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Molecular self-assembled cellulose enabling durable, scalable, high-power osmotic energy harvesting.
Shi, Jianping; Sun, Xuhui; Zhang, Yu; Niu, Shengyue; Wang, Zequn; Wu, Zhuotong; An, Meng; Chen, Lihui; Li, Jianguo.
Afiliación
  • Shi J; College of Material Engineering, National Forestry and Grassland Administration Key Laboratory of Plant Fiber Functional Materials, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
  • Sun X; College of Mechanical and Electrical Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, China.
  • Zhang Y; College of Material Engineering, National Forestry and Grassland Administration Key Laboratory of Plant Fiber Functional Materials, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
  • Niu S; College of Material Engineering, National Forestry and Grassland Administration Key Laboratory of Plant Fiber Functional Materials, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
  • Wang Z; College of Mechanical and Electrical Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, China.
  • Wu Z; College of Material Engineering, National Forestry and Grassland Administration Key Laboratory of Plant Fiber Functional Materials, Fujian Agriculture and Forestry University, Fuzhou 350002, China. Electronic address: wuzt@fafu.edu.cn.
  • An M; College of Mechanical and Electrical Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, China. Electronic address: anmeng@sust.edu.cn.
  • Chen L; College of Material Engineering, National Forestry and Grassland Administration Key Laboratory of Plant Fiber Functional Materials, Fujian Agriculture and Forestry University, Fuzhou 350002, China. Electronic address: lihuichen@fafu.edu.cn.
  • Li J; College of Material Engineering, National Forestry and Grassland Administration Key Laboratory of Plant Fiber Functional Materials, Fujian Agriculture and Forestry University, Fuzhou 350002, China. Electronic address: jianguolicn@fafu.edu.cn.
Carbohydr Polym ; 327: 121656, 2024 Mar 01.
Article en En | MEDLINE | ID: mdl-38171677
ABSTRACT
In recent years, renewable cellulose-based ion exchange membranes have emerged as promising candidates for capturing green, abundant osmotic energy. However, the low power density and structural/performance instability are challenging for such cellulose membranes. Herein, cellulose-molecule self-assembly engineering (CMA) is developed to construct environmentally friendly, durable, scalable cellulose membranes (CMA membranes). Such a strategy enables CMA membranes with ideal nanochannels (∼7 nm) and tailored channel lengths, which support excellent ion selectivity and ion fluxes toward high-performance osmotic energy harvesting. Finite element simulations also verified the function of tailored nanochannel length on osmotic energy conversion. Correspondingly, our CMA membrane shows a high-power density of 2.27 W/m2 at a 50-fold KCl gradient and super high voltage of 1.32 V with 30-pair CMA membranes (testing area of 22.2 cm2). In addition, the CMA membrane demonstrates long-term structural and dimensional integrity in saline solution, due to their high wet strength (4.2 MPa for N-CMA membrane and 0.5 MPa for P-CMA membrane), and correspondingly generates ultrastable yet high power density more than 100 days. The self-assembly engineering of cellulose molecules constructs high-performance ion-selective membranes with environmentally friendly, scalable, high wet strength and stability advantages, which guide sustainable nanofluidic applications beyond the blue energy.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Carbohydr Polym Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Carbohydr Polym Año: 2024 Tipo del documento: Article País de afiliación: China