TiN and TiC as stable and promising supports for oxygen reduction reaction: Theoretical and experimental study
Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger i...
Ausführliche Beschreibung
Autor*in: |
Yue, Rengli [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2019transfer abstract |
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Übergeordnetes Werk: |
Enthalten in: Characterising shape patterns using features derived from best-fitting ellipsoids - Gontar, Amelia ELSEVIER, 2018, a journal devoted to applied physics and chemistry of surfaces and interfaces, Amsterdam |
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Übergeordnetes Werk: |
volume:495 ; year:2019 ; day:30 ; month:11 ; pages:0 |
Links: |
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DOI / URN: |
10.1016/j.apsusc.2019.143620 |
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ELV047948868 |
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520 | |a Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. | ||
520 | |a Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. | ||
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10.1016/j.apsusc.2019.143620 doi GBV00000000000753.pica (DE-627)ELV047948868 (ELSEVIER)S0169-4332(19)32417-1 DE-627 ger DE-627 rakwb eng 000 150 VZ 54.74 bkl Yue, Rengli verfasserin aut TiN and TiC as stable and promising supports for oxygen reduction reaction: Theoretical and experimental study 2019transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. Xia, Meirong oth Wang, Meiqiu oth Chen, Peixian oth Gong, WenMei oth Liao, Shijie oth Li, Zhiping oth Gao, Faming oth Zhang, Lin oth Wang, Jing oth Enthalten in Elsevier Gontar, Amelia ELSEVIER Characterising shape patterns using features derived from best-fitting ellipsoids 2018 a journal devoted to applied physics and chemistry of surfaces and interfaces Amsterdam (DE-627)ELV000097942 volume:495 year:2019 day:30 month:11 pages:0 https://doi.org/10.1016/j.apsusc.2019.143620 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 54.74 Maschinelles Sehen VZ AR 495 2019 30 1130 0 |
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10.1016/j.apsusc.2019.143620 doi GBV00000000000753.pica (DE-627)ELV047948868 (ELSEVIER)S0169-4332(19)32417-1 DE-627 ger DE-627 rakwb eng 000 150 VZ 54.74 bkl Yue, Rengli verfasserin aut TiN and TiC as stable and promising supports for oxygen reduction reaction: Theoretical and experimental study 2019transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. Xia, Meirong oth Wang, Meiqiu oth Chen, Peixian oth Gong, WenMei oth Liao, Shijie oth Li, Zhiping oth Gao, Faming oth Zhang, Lin oth Wang, Jing oth Enthalten in Elsevier Gontar, Amelia ELSEVIER Characterising shape patterns using features derived from best-fitting ellipsoids 2018 a journal devoted to applied physics and chemistry of surfaces and interfaces Amsterdam (DE-627)ELV000097942 volume:495 year:2019 day:30 month:11 pages:0 https://doi.org/10.1016/j.apsusc.2019.143620 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 54.74 Maschinelles Sehen VZ AR 495 2019 30 1130 0 |
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10.1016/j.apsusc.2019.143620 doi GBV00000000000753.pica (DE-627)ELV047948868 (ELSEVIER)S0169-4332(19)32417-1 DE-627 ger DE-627 rakwb eng 000 150 VZ 54.74 bkl Yue, Rengli verfasserin aut TiN and TiC as stable and promising supports for oxygen reduction reaction: Theoretical and experimental study 2019transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. Xia, Meirong oth Wang, Meiqiu oth Chen, Peixian oth Gong, WenMei oth Liao, Shijie oth Li, Zhiping oth Gao, Faming oth Zhang, Lin oth Wang, Jing oth Enthalten in Elsevier Gontar, Amelia ELSEVIER Characterising shape patterns using features derived from best-fitting ellipsoids 2018 a journal devoted to applied physics and chemistry of surfaces and interfaces Amsterdam (DE-627)ELV000097942 volume:495 year:2019 day:30 month:11 pages:0 https://doi.org/10.1016/j.apsusc.2019.143620 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 54.74 Maschinelles Sehen VZ AR 495 2019 30 1130 0 |
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10.1016/j.apsusc.2019.143620 doi GBV00000000000753.pica (DE-627)ELV047948868 (ELSEVIER)S0169-4332(19)32417-1 DE-627 ger DE-627 rakwb eng 000 150 VZ 54.74 bkl Yue, Rengli verfasserin aut TiN and TiC as stable and promising supports for oxygen reduction reaction: Theoretical and experimental study 2019transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. Xia, Meirong oth Wang, Meiqiu oth Chen, Peixian oth Gong, WenMei oth Liao, Shijie oth Li, Zhiping oth Gao, Faming oth Zhang, Lin oth Wang, Jing oth Enthalten in Elsevier Gontar, Amelia ELSEVIER Characterising shape patterns using features derived from best-fitting ellipsoids 2018 a journal devoted to applied physics and chemistry of surfaces and interfaces Amsterdam (DE-627)ELV000097942 volume:495 year:2019 day:30 month:11 pages:0 https://doi.org/10.1016/j.apsusc.2019.143620 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 54.74 Maschinelles Sehen VZ AR 495 2019 30 1130 0 |
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10.1016/j.apsusc.2019.143620 doi GBV00000000000753.pica (DE-627)ELV047948868 (ELSEVIER)S0169-4332(19)32417-1 DE-627 ger DE-627 rakwb eng 000 150 VZ 54.74 bkl Yue, Rengli verfasserin aut TiN and TiC as stable and promising supports for oxygen reduction reaction: Theoretical and experimental study 2019transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. Xia, Meirong oth Wang, Meiqiu oth Chen, Peixian oth Gong, WenMei oth Liao, Shijie oth Li, Zhiping oth Gao, Faming oth Zhang, Lin oth Wang, Jing oth Enthalten in Elsevier Gontar, Amelia ELSEVIER Characterising shape patterns using features derived from best-fitting ellipsoids 2018 a journal devoted to applied physics and chemistry of surfaces and interfaces Amsterdam (DE-627)ELV000097942 volume:495 year:2019 day:30 month:11 pages:0 https://doi.org/10.1016/j.apsusc.2019.143620 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 54.74 Maschinelles Sehen VZ AR 495 2019 30 1130 0 |
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TiN and TiC as stable and promising supports for oxygen reduction reaction: Theoretical and experimental study |
abstract |
Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. |
abstractGer |
Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. |
abstract_unstemmed |
Instability of catalyst supports is a primary reason for energy loss in proton exchange membrane fuel cells. In this study, Pt/TiN and Pt/TiC catalysts were synthesized by a solvothermal process. Density functional theory calculations revealed smaller distortion energies of Pt13 cluster and larger interaction between the Pt-TiN and Pt-TiC systems. The partial density of state calculations demonstrated that the Pt-d and C-p states and Ti-d and N-p states are energetically favorable and allow Pt-C-Ti and Pt-N-Ti to strongly bind to the TiC or TiN supports. As a result, Pt/TiN and Pt/TiC showed excellent durability as electrocatalysts. |
collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U |
title_short |
TiN and TiC as stable and promising supports for oxygen reduction reaction: Theoretical and experimental study |
url |
https://doi.org/10.1016/j.apsusc.2019.143620 |
remote_bool |
true |
author2 |
Xia, Meirong Wang, Meiqiu Chen, Peixian Gong, WenMei Liao, Shijie Li, Zhiping Gao, Faming Zhang, Lin Wang, Jing |
author2Str |
Xia, Meirong Wang, Meiqiu Chen, Peixian Gong, WenMei Liao, Shijie Li, Zhiping Gao, Faming Zhang, Lin Wang, Jing |
ppnlink |
ELV000097942 |
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hochschulschrift_bool |
false |
author2_role |
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doi_str |
10.1016/j.apsusc.2019.143620 |
up_date |
2024-07-06T17:33:16.015Z |
_version_ |
1803851866850721792 |
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7.399768 |