Liu Pei, Sun Yue, Zhu Congcong, Niu Bo, Huang Xiaodong, Kong Xiang-Yu, Jiang Lei, Wen Liping
CAS Key Laboratory of Bio-inspired Materials and Interfacial Science, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
School of Future Technology, University of Chinese Academy of Sciences, Beijing 100049, China.
Nano Lett. 2020 May 13;20(5):3593-3601. doi: 10.1021/acs.nanolett.0c00526. Epub 2020 Apr 8.
Chemical potential energy harvesting from the concentration gradient has been largely improved recently due to the development of nanofluidic energy conversion systems. However, the reported systems mainly focus on improving the membrane's performance but neglect the forms of concentration gradient. Here, we demonstrate the chemical reaction assisted chemical-potential-driven directional ion transport through layered titanium carbides membranes for energy harvesting. The MXene membrane with negatively charged nanochannels shows excellent cation selectivity and could reach 1.1 W/m for a 500-fold salinity gradient. By adopting the traditional neutralization reaction, HCl/KOH as the acid-base pair (ABP), the power density can reach 7.89 W/m with 1 M ABP due to the maintained transmembrane proton gradient. Besides, the membrane's excellent acid-base stability renders the power density stable for ∼192 h without obvious damping. This work provides new inspiration for industrial waste treatment issues and would be worth exploring its potential applications in extreme environments.
近年来,由于纳米流体能量转换系统的发展,从浓度梯度中获取化学势能有了很大的改进。然而,已报道的系统主要集中在改善膜的性能,而忽略了浓度梯度的形式。在此,我们展示了通过层状碳化钛膜进行化学反应辅助的化学势驱动定向离子传输以实现能量收集。具有带负电荷纳米通道的MXene膜表现出优异的阳离子选择性,对于500倍的盐度梯度,功率可达1.1 W/m²。通过采用传统的中和反应,以HCl/KOH作为酸碱对(ABP),由于跨膜质子梯度得以维持,1 M ABP时功率密度可达到7.89 W/m²。此外,该膜优异的酸碱稳定性使功率密度在约192小时内保持稳定,无明显衰减。这项工作为工业废物处理问题提供了新的思路,其在极端环境中的潜在应用值得探索。