In Situ Reconstruction of a Highly Integrated Cu/Cu <sub>2</sub> O/MoO <sub>2</sub> Dual Heterojunctions for High‐Performance CO <sub>2</sub> Photothermal Catalysis

X Xingjuan Li Y Yuhao Guo Q Qinhui Guan (College of Chemistry and Chemical Engineering Shaanxi University of Science and Technology Xi'an People's Republic of China) N Na Li Z Zheyi Sun (College of Chemistry and Chemical Engineering Shaanxi University of Science and Technology Xi'an People's Republic of China) Y Yiyao Sun (School of Chemistry and Chemical Engineering Qufu Normal University Qufu People's Republic of China) W Weiguo Huang H Huiyu Luo S Shengqun Tang (Chilwee Power Group Co. Ltd. Changxing People's Republic of China) C Canyu Yuan (School of Chemistry and Chemical Engineering Qufu Normal University Qufu People's Republic of China) B Bao Pan (College of Chemistry and Chemical Engineering Shaanxi University of Science and Technology Xi'an People's Republic of China) J Jiani Qin (School of Environmental Science and Engineering Shaanxi University of Science and Technology Xi'an People's Republic of China) J Jing Li T Tingjiang Yan (College of Chemistry and Chemical Engineering Shaanxi University of Science and Technology Xi'an People's Republic of China)

Abstract

ABSTRACT During heterogeneous photothermal catalysis, catalysts are prone to undergo random and disordered structural evolution, which poses a severe challenge to the construction of advanced photothermal catalytic systems integrating photoexcited charge carrier separation, molecular activation, and active‐site engineering. In this work, we employ an in situ reconstruction strategy to fabricate a highly integrated Cu/Cu 2 O/MoO 2 composite catalyst using Cu 3 Mo 2 O 9 as the precursor under a CO 2 /H 2 reaction atmosphere. The as‐constructed Cu/Cu 2 O Schottky junction and Cu 2 O/MoO 2 p‐n junction form a dual‐heterojunction structure, enabling efficient separation of photogenerated charge carriers. Meanwhile, amorphous MoO 2 with abundant oxygen vacancies and Cu/Cu 2 O provide functionally complementary activation sites for CO 2 activation and H 2 dissociation/spillover, respectively. Benefiting from the efficient synergistic interplay among the three components (Cu, Cu 2 O, and MoO 2 ), the Cu/Cu 2 O/MoO 2 catalyst enables the efficient conversion of CO 2 via the photothermal reverse water‐gas shift (RWGS) reaction, delivering a superior CO production rate of 14.65 mmol g −1  h −1 alongside ultra‐long stability, retaining high activity across an impressive 215‐h continuous reaction run. This study offers a new avenue for the construction of integrated functional photothermal catalysts with high performance via an in situ reconstruction approach.

Article Details

Volume / Issue Vol. 1, Issue 1
Published August 19, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

X

Xingjuan Li

Y

Yuhao Guo

Q

Qinhui Guan

College of Chemistry and Chemical Engineering Shaanxi University of Science and Technology Xi'an People's Republic of China

N

Na Li

Z

Zheyi Sun

College of Chemistry and Chemical Engineering Shaanxi University of Science and Technology Xi'an People's Republic of China

Y

Yiyao Sun

School of Chemistry and Chemical Engineering Qufu Normal University Qufu People's Republic of China

W

Weiguo Huang

H

Huiyu Luo

S

Shengqun Tang

Chilwee Power Group Co. Ltd. Changxing People's Republic of China

C

Canyu Yuan

School of Chemistry and Chemical Engineering Qufu Normal University Qufu People's Republic of China

B

Bao Pan

College of Chemistry and Chemical Engineering Shaanxi University of Science and Technology Xi'an People's Republic of China

J

Jiani Qin

School of Environmental Science and Engineering Shaanxi University of Science and Technology Xi'an People's Republic of China

J

Jing Li

T

Tingjiang Yan

College of Chemistry and Chemical Engineering Shaanxi University of Science and Technology Xi'an People's Republic of China