51:
276:
201:
60:
42:
431:
444:
618:
315:
566:. An interface layer between tetracene and silicon transfers them into the silicon layer, where most of their energy can be converted into electricity.
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Junk
Science: An Overdue Indictment of Government, Industry, and Faith Groups That Twist Science for Their Own Gain
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reported an ambipolar light-emitting transistor made of a single tetracene crystal. Ambipolar means that the
138:
59:
408:
196:
714:
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482:
474:. It has the appearance of a pale orange powder. Tetracene is the four-ringed member of the series of
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72:
41:
905:
271:
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In 2024, it was used to produce lower-energy excitations in solar cells in a process known as
540:
506:
528:
claimed to have developed an electrically pumped laser based on tetracene during his time at
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870:
865:
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532:(1997–2002). However, his results could not be reproduced, and this is considered to be a
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Nomenclature of
Organic Chemistry: IUPAC Recommendations and Preferred Names 2013
222:
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1028:
926:
803:
581:
494:
299:
InChI=1S/C18H12/c1-2-6-14-10-18-12-16-8-4-3-7-15(16)11-17(18)9-13(14)5-1/h1-12H
972:
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829:
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357:
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1165:
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839:
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17:
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1038:
992:
880:
834:
793:
1129:
1109:
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890:
687:"Ambipolar Light-Emitting Transistors of a Tetracene Single Crystal"
421:
Except where otherwise noted, data are given for materials in their
1145:
475:
149:
137:
127:
752:
259:
685:
T. Takahashi; T. Takenobu; J. Takeya; Y. Iwasa (2007).
595:
New
Designs Could Boost Solar Cells Beyond Their Limits
439:
1138:
1057:
1011:
914:
853:
812:
786:
730:"Hawk Supercomputer Improves Solar Cell Efficiency"
619:International Union of Pure and Applied Chemistry
221:
92:Tetracyclooctadeca-1,3,5,7,9,11,13,15,17-nonaene
113:
764:
8:
390:436.7 °C (818.1 °F; 709.8 K)
771:
757:
749:
551:is transported by both positively charged
509:. Napthacene is the main component of the
274:
199:
177:
33:
241:
610:
539:In May 2007, Japanese researchers from
320:
295:
270:
380:357 °C (675 °F; 630 K)
190:
302:Key: IFLREYGFSNHWGE-UHFFFAOYSA-N
157:
7:
493:(OLEDs). Tetracene can be used as a
728:Paderborn University (2024-03-09).
212:
27:For the initiating explosive, see
25:
1187:Polycyclic aromatic hydrocarbons
780:Polycyclic aromatic hydrocarbons
487:organic field-effect transistors
429:
58:
49:
40:
472:polycyclic aromatic hydrocarbon
425:(at 25 °C , 100 kPa).
627:The Royal Society of Chemistry
578:, also known as benzanthracene
1:
691:Advanced Functional Materials
491:organic light-emitting diodes
1223:
362:228.29 g/mol
323:c1c2cc3cc4ccccc4cc3cc2ccc1
26:
481:Tetracene is a molecular
419:
331:
311:
286:
97:
83:
71:
66:
57:
48:
39:
946:-Benzopyrene(Olympicene)
555:and negatively charged
409:Magnetic susceptibility
370:Yellow to orange solid
1192:Organic semiconductors
703:10.1002/adfm.200700046
1202:Tetracyclic compounds
922:Benzacephenanthrylene
635:10.1039/9781849733069
483:organic semiconductor
73:Preferred IUPAC name
906:Tricyclobutabenzene
397:Solubility in water
36:
29:tetrazene explosive
658:Agin, Dan (2007).
511:tetracycline class
452:Infobox references
90:2,3-Benzanthracene
34:
1174:
1173:
1085:Hexabenzocoronene
968:Benzofluoranthene
963:Benzofluoranthene
958:Benzofluoranthene
953:Benzofluoranthene
876:Benzophenanthrene
697:(10): 1623–1628.
671:978-0-312-37480-8
644:978-0-85404-182-4
593:Daniel Oberhaus,
541:Tohoku University
526:Jan Hendrik Schön
507:chemoluminescence
460:Chemical compound
458:
457:
415:-168.0·10 cm/mol
255:CompTox Dashboard
139:Interactive image
16:(Redirected from
1214:
1197:Laser gain media
1075:Diindenoperylene
983:Dibenzanthracene
978:Dibenzanthracene
973:trans-Bicalicene
773:
766:
759:
750:
744:
743:
741:
740:
725:
719:
718:
713:. Archived from
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675:
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649:
648:
615:
601:, July 11th 2019
545:Osaka University
534:scientific fraud
513:of antibiotics.
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339:Chemical formula
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1139:General classes
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629:. p. 208.
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564:singlet fission
549:electric charge
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447: ?)
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1133:
1132:
1127:
1125:Trinaphthylene
1122:
1120:Superphenalene
1117:
1112:
1107:
1102:
1097:
1092:
1082:
1077:
1072:
1067:
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1034:Dibenzopyrenes
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1021:
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1003:Tetraphenylene
1000:
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861:Benzanthracene
857:
855:
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848:
847:
842:
837:
832:
827:
825:Acenaphthylene
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717:on 2012-12-10.
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466:, also called
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423:standard state
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88:Benzanthracene
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1024:Benzoperylene
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1016:
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989:
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871:Benzofluorene
869:
867:
866:Benzofluorene
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734:CleanTechnica
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664:. Macmillan.
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386:Boiling point
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376:Melting point
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272:DTXSID4059045
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191:ECHA InfoCard
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38:
30:
19:
1070:Dicoronylene
1019:Anthanthrene
943:
901:Triphenylene
895:
886:Fluoranthene
845:Phenanthrene
820:Acenaphthene
737:. Retrieved
733:
723:
715:the original
694:
690:
680:
660:
653:
622:
613:
561:
538:
520:
489:(OFETs) and
480:
467:
463:
462:
98:Identifiers
84:Other names
18:Naphthacenes
1044:Triangulene
1029:Corannulene
937:Benzopyrene
932:Benzopyrene
927:Benzopyrene
804:Naphthalene
582:Doxycycline
495:gain medium
468:naphthacene
367:Appearance
332:Properties
197:100.001.945
159:CHEBI:32600
86:Naphthacene
1181:Categories
1089:Hexa-cata-
830:Anthracene
739:2024-03-10
606:References
576:Tetraphene
503:sensitiser
499:dye lasers
485:, used in
402:Insoluble
358:Molar mass
243:QYJ5Z6712R
170:ChemSpider
126:3D model (
105:CAS Number
35:Tetracene
1166:Phenacene
1156:Cyclacene
1151:Circulene
1080:Heptacene
988:Pentacene
896:Tetracene
840:Phenalene
711:135786504
557:electrons
530:Bell Labs
523:physicist
464:Tetracene
77:Tetracene
1161:Helicene
1115:Sumanene
1105:Rubicene
1095:Kekulene
1065:Coronene
1058:7+ rings
1049:Zethrene
1039:Hexacene
993:Perylene
881:Chrysene
835:Fluorene
794:Butalene
621:(2014).
570:See also
411:(χ)
1130:Truxene
1110:Rubrene
1100:Ovalene
1012:6 rings
915:5 rings
854:4 rings
813:3 rings
799:Azulene
787:2 rings
521:German
517:History
470:, is a
445:what is
443: (
352:
210:PubChem
115:92-24-0
1207:Acenes
998:Picene
891:Pyrene
709:
668:
641:
476:acenes
440:verify
437:
316:SMILES
67:Names
1146:Acene
707:S2CID
599:Wired
588:Notes
553:holes
501:as a
291:InChI
150:ChEBI
128:JSmol
666:ISBN
639:ISBN
559:.
543:and
234:UNII
223:7080
179:6813
699:doi
631:doi
505:in
497:in
260:EPA
213:CID
1183::
732:.
705:.
695:17
693:.
689:.
637:.
625:.
597:,
536:.
478:.
350:12
346:18
1091:)
1087:(
944:H
942:6
772:e
765:t
758:v
742:.
701::
674:.
647:.
633::
435:Y
348:H
344:C
262:)
258:(
130:)
31:.
20:)
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.