Telluride phosphide: Difference between revisions
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{{short description|Class of chemical compounds}} |
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The '''telluride phosphides''' are a class of [[mixed anion compounds]] containing both [[Telluride (chemistry)|telluride]] and [[phosphide]] ions (Te<sup>2−</sup> P<sup>3−</sup>). The phosphidotelluride or telluridophosphide compounds have a [TeP]<sup>3−</sup> group in which the tellurium atom has a bond to the phosphorus atom. A formal charge of −2 is on the phosphorus and −1 on the tellurium. There is no binary compound of [[tellurium]] and [[phosphorus]]. Not many telluride phosphides are known, but they have been discovered for [[noble metal]]s, [[actinide]]s, and [[group 4 element]]s. |
The '''telluride phosphides''' are a class of [[mixed anion compounds]] containing both [[Telluride (chemistry)|telluride]] and [[phosphide]] ions (Te<sup>2−</sup> P<sup>3−</sup>). The phosphidotelluride or telluridophosphide compounds have a [TeP]<sup>3−</sup> group in which the tellurium atom has a bond to the phosphorus atom. A formal charge of −2 is on the phosphorus and −1 on the tellurium. There is no binary compound of [[tellurium]] and [[phosphorus]]. Not many telluride phosphides are known, but they have been discovered for [[noble metal]]s, [[actinide]]s, and [[group 4 element]]s. |
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== Structure == |
== Structure == |
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The titanium group elements form layered hexagonal crystals that can be [[Intercalation (chemistry)|exfoliated]] to [[monolayer]]s. These contain [[ditelluride]] Te<sub>2</sub><sup>2-</sup> units.<ref name=":2">{{Cite journal| |
The titanium group elements form layered hexagonal crystals that can be [[Intercalation (chemistry)|exfoliated]] to [[monolayer]]s. These contain [[ditelluride]] Te<sub>2</sub><sup>2-</sup> units.<ref name=":2">{{Cite journal|last1=Chen|first1=K-W|last2=Das|first2=S|last3=Rhodes|first3=D|last4=Memaran|first4=S|last5=Besara|first5=T|last6=Siegrist|first6=T|last7=Manousakis|first7=E|last8=Balicas|first8=L|last9=Baumbach|first9=R E|date=2016-04-13|title=Uncovering the behavior of Hf 2 Te 2 P and the candidate Dirac metal Zr 2 Te 2 P|journal=Journal of Physics: Condensed Matter|volume=28|issue=14|pages=14LT01|doi=10.1088/0953-8984/28/14/14LT01|pmid=26953683|issn=0953-8984|arxiv=1602.03252|bibcode=2016JPCM...28nLT01C|s2cid=40508370}}</ref> These layered compounds can be [[Intercalation (chemistry)|intercalated]] to form [[non-stoichiometric compound]]s with [[zinc]], [[copper]] or [[cadmium]] by heating with the metals.<ref>{{Cite journal|last1=Yajima|first1=Takeshi|last2=Koshiko|first2=Masaki|last3=Zhang|first3=Yaoqing|last4=Oguchi|first4=Tamio|last5=Yu|first5=Wen|last6=Kato|first6=Daichi|last7=Kobayashi|first7=Yoji|last8=Orikasa|first8=Yuki|last9=Yamamoto|first9=Takafumi|last10=Uchimoto|first10=Yoshiharu|last11=Green|first11=Mark A.|date=December 2016|title=Selective and low temperature transition metal intercalation in layered tellurides|journal=Nature Communications|language=en|volume=7|issue=1|pages=13809|doi=10.1038/ncomms13809|issn=2041-1723|pmc=5171714|pmid=27966540|bibcode=2016NatCo...713809Y}}</ref> Actinide telluride phosphides contain diphosphide anions P<sub>2</sub>.<ref>{{Cite journal|last1=Stolze|first1=Karoline|last2=Isaeva|first2=Anna|last3=Schwarz|first3=Ulrich|last4=Doert|first4=Thomas|date=February 2015|title=UPTe, ThPTe and U 2 PTe 2 O: Actinide Pnictide Chalcogenides with Diphosphide Anions: Actinide Pnictide Chalcogenides with Diphosphide Anions|journal=European Journal of Inorganic Chemistry|language=en|volume=2015|issue=5|pages=778–785|doi=10.1002/ejic.201402951}}</ref> |
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==List== |
==List== |
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=== Artificial === |
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|<ref name=":1">{{Cite web|title=Prinzipien der Syntheseplanung in der anorganischen Festkörperchemie: Analyse der Phasenbildung in Systemen M/P/Te, M = Ti, Ce, Si|url=https://tud.qucosa.de/enwiki/api/qucosa%3A23662/attachment/ATT-0/|last=Philipp|first=Frauke|date=16 October 2008|website=Qucosa |
|<ref name=":1">{{Cite web|title=Prinzipien der Syntheseplanung in der anorganischen Festkörperchemie: Analyse der Phasenbildung in Systemen M/P/Te, M = Ti, Ce, Si|url=https://tud.qucosa.de/enwiki/api/qucosa%3A23662/attachment/ATT-0/|last=Philipp|first=Frauke|date=16 October 2008|website=Qucosa}}</ref><ref name=":3">{{Cite journal|last1=Baldus|first1=Hans Peter|last2=Blachnik|first2=Roger|date=1990-12-01|title=Neue A4B3-Moleküle: P3SbS3, P4S2Te und P4STe2 / New A4B3 Molecules: P3SbS3, P4S2Te and P4STe2|journal=Zeitschrift für Naturforschung B|volume=45|issue=12|pages=1605–1609|doi=10.1515/znb-1990-1201|s2cid=97778193|issn=1865-7117|doi-access=free}}</ref> |
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|<ref name=":1" /> |
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|Mn<sub>x</sub>Ti<sub>2</sub>PTe<sub>2</sub> |
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|''R''{{overbar|3}}''m''1 |
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|a=3.648 c=9.628 |
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|<ref name=":12">{{Cite journal |last1=Yajima |first1=Takeshi |last2=Koshiko |first2=Masaki |last3=Zhang |first3=Yaoqing |last4=Oguchi |first4=Tamio |last5=Yu |first5=Wen |last6=Kato |first6=Daichi |last7=Kobayashi |first7=Yoji |last8=Orikasa |first8=Yuki |last9=Yamamoto |first9=Takafumi |last10=Uchimoto |first10=Yoshiharu |last11=Green |first11=Mark A. |last12=Kageyama |first12=Hiroshi |date=2016-12-14 |title=Selective and low temperature transition metal intercalation in layered tellurides |journal=Nature Communications |language=en |volume=7 |issue=1 |page=13809 |doi=10.1038/ncomms13809 |issn=2041-1723 |pmc=5171714 |pmid=27966540}}</ref> |
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|Fe<sub>x</sub>Ti<sub>2</sub>PTe<sub>2</sub> |
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|''R''{{overbar|3}}''m''1 |
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|a=3.6356 c=9.639 |
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|Cu<sub>0.282</sub>Ti<sub>2</sub>PTe<sub>2</sub> |
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|''R''{{overbar|3}}''m''1 |
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|a=3.6726 c=9.7822 |
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|Zn<sub>0.36</sub>Ti<sub>2</sub>PTe<sub>2</sub> |
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|''R''{{overbar|3}}''m''1 |
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|a=3.6917 c=9.8480 |
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|Cd<sub>x</sub>Ti<sub>2</sub>PTe<sub>2</sub> |
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|''R''{{overbar|3}}''m''1 |
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|a=3.6806 c=10.238 |
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|also monolayer |
|also monolayer |
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|<ref>{{Cite journal| |
|<ref>{{Cite journal|last1=Tschulik|first1=Kristina|last2=Ruck|first2=Michael|last3=Binnewies|first3=Michael|last4=Milke|first4=Edgar|last5=Hoffmann|first5=Stefan|last6=Schnelle|first6=Walter|last7=Fokwa|first7=Boniface P. T.|last8=Gilleßen|first8=Michael|last9=Schmidt|first9=Peer|date=July 2009|title=Chemistry and Physical Properties of the Phosphide Telluride Zr 2 PTe 2|journal=European Journal of Inorganic Chemistry|language=en|volume=2009|issue=21|pages=3102–3110|doi=10.1002/ejic.200900346}}</ref> |
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|Cu<sub>x</sub>Zr<sub>2</sub>PTe<sub>2</sub> |
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|''R''{{overbar|3}}''m''1 |
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|a=3.8445 c=10.1082 |
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|Zn<sub>0.337</sub>Zr<sub>2</sub>PTe<sub>2</sub> |
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|''R''{{overbar|3}}''m''1 |
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|a=3.85873 c=10.1664 |
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|Cd<sub>0.194</sub>Zr<sub>2</sub>PTe<sub>2</sub> |
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|''R''{{overbar|3}}''m''1 |
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|a=3.8469 c=10.4197 |
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|<ref>{{Cite journal|last=Zintl|first=E.|date=1939-01-07|title=Intermetallische Verbindungen |
|<ref>{{Cite journal|last=Zintl|first=E.|date=1939-01-07|title=Intermetallische Verbindungen|journal=Angewandte Chemie|language=de|volume=52|issue=1|pages=1–6|doi=10.1002/ange.19390520102|bibcode=1939AngCh..52....1Z }}</ref> |
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|<ref name=":1" /><ref>{{Cite journal| |
|<ref name=":1" /><ref>{{Cite journal|last1=Jörgens|first1=Stefan|last2=Johrendt|first2=Dirk|last3=Mewis|first3=Albrecht|date=2003-06-06|title=BaP4Te2—A Ternary Telluride with P-Te Bonds and a Structural Fragment of Black Phosphorus|journal=Chemistry - A European Journal|volume=9|issue=11|pages=2405–2410|doi=10.1002/chem.200304858|pmid=12794885}}</ref> |
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|<ref>{{Cite journal|last1=Schmidt|first1=Peer|last2=Dallmann|first2=Hannelore|last3=Kadner|first3=Gudrun|last4=Krug|first4=Jutta|last5=Philipp|first5=Frauke|last6=Teske|first6=Klaus|date=October 2009|title=The thermochemical behaviour of Te8O10(PO4)4 and its use for phosphide telluride synthesis|url=https://hal.archives-ouvertes.fr/hal-00525849|journal=Journal of Inorganic and General Chemistry |
|<ref>{{Cite journal|last1=Schmidt|first1=Peer|last2=Dallmann|first2=Hannelore|last3=Kadner|first3=Gudrun|last4=Krug|first4=Jutta|last5=Philipp|first5=Frauke|last6=Teske|first6=Klaus|date=October 2009|title=The thermochemical behaviour of Te8O10(PO4)4 and its use for phosphide telluride synthesis|url=https://hal.archives-ouvertes.fr/hal-00525849|journal=Journal of Inorganic and General Chemistry |volume=635|issue=13–14|pages=2153|doi=10.1002/zaac.200900350|s2cid=98117179 |doi-access=free}}</ref> |
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|<ref>{{Cite journal|last=Kliche|first=Gerhard|date=1986-01-01|title=NOTIZEN: Iridiumphosphidtellurid, IrPTe / Iridium Phosphide Telluride, IrPTe |
|<ref>{{Cite journal|last=Kliche|first=Gerhard|date=1986-01-01|title=NOTIZEN: Iridiumphosphidtellurid, IrPTe / Iridium Phosphide Telluride, IrPTe|journal=Zeitschrift für Naturforschung B|volume=41|issue=1|pages=130–131|doi=10.1515/znb-1986-0126|s2cid=98059160|issn=1865-7117|doi-access=free}}</ref> |
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|<ref>{{Cite journal| |
|<ref>{{Cite journal|last1=Lutz|first1=H. D.|last2=Schmidt|first2=Th.|last3=Wäschenbach|first3=G.|date=1988|title=Phasendiagramme von Chalkogeniden und Pnictiden des Rutheniums und Osmiums mit Pyrit-, Markasit-, Löllingit‐ und Arsenopyritstruktur|journal=Zeitschrift für anorganische und allgemeine Chemie|language=de|volume=562|issue=1|pages=7–16|doi=10.1002/zaac.19885620102|issn=0044-2313}}</ref> |
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|<ref name=":0">{{Cite book| |
|<ref name=":0">{{Cite book|isbn=9783540456841|pages=153–154|first1= D.|last1= Kaczorowski|title= Pnictides and Chalcogenides iii: Ternary Actinide Pnictides and Chalcogenides}}</ref> |
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== References == |
== References == |
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{{Reflist}} |
{{Reflist}} |
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{{Tellurium compounds}} |
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{{Phosphorus compounds}} |
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{{Phosphides}} |
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[[Category:Tellurides]] |
[[Category:Tellurides]] |
Latest revision as of 19:33, 8 November 2023
The telluride phosphides are a class of mixed anion compounds containing both telluride and phosphide ions (Te2− P3−). The phosphidotelluride or telluridophosphide compounds have a [TeP]3− group in which the tellurium atom has a bond to the phosphorus atom. A formal charge of −2 is on the phosphorus and −1 on the tellurium. There is no binary compound of tellurium and phosphorus. Not many telluride phosphides are known, but they have been discovered for noble metals, actinides, and group 4 elements.
Structure
[edit]The titanium group elements form layered hexagonal crystals that can be exfoliated to monolayers. These contain ditelluride Te22- units.[1] These layered compounds can be intercalated to form non-stoichiometric compounds with zinc, copper or cadmium by heating with the metals.[2] Actinide telluride phosphides contain diphosphide anions P2.[3]
List
[edit]name | formula | MW | ratio
Te:P |
system | space group | unit cell
Å |
volume | density | optical | band gap | CAS | references | |
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P4S2Te | molecular | [4][5] | |||||||||||
P4STe2 | molecular | [4][5] | |||||||||||
Ti2PTe2 | hexagonal | R3m | a=3.6387 c=28.486 | metallic | on c axis | also monolayer | [4] | ||||||
MnxTi2PTe2 | R3m1 | a=3.648 c=9.628 | [6] | ||||||||||
FexTi2PTe2 | R3m1 | a=3.6356 c=9.639 | [6] | ||||||||||
Cu0.282Ti2PTe2 | R3m1 | a=3.6726 c=9.7822 | [6] | ||||||||||
Zn0.36Ti2PTe2 | R3m1 | a=3.6917 c=9.8480 | [6] | ||||||||||
CdxTi2PTe2 | R3m1 | a=3.6806 c=10.238 | [6] | ||||||||||
Zr2PTe2 | rhombohedral | R3m | a=3.8117 c=29.189 Z=3 | 367.27 | 6.356 | black | also monolayer | [7] | |||||
CuxZr2PTe2 | R3m1 | a=3.8445 c=10.1082 | [6] | ||||||||||
Zn0.337Zr2PTe2 | R3m1 | a=3.85873 c=10.1664 | [6] | ||||||||||
Cd0.194Zr2PTe2 | R3m1 | a=3.8469 c=10.4197 | [6] | ||||||||||
RuTeP | [8] | ||||||||||||
BaP4Te | orthorhombic | Pnma with | a =16.486 b =6.484 c =7.076 Z =4 | [4][9] | |||||||||
CeP0.4Te1.6 | [4] | ||||||||||||
CeP1.1Te0.9 | [4] | ||||||||||||
cerium phosphide telluride | Ce3Te3P | 3:1 | [10] | ||||||||||
Hf2Te2P | R3m | a=3.7946 c=29.14 | also monolayer | [1] | |||||||||
IrTeP | orthorhombic | a=6.030 b=6.131 c=12.132 | [11] | ||||||||||
OsTeP | 1:1 | arsenopyrite structure | P21/c | a = 6.2291 b = 6.1604 c = 6.2449 β = 112.01° | 222.2 | 10.43 | [12] | ||||||
ThPTe | 1:1 | tetragonal | a = 4.2505 and c = 17.268 | [13] | |||||||||
UPTe | tetragonal | a=4.100 c=17.026 | [13] | ||||||||||
U2PTe2O | pseudo tetragonal | a = 40.37c = 32.07 | |||||||||||
NpPTe | tetragonal | P4/nmm | a=4.265 c=9.067 | [13] | |||||||||
PuPTe | tetragonal | P4/nmm | a=4.289 c=9.098 | [13] | |||||||||
AmPTe | tetragonal | P4/nmm | a=4.269 c=9.050 | [13] |
References
[edit]- ^ a b Chen, K-W; Das, S; Rhodes, D; Memaran, S; Besara, T; Siegrist, T; Manousakis, E; Balicas, L; Baumbach, R E (2016-04-13). "Uncovering the behavior of Hf 2 Te 2 P and the candidate Dirac metal Zr 2 Te 2 P". Journal of Physics: Condensed Matter. 28 (14): 14LT01. arXiv:1602.03252. Bibcode:2016JPCM...28nLT01C. doi:10.1088/0953-8984/28/14/14LT01. ISSN 0953-8984. PMID 26953683. S2CID 40508370.
- ^ Yajima, Takeshi; Koshiko, Masaki; Zhang, Yaoqing; Oguchi, Tamio; Yu, Wen; Kato, Daichi; Kobayashi, Yoji; Orikasa, Yuki; Yamamoto, Takafumi; Uchimoto, Yoshiharu; Green, Mark A. (December 2016). "Selective and low temperature transition metal intercalation in layered tellurides". Nature Communications. 7 (1): 13809. Bibcode:2016NatCo...713809Y. doi:10.1038/ncomms13809. ISSN 2041-1723. PMC 5171714. PMID 27966540.
- ^ Stolze, Karoline; Isaeva, Anna; Schwarz, Ulrich; Doert, Thomas (February 2015). "UPTe, ThPTe and U 2 PTe 2 O: Actinide Pnictide Chalcogenides with Diphosphide Anions: Actinide Pnictide Chalcogenides with Diphosphide Anions". European Journal of Inorganic Chemistry. 2015 (5): 778–785. doi:10.1002/ejic.201402951.
- ^ a b c d e f Philipp, Frauke (16 October 2008). "Prinzipien der Syntheseplanung in der anorganischen Festkörperchemie: Analyse der Phasenbildung in Systemen M/P/Te, M = Ti, Ce, Si". Qucosa.
- ^ a b Baldus, Hans Peter; Blachnik, Roger (1990-12-01). "Neue A4B3-Moleküle: P3SbS3, P4S2Te und P4STe2 / New A4B3 Molecules: P3SbS3, P4S2Te and P4STe2". Zeitschrift für Naturforschung B. 45 (12): 1605–1609. doi:10.1515/znb-1990-1201. ISSN 1865-7117. S2CID 97778193.
- ^ a b c d e f g h Yajima, Takeshi; Koshiko, Masaki; Zhang, Yaoqing; Oguchi, Tamio; Yu, Wen; Kato, Daichi; Kobayashi, Yoji; Orikasa, Yuki; Yamamoto, Takafumi; Uchimoto, Yoshiharu; Green, Mark A.; Kageyama, Hiroshi (2016-12-14). "Selective and low temperature transition metal intercalation in layered tellurides". Nature Communications. 7 (1): 13809. doi:10.1038/ncomms13809. ISSN 2041-1723. PMC 5171714. PMID 27966540.
- ^ Tschulik, Kristina; Ruck, Michael; Binnewies, Michael; Milke, Edgar; Hoffmann, Stefan; Schnelle, Walter; Fokwa, Boniface P. T.; Gilleßen, Michael; Schmidt, Peer (July 2009). "Chemistry and Physical Properties of the Phosphide Telluride Zr 2 PTe 2". European Journal of Inorganic Chemistry. 2009 (21): 3102–3110. doi:10.1002/ejic.200900346.
- ^ Zintl, E. (1939-01-07). "Intermetallische Verbindungen". Angewandte Chemie (in German). 52 (1): 1–6. Bibcode:1939AngCh..52....1Z. doi:10.1002/ange.19390520102.
- ^ Jörgens, Stefan; Johrendt, Dirk; Mewis, Albrecht (2003-06-06). "BaP4Te2—A Ternary Telluride with P-Te Bonds and a Structural Fragment of Black Phosphorus". Chemistry - A European Journal. 9 (11): 2405–2410. doi:10.1002/chem.200304858. PMID 12794885.
- ^ Schmidt, Peer; Dallmann, Hannelore; Kadner, Gudrun; Krug, Jutta; Philipp, Frauke; Teske, Klaus (October 2009). "The thermochemical behaviour of Te8O10(PO4)4 and its use for phosphide telluride synthesis". Journal of Inorganic and General Chemistry. 635 (13–14): 2153. doi:10.1002/zaac.200900350. S2CID 98117179.
- ^ Kliche, Gerhard (1986-01-01). "NOTIZEN: Iridiumphosphidtellurid, IrPTe / Iridium Phosphide Telluride, IrPTe". Zeitschrift für Naturforschung B. 41 (1): 130–131. doi:10.1515/znb-1986-0126. ISSN 1865-7117. S2CID 98059160.
- ^ Lutz, H. D.; Schmidt, Th.; Wäschenbach, G. (1988). "Phasendiagramme von Chalkogeniden und Pnictiden des Rutheniums und Osmiums mit Pyrit-, Markasit-, Löllingit‐ und Arsenopyritstruktur". Zeitschrift für anorganische und allgemeine Chemie (in German). 562 (1): 7–16. doi:10.1002/zaac.19885620102. ISSN 0044-2313.
- ^ a b c d e Kaczorowski, D. Pnictides and Chalcogenides iii: Ternary Actinide Pnictides and Chalcogenides. pp. 153–154. ISBN 9783540456841.