TY - JOUR
T1 - Fabrication of TiO2 with Ru-induced lattice strain for enhancing photocatalytic nitrogen fixation in gas–solid reaction system
AU - Yue, Yufei
AU - Jin, Yu
AU - Yan, Xiaoqing
AU - Hou, Xuelan
AU - Ou, Honghui
AU - Huang, Qizhong
AU - Hu, Huagui
AU - Yang, Guidong
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2025/2/1
Y1 - 2025/2/1
N2 - Photocatalytic nitrogen (N2) fixation is a promising strategy for green ammonia (NH3) synthesis. However, the design of catalysts possessing high nitrogen adsorption capacity and efficient N2 dissociation remains a significant challenge, owing to the poor solubility of N2 in aqueous solutions coupled with its high chemical stability. Herein, we prepared Ru-TiO2 with metal lattice strain and applied it to a gas–solid two-phase system (G-S). Compared to the conventional gas–liquid-solid three-phase system (G-L-S), the G-S system can effectively enhance N2 adsorption and shorten the diffusive mass transfer path. Additionally, Ru-TiO2 demonstrates improved N2 adsorption capacity and activation efficiency, giving the maximum NH3 production rate of 38.7 μmol g−1 h−1, which is about four times higher than that in the G-L-S system. Density functional theory results demonstrate that N2 adsorption and activation are optimized over the lattice-strained Ru surface. This work provides an innovative approach to developing advanced photocatalysts and NRR systems.
AB - Photocatalytic nitrogen (N2) fixation is a promising strategy for green ammonia (NH3) synthesis. However, the design of catalysts possessing high nitrogen adsorption capacity and efficient N2 dissociation remains a significant challenge, owing to the poor solubility of N2 in aqueous solutions coupled with its high chemical stability. Herein, we prepared Ru-TiO2 with metal lattice strain and applied it to a gas–solid two-phase system (G-S). Compared to the conventional gas–liquid-solid three-phase system (G-L-S), the G-S system can effectively enhance N2 adsorption and shorten the diffusive mass transfer path. Additionally, Ru-TiO2 demonstrates improved N2 adsorption capacity and activation efficiency, giving the maximum NH3 production rate of 38.7 μmol g−1 h−1, which is about four times higher than that in the G-L-S system. Density functional theory results demonstrate that N2 adsorption and activation are optimized over the lattice-strained Ru surface. This work provides an innovative approach to developing advanced photocatalysts and NRR systems.
KW - Adsorption and activation
KW - Lattice strain
KW - Photocatalytic nitrogen fixation
KW - Ru-TiO
KW - Two-phase reaction system
UR - https://www.scopus.com/pages/publications/85212348091
U2 - 10.1016/j.ces.2024.121071
DO - 10.1016/j.ces.2024.121071
M3 - 文章
AN - SCOPUS:85212348091
SN - 0009-2509
VL - 304
JO - Chemical Engineering Science
JF - Chemical Engineering Science
M1 - 121071
ER -