Rapid solar-driven atmospheric water-harvesting with MAF-4-derived nitrogen-doped nanoporous carbon

被引:0
|
作者
Feng, Jin-Hua [1 ]
Lu, Feng [1 ]
Chen, Zhen [1 ]
Jia, Miao-Miao [1 ]
Chen, Yi-Le [1 ]
Lin, Wei-Hai [1 ]
Wu, Qing-Yun [1 ]
Li, Yi [1 ]
Xue, Ming [1 ]
Chen, Xiao-Ming [1 ]
机构
[1] Sun Yat sen Univ, Sch Chem Engn & Technol, Sch Chem, GBRCE Funct Mol Engn, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; POTABLE WATER; ADSORPTION; CAPTURE; VAPOR;
D O I
10.1039/d4sc01802h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Sorption-based atmospheric water-harvesting (AWH) could help to solve global freshwater scarcity. The search for adsorbents with high water-uptake capacity at low relative humidity, rapid adsorption-desorption kinetics and high thermal conductivity is a critical challenge in AWH. Herein, we report a MAF-4 (aka ZIF-8)-derived nanoporous carbon (NPCMAF-4-800) with multiple N-doped sites, considerable micropore characteristics and inherent photothermal properties, for efficient water production in a relatively arid climate. NPCMAF-4-800 exhibited optimal water-sorption performance of 306 mg g-1 at 40% relative humidity (RH). An excellent sunlight-absorption rate was realized (97%) attributed to its high degree of graphitization. A proof-of-concept device was designed and investigated for the practical harvesting of water from the atmosphere using natural sunlight. NPCMAF-4-800 achieved an unprecedentedly high water production rate of 380 mg g-1 h-1 at 40% RH, and could produce 1.77 L kg-1 freshwater during daylight hours in an outdoor low-humidity climate of similar to 25 degrees C and 40% RH. These findings may shed light on the potential of MOF-derived porous carbons in the AWH field, and inspire the future development of solar-driven water-generation systems. A MOF-derived nanoporous carbon (NPCMAF-4-800) with multiple N-doped sites, considerable porous characteristics and inherent photothermal properties demonstrated a superior water-production rate under a relatively arid climate.
引用
收藏
页码:9557 / 9565
页数:10
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