渗透力
反向电渗析
自愈水凝胶
膜
化学工程
化学
盐度
电负性
功率密度
能量转换
离子
储能
环氧氯丙烷
材料科学
能量转换效率
吉布斯自由能
缓压渗透
唐南势
纳米技术
制作
无机化学
比能量
木质素磺酸盐
电解质
渗透
限制
超级电容器
水化能
离子交换
作者
Fengyun Liu,Caiqin Wu,Guilong Li,Jialing Zhou,Huanlin Yang,Ye Kang,Chunmei Zhang,Yì Wáng
标识
DOI:10.1021/acssuschemeng.6c00038
摘要
Direct conversion of Gibbs free energy from salinity gradients into electrical power through ion-exchange membranes holds great promise for mitigating the energy crisis. However, traditional ion-exchange membranes generally suffer from high internal resistance, poor ion selectivity, and low ion permeability, resulting in suboptimal power density and limiting their practical applications. Herein, we develop a series of ion-selective membranes with a three-dimensional (3D) interconnected network for salinity gradient energy (SGE) harvesting by incorporating acidic anions with different electronegativity into a poly(vinyl alcohol) (PVA)-chitosan (CS)-acrylamide (AM) hydrogel. Compared with the weak acidic compound (acrylic acid, AA), the stronger acidic anions (methanesulfonic acid, MSA, and phosphoric acid, H3PO4) can effectively improve ion selectivity and permeability, thereby enhancing the osmotic energy conversion efficiency. The results show that the MSA-modified (NS) and H3PO4-modified (NP) hydrogels achieved maximum power outputs of 29.15 and 16.96 W m–2, respectively, at a 50-fold concentration gradient (0.5 M/0.01 M NaCl), significantly exceeding the commercial benchmark of 5 W m–2. The acid-modified hydrogels also maintained good structural integrity and stable output during long-term operation. This composite hydrogel fabrication strategy offers a viable, cost-effective, and scalable approach to boost SGE conversion in ion-selective membranes, paving the way for their application in sustainable energy harvesting.
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