Introducing Bidirectional Axial Coordination into BiVO @Metal Phthalocyanine Core-Shell Photoanodes for Efficient Water Oxidation.

Core-shell photoanodes have shown great potential for photoelectrochemical (PEC) water oxidation. However, the construction of a high-quality interface between the core and shell, as well as a highly catalytic surface, remains a challenge. Herein, guided by computation, we present a BiVO photoanode coated with ZnCoFe polyphthalocyanine using pyrazine as a coordination agent.

WO Photoanode with Predominant Exposure of {202} Facets for Enhanced Selective Oxidation of Glycerol to Glyceraldehyde.

The photoelectrocatalytic (PEC) oxidation of glycerol into highly value-added products is attractive, but it is extremely challenging to limit the oxidation products to the valuable C3 chemicals. The hole concentration and surface atomic arrangement of a photoanode can be modulated by controlling facet exposure, thus tuning the activity and selectivity. Herein, we report for the first time the formation of a WO photoanode with predominant exposure of {202} facets by a secondary hydrothermal method.

Activity and Stability Boosting of an Oxygen-Vacancy-Rich BiVO Photoanode by NiFe-MOFs Thin Layer for Water Oxidation.

The introduction of oxygen vacancies (Ov) has been regarded as an effective method to enhance the catalytic performance of photoanodes in oxygen evolution reaction (OER). However, their stability under highly oxidizing environment is questionable but was rarely studied. Herein, NiFe-metal-organic framework (NiFe-MOFs) was conformally coated on oxygen-vacancy-rich BiVO (Ov-BiVO ) as the protective layer and cocatalyst, forming a core-shell structure with caffeic acid as bridging agent.

Sequence of Silicon Monolayer Structures Grown on a Ru Surface: from a Herringbone Structure to Silicene.

Silicon-based two-dimensional (2D) materials are uniquely suited for integration in Si-based electronics. Silicene, an analogue of graphene, was recently fabricated on several substrates and was used to make a field-effect transistor. Here, we report that when Ru(0001) is used as a substrate, a range of distinct monolayer silicon structures forms, evolving toward silicene with increasing Si coverage.