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Role of Nitrogen Moieties in N-Doped 3D-Graphene Nanosheets for Oxygen Electroreduction in Acidic and Alkaline Media

机译:氮气部分在酸性和碱性介质中的氧气电氧化氮中的作用

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This study elucidates the synthesis-structure property correlations of nitrogen moieties present in nitrogen-functionalized graphene nanomaterials toward oxygen reduction reactions (ORRs) and their electrochemical pathways in acidic and alkaline electrolytes. Porous three-dimensional nitrogen doped graphene nanosheets (N/3D-GNSs) were fabricated using the sacrificial support method and doped with nitrogen using 10 atom % NH3 under thermal pyrolysis at T = 650, 850, and 1050 degrees C for evaluating the nitrogen species formed under different temperatures. The abundances of the various nitrogen species formed under pyrolytic conditions were evaluated with X-ray photoelectron spectroscopy. Using rotating ring-disk electrode, we analyzed the role played by the nitrogen moieties influencing the electrochemical activity of the N/3D-GNS supports for oxygen reduction reactions (ORRs) in both acidic and alkaline media. It was demonstrated that the concentrations of the nitrogen moieties: graphitic-N, quaternary, hydrogenated-N (hydrogenated nitrogen combined pyrrolic nitrogen and hydrogenated pyridine) and pyridinic-N varied considerably with pyrolysis temperatures. A decrease in graphitic-N content and an increase in the ratio of hydrogenated-N/pyridinic-N significantly improved the activity of the material. The half-wave and onset potentials as well as the current densities and hydrogen peroxide (H2O2)/(HO2-) yields of the N/3D-GNS materials also varied between acidic and alkaline electrolytes but followed the general trend in terms of pyrolysis temperatures and abundance of the nitrogen moieties. Among the synthesized materials, the 3D-graphene nanosheets that were doped with nitrogen at 850 degrees C, optimized to have the highest hydrogenated-N and lowest pyridinic-N as well as better catalyst-ionomer integration, showed the highest ORR performance. This strategy for the tunable synthesis of nitrogen-doped graphene materials with controlled nitrogen functionalization offers a platform for developing active supports or catalytic nanomaterials for fuel cell applications.
机译:本研究阐明了氮气官能化石墨烯纳米材料中存在的氮部分的合成结构性质相关性朝向氧还原反应(ORRS)及其在酸性和碱性电解质中的电化学途径。使用牺牲支撑方法制造多孔的三维氮掺杂石墨烯纳米烯纳米片(N / 3D-GNSS),并在T = 650,850和1050℃的热热解中使用10原子%NH 3掺杂氮气,用于评估氮物质在不同的温度下形成。用X射线光电子能谱评价在热解条件下形成的各种氮物质的丰度。使用旋转环盘电极,我们分析了氮气部分发挥的作用,影响酸性和碱性介质中的N / 3D-GNS支撑氧还原反应(ORRS)的电化学活性。结果表明,氮气部分的浓度:石墨-N,季铵氢化-N(氢化氮气组合吡咯氮和氢化吡啶)和吡啶-N随热解温度而变化。石墨氮含量的降低和氢化-N /吡啶-N的比例的增加显着改善了材料的活性。半波和发病电位以及N / 3D-GNS材料的当前密度和过氧化氢(H 2 O 2)/(HO2-)产率在酸性和碱性电解质之间也变化,但随后在热解温度方面进行了一般趋势和丰富的氮部分。在合成的材料中,在850℃下掺杂氮的3D-石墨烯纳米片,优化为具有最高的氢化-N和最低吡啶-N以及更好的催化剂 - 离聚物集成,显示出最高的ORR性能。具有受控氮官能化的可调谐合成氮掺杂石墨烯材料的该策略提供了用于开发用于燃料电池应用的活性载体或催化纳米材料的平台。

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