Arnau Marc, Pielsticker Lukas, Hetaba Walid, Casanovas Jordi, Turon Pau, Alemán Carlos, Sans Jordi
Departament d'Enginyeria Química, EEBE, Universitat Politècnica de Catalunya, C/Eduard Maristany, 10-14, Ed. I2, 08019, Barcelona, Spain.
Barcelona Research Center in Multiscale Science and Engineering, Universitat Politècnica de Catalunya, C/Eduard Maristany, 10-14, 08019, Barcelona, Spain.
ACS Catal. 2025 Jun 12;15(13):11150-11162. doi: 10.1021/acscatal.5c02426. eCollection 2025 Jul 4.
Catalytically active hydroxyapatite (ca-HAp) decorated with zirconia nanoparticles (ZrO NPs) is presented as a nanocomposite catalyst (ca-HAp/ZrO) capable of performing highly efficient nitrogen to ammonia (N-to-NH) fixation reactions under mild conditions. Accordingly, reactions were carried out in a batch reactor operating at 120 °C, 6 bar of N, and 20 mL of water, under UV irradiation (14 W) for 72 h. The yield of NH obtained was 1.592 ± 0.146 mmol·g , which represents a N fixation efficiency of 6.4%. Near ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) studies under conditions (i.e., at elevated pressure and temperature and during UV irradiation) and density functional theory simulations (DFT) allowed us to elucidate the catalytic mechanism of the system. The ca-HAp/ZrO nanocomposites exhibit a strong synergy arising from the initial photoactivation of N by means of the π-backdonation mechanism in ZrO (N is anchored by four Zr atoms) followed by the dinitrogen spillover toward the Ca-(I) binding sites. Such sites, preferentially exposed in the (001) crystallographic planes of ca-HAp, show high activity due to the enhanced electron transfer properties of ca-HAp. These catalytic nanocomposites represent a viable alternative to the conventional catalysts used for N-to-NH fixation reactions.
负载氧化锆纳米颗粒(ZrO NPs)的具有催化活性的羟基磷灰石(ca-HAp)作为一种纳米复合催化剂(ca-HAp/ZrO)被提出,该催化剂能够在温和条件下高效地进行氮气到氨(N-to-NH)的固定反应。因此,反应在间歇式反应器中进行,反应条件为120℃、6巴氮气和20毫升水,在14瓦紫外线照射下反应72小时。获得的NH产量为1.592±0.146 mmol·g ,这代表了6.4%的氮固定效率。在特定条件下(即在高压和高温以及紫外线照射期间)进行的近常压X射线光电子能谱(NAP-XPS)研究和密度泛函理论模拟(DFT)使我们能够阐明该体系的催化机理。ca-HAp/ZrO纳米复合材料表现出很强的协同作用,这种协同作用源于通过ZrO中的π-反馈机制对N进行初始光活化(N由四个Zr原子锚定),随后双氮溢流到Ca-(I)结合位点。这些位点优先暴露在ca-HAp的(001)晶面上,由于ca-HAp增强的电子转移特性而表现出高活性。这些催化纳米复合材料是用于N-to-NH固定反应的传统催化剂的可行替代品。