摘要：The oxygen reduction reaction （ORR） is essential in research pertaining to life science and energy. In applications, platinum-based catalysts give ideal reactivity, but, in practice, are often subject to high costs and poor stability. Some costefficient transition metal oxides have exhibited excellent ORR reactivity, but the stability and durability of such alternative catalyst materials pose serious challenges. Here, we present a facile method to fabricate uniform CoxOy nanoparticles and embed them into N-doped carbon, which results in a composite of extraordinary stability and durability, while maintaining its high reactivity. The half-wave potential shows a negative shift of only 21 mV after 10,000 cycles, only one third of that observed for Pt/C （63 mV）. Furthermore, after 100,000 s testing at a constant potential, the current decreases by only 17%, significantly less than for Pt/C （35%）. The exceptional stability and durability results from the system architecture, which comprises a thin carbon shell that prevents agglomeration of the CoxOy nanoparticles and their detaching from the substrate.

摘要：Single-component anode materials can barely satisfy the growing demand for next-generation Li-ion batteries with higher capacity and cyclability. Thus developing multi-component synergistic electrodes has become a critical issue. Herein, inspired by natural corn, a ternary hierarchical self-supported array design is proposed. Based on a sequential transformation route, Si/C-modified C0304 nanowire arrays are constructed on 3D Ni foams to form a binder-free integrated electrode. Specifically, an ionic liquid-assisted electrodeposition strategy is employed to prepare discrete ultrafine Si nanoparticles on nanoscale array substrates, which follow the Volmer-Weber island growth mode. In this corn-mimetic system, kernel-like Si nanoparticles and a husk-like carbon coating layer function as enhancing and protecting units, respectively, to improve the capacity and stability of the cobalt oxide basic unit. Taking advantage of a synergistic effect, the ternary nanoarray anode achieves a significant performance enhancement compared to pristine Co304, showing a special capacity as high as -1,000 mAh·g^-1 at 100 mA·g^-1. By extending this corn-mimetic hierarchical array design to other basic, enhancing, and protecting units, new ideas for constructing synergistic nano-architectures for energy conversion and storage field are developed.

摘要：Low-temperature CO oxidation has attracted extensive interest in heterogeneous catalysis because of the potential applications in fuel cells,air cleaning,and automotive emission *** the present study,theoretical investigations have been performed using density functional theory to elucidate the crystal plane effect and structure sensitivity of Co3O4 nano-catalysts toward catalyzing CO *** is shown that the surface Co–O ion pairs are the active site for CO oxidation on the Co3O4 *** of stronger CO adsorption and easier removal of lattice oxygen ions,the Co3O4（011）surface is shown to be more reactive for CO oxidation than the Co3O4（001）surface,which is consistent with previous experimental *** comparing the reaction pathways at different sites on each surface,we have further elucidated the nature of the crystal plane effect on Co3O4 surfaces and attributed the reactivity to the surface *** results suggest that CO oxidation catalyzed by Co3O4 nanocrystals has a strong crystal plane effect and structure *** the vacancy formation energy of the oxide surface is key for high CO oxidation reactivity.

摘要：Two polypyridine complexes containingμ‐OH,μ‐O2dicobalt(III)cores,[(TPA)CoIII(μ‐OH)(μ‐O2)CoIII(TPA)](ClO4)3and[(BPMEN)CoIII(μ‐OH)(μ‐O2)CoIII(BPMEN)](ClO4)3(TPA=tris(2‐pyridylmethyl)amine,BPMEN=N,N′‐dimethyl‐N,N′‐bis(pyridin‐2‐ylmethyl)ethane‐1,2‐diamine),have previously been reported as inactive in the light‐driven water oxidation reaction(ACS Catal.,2016,6,5062?5068).Herein,another dicobalt(III)compound,μ‐OH,μ‐O2‐[{(enN4)2Co2}](ClO4)3(enN4=1,6‐bis(2‐pyridyl‐2,5‐diazaocta‐2,6‐diene),with a similar core structure was synthesized,characterized,and applied to the light‐driven water oxidation *** experiments showed that the complex itself was also inactive in the light‐driven water oxidation,and that the activity observed originated from Co(II)*** research establishes that complexes possessing aμ‐OH,μ‐O2dicobalt(III)core structure are not appropriate choices for true molecular catalysts ofwater oxidation.

摘要：The continuously dynamic-controlled combustion synthesis （CDCCS） was developed based on the continuous fluidization and combustion synthesis technologies. CoC2O4·2H2O powders were transformed to Co3O4 in a gas-solid fluid bed unit designed and build independently, where the reactant of CoC2O4·2H2O powders and the reactant of air were poured and introduced from the top and the bottom of the bed at a certain rates respectively. The reagents met in the bed and ignited at a given low temperature, resulting in formation of Co3O4. The results show a significant difference in combustion wave models. In the case of CDCCS, there was an immobile combustion wave, floating in the combustion zone located in the middle of the bed, instead of propagating of the combustion wave. The temperature of the combustion wave can be controlled by adjusting the flow rate of carrier gas. The resultant Co3O4 powders （diameter size ≤0.8 μm） have a narrow particle size distribution and spherical or quasi-spherical shape. This novel technique has many advantages, such as continuation, efficiency, energy conservation and environmental friendly and has been used in mass production.