Photocatalytic oxidation of ammonia in wastewater has been abundantly investigated in lab − scale, but there are still many issues to be solved towards practical application. Herein, we have immobilized Cu/TiO2 photocatalyst on different solid substrates in order to practically utilize and recycle the photocatalyst during wastewater treatment, on the basis of exploring the effects of different influencing factors such as pH, temperature and salinity on the photocatalytic oxidation of ammonia in this work. The performance of Cu/TiO2 films was evaluated by circulated treatment of different types of wastewater including high salinity ammonia wastewater, copper − ammonia wastewater and liquid − ammonia mercerization wastewater. The characters of wastewater matrices significantly influence the performance for ammonia oxidation. Different from the slurry test of photocatalyst power that operated in a closed reactor, it is importantly found that oxygen in air plays significant role in photocatalytic oxidation of ammonia into dinitrogen in the aerobic oxidation process, when the Cu/TiO2 films were employed. The possible oxidation mechanism has been proposed to elucidate the ammonia oxidation process.
Over the past few decades, organic–inorganic halide perovskites (OIHPs) as novel photocatalyst materials have attracted intensive attention for an impressive variety of photocatalytic applications due to their excellent photophysical (chemical) properties. Regarding practical application and future commercialization, the air–water stability and photocatalytic performance of OIHPs need to be further improved. Accordingly, studying modification strategies and interfacial interaction mechanisms is crucial. In this review, the current progress in the development and photocatalytic fundamentals of OIHPs is summarized. Furthermore, the structural modification strategies of OIHPs, including dimensionality control, heterojunction design, encapsulation techniques, and so on for the enhancement of charge‐carrier transfer and the enlargement of long‐term stability, are elucidated. Subsequently, the interfacial mechanisms and charge‐carrier dynamics of OIHPs during the photocatalytic process are systematically specified and classified via diverse photophysical and electrochemical characterization methods, such as time‐resolved photoluminescence measurements, ultrafast transient absorption spectroscopy, electrochemical impedance spectroscopy measurements, transient photocurrent densities, and so forth. Eventually, various photocatalytic applications of OIHPs, including hydrogen evolution, CO2 reduction, pollutant degradation, and photocatalytic conversion of organic matter.
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