Ding Shichao, Lyu Zhaoyuan, Zhong Hong, Liu Dong, Sarnello Erik, Fang Lingzhe, Xu Mingjie, Engelhard Mark H, Tian Hangyu, Li Tao, Pan Xiaoqing, Beckman Scott P, Feng Shuo, Du Dan, Li Jin-Cheng, Shao Minhua, Lin Yuehe
School of Mechanical and Materials Engineering, Washington State University, Pullman, WA, 99164, USA.
Department of Chemistry and Biochemistry, Northern Illinois University, DeKalb, IL, 60115, USA.
Small. 2021 Apr;17(16):e2004454. doi: 10.1002/smll.202004454. Epub 2020 Dec 11.
Carbon-based single-atom catalysts (CSACs) have recently received extensive attention in catalysis research. However, the preparation process of CSACs involves a high-temperature treatment, during which metal atoms are mobile and aggregated into nanoparticles, detrimental to the catalytic performance. Herein, an ion-imprinting derived strategy is proposed to synthesize CSACs, in which isolated metal-nitrogen-carbon (Me-N -C ) moiety covalently binds oxygen atoms in Si-based molecular sieve frameworks. Such a feature makes Me-N -C moiety well protected/confined during the heat treatment, resulting in the final material enriched with single-atom metal active sites. As a proof of concept, a single-atom Fe-N-C catalyst is synthesized by using this ion-imprinting derived strategy. Experimental results and theoretical calculations demonstrate high concentration of single FeN active sites distributed in this catalyst, resulting in an outstanding oxygen reduction reaction (ORR) performance with a half-wave potential of 0.908 V in alkaline media.
碳基单原子催化剂(CSACs)最近在催化研究中受到了广泛关注。然而,CSACs的制备过程涉及高温处理,在此过程中金属原子具有流动性并聚集成纳米颗粒,这对催化性能不利。在此,提出了一种离子印迹衍生策略来合成CSACs,其中孤立的金属-氮-碳(Me-N-C)部分与硅基分子筛骨架中的氧原子共价结合。这一特性使得Me-N-C部分在热处理过程中得到良好的保护/限制,从而使最终材料富含单原子金属活性位点。作为概念验证,采用这种离子印迹衍生策略合成了单原子Fe-N-C催化剂。实验结果和理论计算表明,该催化剂中分布着高浓度的单FeN活性位点,在碱性介质中具有0.908 V的半波电位,氧还原反应(ORR)性能优异。