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p-doped, or reduced, causing n-doping. Upon charging, the radical is oxidized to an oxoammonium cation, and at the cathode, the radical is reduced to an aminoxyl anion. These processes are reversed upon discharge, and the radicals are regenerated. For stable charge and discharge, both the radical and doped form of the radical must be chemically stable. These batteries exhibit excellent cyclability and power density, attributed to the stability of the radical and the simple one-electron transfer reaction. Slight decrease in capacity after repeated cycling is likely due to a build up of swollen polymer particles which increase the resistance of the electrode. Because the radical polymers are considerably insulating, conductive additives are often added that which lower the theoretical specific capacity. Nearly all organic radical batteries feature a nearly constant voltage during discharge, which is an advantage over
644:
are difficult to find, new organic polymers can be much more easily synthesized. Another advantage is that polymer electrode materials may have lower redox potentials, but they have a higher energy density than inorganic materials. And, because the redox reaction kinetics for organics is higher than that for inorganics, they have a higher power density and rate performance. Because of the inherent flexibility and light weight of organic materials as compared to inorganic materials, polymeric electrodes can be printed, cast, and vapor deposited, enabling application in thinner and more flexible devices. Further, most polymers can be synthesized at low cost or extracted from biomass and even recycled, while inorganic metals are limited in availability and can be harmful to the environment.
622:
a much higher capacity (183 mAh g) as compared to bulk PPy (34.8 mAh g). The structure of the submicron polypyrrole anode allowed for increased electrical contact between the particles, and the electrolyte was able to further penetrate the polymeric active material. It has also been reported that amorphous polymeric active materials performs better than the crystalline counterpart. In 2014, it was demonstrated that crystalline oligopyrene exhibited a discharge capacity of 42.5 mAh g, while the amorphous oligopyrene has a higher capacity of 120 mAh g. Further, the crystalline version experienced a sloped charge and discharge voltage and considerable overpotential due to slow diffusion of ClO
601:
381:
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capacity. This issue can be lessened by incorporating the redox-active unit in the polymeric backbone, but this can decrease the theoretical specific capacity and increase electrochemical polarization. Another challenge is that besides conductive polymers, most polymeric electrodes are electrically insulating and therefore require conductive additives, reducing the battery's overall capacity. While polymers do have a low mass density, they have a greater volumetric energy density which in turn would require an increase in volume of devices being powered.
324:. They are ideal electrode materials due to their conductivity and redox activity, therefore not requiring large quantities of inactive conductive fillers. However they also tend to have low coulombic efficiency and exhibit poor cyclability and self-discharge. Due to the poor electronic separation of the polymer's charged centers, the redox potentials of conjugated polymers change upon charge and discharge due to a dependence on the dopant levels. As a result of this complication, the discharge profile (cell voltage vs. capacity) of
123:. An electrolyte transports charges between these electrodes. For a substance to be a suitable battery active material, it must be able to participate in a chemically and thermodynamically reversible redox reaction. Unlike metal-based batteries, whose redox process is based on the valence charge of the metals, the redox process of polymer-based batteries is based on a change of state of charge in the organic material. For a high energy density, the electrodes should have similar
403:
43:
are being explored, including conductive, non-conductive, and radical polymers. Batteries with a combination of electrodes (one metal electrode and one polymeric electrode) are easier to test and compare to current metal-based batteries, however batteries with both a polymer cathode and anode are also a current research focus. Polymer-based batteries, including metal/polymer electrode combinations, should be distinguished from metal-polymer batteries, such as a
364:
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charged upon assembly and the n-type material is reduced during discharge, while the metal is oxidized. For p-type organics in a metal-polymer test, the battery is already discharged upon assembly. During initial charging, electrolyte salt cations are reduced and mobilized to the polymeric anode while the organic is oxidized. During discharging, the polymer is reduced while the metal is oxidized to its cation.
635:
50/1 to 1000/1, five different sizes were achieved from 66 to 704 degrees of polymerization. A strong dependence on molecular weight was established, as the higher the molecular weight polymers exhibited a higher specific discharge capacity and better cyclability. This effect was attributed to a reciprocal relationship between molecular weight and solubility in the electrolyte.
394:
thiolate anion, formed by a reversible two-electron oxidation of the disulfide bond. Electrochemical storage in thioethers is achieved by the two-electron oxidation of a neutral thioether to a thioether with a +2 charge. As active materials, however, organosulfur compounds, however, exhibit weak cyclability.
621:
Electrochemical performance of polymer electrodes is affected by polymer size, morphology, and degree of crystallinity. In a polypyrrole (PPy)/Sodium ion hybrid battery, a 2018 study demonstrated that the polymer anode with a fluffy structure consisting of chains of submicron particles performed with
665:
A 2009 study evaluated the safety of a hydrophilic radical polymer and found that a radical polymer battery with an aqueous electrolyte is nontoxic, chemically stable, and non-explosive, and is thus a safer alternative to traditional metal-based batteries. Aqueous electrolytes present a safer option
634:
The molecular weight of polymers effects their chemical and physical properties, and thus the performance of a polymer electrode. A 2017 study evaluated the effect of molecular weight on electrochemical properties of poly(TEMPO methacrylate) (PTMA). By increasing the monomer to initiator ratio from
643:
Polymer-based batteries have many advantages over metal-based batteries. The electrochemical reactions involved are more simple, and the structural diversity of polymers and method of polymer synthesis allows for increased tunability for desired applications. While new types of inorganic materials
414:
are electrochemically active with stable organic radical pendant groups that have an unpaired electron in the uncharged state. Nitroxide radicals are the most commonly applied, though phenoxyl and hydrazyl groups are also often used. A nitroxide radical could be reversibly oxidized and the polymer
164:
is applied to oxidize the positive electrode and reduce the negative electrode. The electrolyte salt compensates the charges formed. The limiting factors upon charging a polymer-based battery differ from metal-based batteries and include the full oxidation of the cathode organic, full reduction of
42:
in batteries due to their synthetic availability, high-capacity, flexibility, light weight, low cost, and low toxicity. Recent studies have explored how to increase efficiency and reduce challenges to push polymeric active materials further towards practicality in batteries. Many types of polymers
393:
Sulfur is one of earth's most abundant elements and thus are advantageous for active electrode materials. Small molecule organosulfur active materials exhibit poor stability, which is partially resolved via incorporation into a polymer. In disulfide polymers, electrochemical charge is stored in a
656:
Though superior in this sense to small organic molecules, polymers still exhibit solubility in electrolytes, and battery stability is threatened by dissolved active material that can travel between electrodes, leading to decreased cyclability and self-discharge, which indicates weaker mechanical
376:
Carbonyl compounds have been heavily studied, and thus present an advantage, as new active materials with carbonyl pendant groups can be achieved by many different synthetic properties. Polymers with carbonyl groups can form multivalent anions. Stabilization depends on the substituents; vicinal
283:
Most polymer electrodes are tested in a metal-organic battery for ease of comparison to metal-based batteries. In this testing setup, the metal acts as the anode and either n- or p-type polymer electrodes can be used as the cathode. When testing the n-type organic, this metal-polymer battery is
612:
During discharge, conductive polymers have a sloping voltage that hinders their practical applications. This sloping curve indicates electrochemical instability which could be due to morphology, size, the charge repulsions within the polymer chain during the reaction, or the amorphous state of
185:
This electron transfer rate constant provides a benefit of polymer-based batteries, which typically have high values on the order of 10 cm s. The organic polymer electrodes are amorphous and swollen, which allows for a higher rate of ionic diffusion and further contributes to a better rate
360:, and other redox-active molecules with high reactivity and stable voltage upon charge and discharge. These polymers present an advantage over conjugated polymers due to their localized redox sites and more constant redox potential over charge/discharge.
173:
Upon discharge, the electrons go from the anode to cathode externally, while the electrolyte carries the released ions from the polymer. This process, and therefore the rate performance, is limited by the electrolyte ion travel and the electron-transfer
65:
An article titled "Plastic-Metal
Batteries: New promise for the electric car" wrote in 1982: "Two different organic polymers are being investigated for possible use in batteries" and indicated that the demo he gave was based on work begun in 1976.
1238:
Chen, Xiaoying; Liu, Li; Yan, Zichao; Huang, Zhifeng; Zhou, Qian; Guo, Guoxiong; Wang, Xianyou (2016). "The excellent cycling stability and superior rate capability of polypyrrole as the anode material for rechargeable sodium ion batteries".
186:
performance. Different polymer reactions, however, have different reaction rates. While a nitroxyl radical has a high reaction rate, organodisulfades have significantly lower rates because bonds are broken and new bonds are formed.
647:
Organic small molecules also possess many of these advantages, however they are more susceptible to dissolving in the electrolyte. Polymeric organic active materials less easily dissolve and thus exhibit superior cyclability.
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Despite the conductivity advantage of conjugated polymers, their many drawbacks as active materials have furthered the exploration of polymers with redox active pendant groups. Groups frequently explored include
102:
polymer that has been used for transistors and solar cells. Doped with lithium ions it offered significant electronic conductivity and remained stable through 3,000 charge/discharge cycles. Polymers that conduct
151:
and can generate heat during charge or discharge. Polymer-based batteries, however, have a more efficient charge/discharge process, resulting in improved theoretical rate performance and increased cyclability.
33:
materials instead of bulk metals to form a battery. Currently accepted metal-based batteries pose many challenges due to limited resources, negative environmental impact, and the approaching limit of progress.
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struggle with stability due to high levels of charge, failing to reach the ideal of one charge per monomer unit of polymer. Stabilizing additives can be incorporated, but these decrease the specific capacity.
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Charge and discharge of a Li/radical polymer battery, consisting of a Li anode and nitroxide radical group polymer. This is an example of a semi polymer based battery, where only one electrode is polymeric.
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over organic electrolytes which can be toxic and can form HF acid. The one-electron redox reaction of a radical polymer electrode during charging generates little heat and therefore has a reduced risk of
139:. During charging, p-type materials are oxidized and produce cations, while n-types are reduced and produce anions. B-type organics could be either oxidized or reduced during charging or discharging.
951:
Friebe, Christian; Schubert, Ulrich S. (December 2015). "Development of Active
Organic and Polymeric Materials for Batteries and Solar Cells: Introduction to Essential Characterization Techniques".
189:
Batteries are commonly evaluated by their theoretical capacity (the total capacity of the battery if 100% of active material were utilized in the reaction). This value can be calculated as follows:
271:
275:
where m is the total mass of active material, n is the number of transferred electrons per molar mass of active material, M is the molar mass of active material, and F is
Faraday's constant.
1274:
Han, Su Cheol; Bae, Eun Gyoung; Lim, Heatsal; Pyo, Myoungho (May 2014). "Non-crystalline oligopyrene as a cathode material with a high-voltage plateau for sodium ion batteries".
916:
Bhosale, Manik E.; Chae, Sudong; Kim, Ji Man; Choi, Jae-Young (2018). "Organic small molecules and polymers as an electrode material for rechargeable lithium ion batteries".
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for an organic material under practical measurement conditions. A battery could be 80% charged within 6 seconds. Energy density remained lower than inorganic batteries.
1351:
Koshika, K.; Kitajima, M.; Oyaizu, K.; Nishide, H. (September 2009). "A rechargeable battery based on hydrophilic radical polymer electrode and its green assessment".
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carbonyls are stabilized by enolate formation, aromatic carbonyls are stabilized by delocalization of charge, and quinoidal carbonyls are stabilized by aromaticity.
76:
in 2001, and began to focus on the organic batteries. In 2002, NEC researcher presented a paper on
Piperidinoxyl Polymer technology, and by 2005 they presented an
1136:
Xie, Jian; Gu, Peiyang; Zhang, Qichun (2017-09-08). "Nanostructured
Conjugated Polymers: Toward High-Performance Organic Electrodes for Rechargeable Batteries".
1316:; Fan, Jiyu; Monteiro, Michael J.; Jia, Zhongfan (2017). "The impact of the molecular weight on the electrochemical properties of poly(TEMPO methacrylate)".
860:
Muench, Simon; Wild, Andreas; Friebe, Christian; Häupler, Bernhard; Janoschka, Tobias; Schubert, Ulrich S. (2016-08-24). "Polymer-Based
Organic Batteries".
94:
In 2015 researchers developed an efficient, conductive, electron-transporting polymer. The discovery employed a "conjugated redox polymer" design with a
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can be n-doped or p-doped to form an electrochemically active material with conductivity due to dopant ions on a conjugated polymer backbone.
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Janoschka, Tobias; Hager, Martin D.; Schubert, Ulrich S. (2012-12-18). "Powering up the Future: Radical
Polymers for Battery Applications".
119:
Like metal-based batteries, the reaction in a polymer-based battery is between a positive and a negative electrode with different
91:. In 2007, Waseda announced a new ORB technology based on "soluble polymer, polynorborene with pendant nitroxide radical groups."
62:
Organic batteries are an alternative to the metal reaction battery technologies, and much research is taking place in this area.
626:. The amorphous oligopyrene had a voltage plateau during charge and discharge, as well as significantly less overpotential.
194:
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techniques can be tuned to minimize the solubility of the polymer in the electrolyte, thereby minimizing self-discharge.
54:
Organic polymers can be processed at relatively low temperatures, lowering costs. They also produce less carbon dioxide.
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battery, compared to the voltage plateau of a non-conjugated or organic radical polymer batter discharge curve (green).
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In a polystyrene chain, the phenyl groups are the pendant groups attached to the polymer's backbone chain.
600:
830:
148:
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Naegele, D (September 1988). "Electrically conductive polymers as rechargeable battery electrodes".
1392:, September 29, 2011, National University of Singapore's Nanoscience and Nanotechnology Initiative
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In a commercially available Li-ion battery, the Li+ ions are diffused slowly due to the required
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44:
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This graph is a schematic representation of the problematic sloping discharge curve (blue) of a
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175:
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Kever, Jeannie (2015-04-06). "Researchers discover N-type polymer for fast organic battery".
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25:
670:. Further studies are required to fully understand the safety of all polymeric electrodes.
80:(ORB) based on a modified PTMA, poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl meth-acrylate).
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1184:
667:
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Daniel Ruby (February 1982). "Plastic-Metal
Batteries: New promise for the electric car".
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316:(i.e. conjugated polymers) are embedded with the redox active group, as opposed to having
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Schon, Tyler B.; McAllister, Bryony T.; Li, Peng-Fei; Seferos, Dwight S. (2016).
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1390:"New material claimed to store more energy and cost less money than batteries"
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Nishide, Hiroyuki; Koshika, Kenichiroh; Oyaizu, Kenichi (2009-10-15).
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have been available for some time. The polymer exhibits the greatest
39:
1097:"Environmentally benign batteries based on organic radical polymers"
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300:. In these polymers, the redox group is embedded into the backbone.
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21:
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Kim, Jeonghun; Kim, Jung Ho; Ariga, Katsuhiko (December 2017).
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735:"Redox-Active Polymers for Energy Storage Nanoarchitectonics"
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Performance summary comparison of key polymer electrode types
35:
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1003:"The rise of organic electrode materials for energy storage"
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Charge/discharge redox reaction of thioether pendant group.
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Zhao, Qinglan; Whittaker, Andrew; Zhao, X. (2018-12-17).
73:
1000:
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1173:"Polymer Electrode Materials for Sodium-ion Batteries"
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the anode organic, or consumption of the electrolyte.
703:"Brown engineers build a better battery with plastic"
266:{\displaystyle C_{t}(mA\ h\ g^{-1})={\frac {mnF}{M}}}
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1396:"Organic Radical Battery with Piperidinoxyl Polymer"
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38:active polymers are attractive options for
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135:The active organic material could be a
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829:Nishide, Hiroyuki; Takeo Suga (2005).
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419:batteries. The polymer backbone and
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131:Classification of active materials
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918:Journal of Materials Chemistry A
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87:announced a technology based on
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328:batteries has a sloped curve.
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1150:10.1021/acsenergylett.7b00494
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988:10.1016/0167-2738(88)90316-5
617:Effect of polymer morphology
279:Charge and discharge testing
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874:10.1021/acs.chemrev.6b00070
752:10.1016/j.joule.2017.08.018
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10:
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1101:Pure and Applied Chemistry
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1365:10.1080/17518250903251775
1312:Zhang, Kai; Hu, Yuxiang;
953:Advanced Energy Materials
831:"Organic Radical Battery"
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412:organic radical batteries
288:Types of active materials
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137:p-type, n-type, or b-type
1402:"Flexible battery power"
1276:Journal of Power Sources
1114:10.1351/PAC-CON-08-12-03
1007:Chemical Society Reviews
630:Molecular weight control
410:Polymeric electrodes in
427:Control and performance
372:Carbonyl pendant groups
78:organic radical battery
45:lithium polymer battery
1071:10.1002/adma.201203119
965:10.1002/aenm.201500858
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354:organosulfur compounds
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296:Structures of various
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1423:Plastics applications
680:List of battery types
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486:75.7 after 80 cycles
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594:68 after 500 cycles
573:560 after 20 cycles
538:580 after 90 cycles
536:70 after 100 cycles
462:Cyclability (mAh g)
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143:Charge and discharge
1288:2014JPS...254...73H
1189:2018Mate...11.2567Z
924:(41): 19885–19911.
556:10 after 10 cycles
389:Organosulfur groups
332:Conductive polymers
322:conductive polymers
314:Conductive polymers
310:Conductive polymers
305:Conductive polymers
298:conductive polymers
182:, of the reaction.
1330:10.1039/C7PY00151G
1253:10.1039/C5RA22607D
1198:10.3390/ma11122567
1138:ACS Energy Letters
1059:Advanced Materials
1020:10.1039/C6CS00173D
982:. 28–30: 983–989.
980:Solid State Ionics
930:10.1039/C8TA04906H
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606:conductive polymer
417:conductive polymer
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326:conductive polymer
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72:was approached by
1324:(11): 1815–1823.
1318:Polymer Chemistry
1107:(11): 1961–1970.
1065:(48): 6397–6409.
1013:(22): 6345–6404.
868:(16): 9438–9484.
818:. pp. 89–91.
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