In the present work, nitrogen‐doped carbon spheres were synthesized through a simple hydro‐thermal treatment using glucose and melamine as inexpensive carbon and nitrogen sources, re‐spectively. The ratio of melami...In the present work, nitrogen‐doped carbon spheres were synthesized through a simple hydro‐thermal treatment using glucose and melamine as inexpensive carbon and nitrogen sources, re‐spectively. The ratio of melamine to glucose and annealing temperature were optimized. The final optimal sample exhibited a catalytic activity for the oxygen reduction reaction（ORR） that was supe‐rior than that of commercial 20%Pt/C in 0.1 mol/L KOH. It revealed an onset potential of –22.6 mV and a half‐wave potential of –133.6 mV （vs. Ag/AgCl）, which are 7.2 and 5.9 mV more positive than those of the 20%Pt/C catalyst, respectively, as well as a limiting current density of 4.6 mA/cm^2, which is 0.2 mA/cm^2 higher than that of the 20%Pt/C catalyst. The catalyst also exhibited higher stability and superior durability against methanol than 20%Pt/C. Moreover, ORRs on this catalyst proceed through a more effective 4 e^– path. The above mentioned superiority of the as‐prepared catalyst makes it promising for fuel cells.展开更多
We recently reported an N‐doped mesoporous carbon(N‐MC)extrudate,with major quaternary N species,prepared by a cheap and convenient method through direct carbonization of wheat flour with silica,which has excellent ...We recently reported an N‐doped mesoporous carbon(N‐MC)extrudate,with major quaternary N species,prepared by a cheap and convenient method through direct carbonization of wheat flour with silica,which has excellent catalytic performance in acetylene hydrochlorination.Herein,we examined the activity of Au supported on N‐MC(Au/N‐MC)and compared it with that of Au supported on nitrogen‐free mesoporous carbon(Au/MC).The acetylene conversion of Au/N‐MC was 50%at 180°C with an acetylene space velocity of 600 h–1 and VHCl/VC2H2 of 1.1,which was double the activity of Au/MC(25%).The introduced nitrogen atoms acted as anchor sites that stabilized the Au3+species and inhibited the reduction of Au3+to Au0 during the preparation of Au/N‐MC catalysts.展开更多
Oxygen evolution reaction(OER), as the primary anodic reaction, plays a critical role in many electrochemical energy conversion processes. As the state-of-the-art OER catalysts, iridium-based materials are largely hin...Oxygen evolution reaction(OER), as the primary anodic reaction, plays a critical role in many electrochemical energy conversion processes. As the state-of-the-art OER catalysts, iridium-based materials are largely hindered from practical applications mainly due to the extreme scarcity of iridium. Here we demonstrate the successful fabrication of boron-doped amorphous iridium oxide(IrO_(x)-B) via a facile boric acid-assisted method, which realizes an ultrahigh OER mass activity of 2779 A g^(-1)Irat 300 mV overpotential, representing one of the best acidic OER catalysts reported so far.It is found that boric acid can not only facilitate the exposure of Ir, but also dope the amorphous IrOxwith a form of metaborate, which could further modify the electronic and local ligand structure of Ir for the improved intrinsic activity. Interestingly, the reported strategy is universal that can be applied to improve other metal oxide OER catalysts, highlighting a versatile strategy for creating high-performance electrocatalysts with ultrahigh mass activity for OER and beyond.展开更多
文摘In the present work, nitrogen‐doped carbon spheres were synthesized through a simple hydro‐thermal treatment using glucose and melamine as inexpensive carbon and nitrogen sources, re‐spectively. The ratio of melamine to glucose and annealing temperature were optimized. The final optimal sample exhibited a catalytic activity for the oxygen reduction reaction（ORR） that was supe‐rior than that of commercial 20%Pt/C in 0.1 mol/L KOH. It revealed an onset potential of –22.6 mV and a half‐wave potential of –133.6 mV （vs. Ag/AgCl）, which are 7.2 and 5.9 mV more positive than those of the 20%Pt/C catalyst, respectively, as well as a limiting current density of 4.6 mA/cm^2, which is 0.2 mA/cm^2 higher than that of the 20%Pt/C catalyst. The catalyst also exhibited higher stability and superior durability against methanol than 20%Pt/C. Moreover, ORRs on this catalyst proceed through a more effective 4 e^– path. The above mentioned superiority of the as‐prepared catalyst makes it promising for fuel cells.
基金Zhejiang Provincial Natural Science Foundation of China(LY17B030010)~~
文摘We recently reported an N‐doped mesoporous carbon(N‐MC)extrudate,with major quaternary N species,prepared by a cheap and convenient method through direct carbonization of wheat flour with silica,which has excellent catalytic performance in acetylene hydrochlorination.Herein,we examined the activity of Au supported on N‐MC(Au/N‐MC)and compared it with that of Au supported on nitrogen‐free mesoporous carbon(Au/MC).The acetylene conversion of Au/N‐MC was 50%at 180°C with an acetylene space velocity of 600 h–1 and VHCl/VC2H2 of 1.1,which was double the activity of Au/MC(25%).The introduced nitrogen atoms acted as anchor sites that stabilized the Au3+species and inhibited the reduction of Au3+to Au0 during the preparation of Au/N‐MC catalysts.
基金financially supported by the Ministry of Science and Technology (2017YFA0208200 and 2016YFA0204100)the National Natural Science Foundation of China (22025108 and 51802206)+3 种基金the Natural Science Foundation of Jiangsu Province (BK20180846)the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)the Project of Scientific and Technologic Infrastructure of Suzhou (SZS201905)the Start-up Supports from Xiamen University。
文摘Oxygen evolution reaction(OER), as the primary anodic reaction, plays a critical role in many electrochemical energy conversion processes. As the state-of-the-art OER catalysts, iridium-based materials are largely hindered from practical applications mainly due to the extreme scarcity of iridium. Here we demonstrate the successful fabrication of boron-doped amorphous iridium oxide(IrO_(x)-B) via a facile boric acid-assisted method, which realizes an ultrahigh OER mass activity of 2779 A g^(-1)Irat 300 mV overpotential, representing one of the best acidic OER catalysts reported so far.It is found that boric acid can not only facilitate the exposure of Ir, but also dope the amorphous IrOxwith a form of metaborate, which could further modify the electronic and local ligand structure of Ir for the improved intrinsic activity. Interestingly, the reported strategy is universal that can be applied to improve other metal oxide OER catalysts, highlighting a versatile strategy for creating high-performance electrocatalysts with ultrahigh mass activity for OER and beyond.
