50th Anniversary Perspective: Solid-State Multistimuli, Multiresponsive Polymeric Materials

2017 ◽  
Vol 50 (22) ◽  
pp. 8845-8870 ◽  
Author(s):  
Katie M. Herbert ◽  
Stephen Schrettl ◽  
Stuart J. Rowan ◽  
Christoph Weder
Batteries ◽  
2021 ◽  
Vol 7 (4) ◽  
pp. 75
Author(s):  
Shuo Yan ◽  
Chae-Ho Yim ◽  
Vladimir Pankov ◽  
Mackenzie Bauer ◽  
Elena Baranova ◽  
...  

Solid-state lithium metal batteries (LMBs) have become increasingly important in recent years due to their potential to offer higher energy density and enhanced safety compared to conventional liquid electrolyte-based lithium-ion batteries (LIBs). However, they require highly functional solid-state electrolytes (SSEs) and, therefore, many inorganic materials such as oxides of perovskite La2/3−xLi3xTiO3 (LLTO) and garnets La3Li7Zr2O12 (LLZO), sulfides Li10GeP2S12 (LGPS), and phosphates Li1+xAlxTi2−x(PO4)3x (LATP) are under investigation. Among these oxide materials, LLTO exhibits superior safety, wider electrochemical window (8 V vs. Li/Li+), and higher bulk conductivity values reaching in excess of 10−3 S cm−1 at ambient temperature, which is close to organic liquid-state electrolytes presently used in LIBs. However, recent studies focus primarily on composite or hybrid electrolytes that mix LLTO with organic polymeric materials. There are scarce studies of pure (100%) LLTO electrolytes in solid-state LMBs and there is a need to shed more light on this type of electrolyte and its potential for LMBs. Therefore, in our review, we first elaborated on the structure/property relationship between compositions of perovskites and their ionic conductivities. We then summarized current issues and some successful attempts for the fabrication of pure LLTO electrolytes. Their electrochemical and battery performances were also presented. We focused on tape casting as an effective method to prepare pure LLTO thin films that are compatible and can be easily integrated into existing roll-to-roll battery manufacturing processes. This review intends to shed some light on the design and manufacturing of LLTO for all-ceramic electrolytes towards safer and higher power density solid-state LMBs.


Molecules ◽  
2021 ◽  
Vol 26 (21) ◽  
pp. 6370
Author(s):  
Nadegda Bozova ◽  
Petar D. Petrov

Biopolymer materials have been considered a “green” alternative to petroleum-based polymeric materials. Biopolymers cannot completely replace synthetic polymers, but their application should be extended as much as possible, exploiting the benefits of their low toxicity and biodegradability. This contribution describes a novel strategy for the synthesis of super-macroporous 2-hydroxyethylcellulose (HEC) cryogels. The method involves cryogenic treatment of an aqueous solution of HEC and citric acid (CA), freeze drying, and thermally induced crosslinking of HEC macrochains by CA in a solid state. The effect of reaction temperature (70–180 °C) and CA concentration (5–20 mass % to HEC) on the reaction efficacy and physico-mechanical properties of materials was investigated. Highly elastic cryogels were fabricated, with crosslinking carried out at ≥ 100 °C. The storage modulus of the newly obtained HEC cryogels was ca. 20 times higher than the modulus of pure HEC cryogels prepared by photochemical crosslinking. HEC cryogels possess an open porous structure, as confirmed by scanning electron microscopy (SEM), and uptake a relatively large amount of water. The swelling degree varied between 17 and 40, depending on the experimental conditions. The degradability of HEC cryogels was demonstrated by acid hydrolysis experiments.


2021 ◽  
Author(s):  
Hong Yee Low ◽  
Anupama Ranganath ◽  
Chitrakala Ramasamy ◽  
ingrid Albertina

2008 ◽  
Vol 42 (5) ◽  
pp. 565-574 ◽  
Author(s):  
N. A. Belyaeva ◽  
A. M. Stolin ◽  
L. S. Stel’makh

2018 ◽  
Vol 17 ◽  
pp. 175-203
Author(s):  
Paweł E. Tomaszewski ◽  

Institute of Low Temperature and Structure Research of Polish Academy of Sciences celebrated its 50th anniversary in November 2016. The paper presents the history of the Institute going backward to the history of other ten scientific institutions from which the Institute was finally founded in 1966. It shows the efforts of Prof. Roman Ingarden and Prof. Włodzimierz Trzebiatowski to establish a powerful center of physics and physico-chemistry of solid state in Wrocław.


1990 ◽  
Vol 210 ◽  
Author(s):  
M. M. Lerner ◽  
S. J. Visco ◽  
M. Ue ◽  
M. M. Doeff ◽  
L C. Dejonghe

AbstractRecent work in our laboratory on polymeric organodisulfides has shown these materials to perform well as positive electrodes in solid-state batteries. The polymeric materials have been named solid redox polymerization electrodes (SRPE's) due to the reversible polymerization/depolymerization reaction that occurs on charge/discharge of the electrode. The cell reaction for SRPE-based cells can be described fora simple case as, 2n M + (SRS)n = n M2SRS, where M is an alkali metal (LiNaK) and R is an organic group. In the broader sense SRPE's can have more than two S groups per monomer R unit, and are reversible to other monovalent and divalent metals. In thefully charged state SRPE's consist of polydisulfide polymers and are depolymerized on discharge by scission of sulfur-sulfur bonds, leading to the formation of dithiolate salts in the fully discharged cell. SRPE's are easy to synthesize, are air stable, and should be very inexpensive in bulk quantities. Depending on the redox potential of the polydisulfide and reaction conditions, manydisulfides can be copolymerized by oxidizing a mixture of dithiols, x HSRSH + y HSR'SH + (x+y) l2 = (SRS)x(SR'S)y + 2(x+y) HI, allowing modification of the physical and/or redox properties of the SRPE's. A series of simple aliphatic dithiols including (HSCH2CH2SH), (HSCH2CH2OCH2CH2 SH), and (HSCH2CH2SCH2CH2SH) have been oxidized to polydisulfides and mixtures of the dithiols have been copolymerized. All of the resulting polymers and copolymers were evaluated in solid-state lithium cells, with some of the new materials demonstrating high levels of performance. The utilization of available capacity in the positive electrode was observed to be independent of electrode thickness for a number of SRPE's at loading levels up to 45% by weight. At 90°C, relatively thick positive electrodes based on (SCH2CH2S)n have been discharged to surface capacities of over 20 coulombs/cm2 at a current density of 0.5 mA/cm2. The discharge profiles for most of the aliphatic polydisulfides are exceedingly flat at slightly over 2 volts versus lithium. Although other polydisulfides such as those derived from the dithiazoles exhibit higher cell voltages, the low equivalent weight of materials such as (SCH2CH2S)n [46 g/equiv] and the low cost of such polymers indicates a potential for commercial application.


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