Toward digitally controlled catalyst architectures: Hierarchical nanoporous gold via 3D printing

被引:186
作者
Zhu, Cheng [1 ]
Qi, Zhen [1 ]
Beck, Victor A. [1 ]
Luneau, Mathilde [2 ]
Lattimer, Judith [2 ]
Chen, Wen [1 ]
Worsley, Marcus A. [1 ]
Ye, Jianchao [1 ]
Duoss, Eric B. [1 ]
Spadaccini, Christopher M. [1 ]
Friend, Cynthia M. [2 ]
Biener, Juergen [1 ]
机构
[1] Lawrence Livermore Natl Lab, 7000 East Ave, Livermore, CA 94550 USA
[2] Harvard Univ, Cambridge, MA 02138 USA
来源
SCIENCE ADVANCES | 2018年 / 4卷 / 08期
关键词
POROUS GOLD; EVOLUTION; METALS;
D O I
10.1126/sciadv.aas9459
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Monolithic nanoporous metals, derived from dealloying, have a unique bicontinuous solid/void structure that provides both large surface area and high electrical conductivity, making them ideal candidates for various energy applications. However, many of these applications would greatly benefit from the integration of an engineered hierarchical macroporous network structure that increases and directs mass transport. We report on 3D (three-dimensional) printed hierarchical nanoporous gold (3DP-hnp-Au) with engineered nonrandom macroarchitectures by combining 3D printing and dealloying. The material exhibits three distinct structural length scales ranging from the digitally controlled macroporous network structure (10 to 1000 mu m) to the nanoscale pore/ligament morphology (30 to 500 nm) controlled by dealloying. Supercapacitance, pressure drop, and catalysis measurements reveal that the 3D hierarchical nature of our printed nanoporous metals markedly improves mass transport and reaction rates for both liquids and gases. Our approach can be applied to a variety of alloy systems and has the potential to revolutionize the design of (electro-)chemical plants by changing the scaling relations between volume and catalyst surface area.
引用
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页数:8
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