Significant enhancement of the performance of hydrogen evolution reaction through shape-controlled synthesis of hierarchical dendrite-like platinum

Herein, hierarchical dendrite-like Pt crystals with a distinct morphology were synthesized via a facile one-pot method without any templates. Formation of this hierarchical structure is dependent on the reaction duration. Interestingly, different hierarchical structures show different catalytic acti...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (17), p.868-877
Hauptverfasser: Lin, Liu, Sun, Zemin, Yuan, Mengwei, He, Jinlu, Long, Run, Li, Huifeng, Nan, Caiyun, Sun, Genban, Ma, Shulan
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Sprache:eng
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Zusammenfassung:Herein, hierarchical dendrite-like Pt crystals with a distinct morphology were synthesized via a facile one-pot method without any templates. Formation of this hierarchical structure is dependent on the reaction duration. Interestingly, different hierarchical structures show different catalytic activities. After a 12 hour reaction, tertiary structures of Pt are formed, which can act as outstanding catalysts in the hydrogen evolution reaction (HER). The onset potential of this dendrite-like Pt catalyst for the HER in a 0.5 M H 2 SO 4 solution is 15 mV, which outperforms that of commercial Pt/C (30 mV). Moreover, it shows significantly improved stability for HER as the polarization curve after 10 000 cycles retains a similar performance as in the initial test; this results in a loss of only 2.6% of its initial current density at an overpotential of 0.05 V. The distinct hierarchical dendrite-like structures are maintained after cycling and current-time tests, which can be responsible for the excellent performance of this catalyst. Hierarchically structured Pt micro-pine dendrites were prepared via a one-step solvothermal method, which exhibited excellent catalytic activity and significantly enhanced stability in comparison with the commercial Pt/C.
ISSN:2050-7488
2050-7496
DOI:10.1039/c8ta00993g