Ma Junqing, Luo Wenshu, Wang Xunlu, Yu Xu, Wang Jiacheng Jayden, Hu Huashuai, Du Hanxiao, Zeng Jianrong, Chen Wei, Yang Minghui, Wang Jiacheng, Cui Xiangzhi
State Key Laboratory of High-Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics Chinese Academy of Sciences, Shanghai, 200050, People's Republic of China.
Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing, 100049, People's Republic of China.
Nanomicro Lett. 2025 Aug 25;18(1):39. doi: 10.1007/s40820-025-01893-z.
Investigating structural and hydroxyl group effects in electrooxidation of alcohols to value-added products by solid-acid electrocatalysts is essential for upgrading biomass alcohols. Herein, we report efficient electrocatalytic oxidations of saturated alcohols (C-C) to selectively form formate using NiCo hydroxide (NiCo-OH) derived NiCoO solid-acid electrocatalysts with balanced Lewis acid (LASs) and Brønsted acid sites (BASs). Thermal treatment transforms BASs-rich (89.6%) NiCo-OH into NiCoO with nearly equal distribution of LASs (53.1%) and BASs (46.9%) which synergistically promote adsorption and activation of OH and alcohol molecules for enhanced oxidation activity. In contrast, BASs-enriched NiCo-OH facilitates formation of higher valence metal sites, beneficial for water oxidation. The combined experimental studies and theoretical calculation imply the oxidation ability of C-C alcohols increases as increased number of hydroxyl groups and decreased HOMO-LUMO gaps: methanol (C) < ethylene glycol (C) < glycerol (C) < meso-erythritol (C) < xylitol (C) < sorbitol (C), while the formate selectivity shows the opposite trend from 100 to 80%. This study unveils synergistic roles of LASs and BASs, as well as hydroxyl group effect in electro-upgrading of alcohols using solid-acid electrocatalysts.
研究固体酸电催化剂将醇电氧化为增值产品中的结构和羟基效应对于生物质醇的升级至关重要。在此,我们报道了使用具有平衡的路易斯酸(LASs)和布朗斯特酸位点(BASs)的由氢氧化镍钴(NiCo-OH)衍生的NiCoO固体酸电催化剂,将饱和醇(C-C)高效电催化氧化以选择性地形成甲酸盐。热处理将富含BASs(89.6%)的NiCo-OH转变为LASs(53.1%)和BASs(46.9%)分布近乎相等的NiCoO,它们协同促进OH和醇分子的吸附和活化以增强氧化活性。相比之下,富含BASs的NiCo-OH有利于形成更高价态的金属位点,有利于水氧化。结合实验研究和理论计算表明,C-C醇的氧化能力随着羟基数量的增加和HOMO-LUMO能隙的减小而增加:甲醇(C)<乙二醇(C)<甘油(C)<内消旋赤藓糖醇(C)<木糖醇(C)<山梨醇(C),而甲酸盐选择性呈现从100%到80%的相反趋势。本研究揭示了LASs和BASs的协同作用以及在使用固体酸电催化剂对醇进行电升级中的羟基效应。