer gives a 50 % mixture of H₂O₂ and H₂O. Bimolecular pathways have been implicated in facilitating H₂O formation, therefore, we attribute this high H₂O₂ selectivity to site isolation of the discrete molecular units in each supramolecule. The ability to control reaction selectivity in supramolecular structures beyond traditional host–guest interactions offers new opportunities for designing such architectures for a broader range of catalytic applications.