Synthesis and photoluminescence of graphdiyne
Graphdiyne was prepared by a cross coupling reaction and characterized by SEM, TEM, XRD, Raman spectroscopy and XPS. Its photoluminescence (PL) properties were investigated. It was found that the graphdiyne has a thickness of ca. 1 μm, a O/C atomic ratio of ca. 0.1741 and many oxygen-containing func...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Zheng, Yong-ping [verfasserIn] Feng, Qian [verfasserIn] Tang, Nu-jiang [verfasserIn] Du, You-wei [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2018 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: New carbon materials - Amsterdam [u.a.] : Elsevier, 2006, 33, Seite 516-521 |
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| Übergeordnetes Werk: |
volume:33 ; pages:516-521 |
| DOI / URN: |
10.1016/S1872-5805(18)60354-3 |
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| Katalog-ID: |
ELV001456679 |
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| 520 | |a Graphdiyne was prepared by a cross coupling reaction and characterized by SEM, TEM, XRD, Raman spectroscopy and XPS. Its photoluminescence (PL) properties were investigated. It was found that the graphdiyne has a thickness of ca. 1 μm, a O/C atomic ratio of ca. 0.1741 and many oxygen-containing functional groups. It exhibits strong ultraviolet (UV) PL at 397 nm and optical absorption at ca. 280 nm. It is proposed that the oxygen-containing functional groups in the graphdiyne induce charge transfer, leading to the PL properties. As a new kind of artificially synthesized carbon allotrope, graphdiyne with UV PL have many applications. | ||
| 650 | 4 | |a Polybenzoxazine | |
| 650 | 4 | |a Heteroatom | |
| 650 | 4 | |a Porous carbons | |
| 650 | 4 | |a CO | |
| 700 | 1 | |a Feng, Qian |e verfasserin |4 aut | |
| 700 | 1 | |a Tang, Nu-jiang |e verfasserin |4 aut | |
| 700 | 1 | |a Du, You-wei |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t New carbon materials |d Amsterdam [u.a.] : Elsevier, 2006 |g 33, Seite 516-521 |h Online-Ressource |w (DE-627)534678270 |w (DE-600)2374609-9 |w (DE-576)284927015 |x 1872-5805 |7 nnns |
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2018 |
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2018 |
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10.1016/S1872-5805(18)60354-3 doi (DE-627)ELV001456679 (ELSEVIER)S1872-5805(18)60354-3 DE-627 ger DE-627 rda eng 620 660 DE-600 Zheng, Yong-ping verfasserin aut Synthesis and photoluminescence of graphdiyne 2018 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Graphdiyne was prepared by a cross coupling reaction and characterized by SEM, TEM, XRD, Raman spectroscopy and XPS. Its photoluminescence (PL) properties were investigated. It was found that the graphdiyne has a thickness of ca. 1 μm, a O/C atomic ratio of ca. 0.1741 and many oxygen-containing functional groups. It exhibits strong ultraviolet (UV) PL at 397 nm and optical absorption at ca. 280 nm. It is proposed that the oxygen-containing functional groups in the graphdiyne induce charge transfer, leading to the PL properties. As a new kind of artificially synthesized carbon allotrope, graphdiyne with UV PL have many applications. Polybenzoxazine Heteroatom Porous carbons CO Feng, Qian verfasserin aut Tang, Nu-jiang verfasserin aut Du, You-wei verfasserin aut Enthalten in New carbon materials Amsterdam [u.a.] : Elsevier, 2006 33, Seite 516-521 Online-Ressource (DE-627)534678270 (DE-600)2374609-9 (DE-576)284927015 1872-5805 nnns volume:33 pages:516-521 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 AR 33 516-521 |
| spelling |
10.1016/S1872-5805(18)60354-3 doi (DE-627)ELV001456679 (ELSEVIER)S1872-5805(18)60354-3 DE-627 ger DE-627 rda eng 620 660 DE-600 Zheng, Yong-ping verfasserin aut Synthesis and photoluminescence of graphdiyne 2018 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Graphdiyne was prepared by a cross coupling reaction and characterized by SEM, TEM, XRD, Raman spectroscopy and XPS. Its photoluminescence (PL) properties were investigated. It was found that the graphdiyne has a thickness of ca. 1 μm, a O/C atomic ratio of ca. 0.1741 and many oxygen-containing functional groups. It exhibits strong ultraviolet (UV) PL at 397 nm and optical absorption at ca. 280 nm. It is proposed that the oxygen-containing functional groups in the graphdiyne induce charge transfer, leading to the PL properties. As a new kind of artificially synthesized carbon allotrope, graphdiyne with UV PL have many applications. Polybenzoxazine Heteroatom Porous carbons CO Feng, Qian verfasserin aut Tang, Nu-jiang verfasserin aut Du, You-wei verfasserin aut Enthalten in New carbon materials Amsterdam [u.a.] : Elsevier, 2006 33, Seite 516-521 Online-Ressource (DE-627)534678270 (DE-600)2374609-9 (DE-576)284927015 1872-5805 nnns volume:33 pages:516-521 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 AR 33 516-521 |
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10.1016/S1872-5805(18)60354-3 doi (DE-627)ELV001456679 (ELSEVIER)S1872-5805(18)60354-3 DE-627 ger DE-627 rda eng 620 660 DE-600 Zheng, Yong-ping verfasserin aut Synthesis and photoluminescence of graphdiyne 2018 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Graphdiyne was prepared by a cross coupling reaction and characterized by SEM, TEM, XRD, Raman spectroscopy and XPS. Its photoluminescence (PL) properties were investigated. It was found that the graphdiyne has a thickness of ca. 1 μm, a O/C atomic ratio of ca. 0.1741 and many oxygen-containing functional groups. It exhibits strong ultraviolet (UV) PL at 397 nm and optical absorption at ca. 280 nm. It is proposed that the oxygen-containing functional groups in the graphdiyne induce charge transfer, leading to the PL properties. As a new kind of artificially synthesized carbon allotrope, graphdiyne with UV PL have many applications. Polybenzoxazine Heteroatom Porous carbons CO Feng, Qian verfasserin aut Tang, Nu-jiang verfasserin aut Du, You-wei verfasserin aut Enthalten in New carbon materials Amsterdam [u.a.] : Elsevier, 2006 33, Seite 516-521 Online-Ressource (DE-627)534678270 (DE-600)2374609-9 (DE-576)284927015 1872-5805 nnns volume:33 pages:516-521 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 AR 33 516-521 |
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10.1016/S1872-5805(18)60354-3 doi (DE-627)ELV001456679 (ELSEVIER)S1872-5805(18)60354-3 DE-627 ger DE-627 rda eng 620 660 DE-600 Zheng, Yong-ping verfasserin aut Synthesis and photoluminescence of graphdiyne 2018 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Graphdiyne was prepared by a cross coupling reaction and characterized by SEM, TEM, XRD, Raman spectroscopy and XPS. Its photoluminescence (PL) properties were investigated. It was found that the graphdiyne has a thickness of ca. 1 μm, a O/C atomic ratio of ca. 0.1741 and many oxygen-containing functional groups. It exhibits strong ultraviolet (UV) PL at 397 nm and optical absorption at ca. 280 nm. It is proposed that the oxygen-containing functional groups in the graphdiyne induce charge transfer, leading to the PL properties. As a new kind of artificially synthesized carbon allotrope, graphdiyne with UV PL have many applications. Polybenzoxazine Heteroatom Porous carbons CO Feng, Qian verfasserin aut Tang, Nu-jiang verfasserin aut Du, You-wei verfasserin aut Enthalten in New carbon materials Amsterdam [u.a.] : Elsevier, 2006 33, Seite 516-521 Online-Ressource (DE-627)534678270 (DE-600)2374609-9 (DE-576)284927015 1872-5805 nnns volume:33 pages:516-521 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 AR 33 516-521 |
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| title_sort |
synthesis and photoluminescence of graphdiyne |
| title_auth |
Synthesis and photoluminescence of graphdiyne |
| abstract |
Graphdiyne was prepared by a cross coupling reaction and characterized by SEM, TEM, XRD, Raman spectroscopy and XPS. Its photoluminescence (PL) properties were investigated. It was found that the graphdiyne has a thickness of ca. 1 μm, a O/C atomic ratio of ca. 0.1741 and many oxygen-containing functional groups. It exhibits strong ultraviolet (UV) PL at 397 nm and optical absorption at ca. 280 nm. It is proposed that the oxygen-containing functional groups in the graphdiyne induce charge transfer, leading to the PL properties. As a new kind of artificially synthesized carbon allotrope, graphdiyne with UV PL have many applications. |
| abstractGer |
Graphdiyne was prepared by a cross coupling reaction and characterized by SEM, TEM, XRD, Raman spectroscopy and XPS. Its photoluminescence (PL) properties were investigated. It was found that the graphdiyne has a thickness of ca. 1 μm, a O/C atomic ratio of ca. 0.1741 and many oxygen-containing functional groups. It exhibits strong ultraviolet (UV) PL at 397 nm and optical absorption at ca. 280 nm. It is proposed that the oxygen-containing functional groups in the graphdiyne induce charge transfer, leading to the PL properties. As a new kind of artificially synthesized carbon allotrope, graphdiyne with UV PL have many applications. |
| abstract_unstemmed |
Graphdiyne was prepared by a cross coupling reaction and characterized by SEM, TEM, XRD, Raman spectroscopy and XPS. Its photoluminescence (PL) properties were investigated. It was found that the graphdiyne has a thickness of ca. 1 μm, a O/C atomic ratio of ca. 0.1741 and many oxygen-containing functional groups. It exhibits strong ultraviolet (UV) PL at 397 nm and optical absorption at ca. 280 nm. It is proposed that the oxygen-containing functional groups in the graphdiyne induce charge transfer, leading to the PL properties. As a new kind of artificially synthesized carbon allotrope, graphdiyne with UV PL have many applications. |
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| title_short |
Synthesis and photoluminescence of graphdiyne |
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| author2 |
Feng, Qian Tang, Nu-jiang Du, You-wei |
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| doi_str |
10.1016/S1872-5805(18)60354-3 |
| up_date |
2024-07-06T21:26:13.161Z |
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