A high H2 evolution rate under visible light of a CdS/TiO2NiS catalyst due to a directional electron transfer between the phases
The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electro...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Meng, Jianling [verfasserIn] |
|---|
| Format: |
E-Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
2019transfer abstract |
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| Umfang: |
5 |
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| Übergeordnetes Werk: |
Enthalten in: Keywords - 2013, [S.l.] |
|---|---|
| Übergeordnetes Werk: |
volume:27 ; year:2019 ; number:3 ; pages:544-548 ; extent:5 |
| Links: |
|---|
| DOI / URN: |
10.1016/j.cjche.2018.04.023 |
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ELV046505385 |
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| 245 | 1 | 2 | |a A high H2 evolution rate under visible light of a CdS/TiO2NiS catalyst due to a directional electron transfer between the phases |
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| 520 | |a The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. | ||
| 520 | |a The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. | ||
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10.1016/j.cjche.2018.04.023 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001045.pica (DE-627)ELV046505385 (ELSEVIER)S1004-9541(18)30296-9 DE-627 ger DE-627 rakwb eng 670 VZ 540 VZ 630 VZ Meng, Jianling verfasserin aut A high H2 evolution rate under visible light of a CdS/TiO2NiS catalyst due to a directional electron transfer between the phases 2019transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. Li, Yongdan oth Enthalten in Elsevier Science Keywords 2013 [S.l.] (DE-627)ELV011733624 volume:27 year:2019 number:3 pages:544-548 extent:5 https://doi.org/10.1016/j.cjche.2018.04.023 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_2008 GBV_ILN_2563 AR 27 2019 3 544-548 5 |
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10.1016/j.cjche.2018.04.023 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001045.pica (DE-627)ELV046505385 (ELSEVIER)S1004-9541(18)30296-9 DE-627 ger DE-627 rakwb eng 670 VZ 540 VZ 630 VZ Meng, Jianling verfasserin aut A high H2 evolution rate under visible light of a CdS/TiO2NiS catalyst due to a directional electron transfer between the phases 2019transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. Li, Yongdan oth Enthalten in Elsevier Science Keywords 2013 [S.l.] (DE-627)ELV011733624 volume:27 year:2019 number:3 pages:544-548 extent:5 https://doi.org/10.1016/j.cjche.2018.04.023 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_2008 GBV_ILN_2563 AR 27 2019 3 544-548 5 |
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10.1016/j.cjche.2018.04.023 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001045.pica (DE-627)ELV046505385 (ELSEVIER)S1004-9541(18)30296-9 DE-627 ger DE-627 rakwb eng 670 VZ 540 VZ 630 VZ Meng, Jianling verfasserin aut A high H2 evolution rate under visible light of a CdS/TiO2NiS catalyst due to a directional electron transfer between the phases 2019transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. Li, Yongdan oth Enthalten in Elsevier Science Keywords 2013 [S.l.] (DE-627)ELV011733624 volume:27 year:2019 number:3 pages:544-548 extent:5 https://doi.org/10.1016/j.cjche.2018.04.023 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_2008 GBV_ILN_2563 AR 27 2019 3 544-548 5 |
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10.1016/j.cjche.2018.04.023 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001045.pica (DE-627)ELV046505385 (ELSEVIER)S1004-9541(18)30296-9 DE-627 ger DE-627 rakwb eng 670 VZ 540 VZ 630 VZ Meng, Jianling verfasserin aut A high H2 evolution rate under visible light of a CdS/TiO2NiS catalyst due to a directional electron transfer between the phases 2019transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. Li, Yongdan oth Enthalten in Elsevier Science Keywords 2013 [S.l.] (DE-627)ELV011733624 volume:27 year:2019 number:3 pages:544-548 extent:5 https://doi.org/10.1016/j.cjche.2018.04.023 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_2008 GBV_ILN_2563 AR 27 2019 3 544-548 5 |
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10.1016/j.cjche.2018.04.023 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001045.pica (DE-627)ELV046505385 (ELSEVIER)S1004-9541(18)30296-9 DE-627 ger DE-627 rakwb eng 670 VZ 540 VZ 630 VZ Meng, Jianling verfasserin aut A high H2 evolution rate under visible light of a CdS/TiO2NiS catalyst due to a directional electron transfer between the phases 2019transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. Li, Yongdan oth Enthalten in Elsevier Science Keywords 2013 [S.l.] (DE-627)ELV011733624 volume:27 year:2019 number:3 pages:544-548 extent:5 https://doi.org/10.1016/j.cjche.2018.04.023 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_2008 GBV_ILN_2563 AR 27 2019 3 544-548 5 |
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high h2 evolution rate under visible light of a cds/tio2nis catalyst due to a directional electron transfer between the phases |
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A high H2 evolution rate under visible light of a CdS/TiO2NiS catalyst due to a directional electron transfer between the phases |
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The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. |
| abstractGer |
The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. |
| abstract_unstemmed |
The photocatalytic activity of CdS can be greatly improved by co-modification of NiS and TiO2 materials; furthermore the order of connection affects much. A directional electron transfer route via CdS → TiO2 → NiS is found crucial to the enhancement of ternary catalyst, where TiO2 acts as an electron reservoir and NiS works as an effective cocatalyst. CdS/TiO2NiS with NiS loaded on TiO2 has an activity of H2 evolution 2.5 times higher than NiS@CdS/TiO2 with NiS pre-loaded on CdS. Faster e−/h+ separation rates is obtained of CdS/TiO2@NiS under visible light than under extra UV light irradiation, which in turn demonstrates the importance of directional electron transfer route. |
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| title_short |
A high H2 evolution rate under visible light of a CdS/TiO2NiS catalyst due to a directional electron transfer between the phases |
| url |
https://doi.org/10.1016/j.cjche.2018.04.023 |
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Li, Yongdan |
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| doi_str |
10.1016/j.cjche.2018.04.023 |
| up_date |
2024-07-06T20:24:13.956Z |
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