Synergistic Ru Species on Poly(heptazine imide) Enabling Efficient Photocatalytic CO <sub>2</sub> Reduction with H <sub>2</sub> O beyond 800 nm

B Bo Su (State Key Laboratory of Medical Chemical Biology and College of Pharmacy) S Sibo Wang W Wandong Xing (State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry) K Kunlong Liu (State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry) S Sung‐Fu Hung (Department of Applied Chemistry National Yang Ming Chiao Tung University Hsinchu Taiwan) X Xiong Chen (State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry) Y Yuanxing Fang (State Key Laboratory of Chemistry for NBC Hazards Protection, State Key Laboratory of Photocatalysis on Energy and Environment, Sino-UK International Joint Laboratory on Photocatalysis for Clean Energy and Advanced Chemicals & Materials, College of Chemistry) G Guigang Zhang (State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry) H Huabin Zhang (Center of Excellence for Renewable Energy and Storage Technologies (CREST), Division of Physical Science and Engineering, King Abdullah University of Science and Technology (KAUST), Thuwal, Kingdom of Saudi Arabia.) X Xinchen Wang (State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry)

Abstract

Abstract Photocatalytic CO 2 conversion with H 2 O to carbonaceous fuels is a desirable strategy for CO 2 management and solar utilization, yet its efficiency remains suboptimal. Herein, efficient and durable CO 2 photoreduction is realized over a Ru NPs /Ru‐PHI catalyst assembled by anchoring Ru single atoms (SAs) and nanoparticles (NPs) onto poly(heptazine imide) (PHI) via the in‐plane Ru‐N 4 coordination and interfacial Ru‐N bonds, respectively. This catalyst shows an unsurpassed CO production (32.8 µmol h −1 ), a record‐high apparent quantum efficiency (0.26%) beyond 800 nm, and the formation of the valuable H 2 O 2 . Ru SAs tune PHI's electronic structure to promote in‐plane charge transfer to Ru NPs, forming a built‐in electron field at the interface, which directs electron‐hole separation and rushes excited electron movement from Ru‐PHI to Ru NPs. Simultaneously, Ru SAs introduce an impurity level in PHI to endow long‐wavelength photoabsorption, while Ru NPs strengthen CO 2 adsorption/activation and expedite CO desorption. These effects of Ru species together effectively ensure CO 2 ‐to‐CO conversion. The CO 2 reduction on the catalyst is revealed to follow the pathway CO 2 → *CO 2 → *COOH→ *CO→ CO, based on the intermediates identified by in situ diffuse reflectance infrared Fourier transform spectroscopy and further supported by density functional theory calculations.

Article Details

Volume / Issue Vol. 64, Issue 27
Published July 01, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

B

Bo Su

State Key Laboratory of Medical Chemical Biology and College of Pharmacy

S

Sibo Wang

W

Wandong Xing

State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry

K

Kunlong Liu

State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry

S

Sung‐Fu Hung

Department of Applied Chemistry National Yang Ming Chiao Tung University Hsinchu Taiwan

X

Xiong Chen

State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry

Y

Yuanxing Fang

State Key Laboratory of Chemistry for NBC Hazards Protection, State Key Laboratory of Photocatalysis on Energy and Environment, Sino-UK International Joint Laboratory on Photocatalysis for Clean Energy and Advanced Chemicals & Materials, College of Chemistry

G

Guigang Zhang

State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry

H

Huabin Zhang

Center of Excellence for Renewable Energy and Storage Technologies (CREST), Division of Physical Science and Engineering, King Abdullah University of Science and Technology (KAUST), Thuwal, Kingdom of Saudi Arabia.

X

Xinchen Wang

State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry