Semiconductor p-n Junction Nanofluidic Channels for Light-driven Ion Transport

被引:0
|
作者
Sun, Mingyan [1 ]
Li, Shuyu [1 ]
Guo, Wenyi [1 ]
Nie, Xiaoyan [1 ]
Xiao, Tianliang [2 ]
Liu, Zhaoyue [1 ]
机构
[1] Beihang Univ, Sch Chem, Beijing 100191, Peoples R China
[2] Yanshan Univ, Sch Environm & Chem Engn, Hebei Key Lab Appl Chem, Hebei Key Lab Nanobiotechnol, Qinhuangdao 066004, Peoples R China
基金
中国国家自然科学基金;
关键词
p-n junction; light-driven; ion transport; nanofluidic channel; polypyrrole; POLYPYRROLE; MEMBRANE; ELECTRODES; BEHAVIOR; PROTEIN; FILMS; XPS;
D O I
10.1021/acsanm.4c01928
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Artificial nanofluidic channels that achieve light-driven ion transport in biological systems based on photoelectric effect have attracted significant attention for signal transduction and light energy conversion. However, the light-responsive performance is limited by the charge separation efficiency on the surface of the channels. Herein, we introduce semiconductor p-n junctions into nanofluidic channels to enhance their light-driven ion transport. The p-n junction is formed by an n-type titanium dioxide (TiO2) nanoparticles layer on an electrochemically fabricated p-type polypyrrole (PPy) membrane. The light-induced charge separation at p-n junctions increases the surface charge density of the positively charged PPy membrane. Consequently, the light-driven ion current through the nanofluidic channels is enhanced from 79.6 to 111.9 nA by 40.6% when compared with a single-component p-type PPy membrane. The proof-of-concept demonstration of enhanced light-driven ion transport by semiconductor p-n junctions provides a route toward high-performance light-responsive nanofluidic channels, which demonstrates potential applications for light-controlled mass transport, signal transduction, and energy conversion.
引用
收藏
页码:13481 / 13488
页数:8
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