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金属有机框架衍生的氮掺杂钴纳米簇镶嵌多孔碳作为先进钾硫电池的高效催化剂

Metal-Organic Framework-Derived Nitrogen-Doped Cobalt Nanocluster Inlaid Porous Carbon as High-Efficiency Catalyst for Advanced Potassium-Sulfur Batteries.

作者信息

Ge Xiaoli, Di Haoxiang, Wang Peng, Miao Xianguang, Zhang Peng, Wang Huiyang, Ma Jingyun, Yin Longwei

机构信息

Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials, Ministry of Education, School of Materials Science and Engineering, Shandong University, Jinan 250061, P.R. China.

School of Materials Science and Engineering, Qilu University of Technology (Shandong Academy of Science), Jinan 250353, P.R. China.

出版信息

ACS Nano. 2020 Nov 24;14(11):16022-16035. doi: 10.1021/acsnano.0c07658. Epub 2020 Nov 10.

Abstract

Despite high theoretical capacity and earth-abundant resources, the potential industrialization of potassium-sulfur (K-S) batteries is severely plagued by poor electrochemical reaction kinetics and a parasitic shuttle effect. Herein, a facile low-temperature pyrolysis strategy is developed to synthesize N-doped Co nanocluster inlaid porous N-doped carbon derived from ZIF-67 as catalytic cathodes for K-S batteries. To maximize the utilization efficiency, the size of Co nanoparticles can be tuned from 7 nm to homogeneously distributed 3 nm clusters to create more active sites to regulate affinity for S/polysulfides, improving the conversion reaction kinetics between captured polysulfides and KS/S, fundamentally suppressing the shuttle effect. Cyclic voltammetry curves, Tafel plots, electrochemical impedance spectroscopy, and density functional theory calculations ascertain that 3 nm Co clusters in S-N-Co-C cathodes exhibit superior catalytic activity to ensure low charge transfer resistance and energy barriers, enhanced exchange current density, and improved conversion reaction rate. The constructed S-N-Co-C cathode delivers a superior reversible capacity of 453 mAh g at 50 mA g after 50 cycles, a dramatic rate capacity of 415 mAh g at 400 mA g, and a long cycling stability. This work provides an avenue to make full use of high catalytic Co nanoclusters derived from metal-organic frameworks.

摘要

尽管钾硫(K-S)电池具有较高的理论容量和丰富的地球资源,但其潜在的工业化应用却受到电化学反应动力学较差和寄生穿梭效应的严重困扰。在此,我们开发了一种简便的低温热解策略,以合成由ZIF-67衍生的N掺杂Co纳米团簇镶嵌的多孔N掺杂碳,作为K-S电池的催化阴极。为了最大限度地提高利用效率,Co纳米颗粒的尺寸可以从7 nm调整为均匀分布的3 nm团簇,以创造更多的活性位点来调节对S/多硫化物的亲和力,改善捕获的多硫化物与KS/S之间的转化反应动力学,从根本上抑制穿梭效应。循环伏安曲线、塔菲尔图、电化学阻抗谱和密度泛函理论计算确定,S-N-Co-C阴极中的3 nm Co团簇表现出优异的催化活性,以确保低电荷转移电阻和能量势垒、增强的交换电流密度以及提高的转化反应速率。构建的S-N-Co-C阴极在50 mA g下经过50次循环后具有453 mAh g的优异可逆容量,在400 mA g下具有415 mAh g的显著倍率容量以及长循环稳定性。这项工作为充分利用源自金属有机框架的高催化活性Co纳米团簇提供了一条途径。

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