Atomic interface effect of a single atom copper catalyst for enhanced oxygen reduction reactions. Issue 12 (20th November 2019)

• Record Type: Journal Article
• Authors: Jiang, Zhuoli; Sun, Wenming; Shang, Huishan; Chen, Wenxing; Sun, Tingting; Li, Haijing; Dong, Juncai; Zhou, Jing; Li, Zhi; Wang, Yu; Cao, Rui; Sarangi, Ritimukta; Yang, Zhengkun; Wang, Dingsheng; Zhang, Jiatao; Li, Yadong
• Is Part Of: Energy & environmental science. Volume 12:Issue 12(2019)
• Page Start: 3508
• Page End: 3514
• Publication Date: 2019-11-20
• Subjects: Energy conversion -- Periodicals; Fuel switching -- Periodicals; Environmental sciences -- Periodicals; Environmental chemistry -- Periodicals; 333.79
• DOI: 10.1039/c9ee02974e
• Languages: English
• ISSNs: 1754-5692

Abstract

Abstract : By the in situ X-ray absorption results, the gradually decrease of Cu oxidation state under applied potential implied that low-valence Cu (+1) species in the atomic interface of Cu–N4 –C8 S2 may work as the catalytic sites during an ORR process. Abstract : The regulation of catalytic activity in the oxygen reduction reaction (ORR) is significant to the development of metal–air batteries and other oxygen involving energy conversion devices. Herein, we propose an atomic interface strategy to construct a single atom copper catalyst (denoted as Cu-SA/SNC) which exhibits enhanced ORR activity with a half-wave potential of 0.893 V vs. RHE in alkaline media. Moreover, synchrotron-radiation-based X-ray absorption fine structure (XAFS) investigations together with density functional theory (DFT) calculations reveal that the isolated bond-shrinking low-valence Cu (+1)–N4 –C8 S2 atomic interface moiety serves as an active site during the ORR process, and the synergistic mechanism between the Cu species and the carbon matrix at the atomic interface plays a critical role in boosting the ORR efficiency, by adjusting the reaction free energy of intermediate adsorption. This atomic interface concept may provide an alternative methodology for the rational design of advanced oxygen electrode materials and new probability to improve their catalytic performance.