材料科学
纳米片
膜
层状结构
水溶液
化学工程
离子
纳米技术
离子运输机
渗透力
渗透
离子键合
离子电导率
反向电渗析
电导率
纳米孔
化学物理
渗透压
储能
基质(化学分析)
发电
电化学
肿胀 的
纳米流体学
缓压渗透
作者
Jiadong Tang,Qianqian Zhang,Mengwei Zhang,Bing Liu,Chengze Lu,Yuhong Jin,Quan‐Fu An
摘要
ABSTRACT Two‐dimensional clay nanofluidic membranes hold great promise for harvesting sustainable osmotic energy, yet their practical application is constrained by two core challenges. (1) The inherently tortuous and inefficient ion transport pathways within stacked nanosheet structures limit cation flux, and (2) the severe swelling of interlayer nanochannels in aqueous environments impairs ion selectivity and long‐term stability. To simultaneously tackle these challenges, we construct a continuous hydrogen‐bond network within the interlayer of a lamellar membrane (CHM) via a sequential crosslinking strategy. This engineered network serves a dual function: (1) establishing low‐energy barrier pathways to facilitate cation transport while (2) acting as a dynamic yet robust crosslinked matrix to anchor clay nanosheets for suppressing interlayer expansion. Experimental and theoretical results confirm that the negatively charged surface, in synergy with the hydrogen‐bond network, enables selective and rapid cation transport. The ionic conductivity of in‐plane transport reaches as high as 22 S m −1 in 1 m electrolyte. When employed for osmotic energy harvesting from artificial seawater and river water, the CHM delivers an impressive high‐power density of 22.7 W m −2 and maintains stable power output for over 30 days. Furthermore, an integrated osmotic power generator successfully drives multiple electronic devices, demonstrating its real‐world applicability.
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