4.3 Article

Millisecond-timescale electrodeposition of platinum atom-doped molybdenum oxide as an efficient electrocatalyst for hydrogen evolution reaction

Journal

FRONTIERS OF MATERIALS SCIENCE
Volume 16, Issue 3, Pages -

Publisher

HIGHER EDUCATION PRESS
DOI: 10.1007/s11706-022-0606-8

Keywords

platinum; molybdenum oxide; electrodeposition; hydrogen evolution reaction; doping; electrocatalyst

Funding

  1. Zhejiang Provincial Natural Science Foundation of China [LY20B030007, LQ20B010012]

Ask authors/readers for more resources

This study presents a straightforward method for one-pot electrodeposition of platinum atoms-doped molybdenum oxide films and demonstrates their superior electrocatalytic activity in the hydrogen evolution reaction. The one-pot electrodeposition method offers a higher current density compared to separately electrodeposited platinum and molybdenum oxide films.
We present a straightforward method for one-pot electrodeposition of platinum atoms-doped molybdenum oxide (Pt center dot MoO3-x) films and show their superior electrocatalytic activity in the hydrogen evolution reaction (HER). A similar to 15-nm-thick Pt center dot MoO3-x film was prepared by one-pot electrodeposition at -0.8 V for 1 ms. Due to considerably different solute concentrations, the content of Pt atoms in the electrode-posited composite electrocatalyst is low. No Pt crystals or islands were observed on the flat Pt center dot MoO3-x films, indicating that Pt atoms were homogeneously dispersed within the MoO3-x thin film. The catalytic performance and physicochemical features of Pt center dot MoO3-x as a HER electrocatalyst were characterized. The results showed that our Pt center dot MoO3-x film exhibits 23- and 11-times higher current density than Pt and MoO3-x electrodeposited individually under the same conditions, respectively. It was found that the dramatic enhancement in the HER performance was principally due to the abundant oxygen defects. The use of the developed one-pot electrodeposition and doping method can potentially be extended to various catalytically active metal oxides or hydroxides for enhanced performance in various energy storage and conversion applications.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available