Results 231 to 240 of about 1,541,061 (327)
Operando hard X‐ray absorption spectroscopy is applied to track the dynamic and interactive metal oxidation changes in iron group bimetallic hydroxides under different chemical and electrochemical conditions. It shows that Co and Fe oxidation are relatively equal and synchronized in CoFeOxHy.
Jinzhen Huang +6 more
wiley +1 more source
Anomalous rotational-symmetry breaking in proton arrangement of surface-confined cyclic hydrogen bonds revealed by atomic force spectroscopy. [PDF]
Gao F +12 more
europepmc +1 more source
The Collectivity of Heavy Mesons in Proton-Nucleus Collisions
Zhang, Cheng +6 more
openalex +1 more source
Precursor‐ and solvent‐mediated synthesis yields four Cu3(HHTP)2 morphologies with distinct physicochemical, sorption, and sensing properties toward SO2. Uptake capacities correlate with BET surface area, while sensing performance scales with particle aspect ratio.
Patrick Damacet +5 more
wiley +1 more source
Non-traditional fluorescence in quadruple hydrogen bonded supramolecular polymers. [PDF]
Zuo H +10 more
europepmc +1 more source
High‐performance SEBS‐PFB AEM is developed by crosslinking SEBS‐amine with polyfluorene‐based crosslinker containing benzene spacer. With the superior electrochemical and mechanical properties, SEBS‐PFB enabled an AEMWE single cell to achieve a high current density of 14.0 A cm−2 at 2.0 V and 80 °C in 1 m KOH, using a PtRu/C cathode and Ni2Fe anode ...
Hyun Soo Kwon +8 more
wiley +1 more source
A novel automated framework for multi-engine Monte Carlo model commissioning in proton therapy. [PDF]
Pi Y +6 more
europepmc +1 more source
A minimally invasive, transepithelial corneal cross‐linking (TE‐CXL) approach is presented using upconversion nanoparticles (UCNPs)‐loaded contact lenses (UCLs), after topical delivery of hyaluronate–riboflavin conjugates. The NIR‐to‐UV/blue light conversion by UCNPs in a UCL can activate riboflavin for TE‐CXL, resulting in the biomechanical strength ...
Gibum Lee +8 more
wiley +1 more source

