Published June 9, 2023 | Version v1
Publication

High-temperature solar-selective coatings based on Cr(Al)N. Part 2: Design, spectral properties and thermal stability of multilayer stacks

Description

Two multilayer solar selective absorber coatings [Al/CrN0.95/Cr0.96Al0.04N1.08/Cr0.53Al0.47N1.12/Al2O3 (stack #1) and Cr0.96Al0.04N0.89/Cr0.62Al0.38N1.00/Cr0.53Al0.47N1.12/Al2O3 (stack #2)] were deposited on 316L steel by combining direct current (DC) and high power impulse magnetron sputtering (HiPIMS) technologies with the aim of increasing the working limit temperature. The composition and thickness of the constituent layers were optimized using CODE software to achieve a high solar absorptance (α) and low values of thermal emittance (ε) in the infrared region. The deposited multilayered stacks were heated during 2 h in air at 600, 700 and 800 ◦C to study their thermal stability and optical performance. Compositional, structural and optical characterization of the stacks (as-prepared and after thermal treatment) was performed. Both stacks presented a good solar selectivity with α > 95% and ε < 15%, were stable up to 600 ◦C and fulfilled the performance criterion PC < 5% after 600 and 700 ◦C treatments. Despite the stacks suffered chemical transformations above 600 ◦C, partial oxidation (stack #1) and Cr2N formation (stack #1 and #2), the optical properties were optimum up to 700 ◦C for stack #1 (α = 94%, ε(25 ◦C) = 12%) and 600 ◦C for stack #2 (α = 93%, ε(25 ◦C) = 13%). The solar-to-mechanical energy conversion efficiencies (η) of the as-deposited and annealed (600 and 700 ◦C) samples were up to 20% points higher than the absorber paint commercially used (Pyromark). At 800 ◦C, they underwent a further structural transformation, provoked by the oxidation of the inner layers, and they consequently lost their solar selectivity.

Abstract

Ministerio de Economía, Industria y Competitividad MAT2015-65539-P

Abstract

Ministerio de Ciencia e Innovación PID2019-104256RB-I00

Abstract

Junta de Andalucía P18-RT-2641

Additional details

Created:
June 10, 2023
Modified:
November 28, 2023