Emerging clean energy technologies such as regenerative fuel cells and rechargeable metal–air batteries have attracted increasing global interest because of their high efficiency and environmental benignity, but the lack of highly active bifunctional electrocatalysts at low cost for both oxygen reduction and evolution reactions (ORR and OER) greatly hinders their commercial applications. Here, we report the multilevel architecture optimization of Co-based nanoparticles (NPs) embedded in hollow N-doped carbon polyhedra for boosting the ORR and OER, which are fabricated by a two-step pyrolysis–oxidation strategy with a Co-based MOF (ZIF-67) as precursor. The key for this strategy lies in the precise and effective control of the oxidation processes of Co NPs, which enables the synthesis of a series of Co–Co3O4-based nanoarchitectures that are embedded in hollow nitrogen-doped carbon polyhedra (HNCP), including core–shell Co/Co3O4, yolk@shell Co@Co3O4, and hollow Co3O4 NPs. Benefiting from its abundant oxygen vacancies and tetrahedral Co2+ and the potential synergies of CoO x species and nitrogen-doped carbon as well as the efficient mass transfer of hollow and yolk–shell structures, the optimal yolk@shell Co3O4/HNCP-40 exhibits high activity for the OER with a low overpotential of 333 mV at 10 mA cm–2 and a small Tafel slope of 69 mV dec–1, which is better than those of commercial IrO2 (its overpotential and Tafel slope are 409 mV at 10 mA cm–2 and 104 mV dec–1, respectively). Meanwhile, the catalyst also exhibits comparable ORR catalytic activity with a half-wave potential of 0.834 V but better stability and methanol tolerance relative to commercial Pt/C (20 wt %), making it a potential bifunctional electrocatalyst for both the OER and ORR. This MOF-templated strategy for multilevel nanostructures provides insights into the development of highly efficient and low-cost bifunctional electrocatalysts for the OER/ORR.

Novel sandwich-shelled ZnCdS/ZnO/ZnCdS dodecahedral cages are synthesized with “one stone”, exhibiting advanced performance towards photocatalytic hydrogen production.

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CdTe/CdSe nanocrystal (NC) solar cells with an inverted structure (ITO/ZnO/CdSe/CdTe/Au) have been successfully fabricated by a simple solution process coupled with layer-by-layer sintering techniques. It was found that the device performance is strongly dependent on the annealing strategy, the thickness of the acceptor layer and on the buffer layer of ZnO when the optimal thickness of CdTe is adopted. Without the ZnO buffer layer, a thin film of the CdSeNCs on an ITO substrate shows a rougher morphology, resulting in device shunting. However, when a 40 nm-thick ZnO buffer layer and 60 nm-thick CdSe were employed, the device shows a much higher PCE of 5.81% under device conditions, post-annealing at 340 8C. This value is the highest efficiency ever reported to date for a CdTe/CdSe NC solar cell. Comparing with CdTe/CdSe NC solar cells with the normal device configuration, this device with an inverted structure simultaneously offers good Ohmic contact for carrier collection and efficient harvesting of solar photons in a wide wavelength.