The modulation of thermal radiation in the infrared region is a highly anticipated method to achieve infrared sensing and camouflage. Here, a multiband metamaterial emitter based on the Al / SiO 2 / Al nanosandwich structure is proposed to provide new ideas for effective infrared and laser-compatible camouflage. By virtue of the intrinsic absorption and magnetic resonance property of lossy materials, the thermal radiation in the infrared region can be rationally modulated. The fabricated samples generally present low emissivity ( ε 3 – 5 μm = 0.21 , ε 8 – 14 μm = 0.19 ) in the atmospheric windows to evade infrared detection as well as high emissivity ( ε 5 – 8 μm = 0.43 ) in the undetected band for energy dissipation. Additionally, the laser camouflage is also realized by introducing a strong absorption at 10.6 μm through the nonlocalized plasmon resonance of the SiO 2 layer. Moreover, the fabricated emitter shows promising prospects in thermal management due to the good radiative cooling property that is comparable to the metallic Al material. This work demonstrates a multiband emitter based on the metasurface structure with compatible infrared-laser camouflage as well as radiative cooling properties, which is expected to pave new routes for the design of thermal radiation devices.

The binding of BSA to AgNPs will open a door to fully understand the essence of the interactions between nanoparticles and proteins.

The excited-state intramolecular proton transfer (ESIPT) reactions of 2-(2′-hydroxyphenyl)benzoxazole (HBO), 5-amino-2-(2′-hydroxyphenyl)benzoxazole (5A-HBO) and 6-amino-2-(2′-hydroxyphenyl)benzoxazole (6A-HBO) were investigated with the time-dependent density functional theory (TD-DFT) method at the B3LYP/6-31G(d,p) theoretical level. The primary bond lengths and infrared (IR) vibrational spectra show that the intramolecular hydrogen bond is significantly strengthened in S₁ state. The Mulliken's charge distribution and the frontier molecular orbitals (MOs) were analyzed. The result is consistent with the ESIPT mechanism proposed by Han and co-workers. Upon photo-excitation, the intramolecular hydrogen bond of 5A-HBO-enol (1.73 Å) and 6A-HBO-enol (1.74 Å) in the S₁ state is weaker than that of HBO-enol (1.69 Å) due to the influence of the amino group in the HBO framework. After vertical excitation to the S₁ state, the electronic density redistributes and migrates from the phenol ring to the benzoxazole ring of HBO. While for 5A-HBO and 6A-HBO, it transfers from the amino-benzoxazole moiety to the phenol ring. The analysis of the potential energy curves of HBO, 5A-HBO and 6A-HBO indicates that the ESIPT process of HBO occurs most easily. It is demonstrated that the presence and the position of the amino group in the HBO framework can change the behavior of the intramolecular hydrogen bonds O–H⋯N in the S₁ state and thus hinder the ESIPT processes to some extent.