Nanoporous Mn-based electrocatalysts through thermal conversion of cyano-bridged coordination polymers toward ultra-high efficiency hydrogen peroxide production. Issue 23 (27th May 2016)

• Record Type: Journal Article
• Authors: Zakaria, Mohamed B.; Li, Cuiling; Pramanik, Malay; Tsujimoto, Yoshihiro; Hu, Ming; Malgras, Victor; Tominaka, Satoshi; Yamauchi, Yusuke
• Is Part Of: Journal of materials chemistry. Volume 4:Issue 23(2016)
• Page Start: 9266
• Page End: 9274
• Publication Date: 2016-05-27
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c6ta01470d
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Nanoporous Mn-based electrocatalysts are realized through thermal conversion of cyano-bridged coordination polymers. Abstract : An oriented and controlled crystal growth of cyano-bridged coordination polymers is realized by a controlling agent ( e.g., trisodium citrate dihydrate (TSCD)) as a reaction precursor. In the presence of TSCD, the reaction is slow as the complex appears to be more stable, leading to a preferentially oriented crystal growth. For instance, after mixing manganese acetate with TSCD, the formed Mn–citrate complex tends to release few Mn 2+ ions steadily and slowly, which then react with the ligands at the initial stage of the reaction. Subsequently, the generated nuclei further grow from the interaction between the released Mn 2+ and [Mn(CN)6 ] 3−, [Co(CN)6 ] 3−, or [Ru(CN)6 ] 4− anions to form several types of cyano-bridged coordination polymers (abbreviated as MnCNMn, MnCNCo, or MnCNRu, respectively). After thermal treatment in air, the as-prepared coordination polymers can be decomposed into their corresponding nanoporous Mn-based oxides. Surprisingly, the electrochemical analysis reveals that the Mn–Ru oxide prepared from MnCNRu is a promising catalyst for the production of H2 O2 by selectively catalyzing the oxygen reduction reaction (ORR) through an exact 2-electron pathway. Compared to previously reported materials, our electrocatalyst demonstrates an outstanding activity, a strict selectivity, and a long-term stability for the production of H2 O2 . The present catalyst design sheds new light on the production of H2 O2 by a safe and sustainable way.