摘要：Fast crystallization of nanosized zeolite crystals is a very popular process used for practical zeolite catalyst applications. Herein, we report a designer crystallization process for nanosized zeolite omega crystals based on the relationship between the crystallization time and temperature in the Arrhenius equation. Compared to the conventional hydrothermal synthesis of zeolite omega(72 h at room temperature and 240 h at 100℃, MAZ-100), the crystallization of zeolite omega presented in this work only requires a very short time interval(5 h at 180℃, MAZ-180). Physicochemical characterizations, including XRD, SEM, N2 sorption isotherms, and 27 Al MAS NMR show that the product of zeolite omega(MAZ-180) has good crystallinity and uniform nanocrystals. More importantly, after the loading of Pt nanoparticles(0.5 wt%), the Pt/H-MAZ-180 catalyst exhibits higher isomer selectivity and lower cracking selectivity than those of the Pt/H-MAZ-100 catalyst in the hydroisomerization of n-dodecane. These results suggest the potential applications of these omega nanocrystals as supporting catalyst compounds in industrial processes.

摘要：The design and preparation of non-noble metal catalysts with high catalytic activity and robust stability are important in the research of metal-air batteries and fuel ***,a three-dimensional(3D)hierarchically ordered porous carbon nanomaterial was conveniently synthesized with zeolite-imidazole framework(ZIF-8)carbonization using the silica-template method and carbon nanotube(CNT)*** addition of an iron source endows the porous mFeNCCNT with Fe-based nanoparticles and abundant atomically dispersive Fe-Nx sites from its nitrogen-incorporated graphitic carbon *** a result,the 3D porous structure reduces the charge transport resistance,and the iron and nitrogen codoped carbon exhibits excellent catalytic activity for oxygen reduction reaction(ORR)similar to that of commercial Pt/***,the interwoven CNTs obtained under urea catalysis further shorten the ion and electron diffusion *** and theoretical analyses revealed that the optimized mFeNC-CNT has a high ORR activity with a half-wave potential of 0.908 V and a large open-circuit voltage(1.556 V)when applied on zinc-air *** work provides a promising strategy for the rational design and facile synthesis of high-performing non-noble metal-based electrocatalysts for energy storage,conversion,and transport applications.

摘要：The design and synthesis of high‐performance and low‐cost electrocatalysts for the hydrogen evolution reaction(HER),a key half‐reaction in water electrolysis,are *** to their modest hydrogen adsorption energy,ruthenium(Ru)‐based nanomaterials are considered outstanding candidates to replace the expensive platinum(Pt)‐based HER *** this study,we developed an adsorption‐pyrolysis method to construct nitrogen(N)‐doped graphene aerogel(N‐GA)‐supported ultrafine Ru nanocrystal(Ru‐NC)nanocomposites(Ru‐NCs/N‐GA).The particle size of the Ru‐NCs and the conductivity of the N‐GA substrate can be controlled by varying the pyrolysis *** experiments reveal revealed that 10 wt%Ru‐NCs/N‐GA nanocomposites require overpotentials of only 52 and 36 mV to achieve a current density of 10 mA cm^(−2) in 1 mol/L HClO4 and 1 mol/L KOH electrolytes for HER,respectively,which is comparable to 20 wt%Pt/C *** from the ultrafine size and uniform dispersion of the Ru‐NCs,the synergy between Ru and the highly conductive substrate,and the anchoring effect of the N atom,the Ru‐NCs/N‐GA nanocomposites exhibit excellent activity and durability in the pH‐universal HER,thereby opening a new avenue for the production of commercial HER electrocatalysts.

摘要：Selective coupling of methyl radicals to produce C_(2) species(C2H4 and C2H6)is a key challenge for oxidative coupling of methane(OCM).In traditional OCM reaction systems,homogeneous transformation of methyl radicals in O_(2)‐containing gases are uncontrollable,resulting in limited C_(2) selectivity and ***,we demonstrate that methyl radicals generated by La_(2)O_(3)at low reaction temperature can selectively couple on the surface of 5 wt%Na2WO4/SiO_(2).The controllable surface coupling against overoxidation barely changes the activity of La_(2)O_(3)but boosts the C_(2)selectivity by three times and achieves a C_(2)yield as high as 10.9%at bed temperature of only 570℃.Structure‐property studies suggest that Na_(2)WO_(4) nanoclusters are the active sites for methyl radical *** strong CH_(3)·affinity of these sites can even endow some methane combustion catalysts with OCM *** findings of the surface coupling of methyl radicals open a new direction to develop OCM *** bifunctional OCM catalyst system,which composes of a methane activation center and a CH_(3)·coupling center,may deliver promising OCM performance at reaction temperatures below the ignition temperature of C2H6 and C2H4(~600℃)and is therefore more controllable,safer,and certainly more attractive as an actual process.