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Porous Organic Polymer-Derived Carbon Composite asa Bimodal Catalyst for Oxygen Evolution Reaction and Nitrophenol Reduction

机译:多孔有机聚合物衍生的碳复合材料氧分解反应和硝基苯酚还原的双峰催化剂

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摘要

Ethylene diamine-based porous organic polymer (EPOP) was synthesized, carbonized at different temperatures, and characterized. The successful formation of the triazine polymer was confirmed by Fourier-transform infrared spectroscopy, 13C, and 15N cross-polarization magic angle spinning solid-state NMR. The two-dimensional layered architecture and graphitic nature of the samples resembled that of nitrogen-doped amorphous carbon, as confirmed by Raman, powder X-ray diffraction, and transmission electron microscopy measurements. The catalytic activity of these materials toward nitrophenol reduction and electrocatalytic activity toward oxygen evolution reaction (OER) were systematically evaluated in detail. Electrocatalytic activity toward oxygen evolution reaction was systematically evaluated by chronoamperometry and linear sweep voltammetry. Results clearly demonstrate that all of these catalysts exhibit good OER activity and excellent stability. Among all catalysts, EPOP-700 showed better OER activity, as reflected by its onset potential and current density, comparable with that ofthe metal-based OER catalysts and better than that of metal-free catalysts.Further, their catalytic activity toward the reduction of 4-nitrophenolto 4-aminophenol was tested with NaBH4; although all ofthese catalysts showed good catalytic activity; EPOP-800 displayedbetter catalytic activity.
机译:合成了乙二胺基多孔有机聚合物(EPOP),并在不同温度下对其进行了碳化和表征。通过傅立叶变换红外光谱, 13 C和 15 N交叉极化幻角旋转固态NMR证实了三嗪聚合物的成功形成。样品的二维分层结构和石墨性质类似于氮掺杂的无定形碳,通过拉曼光谱,粉末X射线衍射和透射电子显微镜测量得到证实。详细评估了这些材料对硝基苯酚还原的催化活性和对氧释放反应(OER)的电催化活性。通过计时电流法和线性扫描伏安法系统地评估了对氧释放反应的电催化活性。结果清楚地表明,所有这些催化剂均显示出良好的OER活性和出色的稳定性。在所有催化剂中,EPOP-700表现出更好的OER活性,反映出它的起始电势和电流密度,与EPOP-700相当。金属基OER催化剂要比无金属催化剂好。此外,它们对还原4-硝基苯酚的催化活性用NaBH4测试得到4-氨基苯酚;虽然所有这些催化剂显示出良好的催化活性。显示EPOP-800更好的催化活性。

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