Sun Jianguo, Yang Jing, Wang Tuo, Zhang Song Lin, Yuan Hao, Zang Wenjie, Liu Yu, Liu Ximeng, Wang Wanwan, Xi Shibo, Kirk Chin Ho, Wang Haimei, Wang Junhui, Wang Xingyang, Bhat Usha, Liu Zhaolin, Wang Shijie, Zhang Yong-Wei, Wang John
Department of Materials Science and Engineering, National University of Singapore, Singapore 117574, Singapore.
Institute of High Performance Computing (IHPC), Agency for Science, Technology and Research (A*STAR), 1 Fusionopolis Way, #16-16 Connexis, Singapore 138632, Republic of Singapore.
Nano Lett. 2024 May 1;24(17):5206-5213. doi: 10.1021/acs.nanolett.4c00455. Epub 2024 Apr 22.
Single Atoms Catalysts (SACs) have emerged as a class of highly promising heterogeneous catalysts, where the traditional bottom-up synthesis approaches often encounter considerable challenges in relation to aggregation issues and poor stability. Consequently, achieving densely dispersed atomic species in a reliable and efficient manner remains a key focus in the field. Herein, we report a new facile electrochemical knock-down strategy for the formation of SACs, whereby the metal Zn clusters are transformed into single atoms. While a defect-rich substrate plays a pivotal role in capturing and stabilizing isolated Zn atoms, the feasibility of this novel strategy is demonstrated through a comprehensive investigation, combining experimental and theoretical studies. Furthermore, when studied in exploring for potential applications, the material prepared shows a remarkable improvement of 58.21% for the Li storage and delivers a capacity over 300 Wh kg after 500 cycles upon the transformation of Zn clusters into single atoms.
单原子催化剂(SACs)已成为一类极具前景的多相催化剂,传统的自下而上合成方法在聚集问题和稳定性差方面常常面临巨大挑战。因此,以可靠且高效的方式实现原子物种的密集分散仍然是该领域的关键重点。在此,我们报告了一种用于形成SACs的新型简便电化学拆解策略,通过该策略金属锌簇被转化为单原子。虽然富含缺陷的基底在捕获和稳定孤立的锌原子方面起着关键作用,但通过结合实验和理论研究的全面调查证明了这种新策略的可行性。此外,在探索潜在应用时研究发现,在锌簇转化为单原子后,所制备的材料在锂存储方面有显著提升,提高了58.21%,并且在500次循环后容量超过300 Wh kg。