Concurrent Ammonia Synthesis and Alcohol Oxidation Boosted by Glutathione-Capped Quantum Dots under Visible Light.
Shu-Lin MengJia-Hao LiChen YeYu-Lin YinXin-Ling ZhangChen ZhangXu-Bing LiChen-Ho TungLi-Zhu WuPublished in: Advanced materials (Deerfield Beach, Fla.) (2024)
Mother nature accomplishes efficient ammonia synthesis via cascade N 2 oxidation by lightning strikes followed with enzyme-catalyzed nitrogen oxyanion (NO x - , x = 2,3) reduction. The protein environment of enzymatic centers for NO x - -to-NH 4 + process greatly inspires the design of glutathione-capped (GSH) quantum dots (QDs) for ammonia synthesis under visible light (440 nm) in tandem with plasma-enabled N 2 oxidation. Mechanistic studies reveal that GSH induces positive shift of surface charge to strengthen the interaction between NO x - and QDs. Upon visible light irradiation of QDs, the balanced and rapid hole and electron transfer furnish GS·radicals for 2e - /2H + alcohol oxidation and H·for 8e - /10H + NO 3 - -to-NH 4 + reduction simultaneously. For the first time, mmol-scale ammonia synthesis is realized with apparent quantum yields of 5.45% ± 0.64%, and gram-scale synthesis of value-added acetophenone and NH 4 Cl proceeds with 1:4 stoichiometry and stability, demonstrating promising multielectron and multiproton ammonia synthesis efficiency and sustainability with nature-inspired artificial photocatalysts.