A P-N Organic Battery, a Method of Fabricating the Battery Thereof
20230343960 · 2023-10-26
Inventors
- Abdullah G. Al-Sehemi (Abha, SA)
- Aysegul Dere (Elazig, TR)
- Ahmed A. Al-Ghamdi (Jeddah, SA)
- Fahrettin YAKUPHANOGLU (Elazig, TR)
- Mehboobali Pannipara (Abha, SA)
Cpc classification
H01M10/36
ELECTRICITY
International classification
Abstract
In the present disclosure, a p-n organic battery comprising a p-type organic semiconductor and n-type organic semiconductor as active electrodes, anode and cathode current electrodes, separator and electrolyte and a method of fabricating the same is disclosed. The p-n organic battery has an p-type organic semiconductor separated from a n type organic semiconductor by an aqueous electrolyte solution, contained in an insulating vessel with suitable terminals (not shown) being provided in electric contact with the anode current electrode and the cathode current electrode. The aqueous electrolyte can comprise water, and a transition metal salt such as NiCl.sub.2, CuCl.sub.2 dissolved in the water.
Claims
1. A p-n organic battery comprising: a p-type organic electrode, a n-type organic electrode, said p-type and n-type organic electrodes being separated by an organic separator in a metal chloride electrolyte, said p-type electrode being an organic semiconductor and said n-type electrode being an organic semiconductor.
2. The p-n organic battery of claim 1, wherein the n-type and p-type organic semiconductors are composed of compressed, nano structured, powdered carbon based organic semiconductors.
3. The p-n organic battery of claim 2, wherein the p-type organic semiconductor is selected from a group of organic semiconductors consisting of any or a combination of nano polyaniline or its nanocomposites having polyaniline and graphene.
4. The p-n organic battery of claim 2, wherein the electrical conductivity of the nano polyaniline is at least 3×10.sup.−6 S/cm.
5. The p-n organic battery of claim 1, wherein the N-type organic semiconductor is selected from a group of organic semiconductors consisting essentially of any or a combination of 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA), fullerene, fullerene 70.
6. The p-n organic battery of claim 5, wherein the electrical conductivity of the 3,4,9,10-perylenetetracarboxylic dianhydride is at least 10.sup.−6 S/cm
7. The p-n organic battery of claim 1, wherein at least one of the organic semiconductors has a conductivity of least 10.sup.−6 S/cm.
8. The p-n organic battery of claim 1, wherein the total thickness of the battery electrodes is in a range of about 0.1 mm to about 1 mm.
9. The p-n organic battery of claim 1 wherein n-type organic semiconductors comprise small molecule compounds and aromatic compounds.
10. The p-n organic battery of claim 1, wherein concentration of CuCl.sub.2 in the metal chloride electrolyte ranges from about 0.5 M to about 5 M.
11. The p-n organic battery of claim 1, wherein the open circuit voltage of said organic battery is at least 1 V.
12. The p-n organic battery of claim 1, wherein the short circuit current of said p-n organic battery is at least 35 mA.
13. The p-n organic battery of claim 1, wherein a maximum power of p-n organic battery is at least 11 mW.
14. The p-n organic battery of claim 1, wherein the p-type electrode composed of nano polyaniline generates a power ranging from 5 mW to 15 mW.
15. A method of fabricating a battery comprising: sandwiching one or more active layers of a battery such that the active layers are connected to one another in series and at least one of the active layer is a p-n organic battery.
16. The method of fabricating a battery of claim 15, wherein each of the active layers of the battery are a p-n organic battery.
17. The method of fabricating a battery of claim 15, wherein the p-type electrode is an organic semiconductor selected from a group of organic semiconductors consisting of any or a combination of nano polyaniline or its nanocomposites having polyaniline and graphene.
18. The method of fabricating a battery of claim 15, wherein the n-type organic semiconductor is selected from a group of organic semiconductors consisting essentially of any or a combination of 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA), fullerene, fullerene 70.
Description
[0027] A more complete appreciation of the disclosure and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:
[0028]
[0029]
[0030]
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[0034]
DETAILED DESCRIPTION
[0035] For simplicity and illustrative purposes, the disclosed systems and methods are described by referring mainly to examples and embodiments thereof. In the following description, numerous specific details are set forth in order to provide a thorough understanding of the disclosed systems and methods. It will be readily apparent, however, that the disclosed systems and methods may be practiced without limitation to these specific details. In other instances, some methods and structures readily understood by one of ordinary skill in the art have not been described in detail so as not to unnecessarily obscure the disclosed systems and methods. As used herein, the terms “a” and “an” are intended to denote at least one of a particular element, the term “includes” means includes but not limited to, the term “including” means including but not limited to, and the term “based on” means based at least in part on.
[0036] The present disclosure provides a p-n organic battery comprising a p-type organic electrode, a n-type organic electrode, said p-type and n-type organic electrodes being separated by an organic separator in a metal chloride electrolyte, said p-type electrode being an organic semiconductor and said n-type electrode being an organic semiconductor.
[0037] In an embodiment, the p-n organic mattery may comprise n-type and p-type organic semiconductors that are composed of compressed, nano structured, powdered carbon based organic semiconductors. The p-n organic electrodes may also be comprised of Cu, and Al.
[0038] In an embodiment, the p-n organic mattery may comprise the p-type organic semiconductor that may be selected from a group of organic semiconductors consisting of any or a combination of nano polyaniline or its nanocomposites having polyaniline and graphene. The electrical conductivity of the p-type electrode made of nano polyaniline may be 3×10.sup.−6 S/cm or more.
[0039] In an embodiment, the p-n organic mattery may comprise, the n-type organic semiconductor that may be selected from a group of organic semiconductors consisting essentially of any or a combination of 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA), fullerene, fullerene 70. The electrical conductivity of the 3,4,9,10-perylenetetracarboxylic dianhydride is at least 10.sup.−6 S/cm.
[0040] In an embodiment, the organic semiconductors comprised in the p-n organic battery may have a conductivity of least 10.sup.−6 S/cm. The thickness of the battery electrodes may be in a range of 0.1 mm to 1 mm. The concentration of CuCl.sub.2 in the metal chloride electrolyte may range from about 0.5 M to about 5 M.
[0041] In the present disclosure, a p-n organic battery comprising a p-type organic semiconductor and n-type organic semiconductor as active electrodes, anode and cathode current electrodes, separator and electrolyte are provided. Referring now to
[0042] The anode of the p-n organic battery can be made of a metal or an alloy. In one embodiment, a current electrode of the battery may be aluminum. In another embodiment, the other current electrode may be copper.
[0043] In another embodiment, n-type organic semiconductor can be 3,4,9,10-perylenetetracarboxylic dianhydride organic semiconductor. In another embodiment, p-type organic semiconductor may be polyaniline. In still another embodiment, the active electrode may be an organic semiconductor selected from the group consisting of the polyaniline, polypyrolle, and 3,4,9,10-perylenetetracarboxylic dianhydride
[0044] In one embodiment, the open circuit voltage of the p-n organic battery is at least 1.0 V. In another embodiment, the open circuit voltage is at least 0.5 V. In another embodiment, the open circuit voltage is at least 0.65 V. In still another embodiment, the open circuit voltage is at least 1 V. In still another embodiment, the open circuit voltage is at least 1.1 V.
[0045] In one another embodiment, the short circuit current is at least 10 mA. In one embodiment, the maximum power of the p-n organic battery is at least 13 mW. In another embodiment, the maximum power of the cell is at least 15 mW. In another embodiment, the maximum power of the cell is at least 18 mW. In still another embodiment, the maximum power of the cell is at least 20 mW. In still another embodiment, the maximum power of the cell is at least 25 mW.
[0046] The open circuit voltage, the short circuit current, and the maximum power are improved by changing of active electrodes as described in the present disclosure. For example, selecting a n-type organic semiconductor or an p-type organic semiconductor as the active electrode may alter the open circuit voltage and short circuit current. The short circuit current may be changed by changing nanostructure as nanoparticles, nanorods or nanocluster of the organic semiconductors.
[0047] In an aspect, a method of fabricating a battery is disclosed. The method includes, sandwiching one or more active layers of a battery such that the active layers are connected to one another in series and at least one of the active layer is a p-n organic battery. The p-n organic battery can be fabricated by sandwiching multi active layers, at least one of which is the p-n organic battery, to one another in series.
[0048] In an embodiment, an exemplary illustration for synthesis of nano polyaniline is disclosed. The Polyaniline for electrodes can be synthesized by a chemical method that includes, distillation of pure Aniline, dissolving the nominal molar value of Aniline into Chloroform, mixing with Ammonium Persulphate and HCl to the Aniline solution which may be continued for at least 1 hour.
[0049] For the synthesis of polyaniline (PANI), firstly, pure aniline was distilled. The nominal molar value of aniline was dissolved in chloroform. Then, ammonium persulphate in HCl was added to aniline solution and the reaction was continued for 1 h. After 1 h, the obtained PANI was washed and dried.
[0050] In another embodiment, an X-Ray Diffraction and SEM Analysis of the obtained PANI can be done. The polyaniline synthesized can be subjected to X-ray diffraction analysis.
[0051] Referring to
[0052] Further, the synthesized PANI sample can be subjected to field emission scanning electron microscopy (FESEM). Referring now to
[0053]
[0054] Further, the current-voltage characteristics of the synthesized PANI sample may be recorded to assess the conductivity and the suitability of the synthesized PANI sample. Referring to
[0055]
[0056] What has been described and illustrated herein are examples of the disclosure along with some variations. The terms, descriptions, and figures used herein are set forth by way of illustration only and are not meant as limitations. Many variations are possible within the scope of the disclosure, which is intended to be defined by the following claims—and their equivalents—in which all terms are meant in their broadest reasonable sense unless otherwise indicated.