Chiral Mesostructured Mo Doped Bi <sub>2</sub> WO <sub>6</sub> Drives Photocatalytic Urea Synthesis From N <sub>2</sub> and CO <sub>2</sub>

J Jiamin Ma (State Key Laboratory of Synergistic Chem‐Bio Synthesis School of Chemistry and Chemical Engineering Frontiers Science Center For Transformative Molecules Shanghai Key Laboratory For Molecular Engineering of Chiral Drugs Shanghai Jiao Tong University Shanghai China) Y Yang Gao W Wanning Zhang (School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs) L Lu Han (School of Chemical Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092, China) S Shunai Che (State Key Laboratory of Synergistic Chem‐Bio Synthesis School of Chemistry and Chemical Engineering Frontiers Science Center For Transformative Molecules Shanghai Key Laboratory For Molecular Engineering of Chiral Drugs Shanghai Jiao Tong University Shanghai China) Y Yuxi Fang (School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs)

Abstract

ABSTRACT Direct synthesis of urea through photocatalytic N 2 and CO 2 reduction (PNCR) offers a sustainable approach to mitigate CO 2 emissions and reduce energy consumption from urea production for industry and agriculture. However, achieving high yield of urea is limited by the high energy barrier for co‐reduction of N 2 and CO 2 with subsequent C–N coupling. Herein, we propose that the spin polarization of chiral mesostructured Mo doped Bi 2 WO 6 (CMMB) can facilitate the formation of triplet 3 NOH by regulating the parallel electron spin alignment and promote the separation and transfer of photogenerated carriers, leading to enhanced C–N formation. The incorporation of Mo sites into Bi 2 WO 6 promotes the adsorption and activation of N 2 . A state‐of‐the‐art urea yield was achieved without additives via PNCR on CMMB, surpassing the best‐reported inorganic catalyst by a significant margin. This study provides an effective strategy for designing catalyst structures for the green synthesis of organonitrogen compounds.

Article Details

Volume / Issue Vol. 65, Issue 15
Published April 06, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (6)

J

Jiamin Ma

State Key Laboratory of Synergistic Chem‐Bio Synthesis School of Chemistry and Chemical Engineering Frontiers Science Center For Transformative Molecules Shanghai Key Laboratory For Molecular Engineering of Chiral Drugs Shanghai Jiao Tong University Shanghai China

Y

Yang Gao

W

Wanning Zhang

School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs

L

Lu Han

School of Chemical Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092, China

S

Shunai Che

State Key Laboratory of Synergistic Chem‐Bio Synthesis School of Chemistry and Chemical Engineering Frontiers Science Center For Transformative Molecules Shanghai Key Laboratory For Molecular Engineering of Chiral Drugs Shanghai Jiao Tong University Shanghai China

Y

Yuxi Fang

School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs