Gravvani Konstantina, Solakidou Maria, Louloudi Maria
University of Ioannina, Department of Chemistry, Laboratory of Biomimetic Catalysis & Hybrid Materials, 45110, Ioannina, Greece.
Chemistry. 2025 Mar 17;31(16):e202404440. doi: 10.1002/chem.202404440. Epub 2025 Feb 5.
The use of hybrids, developed by grafting homogeneous catalysts onto supporting materials, has already demonstrated significant potential in various catalytic processes. These systems combine the advantages of homogeneous catalysts, such as high activity and selectivity, with those of solid supports, including enhanced recyclability. Catalytic hydrogen (H) production via dehydrogenation of C1 organic molecules targeting its use in fuel cells is a contemporary scientific issue directly connected with climate crisis. Here, Iminophospine hybrid [SiO@benzNP] and its reduced analogue [SiO@benzNHP] were synthesized, covalently grafted on colloidal SiO, fully characterized (FT-IR, RAMAN, TGA, ssNMR, BET), and used for in-situ synthesis of [SiO@benzNP-Fe] and [SiO@benzNHP-Fe] catalytic complexes for H production from formic acid (HCOOH) and formaldehyde (HCHO), at 80 °C. In HCOOH, both heterogenized catalysts exhibit high selectivity, producing H and CO in a 1 : 1 ratio, without CO contamination, making them ideal for fuel cell applications. [SiO₂@benzNHP-Fe] catalyst demonstrated superior performance in both substates. In HCOOH dehydrogenation, over 82,000 turnover number (TONs) were achieved and retained its efficiency for over five cycles, without any further metal addition. In HCHO dehydrogenation, it showed excellent efficiency as well, achieving 1.3 L of pure H with TONs exceeding 7,000, in 3 consecutive uses. Advanced spectroscopic analysis confirmed the stability and structural integrity of the catalysts, linking the Schiff base reduction and N-H groups to enhanced activity, durability and reusability. This study demonstrates the potential of hybrid materials with non-noble metals for cost-effective and sustainable H production, paving the way for scalable renewable energy solutions.
通过将均相催化剂接枝到载体材料上而开发的杂化材料,已在各种催化过程中展现出巨大潜力。这些体系将均相催化剂的优势(如高活性和选择性)与固体载体的优势(包括增强的可回收性)结合在一起。通过C1有机分子脱氢生产催化氢(H)以用于燃料电池,是一个与气候危机直接相关的当代科学问题。在此,合成了亚氨基膦杂化材料[SiO@benzNP]及其还原类似物[SiO@benzNHP],将其共价接枝到胶体SiO上,进行了全面表征(傅里叶变换红外光谱、拉曼光谱、热重分析、固体核磁共振、比表面积分析),并用于原位合成[SiO@benzNP-Fe]和[SiO@benzNHP-Fe]催化配合物,以在80°C下由甲酸(HCOOH)和甲醛(HCHO)生产H。在HCOOH中,两种多相催化剂均表现出高选择性,以1:1的比例生成H和CO,无CO污染,使其成为燃料电池应用的理想选择。[SiO₂@benzNHP-Fe]催化剂在两种底物中均表现出优异性能。在HCOOH脱氢反应中,实现了超过82,000的周转数(TONs),并在五个循环以上保持其效率,无需进一步添加金属。在HCHO脱氢反应中,它也表现出优异的效率,在连续三次使用中,实现了1.3升纯H,TONs超过7,000。先进的光谱分析证实了催化剂的稳定性和结构完整性,将席夫碱还原和N-H基团与增强的活性、耐久性和可重复使用性联系起来。这项研究证明了含非贵金属的杂化材料在经济高效且可持续的H生产方面的潜力,为可扩展的可再生能源解决方案铺平了道路。