Liquid and Photoliquefiable Azobenzene Derivatives for Solvent-free Molecular Solar Thermal Fuels

被引:23
|
作者
Yang, Yajing [1 ]
Huang, Shuai [2 ,3 ]
Ma, Yanduo [1 ]
Yi, Jie [1 ]
Jiang, Yuchun [1 ]
Chang, Xiaohong [1 ]
Li, Quan [2 ,3 ,4 ,5 ]
机构
[1] Liaoning Univ, Coll Chem, Liaoning Prov Key Lab Green Synth & Preparat Chem, Shenyang 110036, Peoples R China
[2] Southeast Univ, Inst Adv Mat, Nanjing 211189, Peoples R China
[3] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211189, Peoples R China
[4] Kent State Univ, Adv Mat & Liquid Crystal Inst, Kent, OH 44242 USA
[5] Kent State Univ, Chem Phys Interdisciplinary Program, Kent, OH 44242 USA
关键词
liquid azobenzene; photoliquefiable azobenzene; solvent-free; solar thermal fuel; heat release; ENERGY-STORAGE; PHASE-TRANSITIONS; PHOTOSWITCHES; HYBRID; FILM;
D O I
10.1021/acsami.2c07870
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A series of liquid and photoliquefiable azobenzene (Azo) derivatives (Azo-Cn-Br) have been synthesized for molecular solar thermal fuels. Each of the liquid and photoliquefiable azo derivatives shows a high degree of isomerization, a fast isomerization rate, a long half-life, an appropriate energy storage density, and a solvent-free "charging" and "discharging" process. The photoliquefied azo derivatives can isomerize upon UV light irradiation at low temperatures to give the "UV-charged" azo ones. Therefore, the phase transition enthalpy is stored simultaneously along with the isomerization enthalpy. The "UV-charged" azo derivatives are capable of releasing heat under the manipulation of blue light.
引用
收藏
页码:35623 / 35634
页数:12
相关论文
共 50 条
  • [41] Solvent-free Liquid Crystals and Liquids from DNA
    Liu, Kai
    Shuai, Min
    Chen, Dong
    Tuchband, Michael
    Gerasimov, Jennifer Y.
    Su, Juanjuan
    Liu, Qing
    Zajaczkowski, Wojciech
    Pisula, Wojciech
    Muellen, Klaus
    Clark, Noel A.
    Herrmann, Andreas
    CHEMISTRY-A EUROPEAN JOURNAL, 2015, 21 (13) : 4898 - 4903
  • [42] Liquid Quinones for Solvent-Free Redox Flow Batteries
    Shimizu, Akihiro
    Takenaka, Keisuke
    Handa, Naoyuki
    Nokami, Toshiki
    Itoh, Toshiyuki
    Yoshida, Jun-ichi
    ADVANCED MATERIALS, 2017, 29 (41)
  • [43] Reversible dioxygen binding in solvent-free liquid myoglobin
    Perriman A.W.
    Brogan A.P.S.
    Cölfen H.
    Tsoureas N.
    Owen G.R.
    Mann S.
    Nature Chemistry, 2010, 2 (8) : 622 - 626
  • [44] Multifactor theoretical modeling of solar thermal fuels built on azobenzene and norbornadiene scaffolds
    Szabo, Reuben
    Le, Khoa N.
    Kowalczyk, Tim
    SUSTAINABLE ENERGY & FUELS, 2021, 5 (08) : 2335 - 2346
  • [45] Hyper-thermal stability and unprecedented re-folding of solvent-free liquid myoglobin
    Brogan, Alex P. S.
    Siligardi, Giuliano
    Hussain, Rohanah
    Perriman, Adam W.
    Mann, Stephen
    CHEMICAL SCIENCE, 2012, 3 (06) : 1839 - 1846
  • [46] Eco-friendly solvent-free synthesis of thiazolylpyrazole derivatives
    Samir Bondock
    Hossam El-Azap
    Ez-Eldin M. Kandeel
    Mohamed A. Metwally
    Monatshefte für Chemie - Chemical Monthly, 2008, 139 : 1329 - 1335
  • [47] Synthesis of Thioamidoguanidine Derivatives under Solvent-Free Grinding Conditions
    Liu, Tianbao
    Peng, Yanfen
    Wang, Yajie
    Yong, Jiayuan
    Wang, Xin
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2018, 38 (04) : 969 - 974
  • [48] Michael additions on isoxazole derivatives under solvent-free conditions
    Rajanarendar, E
    Ramesh, P
    Karunakar, D
    INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 2003, 42 (08): : 1994 - 1996
  • [49] Solvent-free one-pot synthesis of pyrane derivatives
    Rostami-Charati, Faramarz
    Hossaini, Zinatossadat
    Khalilzadeh, Mohammad A.
    Moghaddam, Mahboube Islami
    Babaei, Vahid
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2012, 49 (02) : 405 - 408
  • [50] Applying solvent-free conditions to the synthesis of ferrocenyl chalcones derivatives
    Delgado, Fernando J. Correa
    Aponte-Santini, Juan C.
    Montes-Gonzalez, Ingrid
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 244