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Carbon nanolayer-mounted single metal sites enable dipole polarization loss under electromagnetic field

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posted on 2025-03-05, 08:28 authored by Siyao Cheng, Daohu Sheng, Soumya MukherjeeSoumya Mukherjee, Wei Dong, Yuanbiao Huang, Rong Cao, Aming Xie, Roland A. Fischer, Weijin Li

Surface modulation strategies have spurred great interest with regard to regulating the morphology, dispersion and flexible processability of materials. Unsurprisingly, customized modulation of surfaces is primed to offer a route to control their electronic functions. To regulate electromagnetic wave (EMW) absorption applications by surface engineering is an unmet challenge. Thanks to pyrolyzing surface-anchored metal-porphyrin, here we report on the surface modulation of four-nitrogen atoms-confined single metal site on a nitrogen-doped carbon layer (sM(N4)@NC, M = Ni, Co, Cu, Ni/Cu) (sM=single metal; NC= nitrogen-doped carbon layer) that registers electromagnetic wave absorption. Surface-anchored metal-porphyrins are afforded by attaching them onto the polypyrrole surface via a prototypical click reaction. Further, sM(N4)@NC is experimentally found to elicit an identical dipole polarization loss mechanism, overcoming the handicaps of conductivity loss, defects, and interfacial polarization loss among the current EMW absorber models. Importantly, sM(N4)@NC is found to exhibit an effective absorption band-width of 6.44 and reflection loss of −51.7 dB, preceding state-of-the-art carbon-based EMW absorbers. This study introduces a surface modulation strategy to design EMW absorbers based on single metal sites that enable fine-tunable and controlled absorption mechanism with atomistic precision.

Funding

Ionic Ultramicroporous Polymer Adsorbents for Energy-efficient Purification of Commodity Chemicals

Science Foundation Ireland

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History

Publication

Nature Communications 15, 9077

Publisher

Nature Portfolio

Other Funding information

National Natural Science Foundation of China (52273267 to A.M.X., 22271155 to W.J.L., 22220102005 to R.C.), and the Fundamental Research Funds for the Central Universities (NO.30922010203 to W.J.L., NO. 2023203001 to W.J.L.)

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  • Bernal Institute

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  • Chemical Sciences

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