A semiconducting hybrid of RhOx/GaN@InGaN for simultaneous activation of methane and water toward syngas by photocatalysis

Author:

Li Dongke12,Wu Zewen3,Li Yixin1,Fan Xiaoxing2ORCID,Hasan S M Najib4,Arafin Shamsul4ORCID,Rahman Md Afjalur5,Li Jinglin1,Wang Zhouzhou1ORCID,Yu Tianqi1,Kong Xianghua3,Zhu Lei1,Sadaf Sharif Md5,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 , 800 Dongchuan Road , Shanghai 200240, China

2. School of Physics, Liaoning University , No. 66 Chongshan Middle Road, Huanggu District, Shenyang City 110036, Liaoning Province , China

3. College of Physics and Optoelectronic Engineering, Shenzhen University , 3688 Nanhai Avenue, Nanshan District , Shenzhen 518061, China

4. Electrical and Computer Engineering, The Ohio State University , Columbus, OH 43210 , USA

5. Centre Energie, Matériaux et Télécommunications, Institut National de la Recherche Scientifique (INRS)-Université du Québec , 1650 Boulevard Lionel-Boulet , Varennes, Quebec J3X1S2, Canada

Abstract

Abstract Prior to the eventual arrival of carbon neutrality, solar-driven syngas production from methane steam reforming presents a promising approach to produce transportation fuels and chemicals. Simultaneous activation of the two reactants, i.e. methane and water, with notable geometric and polar discrepancy is at the crux of this important subject yet greatly challenging. This work explores an exceptional semiconducting hybrid of RhOx/GaN@InGaN nanowires for overcoming this critical challenge to achieve efficient syngas generation from methane steam reforming by photocatalysis. By coordinating density functional theoretical calculations and microscopic characterizations, with in situ spectroscopic measurements, it is found that the multifunctional RhOx/GaN interface is effective for simultaneously activating both CH4 and H2O by stretching the C–H and O–H bonds because of its unique Lewis acid/base attribute. With the aid of energetic charge carriers, the stretched C–H and O–H bonds of reactants are favorably cleaved, resulting in the key intermediates, i.e. *CH3, *OH, and *H, to sit on Rh sites, Rh sites, and N sites, respectively. Syngas is subsequently produced via energetically favored pathway without additional energy inputs except for light. As a result, a benchmarking syngas formation rate of 8.1 mol·gcat−1·h−1 is achieved with varied H2/CO ratios from 2.4 to 0.8 under concentrated light illumination of 6.3 W·cm−2, enabling the achievement of a superior turnover number of 10,493 mol syngas per mol Rh species over 300 min of long-term operation. This work presents a promising strategy for green syngas production from methane steam reforming by utilizing unlimited solar energy.

Funder

National Natural Science Foundation of China

Shanghai Pilot Program for Basic Research—Shanghai Jiao Tong University

Shanghai Municipal Science and Technology Major Project

Department of Science and Technology of Guangdong Province

Shenzhen Natural Science Fund

Publisher

Oxford University Press (OUP)

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