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Dual Inorganic Sacrificial Template Synthesis of Hierarchically Porous Carbon with Specific N Sites for Efficient Oxygen Reduction

机译:双无机牺牲模板与特定N个位点的分层多孔碳的合成,用于有效氧气还原

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It is still a challenge to achieve efficiently controlled preparation of functional oxygen reduction reaction (ORR) carbon electrocatalysts with multi-preferred structures (hierarchically porous networks and specific carbon–nitrogen bonds) from carbohydrate-containing small molecules via simple one-step pyrolysis. Based on the step-by-step spontaneous gas-foaming strategy, we successfully prepare 3D hierarchically porous networks with tunable N sites (N_(P)/N_(G) ≈ 1:1) by pyrolyzing diverse carbohydrates (glucose, maltose, and cyclodextrin) using nonmetal–metal dual inorganic sacrificial templates. In situ evaporation templates can simplify the procedure of the experiments and avoid the active site loss compared with traditional hard templates. Crucially, dual inorganic sacrificial templates can induce abundant defects and microscopic pore structures (the specific surface area increased from 922.403 to 1898.792 m~(2)·g~(–1)) and tunable N sites compared with single nonmetal sacrificial templates. The regulatory mechanism of dual inorganic templates on N sites (N_(P)/N_(G) ≈ 1:1) is independent of the polymeric state of carbohydrate precursors or even the carbonization condition of the pyrolysis process. A series of carbon materials prepared by this strategy all have ORR-preferred structures and exhibit low ORR overpotentials compared with Pt/C. For instance, the Zn–air battery with βCD-DSC-950-1 exhibits an open-circuit potential of 1.51 V and a peak power density of 180.89 mW·cm~(–2), higher than those of Pt/C (1.47 V, 174.94 mW·cm~(–2)). In general, the conversion of carbohydrate-containing small molecules to functional carbon materials provides a new strategy for the development of carbonaceous electrocatalysts.
机译:通过简单的一步热解,从含碳水化合物的小分子中高效控制制备具有多个优先结构(分层多孔网络和特定碳氮键)的功能性氧还原反应(ORR)碳电催化剂仍然是一个挑战。基于逐步自发气体发泡策略,我们成功地制备了具有可调N位(N_P)/N_G)的三维分层多孔网络≈ 1:1)通过使用非金属-金属双无机牺牲模板热解各种碳水化合物(葡萄糖、麦芽糖和环糊精)。与传统的硬模板相比,原位蒸发模板可以简化实验过程,避免活性位损失。重要的是,与单一的非金属牺牲模板相比,双无机牺牲模板可以诱导大量的缺陷和微观孔隙结构(比表面积从922.403增加到1898.792 m~(2)·g~(-1))和可调的N位。双无机模板对N位(N_P)/N_G的调控机制≈ 1:1)与碳水化合物前体的聚合状态甚至热解过程的碳化条件无关。用这种方法制备的一系列碳材料都具有ORR优先结构,与Pt/C相比,表现出较低的ORR过电位。例如,带有βCD-DSC-950-1的锌空气电池的开路电位为1.51V,峰值功率密度为180.89mW·cm~(-2),高于Pt/C(1.47V,174.94mW·cm~(-2))。总的来说,将含碳水化合物的小分子转化为功能性碳材料为含碳电催化剂的开发提供了新的策略。

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