Intrinsic high water/ion selectivity of graphene oxide lamellar membranes in concentration gradient-driven diffusion

被引:66
|
作者
Sun, Pengzhan [1 ,2 ]
Ma, Renzhi [2 ]
Deng, Hui [1 ]
Song, Zhigong [3 ,4 ]
Zhen, Zhen [1 ,4 ]
Wang, Kunlin [1 ]
Sasaki, Takayoshi [2 ]
Xu, Zhiping [3 ,4 ]
Zhu, Hongwei [1 ,4 ]
机构
[1] Tsinghua Univ, Sch Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
[2] Natl Inst Mat Sci, Int Ctr Mat Nanoarchitecton WPI MANA, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
[3] Tsinghua Univ, Dept Engn Mech, Beijing 100084, Peoples R China
[4] Tsinghua Univ, Ctr Nano & Micro Mech, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
ATOMIC-STRUCTURE; SEPARATION; TRANSPORT; PERMEATION; MOLECULES; ULTRATHIN; SOLVENTS;
D O I
10.1039/c6sc02865a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although graphene oxide lamellar membranes (GOLMs) are effective in blocking large organic molecules and nanoparticles for nanofiltration and ultrafiltration, water desalination with GOLM is challenging, with seriously controversial results. Here, a combined experimental and molecular dynamics simulation study shows that intrinsic high water/ion selectivity of GOLM was achieved in concentration gradient-driven diffusion, showing great promise in water desalination. However, in pressure-driven filtration the salt rejection was poor. This study unveils a long-overlooked reason behind the controversy in water desalination with GOLM and further provides a fundamental understanding on the in-depth mechanism concerning the strong correlation of water/ion selectivity with the applied pressure and GO nanochannel length. Our calculations and experiments show that the applied pressure weakened the water-ion interactions in GO nanochannels and reduced their permeation selectivity, while the length of nanochannels dominated the mass transport processes and the ion selectivity. The new insights presented here may open up new opportunities for the optimization of GOLMs in this challenging area.
引用
收藏
页码:6988 / 6994
页数:7
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