4.7 Article

Cooperative electrocatalytic N2 reduction based on WS2-covered Co9S8 hexagonal heterostructures derived from ZIF-67@POMs

Journal

MATERIALS TODAY ENERGY
Volume 33, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.mtener.2023.101278

Keywords

Polyoxometalates; Polyacid derivative; Metal organic frameworks; Bimetallic sulfide; S -vacancies

Ask authors/readers for more resources

Co9S8@WS2 nanosheets are designed and prepared as electrocatalysts for electrochemical N2 reduction reaction (NRR) to produce NH3 at ambient conditions, showing high NRR activity and excellent ammonia synthesis performance.
Electrochemical N2 reduction reaction (NRR) to produce NH3 at ambient conditions is a promising route to replace the energy-intensive Haber-Bosch process, but electrochemical NRR with satisfied efficiency remains challenging. Therefore, a number of efforts have been committed to develop high-performance NRR electrocatalysts for highly efficient NH3 synthesis. Herein, Co9S8 nanosheets with a WS2 outer layer (Co9S8@WS2) are designed and prepared from ZIF-67@polyoxometalates (polyoxometalates , H3PW12O40$xH2O) and used for NRR at ambient temperature and pressure. The successful introduction of S-vacancies can adjust the electronic structure of the material by forming a electron-deficient envi-ronment, can make N2 molecules easily adsorbed and activated on the W active site of the catalyst surface, and thus, can promote the electrocatalytic NRR activity of the catalyst. In 0.1 M KOH, the opti-mized Co9S8@WS2-900 exhibits enhanced Faradaic efficiency (46.81%) and good NH3 yield (50.25 mg h-1 mgcat. -1 ) at -0.4 V vs. a reversible hydrogen electrode, exceeding many recently reported cobalt-or tungsten-based materials. The superior electrocatalytic activity is attributed to the unique composite structures and synergistic effect of electronic couplings between Co9S8 and sulfur-rich vacancies WS2. A density functional theory calculation indicates that the inert N2 can be activated by bare W atoms on the rim of the S-vacancies in Co9S8@WS2. The protonation of N2 to form N-NH* species is the potential -limiting step (DG = 1.05 eV). Therefore, the unique bimetallic sulfide clad architecture and rich S va-cancies of Co9S8@WS2 provide the reference and inspiration for better designing of high-efficiency ni-trogen-fixing catalysts.(c) 2023 Elsevier Ltd. All rights reserved.

Authors

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

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available