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用于在环境条件下将生物质衍生的5-(羟甲基)糠醛选择性电化学氢化为2,5-双(羟甲基)呋喃的还原金属纳米催化剂。

Reduced metal nanocatalysts for selective electrochemical hydrogenation of biomass-derived 5-(hydroxymethyl)furfural to 2,5-bis(hydroxymethyl)furan in ambient conditions.

作者信息

Muchharla Baleeswaraiah, Dikshit Moumita, Pokharel Ujjwal, Garimella Ravindranath, Adedeji Adetayo, Kumar Kapil, Cao Wei, Elsayed-Ali Hani, Sadasivuni Kishor Kumar, Al-Dhabi Naif Abdullah, Kumar Sandeep, Kumar Bijandra

机构信息

Department of Mathematics, Computer Science and Engineering Technology, Elizabeth City State University, Elizabeth City, NC, United States.

Laboratory of Environmental Sustainability and Energy Research (LESER), National Institute of Technology Delhi, New Delhi, India.

出版信息

Front Chem. 2023 Jun 20;11:1200469. doi: 10.3389/fchem.2023.1200469. eCollection 2023.

DOI:10.3389/fchem.2023.1200469
PMID:37408562
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10318534/
Abstract

Selective electrochemical hydrogenation (ECH) of biomass-derived unsaturated organic molecules has enormous potential for sustainable chemical production. However, an efficient catalyst is essential to perform an ECH reaction consisting of superior product selectivity and a higher conversion rate. Here, we examined the ECH performance of reduced metal nanostructures, i.e., reduced Ag (rAg) and reduced copper (rCu) prepared via electrochemical or thermal oxidation and electrochemical reduction process, respectively. Surface morphological analysis suggests the formation of nanocoral and entangled nanowire structure formation for rAg and rCu catalysts. rCu exhibits a slight enhancement in ECH reaction performance in comparison to the pristine Cu. However, the rAg exhibits more than two times higher ECH performance without compromising the selectivity for 5-(HydroxyMethyl) Furfural (HMF) to 2,5-bis(HydroxyMethyl)-Furan (BHMF) formation in comparison to the Ag film. Moreover, a similar ECH current density was recorded at a reduced working potential of 220 mV for rAg. This high performance of rAg is attributed to the formation of new catalytically active sites during the Ag oxidation and reduction processes. This study demonstrates that rAg can potentially be used for the ECH process with minimum energy consumption and a higher production rate.

摘要

生物质衍生的不饱和有机分子的选择性电化学氢化(ECH)在可持续化学生产方面具有巨大潜力。然而,高效的催化剂对于进行具有优异产物选择性和更高转化率的ECH反应至关重要。在此,我们研究了通过电化学或热氧化以及电化学还原过程分别制备的还原态金属纳米结构,即还原态银(rAg)和还原态铜(rCu)的ECH性能。表面形态分析表明,rAg和rCu催化剂分别形成了纳米珊瑚和缠结纳米线结构。与原始铜相比,rCu在ECH反应性能上略有增强。然而,与银膜相比,rAg在不影响5-(羟甲基)糠醛(HMF)生成2,5-双(羟甲基)呋喃(BHMF)的选择性的情况下,ECH性能高出两倍以上。此外,对于rAg,在220 mV的降低工作电位下记录到了相似的ECH电流密度。rAg的这种高性能归因于在银氧化和还原过程中形成了新的催化活性位点。这项研究表明,rAg有可能以最低的能量消耗和更高的生产率用于ECH过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bb/10318534/4c67a89861b9/fchem-11-1200469-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bb/10318534/5ac9db49a1b7/fchem-11-1200469-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bb/10318534/d021569aa41c/fchem-11-1200469-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bb/10318534/8d02d1a51a80/fchem-11-1200469-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bb/10318534/4c67a89861b9/fchem-11-1200469-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bb/10318534/5ac9db49a1b7/fchem-11-1200469-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bb/10318534/d021569aa41c/fchem-11-1200469-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bb/10318534/8d02d1a51a80/fchem-11-1200469-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bb/10318534/4c67a89861b9/fchem-11-1200469-g004.jpg

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