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Visibly transparent, near-infrared-absorbing and ultraviolet-absorbing photovoltaic devices

A photovoltaic device and near-infrared technology, applied in photovoltaic power generation, photosensitive equipment, luminescent materials, etc., to reduce manufacturing complexity, improve device efficiency and performance, and avoid waste treatment and disposal

Pending Publication Date: 2020-03-31
UBIQUITOUS ENERGY INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, a variety of organic and molecular semiconductors exist, but many exhibit strong absorption in the visible spectrum and are therefore not optimal for use in window glass-based photovoltaics

Method used

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  • Visibly transparent, near-infrared-absorbing and ultraviolet-absorbing photovoltaic devices
  • Visibly transparent, near-infrared-absorbing and ultraviolet-absorbing photovoltaic devices
  • Visibly transparent, near-infrared-absorbing and ultraviolet-absorbing photovoltaic devices

Examples

Experimental program
Comparison scheme
Effect test

example D

[0365] Example DiCN structures include structures according to Formula I:

[0366]

[0367] In compounds of formula I, optionally, Y is F, Cl, Br, alkoxy, alkyl or aryl. In compounds of formula I, optionally, n is an integer of 0-5. In the compound of formula I, optionally, X is C(CN) 2 , O, S, C(O) or SO 2 . Optionally, Ar is an aryl group such as phenyl, thienyl, thiazolyl and the like.

[0368] Examples of fused π systems include, but are not limited to: anthra[1,9-bc:5,10-b'c']dithiophenediyl (e.g., anthra[1,9-bc:5,10- b'c']dithiophene-1,6-diyl); 4,9-dihydro-s-indacene[1,2-b:5,6-b']dithiophenediyl (e.g., 4,9-dihydro-s-indacene[1,2-b:5,6-b′]dithiophene-2,7-diyl); unsubstituted and 5-substituted 5H- Dithieno[3,2-b:2′,3′-h]carbazolediyl (for example, 5-methyl-5H-dithieno[3,2-b:2′,3′-h] carbazole-2,8-diyl); unsubstituted and 4-substituted 4H-dithieno[3,2-b:2′,3′-d]pyrrolediyl (e.g., 4-methyl Base-4H-dithieno[3,2-b:2′,3′-d]pyrrole-2,6-diyl or 4-(4-methylphenyl)-4H-di...

example CBI

[0486] Example CBI compounds include according to formula Xa:

[0487]

[0488] And formula Xb:

[0489] compound of,

[0490] and its derivatives. Optionally, in compounds according to formula Xa and formula Xb, each R is independently selected from the group consisting of H, aryl, heteroaryl, alkyl, alkenyl, alkynyl, cycloalkyl, hetero Cyclic groups and electron-withdrawing groups (eg, CN, halogen, etc.).

[0491] In some embodiments, the acceptor material contains a CBI compound or a CBI derivative, and the donor material includes boron-dipyrromethene (BODIPY) compounds, phthalocyanines, naphthalocyanines, nickel dithiolate (NDT) compounds, Dicyano-indandione (DiCN), benzothiadiazole (BT), benzobisthiadiazole (BBT), diketopyrrolopyrrole diphenylthiopheneamine (DPP-DPTA) or combinations thereof . Examples of useful BODIPY compounds include, but are not limited to, the BODIPY compounds described herein. Examples of useful phthalocyanines and naphthalocyanines inclu...

example

[0506] Example cardiocyclenes comprise compounds according to formula XIIa

[0507]

[0508] and Formula VIIb:

[0509] compound of,

[0510] and its derivatives. Optionally, in compounds according to formula XIIa and formula XIIb, each R is independently selected from the group consisting of H, aryl, heteroaryl, alkyl, alkenyl, alkynyl, cycloalkyl, hetero Cyclic groups and electron-withdrawing groups (eg, CN, halogen, etc.).

[0511] In some embodiments, the acceptor material contains a cardiocycle or a cardiocycle derivative, and the donor material includes a boron-dipyrromethene (BODIPY) compound, phthalocyanine, naphthalocyanine, nickel dithiolate (NDT ) compound, dicyano-indandione (DiCN), benzothiadiazole (BT), benzobisthiadiazole (BBT), diketopyrrolopyrrole diphenylthiopheneamine (DPP-DPTA) or a combination thereof. Examples of useful BODIPY compounds include, but are not limited to, the BODIPY compounds described herein. Examples of useful phthalocyanines an...

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PUM

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Abstract

Visibly transparent photovoltaic devices are disclosed, such as those are transparent to visible light but absorb near-infrared light and / or ultraviolet light. The photovoltaic devices make use of transparent electrodes and near-infrared or ultraviolet absorbing visibly transparent photoactive compounds, optical materials, and / or buffer materials.

Description

[0001] Cross References to Related Applications [0002] This application claims U.S. Provisional Application No. 62 / 521,154, filed June 16, 2017, U.S. Provisional Application No. 62 / 521,158, filed June 16, 2017, U.S. Provisional Application No. 62 / 521,158, filed June 16, 2017 Application No. 62 / 521,160, U.S. Provisional Application No. 62 / 521,211 filed June 16, 2017, U.S. Provisional Application No. 62 / 521,214 filed June 16, 2017 and The benefit and priority of filed U.S. Provisional Application No. 62 / 521,224, each of which is hereby incorporated by reference in its entirety. technical field [0003] The present application relates generally to the field of optically active materials and devices, and more particularly, to visible transparent photovoltaic devices and materials for visible transparent photovoltaic devices. Background technique [0004] The surface area required to harness solar energy remains an obstacle to offsetting a sizable portion of non-renewable ene...

Claims

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Application Information

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IPC IPC(8): C07D333/52H01G9/20H01L51/42H01L51/46C09K11/06C07D333/60
CPCH10K85/621H10K85/636H10K85/6576H10K85/311H10K85/322H10K85/6572H10K30/30H10K30/80H10K30/82Y02E10/549H10K30/85H10K85/331H10K85/631H10K85/657H10K85/655H10K85/381H10K85/324H10K85/40
Inventor 迈尔斯·巴尔里沙·潘迪马修·朱罗波·何
Owner UBIQUITOUS ENERGY INC