化学
膜
能量转换
离子
氧化物
化学工程
生物物理学
生物化学
有机化学
热力学
生物
物理
工程类
作者
Qingchen Wang,Zidi Yan,Yuhao Hu,Qixiang Zhang,Xiang‐Yu Kong,Yongchao Qian,Haoyang Ling,Zhehua Zhang,Tingyang Li,Xin Li,Lei Kang,Linsen Yang,Lei Jiang,Zhen Zhang,Liping Wen
摘要
Two-dimensional (2D) membranes with engineered light-responsive ion transport dynamics have been explored to construct efficient nanofluidic platforms that show great potential in osmotic and solar-osmotic energy conversion. However, the power density is still limited by poor responsivity and the inevitable trade-off effect between ion selectivity and flux. Here, we observed light-pumping ion transport behavior in graphdiyne oxide (GDYO) with a unique carbon hybrid skeleton that provides sensitive photoelectric responsivity and high-speed cation pathways. Molecular dynamics simulations verify that the coexistent interaction effects between cations and the negatively charged sites in GDYO (i.e., oxygen-containing groups and electron-rich acetylenic bonds) could significantly promote cation transmembrane transport via an absorption-acceleration mechanism. Furthermore, the GDYO-based system, possessing a coupled photon-electron-ion transport behavior due to its inherent semiconductor properties, could subtly realize unidirectional ion movement, consuming luminous energy either from low concentration to high concentration or vice versa, flexibly promoting the osmotic power density by ∼195% to 11.91 W m-2.
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