Loading…
Dramatically Enhanced Ambient Ammonia Electrosynthesis Performance by In‐Operando Created Li–S Interactions on MoS 2 Electrocatalyst
The Haber‐Bosch process can be replaced by the ambient electrocatalytic N 2 reduction reaction (NRR) to produce NH 3 if suitable electrocatalysts can be developed. However, to develop high performance N 2 fixation electrocatalysts, a key issue to be resolved is to achieve efficient hydrogenation of...
Saved in:
Published in: | Advanced energy materials 2019-04, Vol.9 (14) |
---|---|
Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The Haber‐Bosch process can be replaced by the ambient electrocatalytic N
2
reduction reaction (NRR) to produce NH
3
if suitable electrocatalysts can be developed. However, to develop high performance N
2
fixation electrocatalysts, a key issue to be resolved is to achieve efficient hydrogenation of N
2
without interference by the thermodynamically favored hydrogen evolution reaction (HER). Herein, in‐operando created strong Li–S interactions are reported to empower the S‐rich MoS
2
nanosheets with superior NRR catalytic activity and HER suppression ability. The Li
+
interactions with S‐edge sites of MoS
2
can effectively suppress hydrogen evolution reaction by reducing H* adsorption free energy from 0.03 to 0.47 eV, facilitate N
2
adsorption by increasing N
2
adsorption free energy from –0.32 to –0.70 eV and enhance electrocatalytic N
2
reduction activity by decreasing the activation energy barrier of the reaction control step (*N
2
→ *N
2
H) from 0.84 to 0.42 eV. A NH
3
yield rate of 43.4 μg h
−1
mg
−1
MoS
2
with a faradaic efficiency (FE) of 9.81% can be achieved in presence of strong Li–S interactions, more than 8 and 18 times by the same electrocatalyst in the absence of Li–S interactions. This report opens a new way to design and develop catalysts and catalysis systems. |
---|---|
ISSN: | 1614-6832 1614-6840 |
DOI: | 10.1002/aenm.201803935 |