Enhanced Humid Reliability of Organic Thermoelectrics via Crosslinking with Glycerol
Jaeyun Kim1, Jae Gyu Jang2, Jeonghun Kwak3
1School of Electrical and Computer Engineering, University of Seoul, Seoul 02504, Korea.
Abstract:
Poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS) has shown significant achievements in organic thermoelectrics (TEs) as an alternative for inorganic counterparts. However, PEDOT:PSS films have limited practical applications because their performance is sensitive to humidity. Crosslinking additives are utilized to improve the reliability of PEDOT:PSS film through enhancing hydrophobicity; among these, polyethylene glycol (PEG) is a widely-used additive. However, ether groups in PEG induce water molecules in the film through the hydrogen bond, which deteriorates the TE reliability. Here, we enhance the TE reliability of the PEDOT:PSS film using glycerol as an additive through the crosslinking reaction between the hydroxyl group in glycerol and the sulfonic acid in PEDOT:PSS. The TE reliability (1/Power factor (PF)) of PEG solution-treated PEDOT:PSS film (PEG solution-treated film) was 57% of its initial absolute value (0 h), after 288 h (two weeks) in a humid environment (95% relative humidity, 27 °C temperature). On the other hand, the glycerol solution-treated PEDOT:PSS film (glycerol solution-treated film) exhibited superior TE reliability and preserved 75% of its initial 1/PF. Furthermore, glycerol vapor treatment enabled the film to have stronger TE humid reliability, maintaining 82% of its initial 1/PF, with the same condition. This enhancement is attributed to the increased hydrophobicity and lower oxygen content of the glycerol vapor-treated PEDOT:PSS film (glycerol vapor-treated film), which provides little change in the chemical composition of PEDOT:PSS.
Related Concept Videos
02:42Aqueous Solutions and Heats of Hydration
When ionic compounds dissolve in water, the ions in the solid separate and disperse uniformly throughout the solution because water molecules surround and solvate the ions, reducing the strong electrostatic forces between them. This process...
02:29Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
01:43Thermosensation
02:15Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
01:26Thermal and Photochemical Electrocyclic Reactions: Overview
01:20Aldehydes and Ketones with Water: Hydrate Formation
The formation of hydrates is a reversible reaction. Hydrate formation is influenced by steric and electronic factors accompanying the alkyl substituents on the carbonyl group: The rate of hydrate formation increases with a decrease in the number of alkyl groups attached to the carbonyl carbon. Hence,...