Air‐Promoted Light‐Driven Hydrogen Production from Bioethanol over Core/Shell Cr2O3@GaN Nanoarchitecture

Author:

Wang Zhouzhou12ORCID,Chen Yiqing3,Sheng Bowen4,Li Jinglin1,Yao Lin5,Yu Ying2,Song Jun3,Yu Tianqi1,Li Yixin1,Pan Hu1,Wang Ping4,Wang Xinqiang467,Zhu Lei1,Zhou Baowen1ORCID

Affiliation:

1. Key Laboratory for Power Machinery and Engineering of Ministry of Education, Research Center for Renewable Synthetic Fuel, School of Mechanical Engineering Shanghai Jiao Tong University Shanghai 200240 China

2. Institute of Nanoscience and Nanotechnology, College of Physical Science and Technology Central China Normal University Wuhan 430079 China

3. Department of Mining and Materials Engineering McGill University Montreal QC H3A0C9 Canada

4. State Key Laboratory of Artificial Microstructure and Mesoscopic Physics, School of Physics, Nano-Optoelectronics Frontier Center of Ministry of Education (NFC-MOE) Peking University Beijing 100871 China

5. China-UK Low Carbon College Shanghai Jiao Tong University Shanghai 201306 China

6. Yangtze Delta Institute of Optoelectronics Peking University Nantong 226010 China

7. Collaborative Innovation Center of Quantum Matter, School of Physics Peking University Beijing 100871 China

Abstract

AbstractLight‐driven hydrogen production from biomass derivatives offers a path towards carbon neutrality. It is often however operated with the limitations of sluggish kinetics and severe coking. Herein, a disruptive air‐promoted strategy is explored for efficient and durable light‐driven hydrogen production from ethanol over a core/shell Cr2O3@GaN nanoarchitecture. The correlative computational and experimental investigations show ethanol is energetically favorable to be adsorbed on the Cr2O3@GaN interface, followed by dehydrogenation toward acetaldehyde and protons by photoexcited holes. The released protons are then consumed for H2 evolution by photogenerated electrons. Afterward, O2 can be evolved into active oxygen species and promote the deprotonation and C−C cleavage of the key C2 intermediate, thus significantly lowering the reaction energy barrier of hydrogen evolution and removing the carbon residual with inhibited overoxidation. Consequently, hydrogen is produced at a high rate of 76.9 mole H2 per gram Cr2O3@GaN per hour by only feeding ethanol, air, and light, leading to the achievement of a turnover number of 266,943,000 mole H2 per mole Cr2O3 over a long‐term operation of 180 hours. Notably, an unprecedented light‐to‐hydrogen efficiency of 17.6 % is achieved under concentrated light illumination. The simultaneous generation of aldehyde from ethanol dehydrogenation enables the process more economically promising.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Natural Science Foundation of Beijing Municipality

Publisher

Wiley

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