文献类型：期刊文献

中文题名：Rh掺杂的Cu纳米线催化剂促进5-羟甲基糠醛电催化加氢

英文题名：Rh-dispersed Cu nanowire catalyst for boosting electrocatalytic hydrogenation of 5-hydroxymethylfurfural

作者：张文飞[1,2];齐宴宾[2];赵渊[1];葛胜鑫[2];董磊[1];沈建华[2];江宏亮[1];李春忠[1,2]

机构：[1]East China Univ Sci & Technol, Shanghai Engn Res Ctr Hierarch Nanomat, Sch Chem Engn, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Sch Mat Sci & Engn, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China

年份：2023

卷号：68

期号：19

起止页码：2190

中文期刊名：Science Bulletin

外文期刊名：科学通报（英文版）

收录：CSTPCD;;EI(收录号：20233414605376);Scopus;WOS:【SCI-EXPANDED(收录号:WOS:001097887200001)】；CSCD:【CSCD2023_2024】；PubMed;

基金：This work was supported by the National Key R&D Program of China (2022YFB3808400) , the National Natural Science Foundation of China (22222804 and U22B20143) , the Science and Technology Commission of Shanghai Municipality (22dz1205900) , and the Shanghai Municipal Science and Technology Major Project. The authors thank the Shanghai Synchrotron Radiation Facility (BL14W1, SSRF) .

语种：中文

中文关键词：催化剂设计;高选择性;活性氢;水解离;HMF;可再生能源;可再生资源;催化转化;

外文关键词：Electrocatalysis;Biomass;Water dissociation;Hydrogenation;Value-added products

摘要：生物质是世界上广泛存在的可再生资源,可以转化成高价值燃料和化学品.基于可再生能源产生的电力,将生物质衍生的5-羟甲基糠醛(HMF)电催化转化为2,5-呋喃二甲醇(BHMF)具有重要的研究意义和应用价值.HMF在电转化过程中容易发生二聚反应,从而导致BHMF的选择性较低,产物分离难度大.因此,探索获得高选择性BHMF的高效催化体系极为重要.在此,本文报道了Rh掺杂的Cu纳米线催化剂,其在HMF电还原为BHMF反应中表现出较高的转化率,且有效抑制了二聚反应的发生.动力学实验和原位光谱研究表明,Rh的引入可以有效促进水解离形成活性氢物种,促进5-羟甲基糠醛电催化加氢并抑制其二聚.此催化剂设计策略可以拓展到其他生物质衍生分子的电催化转化过程中.
Electrocatalytic conversion of biomass-derived 5-hydroxymethylfurfural(HMF)to 2,5-bis(hydroxymethyl)furan(BHMF)presents a compelling strategy for the production of premium chemicals via the utilization of renewable energy sources.Exploring efficient catalytic systems to obtain highly selective BHMF has remained a giant challenge.A design strategy is proposed here to regulate active hydrogen(Hads)production in rhodium(Rh)nanoparticles grown on Cu nanowires(RhCu NWs)catalyst,which achieves a faradaic efficiency(FE)of 92.6%in the electrocatalytic reduction of HMF to BHMF at-20 mA cm-2 with no degradation in performance after 8 cycles.Kinetic investigations and electron spin resonance(ESR)spectroscopy reveal that the incorporation of Rh accelerates the water dissociation and facilitates the generation of Hads.In situ attenuated total reflection surface enhanced infrared absorption spectroscopy(ATR-SEIRAS)further demonstrates that the Rh component boosts the proportion of ordered weakly hydrogen-bonded water molecules on the catalyst surface,which is much easier to dissociate.The construction of an interfacial Hads-rich environment promotes the HMF intermediates binding with Hads to BMHF,thereby suppressing the formation of undesired dimers.This work demonstrates the promise of altering the interfacial water environment as a strategy to boost the electrosynthetic properties of biomass-derived products toward value-added outcomes.