Structure-Oriented Electrochemical Synthesis of Layered Double Hydroxide Electrocatalytic Materials for 5-Hydroxymethylfurfural Oxidation

IF 7.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Yixuan Feng, Richard L. Smith Jr., Feng Shen* and Xinhua Qi*, 
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Abstract

Quantitative conversion of biomass-derived 5-hydroxymethylfurfural (HMF) to downstream chemicals at room temperature is a critical milestone in sustainable chemistry. Herein, conversion of metal–organic framework (MOF) structures into layered double hydroxide (LDH) electrocatalytic materials (NiFe-LDH/MOF) was fabricated using NiFe-MOF as a structure-oriented sacrificial template via an in situ electrochemical strategy. Results showed that the electrochemical method to convert the material structures not only overcame inherent limitations of MOF structures (inaccessible sites and low conductivity) but also eliminated LDH self-stacking. Hierarchical NiFe-LDH/MOF exhibited high catalytic activity and selectivity in the electrooxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA), which is due to the increased number of catalytically active sites and the extended electron transport channels of uniformly dispersed LDH nanosheets. Optimized Ni2Fe1-LDH/MOF materials achieved FDCA yields of 99% with Faraday efficiencies of 99% in 1 M KOH with 50 mM HMF at an applied potential of 1.40 V vs reversible hydrogen electrode at ambient temperature. This work demonstrates a promising method for fabricating LDH electrocatalytic materials from MOF structures and shows a proof of principle for selective oxidation of HMF to FDCA.

Abstract Image

以结构为导向合成用于 5-羟甲基糠醛氧化的层状双氢氧化物电催化材料
在室温下将生物质衍生的 5-hydroxymethylfurfural (HMF) 定量转化为下游化学品是可持续化学的一个重要里程碑。在此,我们以 NiFe-MOF 为结构导向的牺牲模板,通过原位电化学策略将金属有机框架(MOF)结构转化为层状双氢氧化物(LDH)电催化材料(NiFe-LDH/MOF)。结果表明,通过电化学方法转换材料结构不仅克服了 MOF 结构的固有局限性(难以获得的位点和低导电性),而且消除了 LDH 自堆叠现象。分层 NiFe-LDH/MOF 在将 5-hydroxymethylfurfural (HMF) 电氧化为 2,5-呋喃二甲酸 (FDCA) 的过程中表现出很高的催化活性和选择性,这是由于均匀分散的 LDH 纳米片增加了催化活性位点的数量并扩展了电子传输通道。优化后的 Ni2Fe1-LDH/MOF 材料在 1 M KOH 和 50 mM HMF 溶液中的 FDCA 产率达到 99%,法拉第效率达到 99%,对可逆氢电极的施加电位为 1.40 V,环境温度为 1.40 V。这项工作展示了一种利用 MOF 结构制造 LDH 电催化材料的可行方法,并证明了将 HMF 选择性氧化为 FDCA 的原理。
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来源期刊
ACS Sustainable Chemistry & Engineering
ACS Sustainable Chemistry & Engineering CHEMISTRY, MULTIDISCIPLINARY-ENGINEERING, CHEMICAL
CiteScore
13.80
自引率
4.80%
发文量
1470
审稿时长
1.7 months
期刊介绍: ACS Sustainable Chemistry & Engineering is a prestigious weekly peer-reviewed scientific journal published by the American Chemical Society. Dedicated to advancing the principles of green chemistry and green engineering, it covers a wide array of research topics including green chemistry, green engineering, biomass, alternative energy, and life cycle assessment. The journal welcomes submissions in various formats, including Letters, Articles, Features, and Perspectives (Reviews), that address the challenges of sustainability in the chemical enterprise and contribute to the advancement of sustainable practices. Join us in shaping the future of sustainable chemistry and engineering.
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