The complex electromagnetic applications in harsh corrosive
environments
urgently require research into multifunctional microwave absorption
(MA) materials. The core–shell structure is an effective strategy
to prepare multifunctional MA materials by efficiently combining the
advantages of each component. Nevertheless, it remains a tough challenge
to elucidate the effect of the binding positions of each component
in MA materials on the comprehensive electromagnetic performance.
Herein, two types of core–shell structured composites based
on hollow mesoporous carbon spheres (HMCS), HMCS@MoS2 and
MoS2@HMCS, were prepared via synergistic etch growth and
spatial confinement growth strategies, respectively. Compared with
HMCS, HMCS@MoS2 severely destroys the connection of HMCS,
therefore resulting in impedance mismatching. Comparatively, the growth
of MoS2 within the HMCS reduces the disruption of the HMCS
connection, enabling MoS2@HMCS with enhanced dielectric
loss while optimizing the impedance matching, and therefore, it yields
an optimal reflection loss of −46.91 dB at 2 mm and an effective
bandwidth of 5.78 GHz at 2.4 mm mixed with polydimethylsiloxane (PDMS).
In addition, the combinations of the spatial confinement effect of
HMCS, corrosion resistance of MoS2, and chemical stability
of PDMS resulted in minimal changes in the MA performance of MoS2@HMCS/PDMS after soaking in acidic and alkaline solutions
for 14 days, proving an excellent corrosion resistance property. This
inspiring work proposes an effective spatial confinement growth strategy
to optimize the impedance matching and further tailor the multifunction
for dielectric loss dominated MA materials.