TY - JOUR
T1 - Sono-Piezo-Photosynthesis of Ethylene and Acetylene from Bioethanol under Ambient Conditions
AU - Jiang, Yue
AU - Zhang, Jiajun
AU - Ma, Hongyang
AU - Zhou, Shujie
AU - Lin, Hsun-Yen
AU - Mofarah, Sajjad S.
AU - Lockrey, Mark
AU - Lu, Teng
AU - Ren, Hangjuan
AU - Zheng, Xiaoran
AU - Gunawan, Maichael
AU - Huang, Suchen
AU - Huang, Yu-Chun
AU - Zhuo, Fenglin
AU - Ji, Dali
AU - Hart, Judy N.
AU - Liu, Yun
AU - Wu, Jyh Ming
AU - Ashokkumar, Muthupandian
AU - Wang, Danyang
AU - Koshy, Pramod
AU - Sorrell, Charles Christopher
PY - 2025
Y1 - 2025
N2 - The catalytic conversion of bioethanol to ethylene (C2H4) and acetylene (C2H2) offers a transformative approach to sustainable production of two industrial cornerstones for organic compound and polymer syntheses, thereby offering significant economic and environmental advantages. In contrast, current methods for the synthesis of these C2 hydrocarbons rely on energy- and carbon-intensive processes that require high temperatures and pressures. The present work addresses these limitations with a novel, low-energy, bioethanol-conversion strategy operating at room temperature and ambient pressure using sono-piezo-photocatalysts. A novel heterostructure of graphene oxide fragments (GO) and sodium bismuth titanate (NBT) within a core-shell microstructure achieved outstanding C2H4 and C2H2 production rates of 134.1 and 55.5 µmol/g/h, respectively. The conversion mechanism is driven by (1) bubble collapse during ultrasound irradiation, generating localized high temperatures (≈4000 K) and pressures (≈100 MPa), and (2) piezo-photocatalytic tuning of GO/NBT by enhanced charge separation and transfer. DFT simulations revealed detailed sono-piezo-photocatalytic conversion pathways, showing significant reductions in energy barriers for C2H4 (22.0 kcal mol−1) and C2H2 (48.0 kcal mol−1) formation. These findings emphasize the critical role of the catalyst in cleaving both C─H and C─O bonds effectively, leading to the desired product formation.
AB - The catalytic conversion of bioethanol to ethylene (C2H4) and acetylene (C2H2) offers a transformative approach to sustainable production of two industrial cornerstones for organic compound and polymer syntheses, thereby offering significant economic and environmental advantages. In contrast, current methods for the synthesis of these C2 hydrocarbons rely on energy- and carbon-intensive processes that require high temperatures and pressures. The present work addresses these limitations with a novel, low-energy, bioethanol-conversion strategy operating at room temperature and ambient pressure using sono-piezo-photocatalysts. A novel heterostructure of graphene oxide fragments (GO) and sodium bismuth titanate (NBT) within a core-shell microstructure achieved outstanding C2H4 and C2H2 production rates of 134.1 and 55.5 µmol/g/h, respectively. The conversion mechanism is driven by (1) bubble collapse during ultrasound irradiation, generating localized high temperatures (≈4000 K) and pressures (≈100 MPa), and (2) piezo-photocatalytic tuning of GO/NBT by enhanced charge separation and transfer. DFT simulations revealed detailed sono-piezo-photocatalytic conversion pathways, showing significant reductions in energy barriers for C2H4 (22.0 kcal mol−1) and C2H2 (48.0 kcal mol−1) formation. These findings emphasize the critical role of the catalyst in cleaving both C─H and C─O bonds effectively, leading to the desired product formation.
U2 - 10.1002/adfm.202425784
DO - 10.1002/adfm.202425784
M3 - Article
SN - 1616-301X
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -