Salinity gradient energy is a chemical potential energy between two solutions with different ionic concentrations, which is also an ocean energy at the junction of rivers and seas. In our original work, the device "activated carbon//(0.083 M NaSO, 0.5 M NaSO)//vanadium pentoxide" for the conversion of salinity gradient energy was designed, and the conversion value of 6.29 J g was obtained. However, the low specific surface area of the original VO inevitably resulted in limited active sites and slow ionic transport rates, and the inherent lower conductivity and narrower layer spacing of the original VO also resulted in poor electrode kinetic performance and cycle stability, hindering its practical application. To solve the above problems, the present work provides a strategy of using polyaniline (PANI) molecule chain intercalation to regulate the layer spacing of the original VO, and through the expansion and traction of the layer spacing, the composite PANI/VO (PVO) with high specific surface area is prepared and used as an anode material for electrochemical conversion of salinity gradient energy application. The significantly increased layer spacing of the crystal plane (001) corresponding to the original VO was confirmed with the PANI by the hydrogen bonding and the van der Waals force. The high specific surface area of the composite provides more electrochemical active sites to realize a fast Na migration rate and high specific capacitance. Meanwhile, the inserted PANI molecule chain, which acts not only as a pillar enlarging the Na diffusion channel but also as an anchor locking the gap between VO bilayers, improves the structural stability of the VO electrode during the electrochemical conversion process. The proposed insertion strategy for the conductive polymer PANI has created a new way to improve the cycle stability performance of the salinity gradient energy conversion device.
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http://dx.doi.org/10.1021/acs.langmuir.4c03422 | DOI Listing |
ACS Appl Mater Interfaces
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College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu 610065, China.
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Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Bottlebrush block polymers, characterized by densely grafted side chains extending from a backbone, have recently garnered significant attention. A particularly attractive feature is the accessibility of ordered morphologies with domain spacings exceeding several hundred nanometers, a capability that is challenging to achieve with linear polymers. These large morphologies make bottlebrush block polymers promising for various applications, such as photonic crystals.
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January 2025
School of Information Technology, Jiangsu Open University, Nanjing, 210017, China.
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January 2025
Key Laboratory of Gas and Fire Control for Mines, Ministry of Education, Xuzhou, 221116, China.
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Department of Physics and Chemistry, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Republic of Korea.
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