Chen Si, Huang Fang, Mao Lijie, Zhang Zhimin, Lin Han, Yan Qixin, Lu Xiangyu, Shi Jianlin
Department of Cardiology, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai, 200092, People's Republic of China.
Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050, People's Republic of China.
Nanomicro Lett. 2024 Oct 4;17(1):32. doi: 10.1007/s40820-024-01522-1.
The current single-atom catalysts (SACs) for medicine still suffer from the limited active site density. Here, we develop a synthetic method capable of increasing both the metal loading and mass-specific activity of SACs by exchanging zinc with iron. The constructed iron SACs (h-FNC) with a high metal loading of 6.27 wt% and an optimized adjacent Fe distance of ~ 4 Å exhibit excellent oxidase-like catalytic performance without significant activity decay after being stored for six months and promising antibacterial effects. Attractively, a "density effect" has been found at a high-enough metal doping amount, at which individual active sites become close enough to interact with each other and alter the electronic structure, resulting in significantly boosted intrinsic activity of single-atomic iron sites in h-FNCs by 2.3 times compared to low- and medium-loading SACs. Consequently, the overall catalytic activity of h-FNC is highly improved, with mass activity and metal mass-specific activity that are, respectively, 66 and 315 times higher than those of commercial Pt/C. In addition, h-FNCs demonstrate efficiently enhanced capability in catalyzing oxygen reduction into superoxide anion (O·) and glutathione (GSH) depletion. Both in vitro and in vivo assays demonstrate the superior antibacterial efficacy of h-FNCs in promoting wound healing. This work presents an intriguing activity-enhancement effect in catalysts and exhibits impressive therapeutic efficacy in combating bacterial infections.
目前用于医学的单原子催化剂(SACs)仍然存在活性位点密度有限的问题。在此,我们开发了一种合成方法,通过用铁交换锌来提高SACs的金属负载量和质量比活性。构建的铁单原子催化剂(h-FNC)具有6.27 wt%的高金属负载量和约4 Å的优化相邻铁间距,表现出优异的类氧化酶催化性能,储存六个月后活性无明显衰减,并具有良好的抗菌效果。引人注目的是,在足够高的金属掺杂量下发现了一种“密度效应”,此时单个活性位点彼此足够接近以相互作用并改变电子结构,导致h-FNCs中单个铁原子位点的本征活性相比低负载和中负载SACs显著提高了2.3倍。因此,h-FNC的整体催化活性得到高度提升,其质量活性和金属质量比活性分别比商业Pt/C高66倍和315倍。此外,h-FNCs在催化氧还原为超氧阴离子(O·)和谷胱甘肽(GSH)消耗方面表现出有效增强的能力。体外和体内试验均证明h-FNCs在促进伤口愈合方面具有优异的抗菌效果。这项工作展示了催化剂中一种有趣的活性增强效应,并在对抗细菌感染方面表现出令人印象深刻的治疗效果。