TY - JOUR
T1 - Fe@CNx Nanocapsules for Microwave Absorption at Gigahertz Frequency
AU - Li, Yixing
AU - Gao, Tong
AU - Zhang, Wenting
AU - Hu, Haihua
AU - Rong, Huawei
AU - Zhang, Xuefeng
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/6/28
Y1 - 2019/6/28
N2 - In order to solve growing electromagnetic wave pollution issues, development of high-performance microwave absorption materials composed of dielectric loss and magnetic loss characteristics has been attracting considerable attention. Herein, we demonstrate an effective approach for the transformation of Fe@C into Fe@CNx nanocapsules by in situ microwave-assisted heating effect. Ascribed to the high effective microwave absorption capacity, the microwave energy could be localized around the nanoscale environment of Fe@C nanocapsules, resulting in the in situ chemical decomposition of urea precursor and the transformation of the initial graphitic shells to CNx shells. Microstructure characterizations coupled with complex permittivity spectra further reveal that the intrinsic dielectric enhancement for the Fe@CNx nanocapsules originates from the atomic-scale C-N complexes that induce the space charge separation and form the electric dipoles. The present study indicates a novel approach for in situ synthesizing Fe@CNx nanoparticles and has promising potentials to extend to other carbon-based materials and diverse applications.
AB - In order to solve growing electromagnetic wave pollution issues, development of high-performance microwave absorption materials composed of dielectric loss and magnetic loss characteristics has been attracting considerable attention. Herein, we demonstrate an effective approach for the transformation of Fe@C into Fe@CNx nanocapsules by in situ microwave-assisted heating effect. Ascribed to the high effective microwave absorption capacity, the microwave energy could be localized around the nanoscale environment of Fe@C nanocapsules, resulting in the in situ chemical decomposition of urea precursor and the transformation of the initial graphitic shells to CNx shells. Microstructure characterizations coupled with complex permittivity spectra further reveal that the intrinsic dielectric enhancement for the Fe@CNx nanocapsules originates from the atomic-scale C-N complexes that induce the space charge separation and form the electric dipoles. The present study indicates a novel approach for in situ synthesizing Fe@CNx nanoparticles and has promising potentials to extend to other carbon-based materials and diverse applications.
KW - dielectric polarization
KW - microwave absorption
KW - microwave-assisted heating
KW - nanocapsules
KW - nitrogen substitutions
UR - http://www.scopus.com/inward/record.url?scp=85068597926&partnerID=8YFLogxK
U2 - 10.1021/acsanm.9b00589
DO - 10.1021/acsanm.9b00589
M3 - 文章
AN - SCOPUS:85068597926
SN - 2574-0970
VL - 2
SP - 3648
EP - 3653
JO - ACS Applied Nano Materials
JF - ACS Applied Nano Materials
IS - 6
ER -