4.8 Article

Scalable, inexpensive, one-pot, facile synthesis of crystalline two-dimensional birnessite flakes

期刊

MATTER
卷 5, 期 7, 页码 -

出版社

CELL PRESS
DOI: 10.1016/j.matt.2022.05.038

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资金

  1. Ceramics Division of NSF [1740795]
  2. Murata Manufacturing, Co., Ltd of Japan
  3. WPI TRIAD Seed Grant - Deutsche Forschungsgemeinschaft [324659309, CRC/TRR 270, B02]
  4. WPI TRIAD Seed Grant
  5. Deutsche Forschungsgemeinschaft [324659309, CRC/TRR 270, 233512597]
  6. Interdisciplinary Center for Analytics on the Nanoscale of the University of Duisburg - Essen (DFG) [B02]
  7. DFG [405553726, RI_00313]
  8. U.S. Naval Research Laboratory - Office of Naval Research
  9. Direct For Mathematical & Physical Scien
  10. Division Of Materials Research [1740795] Funding Source: National Science Foundation

向作者/读者索取更多资源

Researchers have successfully synthesized high-quality two-dimensional flakes using a new method that is simple and cost-effective. By converting water-insoluble Mn-bearing precursors into birnesite-based materials, they have achieved remarkable crystallinity for the synthesized flakes.
Synthesis of two-dimensional (2D) materials that is readily scalable, cost-effective, and eco-friendly is important from both scientific and industrial viewpoints. Currently, these 2D materials are synthesized either by selective etching of relatively expensive layered solids, viz. using a top-down approach, or by autoclaving metal salts/organic compounds. Herein, we describe a near-ambient, one-pot, inexpensive, scalable pathway to convert-through a bot-tom-up approach-5 different water-insoluble Mn-bearing precursors, viz. Mn3O4, Mn2O3, MnB, Mn5SiB2, and Mn2AlB2, into birnes-site-based 2D flakes that, in some cases, are remarkably crystalline. The precursor powders are immersed in 25 wt % tetra-methylammonium hydroxide aqueous solutions at 50? to 80? for 2 to 4 days. The structures, compositions, oxidation states, and morphologies of the synthesized flakes are determined using a battery of characterization techniques. The synthesized 2D sheets demonstrate reversible O-2 electrocatalysis with activities comparable with those of a commercial Pt/C catalyst.

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