TY - JOUR
T1 - Nanoporous magnesium
AU - Okulov, Ilya Vladimirovich
AU - Lamaka, Sviatlana V.
AU - Wada, Takeshi
AU - Yubuta, Kunio
AU - Zheludkevich, Mikhail L.
AU - Weissmüller, Jörg
AU - Markmann, Jürgen
AU - Kato, Hidemi
N1 - Funding Information:
I. V. O. thanks Prof. Geslin, Prof. Joo, and Mrs. Sarmanova for valuable discussions. Funding by the Helmholtz Impuls-und Vernetzungsfonds via the Helmholtz-Chinese Academy of Sciences Joint Research Group “Nanoporous transition metals for strength and function–towards a cost-efficient materials base” grant no. HCJRG-315 and by the International Collaboration Center, Institute for Materials Research (ICC-IMR), Tohoku University, Japan are gratefully acknowledged.
Publisher Copyright:
© 2018, Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - In this study, we present freestanding nanoporous magnesium as a novel lightweight material with high potential for structural and functional applications. Thus far, the high reactivity of Mg with oxygen and aqueous media prevented the fabrication of nanoporous Mg. First, in order to synthesize nanoporous Mg, we fabricated a bicontinuous nanocomposite consisting of interpenetrating Mg and non-Mg phases by liquid metal dealloying. The non-Mg phases in the nanocomposite protect Mg against corrosion. Second, we etched the non-Mg phases from the nanocomposite, leaving nanoporous Mg, using HF solution. This process is advantageous because the nanoporous Mg was passivated by a MgF2 layer during the etching. Our approach is very flexible, and we demonstrate that versatile microstructures of the nanoporous Mg—e.g., nanoscale bicontinuous network, hierarchical, or plate-like structures—can be designed for the given needs. More importantly, these nanoporous Mg samples can readily be exposed to air without being harmed by corrosion. [Figure not available: see fulltext.].
AB - In this study, we present freestanding nanoporous magnesium as a novel lightweight material with high potential for structural and functional applications. Thus far, the high reactivity of Mg with oxygen and aqueous media prevented the fabrication of nanoporous Mg. First, in order to synthesize nanoporous Mg, we fabricated a bicontinuous nanocomposite consisting of interpenetrating Mg and non-Mg phases by liquid metal dealloying. The non-Mg phases in the nanocomposite protect Mg against corrosion. Second, we etched the non-Mg phases from the nanocomposite, leaving nanoporous Mg, using HF solution. This process is advantageous because the nanoporous Mg was passivated by a MgF2 layer during the etching. Our approach is very flexible, and we demonstrate that versatile microstructures of the nanoporous Mg—e.g., nanoscale bicontinuous network, hierarchical, or plate-like structures—can be designed for the given needs. More importantly, these nanoporous Mg samples can readily be exposed to air without being harmed by corrosion. [Figure not available: see fulltext.].
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U2 - 10.1007/s12274-018-2167-9
DO - 10.1007/s12274-018-2167-9
M3 - Article
AN - SCOPUS:85052301968
SN - 1998-0124
VL - 11
SP - 6428
EP - 6435
JO - Nano Research
JF - Nano Research
IS - 12
ER -