离子
离子泵
膜
离子运输机
整改
电化学梯度
电位梯度
化学
化学物理
膜电位
反向电渗析
纳米技术
材料科学
电压
电渗析
物理
有机化学
量子力学
生物化学
作者
Xuejiang Li,Bingxin Lu,Jianwei He,Xia Fan,Qianqian Zhang
出处
期刊:Small
[Wiley]
日期:2025-03-19
卷期号:21 (18): e2409834-e2409834
标识
DOI:10.1002/smll.202409834
摘要
Abstract The cation transport pump is a critical process in the realm of organismal energy utilization and acquisition. In this study, a TpPa‐SO 3 /TiO 2 ‐C 3 N 4 nanochannel membrane is fabricated to emulate the energy‐consuming ion pump mechanism of V‐ATPase. The channels exhibit ion rectification properties, excellent cation selectivity due to negatively charged TpPa‐SO 3 groups, while the TiO 2 ‐C 3 N 4 heterojunction acted as the light‐harnessing component for counter‐gradient ion transport, enabling light‐driven cation pumping through their synergistic effect. Asymmetric visible light irradiation on one side of the TpPa‐SO 3 /TiO 2 ‐C 3 N 4 nanochannel membrane generates a built‐in electric field across the membrane due to the intrinsic photoelectronic properties of TiO 2 ‐C 3 N 4 , driving cation transport against the concentration gradients and demonstrating an ion‐pumping effect. Impressively, the nanochannels can utilize external light energy to generate a chemical potential gradient, enabling an entropy reduction process similar to reverse concentration gradient transport in living organisms. These distinctive ion rectification and pumping properties offer great potential for advancements in ion circuits and energy conversion systems, expanding the frontiers of scientific exploration.
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