Sulfur doping optimized intermediate energetics of FeCoOOH for enhanced oxygen evolution catalytic activity
Publication Name
Cell Reports Physical Science
Abstract
Transition metal sulfides have been demonstrated to be more active electrocatalysts than the corresponding (hydr)oxides for oxygen evolution reaction (OER). The nature of active sites, however, remains unclear. Here, we study whether S could promote the OER activity of FeCoOOH and try to identify the catalytically active centers. Density functional theory suggests that two coordinating S could work synergistically with one adjacent Fe to optimize the electronic states of Co, resulting in decreased binding energy of OH∗ (ΔE ) while little changed ΔE , and thus significantly lowering the catalytic overpotential. Further experimental studies validate the synergistic effect between S and Fe on tuning the electronic structure and the greatly improved catalytic activity with a small overpotential of 225.3 mV to drive 20 mA cm . This study reveals the origin of the high catalytic activity of transition metal sulfides and provides insights into the design of efficient OER electrocatalysts. Yuan et al. study the effect of S on the OER activity of FeCoOOH. Results show that two coordinating S and one adjacent Fe synergistically optimize the electronic states of Co, resulting in the decreased binding energy of OH∗ (ΔE ), with little change to ΔE , thus greatly enhancing the catalytic activity. OH O OH O −2
Open Access Status
This publication may be available as open access
Volume
2
Issue
2
Article Number
100331
Funding Number
DE210101102
Funding Sponsor
Australian Research Council