Photocatalytic ammonia synthesis is exciting but quite challenging with a very moderate yield at present. One of the greatest challenges is to develop highly active centers in a photocatalyst for N2 reduction under ambient conditions. Herein, porous carbon‐doped anatase TiOx (C‐TiOx) nanosheets with high‐concentration active sites of Ti3+ are presented, which are produced by layered Ti3SiC2 through a reproducible bottom‐up approach. It is shown that the high‐concentration Ti3+ sites are the major species for the significant increase in N2 photoreduction activity by the C‐TiOx. Such bottom‐up substitutional doping of C into TiO2 is responsible for both visible absorption and generation of Ti3+ concentration. Together with the porous nanosheets morphology and the loading of a Ru/RuO2 nanosized cocatalyst for enhanced charge separation and transfer, the optimal C‐TiOx with a Ti3+/Ti4+ ratio of 72.1% shows a high NH3 production rate of 109.3 µmol g−1 h−1 under visible‐light irradiation and a remarkable apparent quantum efficiency of 1.1% at 400 nm, which is the highest compared to all TiO2‐based photocatalysts at present.

Photocatalytic ammonia (NH3) synthesis from N2 and water driven by solar energy is a sustainable and environment-friend technology, which has gained considerable attention in recent years. In this review, the...

Oxidation of methane into valuable chemicals, such as C 2+ molecules, has been long sought after but the dilemma between high yield and high selectivity of desired products remains. Herein, methane is upgraded through the photocatalytic oxidative coupling of methane (OCM) over a ternary Ag−AgBr/TiO 2 catalyst in a pressurized flow reactor. The ethane yield of 35.4 μmol/h with a high C 2+ selectivity of 79% has been obtained under 6 bar pressure. These are much better than most of the previous benchmark performance in photocatalytic OCM processes. These results are attributed to the synergy between Ag and AgBr, where Ag serves as an electron acceptor and promotes the charge transfer and AgBr forms a heterostructure with TiO 2 not only to facilitate charge separation but also to avoid the overoxidation process. This work thus demonstrates an efficient strategy for photocatalytic methane conversion by both the rational design of the catalyst for the high selectivity and reactor engineering for the high conversion.

Metrics & MoreArticle Recommendations CONSPECTUS: Photocatalytic conversion of small molecules (including H 2 O, CO 2 , N 2 , CH 4 , and benzene) into value-added chemicals or fuels (e.g., H 2 , NH 3 , C 2 + , etc.) is a promising strategy to cope with both the worldwide increasing energy demand and greenhouse gas emission in both energy sectors and chemical industry, thus paving an effective way to carbon neutrality. On the other hand, compared with conventionally thermo-or electrocatalytic processes, photoactivation can convert these very stable small molecules by the unexhausted solar energy, so leading to store solar energy in chemical bonds. Thus, it can effectively reduce the reliance on the nonrenewable fossil fuels and avoid the substantial emission of hazardous gases such as CO 2 , NO x , and so on while producing valued-added chemicals. For example, semiconductors can absorb solar light to split H 2 O into H 2 and O 2 or convert CO 2 to alcohols, which can then be used as zero or neutral carbon energy sources. Although many efforts have already been made on photocatalytic small molecule activation, the light−energy conversion efficiency is still rather moderate and the yield of aimed value-added chemicals cannot meet the requirement of large-scale application. The core for these artificial photocatalytic processes is to discover a novel photocatalyst with high efficiency, low cost, and excellent durability. Over the past two decades, the Tang group has discovered a few benchmark photocatalysts (such as dual-metal-loaded metal oxides, atomic photocatalysts, carbon-doped TiO 2 , and polymer heterojunctions, etc.) and investigated them for photocatalytic conversion of the above-mentioned five robust molecules into value-added chemicals or liquid fuels. Besides, advanced photocatalytic reaction systems including batch and continuous flow membrane reactors have been studied. More importantly, the underlying reaction mechanism of these processes has been thoroughly analyzed using the state-of-the-art static and time-resolved spectroscopies. In this Account, we present the group's recent research progress in search of efficient photocatalysts for these small molecules' photoactivation. First, the strategies used in the group with respect to three key factors in photocatalysis, including light harvesting, charge separation, and reactant adsorption/product desorption, are comprehensively analyzed with the aim to provide a clear strategy for efficient photocatalyst design toward small and robust molecule photoactivation under ambient conditions. The application of in situ and operando techniques on charge carrier dynamics and reaction pathway analysis used in the group are next discussed. Finally, we point out the key challenges and future research directions toward each specific small molecule's photoactivation process.

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A series of monometallic and bimetallic cocatalyst(s), comprising FeO x , CuO x , CoO x , FeO x −CuO x , and FeO x −CoO x loaded TiO 2 catalysts prepared by the surface impregnation method, were investigated for the photocatalytic mineralization of the widely used four herbicides: 2,4-dichlorophenol (2,4-DCP), 2,4,6-trichlorophenol (2,4,6-TCP), 2,4-dichlorophenoxyacetic acid (2,4-D), and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). It was found that FeO x −CoO x /TiO 2 showed the highest photocatalytic efficiency toward mineralization of selected herbicides. FeO x −CoO x /TiO 2 achieves 92% TOC removal in 180 min, representing nearly three time activity of the benchmark PC50 TiO 2 . From XPS analysis, FeOOH, CuO, and CoO were determined to be loaded onto the TiO 2 surface. The outstanding photocatalytic performance of the optimized FeO x −CoO x /TiO 2 sample for herbicides mineralization is due to an increased charge separation and enhanced hydroxyl radicals production monitored by diverse spectroscopies. Based on the proposed charge transfer mechanism, FeO x −CoO x cocatalyst species accelerate the transfer of photogenerated holes on TiO 2 , thus facilitating hydroxyl radicals production.

Photocatalytic water reforming of methanol is viewed as a promising strategy to realize H2 release on demand. Herein, we report highly dispersed CuOx nanoparticles on TiO2 (PC50) for continuous H2...