氮化硼
材料科学
多孔性
介孔材料
化学工程
氮化物
纳米技术
微型多孔材料
化学
催化作用
有机化学
复合材料
工程类
图层(电子)
作者
Sofia Marchesini,Catriona M. McGilvery,Josh J. Bailey,Camille Petit
出处
期刊:ACS Nano
[American Chemical Society]
日期:2017-09-11
卷期号:11 (10): 10003-10011
被引量:135
标识
DOI:10.1021/acsnano.7b04219
摘要
Production of biocompatible and stable porous materials, e . g ., boron nitride, exhibiting tunable and enhanced porosity is a prerequisite if they are to be employed to address challenges such as drug delivery, molecular separations, or catalysis. However, there is currently very limited understanding of the formation mechanisms of porous boron nitride and the parameters controlling its porosity, which ultimately prevents exploiting the material’s full potential. Herein, we produce boron nitride with high and tunable surface area and micro/mesoporosity via a facile template-free method using multiple readily available N-containing precursors with different thermal decomposition patterns. The gases are gradually released, creating hierarchical pores, high surface areas (>1900 m 2 /g), and micropore volumes. We use 3D tomography techniques to reconstruct the pore structure, allowing direct visualization of the mesopore network. Additional imaging and analytical tools are employed to characterize the materials from the micro- down to the nanoscale. The CO 2 uptake of the materials rivals or surpasses those of commercial benchmarks or other boron nitride materials reported to date (up to 4 times higher), even after pelletizing. Overall, the approach provides a scalable route to porous boron nitride production as well as fundamental insights into the material’s formation, which can be used to design a variety of boron nitride structures.
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