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源自无孔配位聚合物的分级多孔碳

Hierarchically Porous Carbons Derived from Nonporous Coordination Polymers.

作者信息

Tong Lei, Zhang Le-Le, Wang Yu-Cheng, Wan Li-Yang, Yan Qiang-Qiang, Hua Cheng, Jiao Chen-Jia, Zhou Zhi-You, Ding Yan-Wei, Liu Bo, Liang Hai-Wei

机构信息

Hefei National Laboratory for Physical Sciences at the Microscale, Department of Chemistry, University of Science and Technology of China, Hefei 230026, China.

State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative innovation center of Chemistry for Energy Materials, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.

出版信息

ACS Appl Mater Interfaces. 2020 Jun 3;12(22):25211-25220. doi: 10.1021/acsami.0c06423. Epub 2020 May 21.

Abstract

Hierarchically porous carbons (HPCs) with multimodal pore systems exhibit great technological potentials, especially in the fields of heterogeneous catalysis, energy storage, and conversion. Here, we establish a simple and general approach to HPCs by carbonization of nonporous coordination polymers that are produced by mixing metal salts with polytopic ligands in alkaline aqueous solutions at room temperature. The proposed approach is applicable to a wide scope of ligand molecules (18 examples), thus affording the synthesized HPCs with high diversity in porosity, morphology, and composition. In particular, the prepared HPCs exhibit high specific surface areas (up to 2647 m g) and large pore volumes (up to 2.39 cm g). The HPCs-supported atomically dispersed Fe-N catalysts show much-improved fuel cell cathode performance over the micropore-dominated carbon black-supported catalysts, demonstrating the structural superiority of the HPCs for enhancing the mass transport properties.

摘要

具有多峰孔系统的分级多孔碳(HPCs)展现出巨大的技术潜力,尤其是在多相催化、能量存储和转换领域。在此,我们通过在室温下于碱性水溶液中将金属盐与多齿配体混合制备的无孔配位聚合物碳化,建立了一种简单通用的制备HPCs的方法。所提出的方法适用于广泛的配体分子(18个实例),从而使合成的HPCs在孔隙率、形态和组成方面具有高度多样性。特别地,制备的HPCs表现出高比表面积(高达2647 m²/g)和大孔体积(高达2.39 cm³/g)。与以微孔为主的炭黑负载催化剂相比,HPCs负载的原子分散Fe-N催化剂显示出显著改善的燃料电池阴极性能,证明了HPCs在增强传质性能方面的结构优越性。

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