Ultra‐Efficient, Non‐Aqueous Solar Urea Synthesis Over Chemical Environment‐Orchestrated Ru
Abstract
ABSTRACT Sunlight‐driven catalytic urea synthesis offers a sustainable ambient‐pressure pathway for fertilizer production, but energy‐intensive liquid‐urea separation limits its practicality. Non‐aqueous photothermal urea synthesis from gaseous NH 3 and CO 2 offers a promising alternative, though molecular activations under dry and mild conditions remain challenging. Here, we report photothermal urea synthesis over Ru nanocrystals supported on acidic Al 2 O 3 , basic MgO, and neutral SiO 2 , achieving an optimal rate of 2745.71 ± 46.91 µmol urea g Ru −1 h −1 , an order‐of‐magnitude higher than state‐of‐the‐arts at ambient pressure. Mechanistic studies elucidate a reaction pathway, initiated photothermally by Ru and orchestrated by an acidic chemical environment that promoted the availability of reactants, in which exothermic N–H bond dissociation of NH 3 matches endothermic C–N coupling with CO 2 in a thermodynamically favorable manner. This work demonstrates an ultra‐efficient pioneering synthesis paradigm under near‐ambient conditions, circumventing industrial reliance on harsh thermochemical conditions.
Article Details
Authors (9)
Guanshu Zhao
Department of Chemistry, University of Toronto
Chengliang Mao
State Key Laboratory of Green Papermaking and Resource Recycling, Shanghai Engineering Research Center of Solid Waste Treatment and Resource Recovery, School of Environmental Science and Engineering
Shuai Yue
Ministry of Education Key Laboratory of Pollution Processes and Environmental Criteria, College of Environmental Science and Engineering, Nankai University
Shufang Ji
Department of Chemistry
Lei Wu
Andrew Wang
Kaiwen Zheng
Chengqi Tao
Department of Chemistry Solar Fuels Group University of Toronto Toronto Ontario Canada
Geoffrey Ozin
Department of Chemistry Solar Fuels Group University of Toronto Toronto Ontario Canada