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一種高效雙功能電催化劑CoP/Co@NPC@rGO的制備

Preparation of CoP/Co@NPC@rGO nanocomposites with an efficient bifunctional electrocatalyst for hydrogen evolution and oxygen evolution reaction

  • 摘要: 簡單的熱處理和熱處理磷化ZIF-67/氧化石墨烯(GO)前驅體得到具有典型的多孔碳結構特征的CoP/Co@NPC@rGO納米復合材料電催化劑。通過掃描電子顯微鏡(SEM)、透射電子顯微鏡(TEM)、X射線衍射(XRD)、X射線光電子能譜(XPS)、拉曼光譜(Raman)和N2等溫吸脫附曲線等對其形貌、成分和結構進行分析和表征。采用線性掃描伏安法、電化學阻抗譜和計時電位法探討了CoP/Co@NPC@rGO納米復合電催化劑對氫氣析出反應(HER)和氧氣析出反應(OER)的電催化活性和穩定性。結果表明,CoP/Co@NPC@rGO?350在1.0 mol·L–1 KOH溶液中達到10 mA·cm?2電流密度的析氫過電位僅127 mV;同時,在1.0 mol·L–1 KOH溶液中顯示出優于貴金屬RuO2的析氧性能,達到10 mA·cm?2電流密度的過電位為276 mV,塔菲爾斜率僅為42 mV·dec?1。這種高析氫和析氧電催化活性主要歸因于高度石墨化的N摻雜多孔碳與N摻雜石墨烯之間的協同效應。CoP/Co@NPC@rGO是電催化全解水電催化劑的候選材料,且為基于金屬有機骨架(MOFs)/氧化石墨烯復合材料的高效電催化劑的設計開辟了一條新的途徑。

     

    Abstract: The construction of the highly active transition-metal phosphide/carbon-based electrocatalyst from metal-organic frameworks (MOFs) precursors is considered as an efficient approach. In this work, ZIF-67/GO precursors were firstly obtained by the in situ controllable growth of ZIF-67 nanocrystals on both surfaces of GO sheets. Then, a highly efficient bifunctional electrocatalyst CoP/Co@NPC@rGO nanocomposite was derived by the thermal pyrolysis of ZIF-67/GO precursors under N2 atmosphere and a subsequent phosphatization process. The structure and elemental composition of the ZIF-67/GO, Co@NPC@rGO, and CoP/Co@NPC@rGO nanocomposites were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and N2 ad-/desorption isotherms analysis. The Co@NPC@rGO?800 nanocomposite exhibits a high Brunauer-Emmett-Teller (BET) surface area of 186.27 m2·g?1, indicating that both micropores and mesopores existed. Subsequently, the electrocatalytic properties of the CoP/Co@NPC@rGO nanocomposites for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) were investigated by electrochemical measurements. The results suggest that the obtained CoP/Co@NPC@rGO?350 nanocomposite only requires an overpotential of 127 mV to reach a current density of 10 mA·cm?2 for HER in 1.0 mol·L–1 KOH solution. For OER, CoP/Co@NPC@rGO?350 nanocomposite can reach a current density of 10 mA·cm?2 at an overpotential of 276 mV, with a Tafel slope of 42 mV·dec?1, in the same alkaline aqueous solution, which is superior to RuO2. In addition, for both HER and OER, CoP/Co@NPC@rGO?350 nanocomposite also shows impressive strong durability in alkaline aqueous solution. The outstanding performance can be attributed to the synergistic effect of coupled highly graphitized N-doped porous carbon and N-doped graphene. The as-prepared CoP/Co@NPC@rGO?350 electrocatalyst is a promising candidate for overall water splitting in the alkaline solution. This development offers an attractive catalyst material based on MOF/GO composites. It is expected that the presented strategy can be extended to the fabrication of other composites electrode materials for more efficient water splitting.

     

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