Abstract
A robust and reliable method for fabricating porous anodic alumina (PAA)-based distributed Bragg reflectors (DBRs), operating in mid-infrared (MIR) spectral region, is presented. The method relies on application of high (UH) and low (UL) voltage pulse sequence repeated in cycles. PAA-based DBR consists of alternating high-(dH) and low-porosity (dL) layers translated directly into periodically varied refractive index. Two anodization modes were used: time- and charge density-controlled mode. The former generated dH + dL pairs with non-uniform thickness (∆d) and effective refractive index (∆neff). It is supposed, that owing to a compensation effect between the ∆d and ∆neff, the photonic stopbands (PSBs) were symmetrical and intensive (transmittance close to zero). Under the charge density-controlled mode dH + dL pairs of uniform thickness were formed. However, the remaining ∆neff provided an asymmetrical broadening of PSBs. Furthermore, it is demonstrated that the spectral position of the PSBs can be precisely tuned in the 3500–5500 nm range by changing duration of voltage pulses, the amount of charge passing under subsequent UH and UL pulses, and by pore broadening after the electrochemical synthesis. The material can be considered to be used as one-dimensional transparent photonic crystal heat mirrors for solar thermal applications.
Highlights
Distributed Bragg reflectors (DBRs) are one-dimensional (1D) photonic structures that consist of dielectric layers of different refractive indices which are regularly and alternately arranged into a stack to modulate the light waves [1,2,3]
Porous anodic alumina (PAA) is a well-known template with a honeycomb-like structure formed by arrays of uniform and parallel pores [4]
In our previous works free-standing structures were prepared by im- inshifts towards blue part of[25,29], the spectrum as theDBR
Summary
The influence of the immersion time in the CuCl2 /HCl solution (tp ) on optical properties of the PAA- based DBR structures was studied. This time a front side of the free-standing DBRs (top view in the Figure 2) was exposed to the contact with the solution, allowing the acid to penetrate to the open pores and react with Al2 O3 .
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