Tian Feiyang, Cheng Ruixue, Shang Yujing, Pan Le, Cui Xiuyun, Jiang Xuekai, Chen Kai, Zhao Huajun, Wang Kuiyuan
School of Chemistry and Chemical Engineering, Huangshan University, Huangshan, Anhui 245041, China.
Collaborative Innovation Center of Atmospheric Environment and Equipment Technology, Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, School of Environmental Science and Engineering, Nanjing University of Information Science & Technology, 210044 Nanjing, China.
Dalton Trans. 2025 May 13;54(19):7753-7764. doi: 10.1039/d5dt00418g.
Cucurbit[]urils, owing to their unique structural features, exhibit versatility in performing tasks such as adsorption, detection, and catalysis. However, the scope of their catalytic applications remains limited, primarily because most cucurbituril-based catalytic reactions take place in either aqueous or organic phases. In this study, we have successfully synthesized porous honeycomb composites of cucurbit[6]uril with cobalt and nickel (denoted as Co@Q[6] and Ni@Q[6], respectively) and applied them in a photothermal synergistic heterogeneous gas-solid reaction for the reduction of nitrogen to ammonia under mild conditions. This represents a groundbreaking achievement, as it is the first instance where a cucurbit[]uril-based material has demonstrated catalytic functionality in its solid-state form, thereby introducing a novel concept for the design and application of cucurbit[]uril-based photocatalysts. To characterize the structure of these composites, we employed a range of techniques including X-ray absorption fine structure (XAFS) analysis, transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and hydrogen temperature-programmed reduction (H-TPR). Our findings revealed that Ni@Q[6] exhibits higher photothermal catalytic ammonia synthesis activity compared to Co@Q[6]. This enhanced activity is attributed to the strong metal-support interaction (MSI) between Ni and Q[6], which facilitates electron transfer and nitrogen activation. Furthermore, the thermal source promotes the transition of electrons from the valence band to the conduction band, thereby enhancing the cleavage of the NN bond. Notably, the band gaps of Co@Q[6] and Ni@Q[6] are significantly reduced. In particular, Ni@Q[6] demonstrates the highest efficiency in electron-hole pair separation, as evidenced by photoluminescence (PL) and electrochemical impedance spectroscopy (EIS) measurements. Overall, Co/Ni@Q[6] provides an effective pathway for nitrogen reduction under mild conditions and advances the application of cucurbituril-based materials in photothermal catalysis. This work also contributes to the development of environmentally sustainable ammonia synthesis technology.
葫芦脲由于其独特的结构特征,在吸附、检测和催化等任务中表现出多功能性。然而,其催化应用的范围仍然有限,主要是因为大多数基于葫芦脲的催化反应发生在水相或有机相中。在本研究中,我们成功合成了葫芦[6]脲与钴和镍的多孔蜂窝状复合材料(分别表示为Co@Q[6]和Ni@Q[6]),并将它们应用于光热协同非均相气固反应,在温和条件下将氮气还原为氨。这代表了一项开创性的成就,因为这是首次有基于葫芦脲的材料以固态形式展现出催化功能,从而为基于葫芦脲的光催化剂的设计和应用引入了一个新概念。为了表征这些复合材料的结构,我们采用了一系列技术,包括X射线吸收精细结构(XAFS)分析、透射电子显微镜(TEM)、扫描电子显微镜(SEM)、X射线光电子能谱(XPS)和氢程序升温还原(H-TPR)。我们的研究结果表明,与Co@Q[6]相比,Ni@Q[6]表现出更高的光热催化氨合成活性。这种增强的活性归因于Ni和Q[6]之间强烈的金属-载体相互作用(MSI),这促进了电子转移和氮活化。此外,热源促进电子从价带跃迁到导带,从而增强N≡N键的裂解。值得注意的是,Co@Q[6]和Ni@Q[6]的带隙显著减小。特别是,光致发光(PL)和电化学阻抗谱(EIS)测量证明,Ni@Q[6]在电子-空穴对分离方面表现出最高效率。总体而言,Co/Ni@Q[6]为温和条件下的氮还原提供了一条有效途径,并推动了基于葫芦脲的材料在光热催化中的应用。这项工作也有助于环境可持续氨合成技术的发展。