Ordering Bimetallic Cu‐Pd Catalysts onto Orderly Mesoporous SrTiO3‐Crystal Nanotubular Networks for Efficient Carbon Dioxide Photoreduction

Author:

Fang Fan12ORCID,Zhang Jie2,Xiang Lijing2,Chen Chong2,Feng Nengjie3,Lv Yanqi4,Chang Kun2,Huang Jun1

Affiliation:

1. Laboratory for Catalysis Engineering, School of Chemical and Biomolecular Engineering & Sydney Nano Institute The University of Sydney Darlington, New South Wales 2008 Australia

2. College of Materials Science and Technology Nanjing University of Aeronautics and Astronautics Nanjing 210016 P. R. China

3. State Key Laboratory of Materials-Oriented Chemical Engineering College of Chemical Engineering Jiangsu National Synergetic Innovation Center for Advanced Materials Jiangsu Collaborative Innovation Center for Advanced Inorganic Function Composites Nanjing Tech University Nanjing 210009 P. R. China

4. School of Management and Engineering Nanjing University Nanjing 210093 P. R. China

Abstract

AbstractArtificial photosynthesis of fuels has garnered significant attention, with SrTiO3 emerging as a potential candidate for photocatalysis due to its exceptional physicochemical properties. However, selectively converting CO2 into fuels with desired reaction products remains a grand challenge. Herein, we design an updated method via an aging strategy based on the electrospinning technique to synthesize a single‐crystalline Al‐doped SrTiO3 nanotubular networks with self‐assembled orderly mesopores, further modified by Cu−Pd alloy. It exhibits both high crystallinity and superior cross‐linked mesoporous structures, effectively facilitating charge carrier transfer, photon utilization, and mass transfer, with a remarkable enhancement from 0.025 mmol h−1 m−2 to 1.090 mmol h−1 m−2 in the CO production rate. Meanwhile, the ordered arrangement of Cu and Pd atoms on the (111) surface can promote the rate‐determining step (*CO2 to *COOH), which is also responsible for its good activity. The presence of CuO in the reaction confers a significant advantage for CO desorption, leading to a remarkable CO selectivity of 95.54 %. This work highlights new insights into developing advanced heterogeneous photocatalysts.

Funder

National Natural Science Foundation of China

Australian Research Council

Natural Science Foundation of Jiangsu Province

Fundamental Research Funds for the Central Universities

Postdoctoral Research Foundation of China

Publisher

Wiley

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