4.7 Article

In situ embedding of Mo2C/MoO3-x nanoparticles within a carbonized wood membrane as a self-supported pH-compatible cathode for efficient electrocatalytic H2 evolution

期刊

DALTON TRANSACTIONS
卷 49, 期 25, 页码 8557-8565

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0dt01690j

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资金

  1. Fundamental Research Funds for the Central Universities at North Minzu University [2019XYZHG07]
  2. West Light Foundation of the Chinese Academy of Sciences [XAB2018AW13]
  3. Natural Science Foundation of Ningxia Province [2018AAC02011]
  4. National Natural Science Foundation of China [21763001]
  5. Foundation of Academic Top-notch Talent Support Program of North Minzu University [2019BGBZ08]
  6. Foundation of Training Program for Yong and Middle-aged Talents of State Ethnic Affairs Commission of China
  7. Foundation of Key Laboratory of Electrochemical Energy Conversion Technology and Application

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A rational design of active, stable, and pH-compatible electrocatalysts is crucial to produce high-purity H(2)viaan electrocatalytic water splitting reaction. Herein, we report a carbonized wood membrane (CWM) embedded with Mo2C/MoO(3-x)nanoparticles (denoted as MCWM) as an efficient and stable self-supported H(2)evolution cathode in both acidic and alkaline solutions. The CWM features a high surface area with numerous aligned and open channels and abundant porosity, greatly facilitating electrolyte transport and gas release. Thein situembedded Mo2C/MoO(3-x)nanoparticles are uniformly dispersed throughout the entire framework of the CWM, providing abundant active sites. These structural synergies endow the as-fabricated MCWM electrodes with excellent electrocatalytic H(2)evolution activity, and the optimal MCWM electrode requires overpotentials of 187 and 275 mV to achieve a current density of 10 mA cm(-2)in 0.5 M H(2)SO(4)and 1.0 M KOH, respectively. Moreover, the MCWM electrode exhibits superior H(2)evolution stability at a high current density of 80 mA cm(-2)in both solutions with nearly 100% faradaic efficiencies. This work provides a promising nature-inspired strategy for the development of self-supported and pH-compatible electrodes for large-scale electrocatalytic H(2)evolution reactions.

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