Tuning Reaction Pathway with Surface Metal Cocatalyst for Ethylene Production via Photocatalytic Methane Conversion
Jiakang You, Yanzhao Zhang, Zhiliang Wang, Hanqing Yin, Guangyu Zhao, Julian A. Steele, Jitraporn Vongsvivut, James D. Riches, Kai Wang, Dazhi Yao, Haijiao Lu, Yifan Bao, Xiyue Peng, Peng Chen, Ping Chen, Aijun Du, Yonggang Jin, Lianzhou Wang
Abstract
Photocatalytic oxidative coupling of methane (POCM) provides a sustainable route to convert methane (CH 4 ) into value-added chemicals. However, the selectivity and production rate of high-value hydrocarbons, such as ethylene, are still bottlenecked by the ambiguous carbon–carbon (C–C) coupling mechanism and inefficient CH 4 activation processes. This work investigated the POCM process based on cocatalysts of palladium (Pd), gold (Au), and their alloy (PdAu) to elucidate the reaction pathway. By studying the intermediates and product selectivity, we reveal that the strong bonding between the metal cocatalyst and hydrocarbon intermediates of *CH x ( x = 2 or 3) is essential for achieving a rapid and selective CH 4 conversion process. The PdAu alloy facilitates the *CH 2 generation and lowers the energy barrier for *CH 2 coupling, thereby selectively tuning the reaction pathway toward ethylene generation. Using a classic TiO 2 photocatalyst loaded with PdAu cocatalysts, an ethylene production rate of 0.18 mmol g –1 h –1 and a CH 4 conversion rate of 13.73 mmol g –1 h –1 are achieved, corresponding to an apparent quantum efficiency (AQE) of 12% at a wavelength of 350 nm. Mechanistic studies establish that an effective cocatalyst for value-added product generation should perform three critical functions, including modulating CH 4 activation, stabilizing the *CH x intermediates, and promoting C–C coupling. Our findings demonstrate that alloy engineering is an effective strategy to balance these three functions to advance methane valorization for the efficient and selective generation of multicarbon products.