TY - JOUR
T1 - Surface Single Atom Alloys for Alkaline Hydrogen Evolution Reaction
AU - Xu, Li
AU - Xu, Yanping
AU - Xia, Bin
AU - Guo, Bingrong
AU - Kamal, Khaja Mohaideen
AU - Likozar, Blaž
AU - Li, Xiumin
AU - Dong, Feifei
AU - Li, Siwei
AU - Ma, Yufei
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025/10/16
Y1 - 2025/10/16
N2 - Single atom catalysts (SACs) achieve 100% utilization of metal atoms and have versatile support effects, whereas single atom alloys (SAAs) with metallic bonds own the free-atom-like electronic structure. Herein, surface single atom alloys (SSAAs) are developed that integrate the advantages of SACs and SAAs via incorporating an ultrathin metallic layer during the synthetic process of SACs. It is shown that the Pt single atom preferentially coordinates with metallic Mo nanolayer, thereby forming a Pt1-MoL surface atom alloy on Mo2C (marked as Pt1-MoL-Mo2C SSAAs). Comprehensive spectroscopic and theoretical calculations reveal that the Mo nanolayer in SSAAs not only functions as an electron buffer between Pt1 and Mo2C, leading to a free-atom-like d state at Pt1 sites and thereby balancing the adsorption and desorption of H, but also enhances the aggregation, adsorption, and activation of H2O. Consequently, the Pt1-MoL-Mo2C SSAAs exhibit superior alkaline hydrogen evolution reaction (HER) performance compared to Pt1/Mo2C SACs, achieving a low overpotential of 12 mV at 10 mA cm−2 and a low Tafel slope of 17 mV dec−1. This work provides novel insights into the design of advanced single-site catalysts.
AB - Single atom catalysts (SACs) achieve 100% utilization of metal atoms and have versatile support effects, whereas single atom alloys (SAAs) with metallic bonds own the free-atom-like electronic structure. Herein, surface single atom alloys (SSAAs) are developed that integrate the advantages of SACs and SAAs via incorporating an ultrathin metallic layer during the synthetic process of SACs. It is shown that the Pt single atom preferentially coordinates with metallic Mo nanolayer, thereby forming a Pt1-MoL surface atom alloy on Mo2C (marked as Pt1-MoL-Mo2C SSAAs). Comprehensive spectroscopic and theoretical calculations reveal that the Mo nanolayer in SSAAs not only functions as an electron buffer between Pt1 and Mo2C, leading to a free-atom-like d state at Pt1 sites and thereby balancing the adsorption and desorption of H, but also enhances the aggregation, adsorption, and activation of H2O. Consequently, the Pt1-MoL-Mo2C SSAAs exhibit superior alkaline hydrogen evolution reaction (HER) performance compared to Pt1/Mo2C SACs, achieving a low overpotential of 12 mV at 10 mA cm−2 and a low Tafel slope of 17 mV dec−1. This work provides novel insights into the design of advanced single-site catalysts.
KW - free-atom-like d state
KW - hydrogen evolution reaction
KW - molybdenum carbide
KW - single atom catalyst
KW - surface single-atom alloys
UR - https://www.scopus.com/pages/publications/105003708605
U2 - 10.1002/adma.202502989
DO - 10.1002/adma.202502989
M3 - 文章
AN - SCOPUS:105003708605
SN - 0935-9648
VL - 37
JO - Advanced Materials
JF - Advanced Materials
IS - 41
M1 - 2502989
ER -