TY - JOUR
T1 - Pd-intercalated black phosphorus
T2 - An efficient electrocatalyst for CO2 reduction
AU - Xiao, Liangping
AU - Zheng, Qizheng
AU - Luo, Shiwen
AU - Ying, Yifan
AU - Zhou, Rusen
AU - Zhou, Shiyuan
AU - Li, Xingyun
AU - Ye, Xiaoyuan
AU - Yu, Zhiyang
AU - Xu, Qingchi
AU - Liao, Honggang
AU - Xu, Jun
N1 - Publisher Copyright:
© 2024 the Authors, some rights reserved;
PY - 2024/6
Y1 - 2024/6
N2 - Nanoconfined catalysts enhance stabilization of reaction intermediates, facilitate electron transfer, and safeguard active centers, leading to superior electrocatalytic activity, particularly in CO2 reduction reactions (CO2RR). Despite their effectiveness, crafting nanoconfined catalysts is challenging due to unclear formation mechanisms. In this study, we introduce an electrochemical method to grow Pd clusters within the interlayers of two-dimensional black phosphorus, creating Pd cluster–intercalated black phosphorus (Pd-i-BP) as an electrocatalyst. Using in situ electrochemical liquid phase transmission electron microscopy (EC-TEM), we revealed the synthesis mechanism of Pd-i-BP, involving electrochemically driven Pd ion intercalation followed by reduction within the BP layers. The Pd-i-BP electrocatalyst exhibits exemplary CO2-to-formate conversion, achieving 90% Faradaic efficiency for formate production, owing to its distinct nanoconfined structure that stabilizes intermediates and enhances electron transfer. Density functional theory (DFT) calculations underscore the structural benefits for enhancing intermediate adsorption and catalyzing the reaction. Our insights deepen understanding of nanoconfined material synthesis, promising advanced, high-efficiency catalysts.
AB - Nanoconfined catalysts enhance stabilization of reaction intermediates, facilitate electron transfer, and safeguard active centers, leading to superior electrocatalytic activity, particularly in CO2 reduction reactions (CO2RR). Despite their effectiveness, crafting nanoconfined catalysts is challenging due to unclear formation mechanisms. In this study, we introduce an electrochemical method to grow Pd clusters within the interlayers of two-dimensional black phosphorus, creating Pd cluster–intercalated black phosphorus (Pd-i-BP) as an electrocatalyst. Using in situ electrochemical liquid phase transmission electron microscopy (EC-TEM), we revealed the synthesis mechanism of Pd-i-BP, involving electrochemically driven Pd ion intercalation followed by reduction within the BP layers. The Pd-i-BP electrocatalyst exhibits exemplary CO2-to-formate conversion, achieving 90% Faradaic efficiency for formate production, owing to its distinct nanoconfined structure that stabilizes intermediates and enhances electron transfer. Density functional theory (DFT) calculations underscore the structural benefits for enhancing intermediate adsorption and catalyzing the reaction. Our insights deepen understanding of nanoconfined material synthesis, promising advanced, high-efficiency catalysts.
UR - https://www.scopus.com/pages/publications/85196684181
U2 - 10.1126/sciadv.adn2707
DO - 10.1126/sciadv.adn2707
M3 - 文章
C2 - 38896618
AN - SCOPUS:85196684181
SN - 2375-2548
VL - 10
JO - Science Advances
JF - Science Advances
IS - 25
M1 - eadn2707
ER -