脱氢
催化作用
光化学
丙烷
材料科学
等离子体子
吸收(声学)
化学
串联
热稳定性
纳米团簇
氢
还原消去
微型反应器
无机化学
吸收带
纳米反应器
丙烯
漫反射红外傅里叶变换
化学工程
光催化
多相催化
纳米材料基催化剂
微型加热器
作者
Gunjan Sharma,Charvi Singhvi,Girish Mishra,Amitabha Nandi,Götz Schuck,Nico Grimm,Dirk Wallacher,Abhishek Kumar,Pavan Nukala,Sukhendu Nath,Soumya Ghosh,Vivek Polshettiwar
标识
DOI:10.1073/pnas.2520317122
摘要
Catalytic CO 2 reduction into value-added products is an energy-intensive process and typically relies on molecular hydrogen as reductant. Coupling CO 2 reduction with propane dehydrogenation for in situ hydrogen generation presents a sustainable alternative but conventionally demands high temperatures, causing undesirable side reactions such as cracking and coke formation. Here, we demonstrate a nonthermal catalytic pathway driven by hot electrons generated via localized surface plasmon resonance. Using a plasmonic catalyst comprising Ga–Ni–Mn active sites anchored on broadband plasmonic “black gold,” we achieve tandem CO 2 reduction and propane dehydrogenation under visible-light irradiation. The catalyst consistently produces equimolar amounts (~1,600 µmol g −1 h −1 ) of CO and propene under flow conditions, maintaining exceptional stability even after 500 h. Notably, light illumination suppresses undesired side reactions, such as dry reforming of propane, cracking, and coking, preserving a stable stoichiometric ratio of CO and propene. Mechanistic studies, including controlled thermal experiments, Arrhenius analysis, and finite-difference time-domain simulations, confirm that catalytic selectivity and stability originate specifically from plasmon-induced hot electrons rather than photothermal effects. Comprehensive structural characterization using X-ray absorption near-edge structure and extended X-ray absorption fine structure, in situ diffuse reflectance infrared Fourier transform spectroscopy, ultrafast transient absorption spectroscopy, and density functional theory calculations elucidate that plasmonic excitation promotes advantageous charge-transfer states within Ga–Ni–Mn ensembles, facilitating selective activation of CO 2 and propane. This study establishes hot electron–driven plasmonic catalysis as a distinctive strategy for tandem propane dehydrogenation and circular CO 2 utilization under mild conditions.
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