A Radiative-Cooling Hierarchical Aligned Porous Poly(vinylidene fluoride)Film by Freeze-Thaw-Promoted Nonsolvent-Induced Phase Separation

Passive daytime radiative cooling(PDRC)is an innovative and sustainable cooling technology that holds immense potential for addressing the energy crisis.Despite the numerous reports on radiative coolers,the design of a straightforward,efficient,and readily producible system remains a challenge.Herein,we present the development of a hierarchical aligned porous poly(vinylidene fluoride)(HAP-PVDF)film through a freeze-thaw-promoted nonsolvent-induced phase separation strategy.This film features oriented microporous arrays in conjunction with random nanopores,enabling efficient radiative cooling performance under direct sunlight conditions.The incorporation of both micro-and nano-pores in the HAP-PVDF film results in a remarkable solar reflectance of 97%and a sufficiently high infrared thermal emissivity of 96%,facilitating sub-environmental cooling at 18.3℃ on sunny days and 13.1℃ on cloudy days.Additionally,the HAP-PVDF film also exhibits exceptional flexibility and hydrophobicity.Theoretical calculations further confirm a radiative cooling power of 94.8 W·m^(-2)under a solar intensity of 1000W·m^(-2),demonstrating a performance comparable to the majority of reported radiative coolers.

Nonsolvent-induced phase separation-derived TiO_(2) nanotube arrays/porous Ti electrode as high-energy-density anode for lithium-ion batteries

TiO_(2) nanotube arrays,growing on three-dimensional(3 D)porous Ti membrane,were synthesized using a facile nonsolvent-induced phase separation and anodization process.The length of those three-dimensional nanotube arrays could be tuned by prolonging the anodizing time.When the anodizing time is 8 h,the three-dimensional TiO_(2) nanotube arrays/porous Ti electrode exhibits well cycling stability and ultra-high specific capacity,which is used in lithium-ion batteries,attributed to the high utilization rate of the substrate and the high growth intensity of the active materials.Three-dimensional TiO_(2) nano tube arrays/porous Ti electrode,at 100μA·cm^(-2) with 8 h anodizing time,shows a typical discharge plateau at 1.78 V and exhibits the specific capacity with 2126.7μAh·cm^(-2),The novel nanotube arrays@3 D porous architecture effectively shortens the electron/ion transmission path,which could pave way for optimizing the design of highperformance anode materials for next-generation energy storage system.

Tuning dual three-dimensional porous copper/graphite composite to achieve diversified utilization of copper current collector for lithium storage

Graphite anode materials are widely used in commercial lithium-ion batteries;however, the long electron/ion transportation path restricted its high energy storage. In this experiment, we designed a copper/graphite composite with a dual three-dimensional(3 D) continuous porous structure combining used nonsolvent-induced phase separation and heat treatment, in which a large amount of graphite is embedded in the 3 D porous copper/carbon architecture. In the novel structure, not only the electron and Li^(+) transmission performances are improved, but also the space of current collector is fully utilized. Meanwhile,carbonized polyacrylonitrile network stabilizes the interface between graphite and copper matrix. The obtained copper/graphite composite anode has an initial discharge capacity of 524.6 mAh·g^(-1), a holding capacity of350 mAh·g^(-1) and excellent cycle stability(299.3 mAh·g^(-1) after 180 cycles at 0.1 C rate), exhibiting good electrochemical performance. The experimental results show that the mass loading of the copper/graphite composite electrode material is about 4.39 mg·cm^(-2). We also envisage replacing graphite with other high-capacity active materials to fill the current collector, which can provide a reference for the future development of next-generation advanced electrodes.