首页|期刊导航|燃料化学学报(中英文)|镍钴锰硫化物电催化氧化5-羟甲基糠醛性能研究

镍钴锰硫化物电催化氧化5-羟甲基糠醛性能研究OA北大核心

Performance study on electrocatalytic oxidation of 5-hydroxymethylfurfural by nickel-cobalt-manganese sulfide

中文摘要英文摘要

利用生物质衍生物 5-羟甲基糠醛(HMF)电催化氧化制备 2,5-呋喃甲酸(FDCA)是一种极具吸引力的可再生绿色发展策略,开发高性能、低成本的HMF电催化剂具有重要意义.本研究采用两步水热法,在泡沫镍(NF)基底上制备了硫化物NiCoMnx-Sy/NF电极材料,考察不同S2-浓度硫化对电催化HMF氧化性能的影响.得益于大的比表面积、较强的电荷转移能力和快的反应动力学,NiCoMn4-S0.10/NF在含有 10 mmol/L HMF的 1 mol/L KOH溶液中表现出优异的HMF氧化性能,在 1.37 V时可以实现 99.41%的HMF转化率、98.84%的FDCA产率和 97.31%的法拉第效率(FE),并在重复使用 10次后仍能保持较高的活性.

As countries'demand for fossil fuels and resources continues to increase,it is particularly critical to reduce dependence on these energy sources and actively promote new green renewable resources.5-Hydroxymethylfurfural(HMF)has been identified as one of the important biomass platform chemicals,which can be converted into a series of valuable chemicals through reaction.Its typical oxidation product,2,5-furanediformic acid(FDCA),can replace petroleum-based terephthalic acid(TPA),and also has important applications in metal-organic framework materials,chemical synthesis,etc.This is essential for mitigating the global fossil resource crisis and achieving carbon peaking and carbon neutrality goals.However,traditional HMF thermochemical oxidation typically requires reactions under harsh conditions to achieve high HMF conversion and FDCA yield.In comparison,the electrocatalytic oxidation of 5-hydroxymethylfurfural(HMFOR)is a clean and environmentally friendly method with mild reaction conditions,simple operation,and high energy efficiency.Its theoretical oxidation potential is 0.3 V,which is lower than the kinetic slow OER(1.23 V).It can replace OER in anodic reactions and generate H2 and high value-added chemicals at the same time,improving energy efficiency.Therefore,it is of great significance to design electrocatalysts with high catalytic activity,high energy utilization and low cost.Transition metal sulfides have attracted much attention due to their abundant raw material storage,simple preparation methods,and high electrical conductivity.Previous studies have shown that transition metal sulfides form layered structures under the influence of van der Waals forces,which can expose more activity check points and increase the specific surface area of activity to participate in the reaction,thereby improving the electrocatalytic performance.Studies have shown that multi-component metal sulfides tend to exhibit higher HMFOR activity than single metal sulfides,due to the synergistic effect of multiple metal ions and the promotion of multiple oxidation-reduction reactions by multiple valence states.Compared with the adhesive required for powder catalysts,the catalyst can be directly grown on conductive substrates such as nickel foam(NF),carbon cloth(CC),and copper foam(CF)with high specific surface area,so that the catalyst can be exposed to more active sites and is more stable.Based on this,NiCoMnx/NF precursors with different Ni/Co ratios were prepared by hydrothermal method using three-dimensional nickel foam as the substrate,and then they were hydrothermally vulcanized to obtain NiCoMnx-Sy/NF sulfides at different concentrations.The catalysts were tested by linear scanning voltammetry(LSV),cyclic voltammetry(CV),electrochemical impedance spectroscopy(EIS)and open circuit potential test(OCPT).The catalysts were characterized by X-ray powder diffraction(XRD),X-ray photoelectron spectroscopy(XPS),scanning electron microscopy(SEM)and specific surface area analysis(BET).The results of electrochemical analysis show that NiCoMn4/NF has relatively better HMFOR performance,and NiCoMn4/NF with better comprehensive performance is selected for the next vulcanization process.NiCoMn4-S0.10/NF with vulcanization concentration of 10 mmol/L has excellent HMFOR performance,and HMFOR reaction is carried out at 300 r/min rotational speed and 1.37 V voltage.The conversion rate of HMF,the yield of FDCA and FE can reach 99.41%,98.84%and 97.31%,respectively.And after 10 consecutive HMF electrolytic oxidation experiments,the catalytic efficiency did not decrease significantly,indicating that NiCoMn4-S0.10/NF has good cycle durability.The results of catalyst characterization showed that the conductivity and specific surface area of the catalyst increased greatly after vulcanization.The surface reconfiguration of the sulfide on the catalyst surface to(Ni,Co)OOH occurs,and(Ni,Co)OOH is the true active site of HMFOR.At the same time,Mn doping can add a new adsorption site for HMF oxidation,and promote the adsorption of HMF molecules on the surface of NiCoMn4-S0.10/NF,which makes NiCoMn4-S0.10/NF have excellent HMFOR performance.

殷啸天;包桂蓉;罗嘉;于方正;潘浩伟;吉学武;谈诚

昆明理工大学冶金与能源工程学院,云南 昆明 650093||省部共建复杂有色金属资源清洁利用国家重点实验室,云南 昆明 650093昆明理工大学冶金与能源工程学院,云南 昆明 650093||省部共建复杂有色金属资源清洁利用国家重点实验室,云南 昆明 650093中国科学院西双版纳热带植物园昆明分部,云南 昆明 650223昆明理工大学冶金与能源工程学院,云南 昆明 650093||省部共建复杂有色金属资源清洁利用国家重点实验室,云南 昆明 650093昆明理工大学冶金与能源工程学院,云南 昆明 650093||省部共建复杂有色金属资源清洁利用国家重点实验室,云南 昆明 650093昆明理工大学冶金与能源工程学院,云南 昆明 650093||省部共建复杂有色金属资源清洁利用国家重点实验室,云南 昆明 650093昆明理工大学冶金与能源工程学院,云南 昆明 650093||省部共建复杂有色金属资源清洁利用国家重点实验室,云南 昆明 650093

化学工程

5-羟甲基糠醛电催化氧化硫化物S2-浓度

5-hydroxymethylfurfuralelectrocatalytic oxidationsulfideS2-concentration

《燃料化学学报(中英文)》 2025 (5)

625-637,13

The project was supported by National Natural Science Foundation of China(52466014)and Yunnan Major Scientific and Technological Projects(202302AG050011). 国家自然科学基金(52466014)和云南省重大科技项目(202302AG050011)资助

10.3724/2097-213X.2024.JFCT.0033

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