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Highly Effective OER Electrocatalysts Generated from a Two-Dimensional Metal–Organic Framework Including a Sulfur-Containing Linker without Doping

过电位 双金属片 化学 塔菲尔方程 硫黄 电化学 硫化钴 化学工程 金属有机骨架 无机化学 分解水 金属 纳米技术 电极 催化作用 材料科学 物理化学 有机化学 吸附 光催化 工程类
作者
Tang-ming Li,Bingqian Hu,Jinghua Han,Wangting Lu,Yu Fan,Bao Li
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:61 (18): 7051-7059 被引量:11
标识
DOI:10.1021/acs.inorgchem.2c00493
摘要

Metal-organic frameworks (MOFs) with different topologies formed by the self-assembly of sulfur-containing inorganic ligands, cobalt ions, and large ligands can be used to prepare electrocatalysts for water splitting in order to fully explore the advantages of MOFs in terms of structural tailoring and quantitative assembly. It is possible to avoid using an extradoped sulfur source to reduce waste as well as to disperse Co and sulfur elements evenly and controllably throughout the final material to maximize the overall synergistic effect. In this work, different kinds of bimetallic MOF materials containing sulfur can be synthesized very conveniently by using an economical and practical diffusion method. These materials are directly used as OER electrocatalysts, and the bimetallic MOFs have the best electrocatalytic performance when the ratio of Co to Fe is 6:4. The overpotential at a current density of 10 mA cm-2 was 260 mV, with a Tafel slope of 56 mV dec-1 and good stability. It was assembled with 20% commercial Pt/C material into a two-electrode system for all-water decomposition, and the decomposition voltage at 10 mA cm-2 was 1.81 V. From the electronic configuration microscopic point of view, the introduction of iron ions changed the original synergistic effect for Co-S-Co, which more easily led to the formation of high-valence Co3+ and finally produced highly active electrocatalytic sites. From a macroscopic point of view, the material produced in situ during the electrochemical reaction process not only retains the original 2D layered structure but also utilizes bubbles to produce a loose structure with defective sites. These structural features are advantageous because they provide not only an abundance of active sites and permeable channels but also the necessary interfaces and electron-transport channels for the formation of electrostatic charge-separation layers, making it easier to intercalate and delaminate the hydroxide ions. Furthermore, the changed hydroxyl ions and nitrogen and sulfur atoms on the channel surface may operate as interaction sites, increasing the surface characteristics, facilitating electron transfer, and reducing electron-transfer resistance. To summarize, the rational design of sulfur-containing layered MOF materials directly as water-splitting catalysts is a crucial next step in developing cost-effective, environmentally friendly, and low-energy-consumption electrocatalysts based on the findings of this study.
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