Enhanced energy harvesting by concentration gradient-driven ion transport in SBA-15 mesoporous silica thin films

被引:71
作者
Hwang, Junho [1 ,2 ]
Kataoka, Sho [2 ,3 ]
Endo, Akira [2 ,3 ]
Daiguji, Hirofumi [1 ,2 ]
机构
[1] Univ Tokyo, Grad Sch Engn, Dept Mech Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
[2] Japan Sci & Technol Agcy JST, CREST, Chiyoda Ku, 7 Gobancho, Tokyo 1020076, Japan
[3] Natl Inst Adv Ind Sci & Technol, AIST Tsukuba Cent 5-2,1-1-1 Higashi, Tsukuba, Ibaraki 3058565, Japan
关键词
NANOFLUIDIC CHANNELS; POWER-GENERATION; REVERSE ELECTRODIALYSIS; PROTON TRANSPORT; CUBIC STRUCTURES; MEMBRANE; ELECTROLYTES; NANOPORES; THERMODYNAMICS; COEFFICIENTS;
D O I
10.1039/c6lc00844e
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nanofluidic energy harvesting systems have attracted interest in the field of battery application, particularly for miniaturized electrical devices, because they possess excellent energy conversion capability for their size. In this study, a mesoporous silica (MPS)-based nanofluidic energy harvesting system was fabricated and selective ion transport in mesopores as a function of the salt gradient was investigated. Aqueous solutions with three different kinds of monovalent electrolytes-KCl, NaCl, and LiCl-with different diffusion coefficients (D+) were considered. The highest power density was 3.90 W m(-2) for KCl, followed by 2.39 W m(-2) for NaCl and 1.29 W m(-2) for LiCl. Furthermore, the dependency of power density on the type of cation employed indicates that the harvested energy increases as the cation mobility increases, particularly at high concentrations. This cation-specific dependency suggests that the maximum power density increases by increasing the diffusion coefficient ratio of cations to anions, making this ratio a critical parameter in enhancing the performance of nanofluidic energy harvesting systems with extremely small pores ranging from 2 to 3 nm.
引用
收藏
页码:3824 / 3832
页数:9
相关论文
共 48 条
[1]   BEHAVIOR OF A PYROGENIC SILICA IN SIMPLE ELECTROLYTES [J].
ABENDROTH, RP .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1970, 34 (04) :591-+
[2]   Fabrication of 10 nm enclosed nanofluidic channels [J].
Cao, H ;
Yu, ZN ;
Wang, J ;
Tegenfeldt, JO ;
Austin, RH ;
Chen, E ;
Wu, W ;
Chou, SY .
APPLIED PHYSICS LETTERS, 2002, 81 (01) :174-176
[3]   Towards understanding the nanofluidic reverse electrodialysis system: well matched charge selectivity and ionic composition [J].
Cao, Liuxuan ;
Guo, Wei ;
Ma, Wen ;
Wang, Lin ;
Xia, Fan ;
Wang, Shutao ;
Wang, Yugang ;
Jiang, Lei ;
Zhu, Daoben .
ENERGY & ENVIRONMENTAL SCIENCE, 2011, 4 (06) :2259-2266
[4]   Electrokinetic energy conversion in micrometer-length nanofluidic channels [J].
Chang, Chih-Chang ;
Yang, Ruey-Jen .
MICROFLUIDICS AND NANOFLUIDICS, 2010, 9 (2-3) :225-241
[5]   Tunable reverse electrodialysis microplatform with geometrically controlled self-assembled nanoparticle network [J].
Choi, Eunpyo ;
Kwon, Kilsung ;
Kim, Daejoong ;
Park, Jungyul .
LAB ON A CHIP, 2015, 15 (01) :168-178
[6]   Ion transport in nanofluidic channels [J].
Daiguji, H ;
Yang, PD ;
Majumdar, A .
NANO LETTERS, 2004, 4 (01) :137-142
[7]   Ion transport in nanofluidic channels [J].
Daiguji, Hirofumi .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (03) :901-911
[8]   Ion Transport in Mesoporous Silica SBA-16 Thin Films with 3D Cubic Structures [J].
Daiguji, Hirofumi ;
Hwang, Junho ;
Takahashi, Asuka ;
Kataoka, Sho ;
Endo, Akira .
LANGMUIR, 2012, 28 (07) :3671-3677
[9]   Review article: Fabrication of nanofluidic devices [J].
Duan, Chuanhua ;
Wang, Wei ;
Xie, Quan .
BIOMICROFLUIDICS, 2013, 7 (02)
[10]   Anomalous ion transport in 2-nm hydrophilic nanochannels [J].
Duan, Chuanhua ;
Majumdar, Arun .
NATURE NANOTECHNOLOGY, 2010, 5 (12) :848-852