Harvesting solar energy for catalytic conversion of CO 2 into valuable chemical fuels/feedstocks is an attractive yet challenging strategy to realize a sustainable carbon-cycle utilization. Homogeneous catalysts typically exhibit higher activity and selectivity as compared with heterogeneous counterparts, benefiting from their atomically dispersed catalytic sites and versatile coordination structures. However, it is still a "black box" how the coordination and electronic structures of catalysts dynamically evolve during the reaction, forming the bottleneck for understanding their reaction pathways. Herein, we demonstrate to track the mechanistic pathway of photocatalytic CO 2 reduction using a terpyridine nickel(II) complex as a catalyst model. Integrated with a typical homogeneous photosensitizer, the catalytic system offers a high selectivity of 99% for CO 2 -to-CO conversion with turnover number and turnover frequency as high as 2.36 × 10 7 and 385.6 s −1 , respectively. We employ operando and time-resolved X-ray absorption spectroscopy, in combination with other in situ spectroscopic techniques and theoretical computations, to track the intermediate species of Ni catalyst in the photocatalytic CO 2 reduction reaction for the first time. Taken together with the charge dynamics resolved by optical transient absorption spectroscopy, the investigation elucidates the full mechanistic reaction pathway including some key factors that have been often overlooked. This work opens the "black box" for CO 2 reduction in the system of homogeneous catalysts and provides key information for developing efficient catalysts toward artificial photosynthesis.

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