A high-efficiency salt-rejecting solar evaporator with optimized porous structure for continuous solar desalination

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A high-efficiency salt-rejecting solar evaporator with optimized porous structure for continuous solar desalination

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Although photothermal reactions have gained extensiveattention,their surface-localized naturewhere heat concentrates on nanoscalesurfacesleads to suboptimal chemical reactivity. This studyestablishes an intrapore-confined thermal-field-driven reaction paradigmwith unprecedented photothermal reactivity, through investigationsof photothermal Congo Red (CR) pyrolysis in three-dimensional orderedmacroporous carbon (OMC) versus nonmacroporous solid carbon (SC).Two model systems are constructed: (1) intrapore-confined configuration:fluorine–cerium nanodomains with ultrahigh CR adsorption capacityare anchored onto macroporous walls to achieve uniform CR distributionin OMC; (2) surface-localized pathway: CR is blended on the externalsurface of SC, decoupling intrapore confinement and surface localizationmechanisms. The intrapore-confined system demonstrates transformativeadvantages: near-complete CR pyrolysis (>99.00 vs 39.89%), a 27.73-foldincrease in rate constants (4.00 vs 0.14%/s), and a 30.71-fold enhancementin energy efficiency. Finite element analysis reveals an intrapore-confinedthermal field within OMC due to its low thermal conductivity. Characterizedby an inward-increasing temperature gradient, this field overcomessurface-localized limitations by reconstructing the temperature distribution,forming effective reaction driving forces. This work transcends conventionalunderstanding of photothermal mechanisms and highlights macroporousarchitecture as a critical design principle for advanced photothermalmaterials.

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Solar-driven interface evaporation recently emerges as one of the most promising methods for seawater desalination and wastewater purification, mainly due to its low energy consumption. However, there still exist special issues in the present material system based on conventional noble metals or two-dimensional (2D) nanomaterials etc., such as high costs, low light-to-heat conversion efficiencies, and unideal channels for water transport. Herein, a composite photothermal membrane based on Ti3C2Tx MXene nanoflakes/copper indium selenide (CIS) nanoparticles is reported for highly efficient solar-driven interface evaporation toward water treatment applications. Results indicate that the introduction of CIS improves the spatial accessibility of the membrane by increasing the interlayer spacings and wettability of MXene nanoflakes and enhances light absorption capability as well as reduces reflection for the photothermal membrane. Simultaneously, utilization of the MXene/CIS composite membrane improves the efficiency of light-to-heat conversion probably due to formation of a Schottky junction between MXene and CIS. The highest water evaporation rate of 1.434 kgm-2 h-1 and a maximum water evaporation efficiency of 90.04% as well as a considerable cost-effectiveness of 62.35 g h-1/$ are achieved by using the MXene/CIS composite membrane for solar interface evaporation, which also exhibits excellent durability and light intensity adaptability. In addition, the composite photothermal membrane shows excellent impurity removal ability, e.g., >98% for salt ions, >99.8% for heavy metal ions, and ∼100% for dyes molecules. This work paves a promising avenue for the practical application of MXene in the field of water treatment.

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