The development of highly efficient catalysts for cathodes remains an important objective of fuel cell research. Here, we report Co3O4 nanoparticles assembled on a polypyrrole/graphene oxide electrocatalyst （C...The development of highly efficient catalysts for cathodes remains an important objective of fuel cell research. Here, we report Co3O4 nanoparticles assembled on a polypyrrole/graphene oxide electrocatalyst （Co3O4/Ppy/GO） as an efficient catalyst for the oxygen reduction reaction （ORR） in alkaline media. The catalyst was prepared via the hydrothermal reaction of Co2＋ ions with Ppy-modified GO. The GO, Ppy/GO, and Co3O4/Ppy/GO were characterized using scanning electron microscopy, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy. The incorporation of Ppy into GO nanosheets resulted in the formation of a nitrogen-modified GO po-rous structure, which acted as an efficient electron-transport network for the ORR. With further anchoring of Co3O4 on Ppy/GO, the as-prepared Co3O4/Ppy/GO exhibited excellent ORR activity and followed a four-electron route mechanism for the ORR in alkaline solution. An onset potential of -0.10 V vs. a saturated calomel electrode and a diffusion limiting current density of 2.30 mA/cm^2 were achieved for the Co3O4/Ppy/GO catalyst heated at 800 ℃; these values are comparable to those for noble-metal-based Pt/C catalysts. Our work demonstrates that Co3O4/Ppy/GO is highly active for the ORR. Notably, the Ppy coupling effects between Co3O4 and GO provide a new route for the preparation of efficient non-precious electrocatalysts with hierarchical porous structures for fuel cell applications.展开更多
Manipulating the chemical reactivity of graphene toward oxygen reduced reduction(ORR)is of particular interest for both fundamental research and practical application in fuel cell.Deposing graphene on selected substra...Manipulating the chemical reactivity of graphene toward oxygen reduced reduction(ORR)is of particular interest for both fundamental research and practical application in fuel cell.Deposing graphene on selected substrate provides a structure-intact strategy to enhance its chemical reactivity due to substrate-induced charge and interface effect.Here,we report the graphene deposited on one-dimensional electride Y5Si3 as an effective ORR catalyst in acidic media.Thermodynamic calculations suggest that depositing graphene on electride materials can facilitate the protonation of O2,which is the rate-determining step based on the four-electron reaction pathway and thus promote the ORR activity.Further electronic calculations reveal that low work function(3.5 eV),superior electrical conductivity and slight charge transfer from substrate to graphene result in the enhanced ORR performance of graphene.These findings shed light on the rational design of ORR catalysts based on graphitic materials and emphasize the critical role of substrates for energy-related electrochemical reactions.展开更多
A Pt/graphene‐TiO2catalyst was prepared by a microwave‐assisted solvothermal method and was characterized by X‐ray diffraction,scanning electron microscopy,transmission electron microscopy,cyclic voltammetry,and li...A Pt/graphene‐TiO2catalyst was prepared by a microwave‐assisted solvothermal method and was characterized by X‐ray diffraction,scanning electron microscopy,transmission electron microscopy,cyclic voltammetry,and linear sweep voltammetry.The cubic TiO2particles were approximately60nm in size and were distributed on the graphene sheets.The Pt nanoparticles were uniformly distributed between the TiO2particles and the graphene sheet.The catalyst exhibited a significant improvement in activity and stability towards the oxygen reduction reaction compared with Pt/C,which resulted from the high electronic conductivity of graphene and strong metal‐support interactions.展开更多
Very recent progress on the graphene derivatives supported variable nanocatalysts for oxygen reduction reaction （ORR） in fuel cell is reviewed. First, common electrochemical techniques to characterize graphene-based...Very recent progress on the graphene derivatives supported variable nanocatalysts for oxygen reduction reaction （ORR） in fuel cell is reviewed. First, common electrochemical techniques to characterize graphene-based electrocatalysts are mentioned. Second, recent updates on gra- phene-derived electrocatalysts are introduced. In this part, both electrochemical activity and stabil- ity of Pt catalysts can be improved when they are supported by reduced graphene oxide （RGO）. Other noble-metal catalysts including Pd, Au, and Ag showing comparable performance have been investigated. The stability of Pd catalyst is enhanced by RGO or few-layered graphene support. Syn- thetic approaches for Au or Ag catalysts supported on graphene oxide are discussed. In addition, non-noble transition metals in N4-chelate complexes can reduce oxygen electrochemically. Fe and Co are cheap alternative catalysts for ORR. In most cases, the stability and tolerance issues are overcome well, but their overall performances don＇t seem to surpass Pt/C catalyst yet,展开更多
Unique MoS_(2)‐SnS_(2)heterogeneous nanoplates have successfully in‐situ grown on poly(3‐(1‐vinylimidazolium‐3‐yl)propane‐1‐sulfonate)functionalized polypyrrole/graphene oxide(PVIPS/PPy/GO).PVIPS can attract h...Unique MoS_(2)‐SnS_(2)heterogeneous nanoplates have successfully in‐situ grown on poly(3‐(1‐vinylimidazolium‐3‐yl)propane‐1‐sulfonate)functionalized polypyrrole/graphene oxide(PVIPS/PPy/GO).PVIPS can attract heptamolybdate ion(Mo7O246−)and Sn^(4+)as the precursors by the ion‐exchange,resulting in the simultaneous growth of 1T’‐MoS2 and the berndtite‐2T‐type hexagonal SnS_(2)by the interfacial induced effect of PVIPS.The obtained MoS_(2)‐SnS_(2)/PVIPS/PPy/GO can serve as electrocatalysts,exhibiting good NRR performance by the synergistic effect.The semi‐conducting SnS_(2)would limit the surface electron accessibility for suppressing HER process of 1T’‐MoS_(2),while metallic 1T’‐MoS_(2)might efficiently improve the NRR electroactivity of SnS_(2)by the creation of Mo‐Sn‐Sn trimer catalytic sites.Otherwise,the irreversible crystal phase transition has taken place during the NRR process.Partial 1T’‐MoS_(2)and SnS_(2)have electrochemically reacted with N_(2),and irreversibly converted into Mo^(2)N and SnxNz due to the formation of Mo−N and Sn−N bonding,meanwhile,partial SnS_(2) has been irreversibly evolved into SnS due to the reduction by the power source in the electrochemical system.It would put forward a new design idea for optimizing the preparation method and electrocatalytic activity of transition metal dichalcogenides.展开更多
基金supported by the National Natural Science Foundation of China(21373042)~~
文摘The development of highly efficient catalysts for cathodes remains an important objective of fuel cell research. Here, we report Co3O4 nanoparticles assembled on a polypyrrole/graphene oxide electrocatalyst （Co3O4/Ppy/GO） as an efficient catalyst for the oxygen reduction reaction （ORR） in alkaline media. The catalyst was prepared via the hydrothermal reaction of Co2＋ ions with Ppy-modified GO. The GO, Ppy/GO, and Co3O4/Ppy/GO were characterized using scanning electron microscopy, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy. The incorporation of Ppy into GO nanosheets resulted in the formation of a nitrogen-modified GO po-rous structure, which acted as an efficient electron-transport network for the ORR. With further anchoring of Co3O4 on Ppy/GO, the as-prepared Co3O4/Ppy/GO exhibited excellent ORR activity and followed a four-electron route mechanism for the ORR in alkaline solution. An onset potential of -0.10 V vs. a saturated calomel electrode and a diffusion limiting current density of 2.30 mA/cm^2 were achieved for the Co3O4/Ppy/GO catalyst heated at 800 ℃; these values are comparable to those for noble-metal-based Pt/C catalysts. Our work demonstrates that Co3O4/Ppy/GO is highly active for the ORR. Notably, the Ppy coupling effects between Co3O4 and GO provide a new route for the preparation of efficient non-precious electrocatalysts with hierarchical porous structures for fuel cell applications.
基金supported by the National Natural Science Foundation of China (No.21573204 and No.21421063)Ministry of Science and Technology of China (No.2016YFA0200602)+2 种基金Anhui Initiative in Quantum Information Technologies, Fundamental Research Funds for the Central UniversitiesNational Program for Support of Top-notch Young Professional, Chinese Academy of Sciences Interdisciplinary Innovation TeamSuper Computer Center of USTC supercomputing center and CAS supercomputing center
文摘Manipulating the chemical reactivity of graphene toward oxygen reduced reduction(ORR)is of particular interest for both fundamental research and practical application in fuel cell.Deposing graphene on selected substrate provides a structure-intact strategy to enhance its chemical reactivity due to substrate-induced charge and interface effect.Here,we report the graphene deposited on one-dimensional electride Y5Si3 as an effective ORR catalyst in acidic media.Thermodynamic calculations suggest that depositing graphene on electride materials can facilitate the protonation of O2,which is the rate-determining step based on the four-electron reaction pathway and thus promote the ORR activity.Further electronic calculations reveal that low work function(3.5 eV),superior electrical conductivity and slight charge transfer from substrate to graphene result in the enhanced ORR performance of graphene.These findings shed light on the rational design of ORR catalysts based on graphitic materials and emphasize the critical role of substrates for energy-related electrochemical reactions.
基金supported by the National Natural Science Foundation of China(21376113)the Jiangsu Specially Appointed Professor Projectthe Graduate Student Scientific Research Innovation Projects in Jiangsu Province(KYZZ15_0384)~~
文摘A Pt/graphene‐TiO2catalyst was prepared by a microwave‐assisted solvothermal method and was characterized by X‐ray diffraction,scanning electron microscopy,transmission electron microscopy,cyclic voltammetry,and linear sweep voltammetry.The cubic TiO2particles were approximately60nm in size and were distributed on the graphene sheets.The Pt nanoparticles were uniformly distributed between the TiO2particles and the graphene sheet.The catalyst exhibited a significant improvement in activity and stability towards the oxygen reduction reaction compared with Pt/C,which resulted from the high electronic conductivity of graphene and strong metal‐support interactions.
文摘Very recent progress on the graphene derivatives supported variable nanocatalysts for oxygen reduction reaction （ORR） in fuel cell is reviewed. First, common electrochemical techniques to characterize graphene-based electrocatalysts are mentioned. Second, recent updates on gra- phene-derived electrocatalysts are introduced. In this part, both electrochemical activity and stabil- ity of Pt catalysts can be improved when they are supported by reduced graphene oxide （RGO）. Other noble-metal catalysts including Pd, Au, and Ag showing comparable performance have been investigated. The stability of Pd catalyst is enhanced by RGO or few-layered graphene support. Syn- thetic approaches for Au or Ag catalysts supported on graphene oxide are discussed. In addition, non-noble transition metals in N4-chelate complexes can reduce oxygen electrochemically. Fe and Co are cheap alternative catalysts for ORR. In most cases, the stability and tolerance issues are overcome well, but their overall performances don＇t seem to surpass Pt/C catalyst yet,
文摘Unique MoS_(2)‐SnS_(2)heterogeneous nanoplates have successfully in‐situ grown on poly(3‐(1‐vinylimidazolium‐3‐yl)propane‐1‐sulfonate)functionalized polypyrrole/graphene oxide(PVIPS/PPy/GO).PVIPS can attract heptamolybdate ion(Mo7O246−)and Sn^(4+)as the precursors by the ion‐exchange,resulting in the simultaneous growth of 1T’‐MoS2 and the berndtite‐2T‐type hexagonal SnS_(2)by the interfacial induced effect of PVIPS.The obtained MoS_(2)‐SnS_(2)/PVIPS/PPy/GO can serve as electrocatalysts,exhibiting good NRR performance by the synergistic effect.The semi‐conducting SnS_(2)would limit the surface electron accessibility for suppressing HER process of 1T’‐MoS_(2),while metallic 1T’‐MoS_(2)might efficiently improve the NRR electroactivity of SnS_(2)by the creation of Mo‐Sn‐Sn trimer catalytic sites.Otherwise,the irreversible crystal phase transition has taken place during the NRR process.Partial 1T’‐MoS_(2)and SnS_(2)have electrochemically reacted with N_(2),and irreversibly converted into Mo^(2)N and SnxNz due to the formation of Mo−N and Sn−N bonding,meanwhile,partial SnS_(2) has been irreversibly evolved into SnS due to the reduction by the power source in the electrochemical system.It would put forward a new design idea for optimizing the preparation method and electrocatalytic activity of transition metal dichalcogenides.
