http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110684041-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5cedae1e4103c4e3719a5e9c94c2b510 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02E10-549 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K85-322 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F5-003 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K30-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01L51-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01L51-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F5-02 |
| filingDate | 2019-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_099e29e0a2576c114871c28510a0d590 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf3d2013dcabd88a6e83990a1a7693b7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3dbbb25b017d3320963dd26074ded25b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f6271c4da65ee13026d24187259fdff http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e0bd2451a8390c55ed912ac944a489d0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67d16ac9e1db883c3168ba0bcee372fe http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_48432aee4632399df0ffb000b5e520ed http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_23d5b5210c448567930663089bb237ee |
| publicationDate | 2020-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-110684041-A |
| titleOfInvention | Subnaphthalocyanine acceptor material and its synthesis method and solar cell |
| abstract | The sub-naphthalocyanine acceptor material, a synthesis method and a solar cell of the invention belong to the technical fields of organic synthesis and optoelectronics. Using 6,7-dicyanonaphthalene monoimide compound and boron trichloride as raw materials, in an organic solvent, the reaction is stirred at a certain temperature to generate chloronaphthalene phthalocyanine triimide. Naphthalocyanine triimide undergoes fluorine substitution, phenoxy substitution or phenylthio substitution, and finally a series of naphthalocyanine molecular acceptor materials are obtained. In the invention, imide groups are designed to be introduced into unsubstituted naphthalene phthalocyanine molecules, and a new type of acceptor material with good solubility, simple separation and purification and suitable LUMO energy level is synthesized. This type of acceptor material has a photoelectric conversion efficiency of up to 6.25% in bulk heterojunction solar cells with simple device structure requirements, and is a solution-processable organic solar energy of subphthalocyanine, subnaphthalocyanine, phthalocyanine and naphthalocyanine. The highest photoelectric conversion efficiency in the battery. |
| priorityDate | 2019-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 82.