NiSX/carbon black hybrids for efficient electrochemical oxidation of 5-hydroxymethyfurfural to 2,5-furandicarboxylic acid

IF 5.2 2区 化学 Q1 CHEMISTRY, APPLIED Catalysis Today Pub Date : 2024-07-29 DOI:10.1016/j.cattod.2024.114967
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Abstract

NiSX stands out in the electrochemical oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) due to the favorable conductivity and diverse chemical composition. However, NiSX usually exhibits few exposed active sites and poor charge transfer kinetics. Moreover, during the electrochemical oxidation of HMF, the conductivity of the catalyst would decrease rapidly with the formation of oxidized Ni species, leading to a rapid decline in catalytic performance. Therefore, a series of NiSX/carbon black (CB) hybrids (NiSX/CB-n) were synthesized via a one-step solvent hydrothermal method in which NiSX displayed a large cubic block structure assembled from small nanosheets. Among the prepared catalysts, NiSX/CB-2, with the optimal amount of introduced CB, exhibited superior electrocatalytic activity for the oxidation of HMF, achieving 100% HMF conversion, 98% FDCA yield, and 100% Faradaic efficiency at 1.45 V (vs. RHE). The outstanding electrocatalytic activity of NiSX/CB-2 was attributed to the suitable CB doping, which not only enhanced the conductivity of catalyst but also separated the small nanosheets, preventing the formation of densely packed NiSX structure and increasing the specific surface area of catalyst, thereby exposing more active sites and improving the availability of material. Furthermore, the formation of C-S bonds facilitated charge interactions between NiSX and CB, promoting the transfer of charges during the electrolysis process and enhancing electrocatalytic kinetics. Open circuit potential tests demonstrated that the introduction of CB also strengthened the adsorption capacity of catalyst for HMF, further benefiting its electrocatalytic activity.

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用于将 5-羟甲基糠醛高效电化学氧化为 2,5-呋喃二甲酸的 NiSX/炭黑混合物
NiS 在 5-hydroxymethylfurfural (HMF) 到 2,5-呋喃二甲酸 (FDCA) 的电化学氧化过程中表现突出,这是因为它具有良好的导电性和多种化学成分。然而,NiS 通常暴露的活性位点较少,电荷转移动力学较差。此外,在 HMF 的电化学氧化过程中,催化剂的电导率会随着氧化镍的形成而迅速降低,导致催化性能迅速下降。因此,研究人员通过一步溶剂水热法合成了一系列 NiS/ 炭黑(CB)杂化物(NiS/CB-n),其中 NiS 呈大立方块状结构,由小纳米片组装而成。在所制备的催化剂中,NiS/CB-2(引入了最佳量的 CB)在 HMF 氧化过程中表现出优异的电催化活性,在 1.45 V(相对于 RHE)电压下,HMF 转化率达到 100%,FDCA 收率达到 98%,Faradaic 效率达到 100%。NiS/CB-2 杰出的电催化活性归功于适当的 CB 掺杂,CB 掺杂不仅增强了催化剂的导电性,而且分离了小纳米片,防止形成密集的 NiS 结构,增加了催化剂的比表面积,从而暴露出更多的活性位点,提高了材料的可用性。此外,C-S 键的形成促进了 NiS 和 CB 之间的电荷相互作用,推动了电解过程中的电荷转移,增强了电催化动力学。开路电位测试表明,CB 的引入还增强了催化剂对 HMF 的吸附能力,进一步提高了催化剂的电催化活性。
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来源期刊
Catalysis Today
Catalysis Today 化学-工程:化工
CiteScore
11.50
自引率
3.80%
发文量
573
审稿时长
2.9 months
期刊介绍: Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues. Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.
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