渗透力
反向电渗析
膜
功率密度
离子
分析化学(期刊)
化学
化学工程
缓压渗透
材料科学
电渗析
纳米技术
正渗透
化学物理
功率(物理)
色谱法
热力学
物理
反渗透
有机化学
生物化学
工程类
作者
Li Ding,Dan Xiao,Lu Zong,Junjie Deng,Yanying Wei,Jürgen Caro,Haihui Wang
标识
DOI:10.1002/ange.201915993
摘要
Abstract Membrane‐based reverse electrodialysis (RED) is considered as the most promising technique to harvest osmotic energy. However, the traditional membranes are limited by high internal resistance and low efficiency, resulting in undesirable power densities. Herein, we report the combination of oppositely charged Ti 3 C 2 T x MXene membranes (MXMs) with confined 2D nanofluidic channels as high‐performance osmotic power generators. The negatively or positively charged 2D MXene nanochannels exhibit typical surface‐charge‐governed ion transport and show excellent cation or anion selectivity. By mixing the artificial sea water (0.5 m NaCl) and river water (0.01 m NaCl), we obtain a maximum power density of ca. 4.6 Wm −2 , higher than most of the state‐of‐the‐art membrane‐based osmotic power generators, and very close to the commercialization benchmark (5 Wm −2 ). Through connecting ten tandem MXM‐RED stacks, the output voltage can reach up 1.66 V, which can directly power the electronic devices.
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