TY - JOUR
T1 - Controlled Fabrication of Ramie Plant Derived Magnetic Helical/Chiral Porous Carbon Fibers (Ni@CNTs@HPCFs) for Highly Efficient Microwave Absorption Performance and EAB across a Broad Temperature Range
AU - Tariq, Muhammad Rizwan
AU - Ahmad, Mudasir
AU - Raza, Zulfiqar Ali
AU - Wu, Jianfeng
AU - Zhang, Baoliang
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/11/6
Y1 - 2024/11/6
N2 - Herein, we report a sustainable catalytic self-deposition (CSD) synthesis approach to fabricate 1D ultralightweight magnetic CNT helical/chiral porous carbon fibers (Nix@CNTs@HPCFt's) that exhibit tremendous absorption performance over a broad range of temperature (700-800 °C) and magnetic contents (1.00-2.00 mmol). The synergistic impact of in situ dipping and the CSD synthesis approach enables the regulation of morphology and CNT density by encapsulating Ni nanocatalysts. Nix@CNTs@HPCFt's unprecedentedly exhibit splendid absorption capabilities over broad spectrum of microwave (4.00-18.00 GHz) with efficient absorption bandwidth (EAB, RL ≤ −10 dB) and 2.00-4.50 mm thickness. Moreover, the unprecedented absorption capabilities of Nix@CNTs@HPCFt's refer to their sophisticated helical/chiral structure, ultralow density, large specific surface area, CNTs, interface polarization, cross-polarization, dielectric loss by integration of 0D/1D dielectric components, magnetic loss, and well-matched impedance. Notably, Ni1.00@CNTs@HPCF700 at 11.92 GHz and 2.41 mm matching thickness exhibits an astronomical RL of −45.20 dB with an EAB of 10.40-18.00 GHz (7.60 GHz) covering 40% of the X band and the entire band. The EAB improves to 8.00 GHz (10.00-18.00 GHz) covering 50% of the whole Ku band at a matching thickness of 2.30 mm. Meanwhile, Ni1.50@CNTs@HPCF800 at just a matching thickness of 4.10 mm and 8.24 GHz gained an RL of −64.40 dB with an EAB of 4.32 GHz (6.80-11.12 GHz) covering 30% of the C band and 78% of the X band. This study opens new doors for the development of absorbers produced at a broad carbonization temperature range with comparable performance.
AB - Herein, we report a sustainable catalytic self-deposition (CSD) synthesis approach to fabricate 1D ultralightweight magnetic CNT helical/chiral porous carbon fibers (Nix@CNTs@HPCFt's) that exhibit tremendous absorption performance over a broad range of temperature (700-800 °C) and magnetic contents (1.00-2.00 mmol). The synergistic impact of in situ dipping and the CSD synthesis approach enables the regulation of morphology and CNT density by encapsulating Ni nanocatalysts. Nix@CNTs@HPCFt's unprecedentedly exhibit splendid absorption capabilities over broad spectrum of microwave (4.00-18.00 GHz) with efficient absorption bandwidth (EAB, RL ≤ −10 dB) and 2.00-4.50 mm thickness. Moreover, the unprecedented absorption capabilities of Nix@CNTs@HPCFt's refer to their sophisticated helical/chiral structure, ultralow density, large specific surface area, CNTs, interface polarization, cross-polarization, dielectric loss by integration of 0D/1D dielectric components, magnetic loss, and well-matched impedance. Notably, Ni1.00@CNTs@HPCF700 at 11.92 GHz and 2.41 mm matching thickness exhibits an astronomical RL of −45.20 dB with an EAB of 10.40-18.00 GHz (7.60 GHz) covering 40% of the X band and the entire band. The EAB improves to 8.00 GHz (10.00-18.00 GHz) covering 50% of the whole Ku band at a matching thickness of 2.30 mm. Meanwhile, Ni1.50@CNTs@HPCF800 at just a matching thickness of 4.10 mm and 8.24 GHz gained an RL of −64.40 dB with an EAB of 4.32 GHz (6.80-11.12 GHz) covering 30% of the C band and 78% of the X band. This study opens new doors for the development of absorbers produced at a broad carbonization temperature range with comparable performance.
UR - http://www.scopus.com/inward/record.url?scp=85208578904&partnerID=8YFLogxK
U2 - 10.1021/acs.iecr.4c02470
DO - 10.1021/acs.iecr.4c02470
M3 - 文章
AN - SCOPUS:85208578904
SN - 0888-5885
VL - 63
SP - 18916
EP - 18930
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 44
ER -