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We described an effective way to generate a Co3O4 mesocrystal array with well-developed porosity, simply by uniting a coupled interface with hydrazine treatment. Due to the fast electron transfer and sufficient active sites, the Ti mesh-supported Co3O4 nanoneedles electrode could provide a current density of 49.9 mA cm−2 at 570 mV OER overpotential and has exceptionally high stability. [ABSTRACT FROM AUTHOR]

As a new type of heterogeneous catalyst with "homogeneous‐like" activity, single‐site transition‐metal materials are usually treated as integrated but separate active centers. A novel grouping effect is reported for single Ni−N4 sites in nitrogen‐doped carbon (Ni/NC), where an effective ligand‐stabilized polycondensation method endows Ni/NC nanocatalysts with a high content of single‐site Ni up to 9.5 wt %. The enhanced electron density at each single Ni−N4 site promotes a highly efficient hydrogen transfer, which is exemplified by the coupling of benzyl alcohol and aniline into N‐benzylaniline with a turnover frequency (TOF) value of 7.0 molN‐benzylaniline molmetal−1 h−1; this TOF outpaces that of reported stable non‐noble‐metal‐based catalysts by a factor of 2. Herd instinct: A grouping effect is observed for single Ni−N4 sites in a Ni catalyst supported by nitrogen‐doped carbon (NC). A high 9.5 wt % Ni content was achieved with a ligand‐stabilized polycondensation method. An enhanced electron density effect manifests at each single Ni−N4 site, which decreases the binding energy of H radicals to Ni and promotes efficient coupling of benzyl alcohol and aniline to form N‐benzylaniline. [ABSTRACT FROM AUTHOR]

The greenhouse effect and global warming are serious problems because the increasing global demand for fossil fuels has led to a rapid rise in greenhouse gas exhaust emissions in the atmosphere and disruptive changes in climate. As a major contributor, CO2 has attracted much attention from scientists, who have attempted to convert it into useful products by electrochemical or photoelectrochemical reduction methods. Facile design of efficient but inexpensive and abundant catalysts to convert CO2 into fuels or valuable chemical products is essential for materials chemistry and catalysis in addressing global climate change as well as the energy crisis. Herein, we show that two-dimensional fewlayer graphitic carbon nitride (g-C3N4) can function as an efficient metal-free electrocatalyst for selective reduction of CO2 to CO at low overpotentials with a high Faradaic efficiency of ~ 80%. The polarized surface of ultrathin g-C3N4 layers (thickness: ~ 1 nm), with a more reductive conduction band, yields excellent electrochemical activity for CO2 reduction. [ABSTRACT FROM AUTHOR]

The oxygen evolution reaction (OER) is the rate-limiting process for water splitting, and highly efficient large-area OER photoanodes have been considered as an essential part in photoelectrochemical water splitting reactors. The high hole–electron separation efficiency of photoanodes is highly required for real applications of photoanodes in sufficiently harvesting solar energy. Herein we show that the inactive g-C3N4 nanolayers can be self-assembled with BiVO4 into a highly coupled BV/CN dyad to significantly enhance the charge separation efficiency of BiVO4 photoelectrodes for the OER. The incident photon-to-current conversion efficiency (IPCE) of visible light (400 nm) provided by the scalable BV/CN-5 photoanode was estimated to be 50% at 1.23 V vs. RHE in 0.5 M Na2SO4 solution and significantly increased to 97% at a bias voltage of 1.6 V vs. RHE. [ABSTRACT FROM AUTHOR]

Oxygen vacancies can help to capture oxygen-containing species and act as active centers for oxygen evolution reaction (OER). Unfortunately, effective methods for generating a high amount of oxygen vacancies on the surface of various nanocatalysts are rather limited. Here, we described an effective way to generate oxygen-vacancy-rich surface of transition metal oxides, exemplified with Co3O4, simply by constructing highly coupled interface of ultrafine Co3O4 nanocrystals and metallic Ti. Impressively, the amounts of oxygen vacancy on the surface of Co3O4/Ti surpassed the reported values of the Co3O4 modified even under highly critical conditions. The Co3O4/Ti electrode could provide a current density of 23 mA cm−2 at an OER overpotential of 570 mV, low Tafel slope, and excellent durability in neutral medium. Because of the formation of a large amount of oxygen vacancies as the active centers for OER on the surface, the TOF value of the Co3O4@Ti electrode was optimized to be 3238 h−1 at an OER overpotential of 570 mV, which is 380 times that of the state-of-the-art non-noble nanocatalysts in the literature. [ABSTRACT FROM AUTHOR]

We described an effective way to generate a Co 3 O 4 mesocrystal array with well-developed porosity, simply by uniting a coupled interface with hydrazine treatment. Due to the fast electron transfer and sufficient active sites, the Ti mesh-supported Co 3 O 4 nanoneedles electrode could provide a current density of 49.9 mA cm -2 at 570 mV OER overpotential and has exceptionally high stability.

As a new type of heterogeneous catalyst with "homogeneous-like" activity, single-site transition-metal materials are usually treated as integrated but separate active centers. A novel grouping effect is reported for single Ni-N 4 sites in nitrogen-doped carbon (Ni/NC), where an effective ligand-stabilized polycondensation method endows Ni/NC nanocatalysts with a high content of single-site Ni up to 9.5 wt %. The enhanced electron density at each single Ni-N 4 site promotes a highly efficient hydrogen transfer, which is exemplified by the coupling of benzyl alcohol and aniline into N-benzylaniline with a turnover frequency (TOF) value of 7.0 mol N-benzylaniline  mol metal -1  h -1 ; this TOF outpaces that of reported stable non-noble-metal-based catalysts by a factor of 2., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The oxygen evolution reaction (OER) is the rate-limiting process for water splitting, and highly efficient large-area OER photoanodes have been considered as an essential part in photoelectrochemical water splitting reactors. The high hole-electron separation efficiency of photoanodes is highly required for real applications of photoanodes in sufficiently harvesting solar energy. Herein we show that the inactive g-C 3 N 4 nanolayers can be self-assembled with BiVO 4 into a highly coupled BV/CN dyad to significantly enhance the charge separation efficiency of BiVO 4 photoelectrodes for the OER. The incident photon-to-current conversion efficiency (IPCE) of visible light (400 nm) provided by the scalable BV/CN-5 photoanode was estimated to be 50% at 1.23 V vs. RHE in 0.5 M Na 2 SO 4 solution and significantly increased to 97% at a bias voltage of 1.6 V vs. RHE.

Oxygen vacancies can help to capture oxygen-containing species and act as active centers for oxygen evolution reaction (OER). Unfortunately, effective methods for generating a high amount of oxygen vacancies on the surface of various nanocatalysts are rather limited. Here, we described an effective way to generate oxygen-vacancy-rich surface of transition metal oxides, exemplified with Co 3 O 4 , simply by constructing highly coupled interface of ultrafine Co 3 O 4 nanocrystals and metallic Ti. Impressively, the amounts of oxygen vacancy on the surface of Co 3 O 4 /Ti surpassed the reported values of the Co 3 O 4 modified even under highly critical conditions. The Co 3 O 4 /Ti electrode could provide a current density of 23 mA cm -2 at an OER overpotential of 570 mV, low Tafel slope, and excellent durability in neutral medium. Because of the formation of a large amount of oxygen vacancies as the active centers for OER on the surface, the TOF value of the Co 3 O 4 @Ti electrode was optimized to be 3238 h -1 at an OER overpotential of 570 mV, which is 380 times that of the state-of-the-art non-noble nanocatalysts in the literature., (© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)