Tailoring the selective adsorption sites of NiMoO by Ni particles for biomass upgrading assisted hydrogen production
作者机构:Guangxi Key Laboratory of Electrochemical Energy MaterialsSchool of Chemistry and Chemical EngineeringSchool of Physical Science and TechnologyGuangxi UniversityNanning 530004GuangxiChina
出 版 物:《Journal of Energy Chemistry》 (能源化学(英文版))
年 卷 期:2023年第86卷第11期
页 面:480-489,I0010页
核心收录:
学科分类:081702[工学-化学工艺] 081704[工学-应用化学] 07[理学] 070304[理学-物理化学(含∶化学物理)] 08[工学] 0817[工学-化学工程与技术] 0703[理学-化学]
基 金:supported by the National Natural Science Foundation of China(22162004) the Natural Science Foundation of Guangxi(2022JJD120011) the High-performance Computing Platform of Guangxi University
主 题:5-Hydroxymethylfurfural electrooxidation Hydrogen evolution reaction Kinetics Nanowires Catalyst
摘 要:5-Hydroxymethylfurfural electrooxidation reaction(HMFOR)is a promising route to produce valueadded chemicals from *** it involves HMF adsorption and C-H/O-H cleavage,understanding the adsorption behavior and catalytic process of organic molecules on catalysts is ***,the selective adsorption sites of NiMoO are tuned by Ni particles for HMFOR-assisted *** and theoretical calculation results indicate that the synergistic interaction between Ni and NiMoO optimizes the adsorption/desorption of HMF/intermediates/2,5-furandicarboxylic acid(FDCA)and promotes the C-H/O-H bond cleavage,thereby improving the HMFOR kinetics(kNiMoO-Ni/kNiMoO=1.97)and FDCA selectivity(99.3%).When coupled as a two-electrode system,it can drive efficient HMF conversion(FDCA yield:98.5%)and H2production(Faradaic efficiency:99.1%)at 1.45 *** work thus offers a strategy to tune the adsorption sites of catalyst for efficient HMFOR-assisted H2production.