4.8 Article

Morphology-Tuned Pt3Ge Accelerates Water Dissociation to Industrial-Standard Hydrogen Production over a wide pH Range

期刊

ADVANCED MATERIALS
卷 34, 期 30, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202202294

关键词

electrochemistry; hydrogen production; intermetallics; water electrolysis

资金

  1. Department of Science and Technology, India (DST) [DST/TMD/HFC/2K18/128(G)]
  2. DST [DST/SJF/CSA-02/2017-18]
  3. DST
  4. Council of Scientific and Industrial Research (CSIR)
  5. University Grant Commission (UGC)
  6. HRI Allahabad
  7. DST-SERB Funding [SRG/2020/001707]
  8. Jawaharlal Nehru Centre for Advanced Scientific Research

向作者/读者索取更多资源

The discovery of novel materials for industrial-standard hydrogen production is crucial for global energy infrastructure. This study introduces a novel electrocatalyst, Pt3Ge, which shows enhanced hydrogen production and operational stability compared to the commercial catalyst platinum.
The discovery of novel materials for industrial-standard hydrogen production is the present need considering the global energy infrastructure. A novel electrocatalyst, Pt3Ge, which is engineered with a desired crystallographic facet (202), accelerates hydrogen production by water electrolysis, and records industrially desired operational stability compared to the commercial catalyst platinum is introduced. Pt3Ge-(202) exhibits low overpotential of 21.7 mV (24.6 mV for Pt/C) and 92 mV for 10 and 200 mA cm(-2) current density, respectively in 0.5 m H2SO4. It also exhibits remarkable stability of 15 000 accelerated degradation tests cycles (5000 for Pt/C) and exceptional durability of 500 h (@10 mA cm(-2)) in acidic media. Pt3Ge-(202) also displays low overpotential of 96 mV for 10 mA cm(-2) current density in the alkaline medium, rationalizing its hydrogen production ability over a wide pH range required commercial operations. Long-term durability (>75 h in alkaline media) with the industrial level current density (>500 mA cm(-2)) has been demonstrated by utilizing the electrochemical flow reactor. The driving force behind this stupendous performance of Pt3Ge-(202) has been envisaged by mapping the reaction mechanism, active sites, and charge-transfer kinetics via controlled electrochemical experiments, ex situ X-ray photoelectron spectroscopy, in situ infrared spectroscopy, and in situ X-ray absorption spectroscopy further corroborated by first principles calculations.

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