New insights into HER catalysis: the effect of nano-silica support on catalysis by silver nanoparticles
文献信息
Gifty Sara Rolly, Guy Yardeni, Ronen Bar-Ziv, Tomer Zidki
Supported metal catalysts have recently attracted considerable attention in the field of catalysis. The effect of surface chemical groups (SiO−/SiOH2+) on SiO2-Ag0-NPs along with the average negative charge induced by (CH3)2COH˙ radicals on the catalytic reduction of H2O/H3O+ towards the hydrogen evolution reaction (HER) is reported. The results indicate that similar effects are observed both above and below the point of zero charge (PZC) of silica. More importantly, it is shown that a high concentration of this catalyst does not necessarily contribute to boosting the hydrogen formation, but instead, the density of charge on its surface is a decisive factor. A mechanistic explanation of the observed effect is given.
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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.













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