锂(药物)
离子
纳米技术
离子交换
电池(电)
膜
材料科学
化学
生物化学
有机化学
内分泌学
医学
功率(物理)
物理
量子力学
作者
Yang Liu,Yongchao Qian,Lin Fu,Congcong Zhu,Xin Li,Qingchen Wang,Haoyang Ling,Huaqing Du,Shengyang Zhou,Xiang‐Yu Kong,Lei Jiang,Liping Wen
出处
期刊:ACS central science
[American Chemical Society]
日期:2024-02-13
卷期号:10 (2): 469-476
被引量:6
标识
DOI:10.1021/acscentsci.3c01179
摘要
With the rapid development of the lithium ion battery industry, emerging lithium (Li) enrichment in nature has attracted ever-growing attention due to the biotoxicity of high Li levels. To date, fast lithium ion (Li+) detection remains urgent but is limited by the selectivity, sensitivity, and stability of conventional technologies based on passive response processes. In nature, archaeal plasma membrane ion exchangers (NCLX_Mj) exhibit Li+-gated multi/monovalent ion transport behavior, activated by different stimuli. Inspired by NCLX_Mj, we design a pH-controlled biomimetic Li+-responsive solid-state nanochannel system for on-demand Li+ detection using 2-(2-hydroxyphenyl)benzoxazole (HPBO) units as Li+ recognition groups. Pristine HPBO is not reactive to Li+, whereas negatively charged HPBO enables specific Li+ coordination under alkaline conditions to decrease the ion exchange capacity of nanochannels. On-demand Li+ detection is achieved by monitoring the decline in currents, thereby ensuring precise and stable Li+ recognition (>0.1 mM) in the toxic range of Li+ concentration (>1.5 mM) for human beings. This work provides a new approach to constructing Li+ detection nanodevices and has potential for applications of Li-related industries and medical services.
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