Solar photoelectrochemical synthesis of electrolyte-free H2O2 aqueous solution without needing electrical bias and H2

Author(s):  
Tae Hwa Jeon ◽  
Bupmo Kim ◽  
Chuhyung Kim ◽  
Chuan Xia ◽  
Haotian Wang ◽  
...  

An external bias-free photoelectrochemical system containing solid polymer electrolytes achieves efficient and durable synthesis of pure (electrolyte-free) aqueous H2O2 solution.

Author(s):  
Jijeesh Nair ◽  
◽  
Matteo Destro ◽  
Claudio Gerbaldi ◽  
Federico Bella

2008 ◽  
Vol 73 (12) ◽  
pp. 1777-1798 ◽  
Author(s):  
Olt E. Geiculescu ◽  
Rama V. Rajagopal ◽  
Emilia C. Mladin ◽  
Stephen E. Creager ◽  
Darryl D. Desmarteau

The present work consists of a series of studies with regard to the structure and charge transport in solid polymer electrolytes (SPE) prepared using various new bis(trifluoromethanesulfonyl)imide (TFSI)-based dianionic dilithium salts in crosslinked low-molecular-weight poly(ethylene glycol). Some of the thermal properties (glass transition temperature, differential molar heat capacity) and ionic conductivities were determined for both diluted (EO/Li = 30:1) and concentrated (EO/Li = 10:1) SPEs. Trends in ionic conductivity of the new SPEs with respect to anion structure revealed that while for the dilute electrolytes ionic conductivity is generally rising with increased length of the perfluoroalkylene linking group in the dianions, for the concentrated electrolytes the trend is reversed with respect to dianion length. This behavior could be the result of a combination of two factors: on one hand a decrease in dianion basicity that results in diminished ion pairing and an enhancement in the number of charge carriers with increasing fluorine anion content, thereby increasing ionic conductivity while on the other hand the increasing anion size and concentration produce an increase in the friction/entanglements of the polymeric segments which lowers even more the reduced segmental motion of the crosslinked polymer and decrease the dianion contribution to the overall ionic conductivity. DFT modeling of the same TFSI-based dianionic dilithium salts reveals that the reason for the trend observed is due to the variation in ion dissociation enthalpy, derived from minimum-energy structures, with respect to perfluoroalkylene chain length.


2021 ◽  
Vol 11 (4) ◽  
pp. 1561
Author(s):  
Gabrielle Foran ◽  
Nina Verdier ◽  
David Lepage ◽  
Arnaud Prébé ◽  
David Aymé-Perrot ◽  
...  

Solid polymer electrolytes have been widely proposed for use in all solid-state lithium batteries. Advantages of polymer electrolytes over liquid and ceramic electrolytes include their flexibility, tunability and easy processability. An additional benefit of using some types of polymers for electrolytes is that they can be processed without the use of solvents. An example of polymers that are compatible with solvent-free processing is epoxide-containing precursors that can form films via the lithium salt-catalyzed epoxide ring opening polymerization reaction. Many polymers with epoxide functional groups are liquid under ambient conditions and can be used to directly dissolve lithium salts, allowing the reaction to be performed in a single reaction vessel under mild conditions. The existence of a variety of epoxide-containing polymers opens the possibility for significant customization of the resultant films. This review discusses several varieties of epoxide-based polymer electrolytes (polyethylene, silicone-based, amine and plasticizer-containing) and to compare them based on their thermal and electrochemical properties.


2021 ◽  
Author(s):  
Heng Zhang ◽  
Ziyu Song ◽  
Weimin Yuan ◽  
Wenfang Feng ◽  
Jin Nie ◽  
...  

Polymer ◽  
2021 ◽  
pp. 123695
Author(s):  
Yubing Chen ◽  
Guangping Chen ◽  
Chaoqun Niu ◽  
Wenyan Shang ◽  
Rentong Yu ◽  
...  

2020 ◽  
pp. 152808372097062
Author(s):  
Muhammad Yameen Solangi ◽  
Umair Aftab ◽  
Muhammad Ishaque ◽  
Aqeel Bhutto ◽  
Ayman Nafady ◽  
...  

Solid polymer electrolytes (SPEs) are the best choice to replace liquid electrolytes in supercapacitors, fuel cells, solar cells and batteries. The main challenge in this filed is the ionic conductivity and thermal stability of SPEs which is still not up to mark, therefore more investigations are needed to address these issues. In this study, PVA/salt based SPEs was fabricated using both solution cast and electro-spinning methods to probe the effect of different salts such as (NaCl, KCl and KI) and their concentrations on the ionic conductivity. Scanning electron microscopy (SEM) x and Fourier Transform Infra-Red (FTIR) have been employed to study the morphology as well as the different functional groups of SPEs, respectively. It was noted that small addition of NaCl, KCl and KI salts in SPEs dramatically increased the ionic conductivity to 5.95×10−6, 5.31×10−6 and 4.83×10−6 S/cm, respectively. Importantly, the SPEs obtained with NaCl via electro-spinning have higher ionic conductivity (5.95×10−6 S/cm) than their casted SPEs (1.87×10−6 S/cm). Thermal stability was also studied at two different temperatures i.e. 80 °C and 100 °C. The weight loss percentage of electrospun SPEs have zero percent weight loss than the solution based SPEs. The combined results clearly indicated that the nature of salt, concentration and fabrication process play a vital role in the ionic conductivity. Also, the NaCl salt with low molecular weight at low concentrations shows an enhanced ionic conductivity.


2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Shujahadeen B. Aziz ◽  
Zul Hazrin Z. Abidin

Solid polymer electrolytes based on chitosan NaCF3SO3 have been prepared by the solution cast technique. X-ray diffraction shows that the crystalline phase of the pure chitosan membrane has been partially disrupted. The fourier transform infrared (FTIR) results reveal the complexation between the chitosan polymer and the sodium triflate (NaTf) salt. The dielectric constant and DC conductivity follow the same trend with NaTf salt concentration. The increase in dielectric constant at different temperatures indicates an increase in DC conductivity. The ion conduction mechanism follows the Arrhenius behavior. The dependence of DC conductivity on both temperature and dielectric constant (σdc(T,ε′)=σ0e−Ea/KBT) is also demonstrated.


Sign in / Sign up

Export Citation Format

Share Document