Multifunctional Energy Storage and Conversion Devices

被引:479
作者
Huang, Yan [1 ]
Zhu, Minshen [1 ]
Huang, Yang [1 ]
Pei, Zengxia [1 ]
Li, Hongfei [1 ]
Wang, Zifeng [1 ]
Xue, Qi [1 ]
Zhi, Chunyi [1 ,2 ]
机构
[1] City Univ Hong Kong, Dept Phys & Mat Sci, 83 Tat Chee Ave, Hong Kong, Hong Kong, Peoples R China
[2] City Univ Hong Kong, Shenzhen Res Inst, Shenzhen 518000, Peoples R China
关键词
energy storage and conversion; fabrication; multifunctional devices; smart functional materials; STATE ASYMMETRIC SUPERCAPACITORS; GLASS-TRANSITION TEMPERATURE; SHAPE-MEMORY SUPERCAPACITOR; SELF-HEALING BEHAVIOR; ON-CHIP; THERMORESPONSIVE POLYMERS; PHOTOELECTRIC CONVERSION; DRUG-DELIVERY; HIGH-CONTRAST; SOLAR-CELL;
D O I
10.1002/adma.201601928
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multifunctional energy storage and conversion devices that incorporate novel features and functions in intelligent and interactive modes, represent a radical advance in consumer products, such as wearable electronics, healthcare devices, artificial intelligence, electric vehicles, smart household, and space satellites, etc. Here, smart energy devices are defined to be energy devices that are responsive to changes in configurational integrity, voltage, mechanical deformation, light, and temperature, called self-healability, electrochromism, shape memory, photodetection, and thermal responsivity. Advisable materials, device designs, and performances are crucial for the development of energy electronics endowed with these smart functions. Integrating these smart functions in energy storage and conversion devices gives rise to great challenges from the viewpoint of both understanding the fundamental mechanisms and practical implementation. Current state-of-art examples of these smart multifunctional energy devices, pertinent to materials, fabrication strategies, and performances, are highlighted. In addition, current challenges and potential solutions from materials synthesis to device performances are discussed. Finally, some important directions in this fast developing field are considered to further expand their application.
引用
收藏
页码:8344 / 8364
页数:21
相关论文
共 219 条
  • [1] Platinum Monolayer Electrocatalysts: Tunable Activity, Stability, and Self-Healing Properties
    Adzic, Radoslav R.
    [J]. ELECTROCATALYSIS, 2012, 3 (3-4) : 163 - 169
  • [2] Ahn BK, 2014, NAT MATER, V13, P867, DOI [10.1038/nmat4037, 10.1038/NMAT4037]
  • [3] Tandem dye-sensitized solar cell-powered electrochromic devices for the photovoltaic-powered smart window
    Ahn, Kwang-Soon
    Yoo, Sung Jong
    Kang, Moon-Sung
    Lee, Ji-Won
    Sung, Yung-Eun
    [J]. JOURNAL OF POWER SOURCES, 2007, 168 (02) : 533 - 536
  • [4] Building better batteries
    Armand, M.
    Tarascon, J. -M.
    [J]. NATURE, 2008, 451 (7179) : 652 - 657
  • [5] Switching the inside and the outside of aggregates of water-soluble block copolymers with double thermoresponsivity
    Arotçaréna, M
    Heise, B
    Ishaya, S
    Laschewsky, A
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (14) : 3787 - 3793
  • [6] Approaching the limits of transparency and conductivity in graphitic materials through lithium intercalation
    Bao, Wenzhong
    Wan, Jiayu
    Han, Xiaogang
    Cai, Xinghan
    Zhu, Hongli
    Kim, Dohun
    Ma, Dakang
    Xu, Yunlu
    Munday, Jeremy N.
    Drew, H. Dennis
    Fuhrer, Michael S.
    Hu, Liangbing
    [J]. NATURE COMMUNICATIONS, 2014, 5
  • [7] COMPUTATIONAL THERMODYNAMICS-BASED DESIGN OF NANODISPERSION-STRENGTHENED SHAPE MEMORY ALLOYS
    Bender, M. D.
    Olson, G. B.
    [J]. SMST-2007: PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON SHAPE MEMORY AND SUPERELASTIC TECHNOLOGIES, 2008, : 115 - 122
  • [8] Mendable polymers
    Bergman, Sheba D.
    Wudl, Fred
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2008, 18 (01) : 41 - 62
  • [9] Bharti B, 2015, NAT MATER, V14, P1104, DOI [10.1038/NMAT4364, 10.1038/nmat4364]
  • [10] Surface glass transition temperature of amorphous polymers. A new insight with SFM
    Bliznyuk, VN
    Assender, HE
    Briggs, GAD
    [J]. MACROMOLECULES, 2002, 35 (17) : 6613 - 6622