4.6 Article

First electrochemical synthesis of mesoporous RhNi alloy films for an alkali-mediated hydrogen evolution reaction

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 9, 期 5, 页码 2754-2763

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ta09348c

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资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2020R1A6A3A03039037]
  2. ANSTO
  3. National Research Foundation of Korea [2020R1A6A3A03039037] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study presents a method for generating mesoporous RhNi alloy films via electrochemical co-deposition, enhancing the performance of catalytic electrodes. The control of Rh precursor concentration and Rh3+ : Ni2+ ratio can adjust alloy compositions, with further investigation into the impact of pH and deposition potentials.
Synthesizing mesoporous alloys composed of metals with divergent reactivities and standard redox potentials (E-0) is challenging because the kinetics of metal deposition is totally different. Herein, we report the first method to generate mesoporous RhNi alloy films via electrochemical co-deposition using self-assembled micelle templates. The concentration of Rh precursor (Rh3+) is crucial to control reaction kinetics and morphology because Rh deposition is the trigger of Ni co-deposition. The ratio of Rh3+ : Ni2+ (in the precursor) can be altered to generate different alloy compositions, and the impact of pH and deposition potentials is also investigated. We examine the mesoporous RhNi films as electrocatalytic electrodes for the hydrogen evolution reaction (HER). Ni-doping serves to enhance the HER performance of the mesoporous films, and the 1 : 1 alloy (mesoporous Rh49Ni51 film) shows the best performance with the overpotential of 59 mV @ 10 mA cm(-2) and Tafel slope of 67 mV dec(-1). The insight gained here will enable researchers to experiment with different noble-transition metal alloys to generate better porous electrodes for electrocatalysis.

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