Ji-Chao Wang

Indirect Z-Scheme BiOI/g-C3N4 Photocatalysts with Enhanced Photoreduction CO2 Activity under Visible Light Irradiation

Rational design and construction of Z-scheme photocatalysts has received much attention in the field of CO2 reduction because of its great potential to solve the current energy and environmental crises. In this study, a series of Z-scheme BiOI/g-C3N4 photocatalysts are synthesized and their photocatalytic performance for CO2 reduction to produce CO, H2 and/or CH4 is evaluated under visible light irradiation (λ > 400 nm). The results show that the as-synthesized composites exhibit more highly efficient photocatalytic activity than pure g-C3N4 and BiOI and that the product yields change remarkably depending on the reaction conditions such as irradiation light wavelength. Emphasis is placed on identifying how the charge transfers across the heterojunctions and an indirect Z-scheme charge transfer mechanism is verified by detecting the intermediate I3(-) ions. The reaction mechanism is further proposed based on the detection of the intermediate (•)OH and H2O2. This work may be useful for rationally designing of new types of Z-scheme photocatalyst and provide some illuminating insights into the Z-scheme transfer mechanism.

Enhanced Photoreduction CO2 Activity over Direct Z-Scheme α-Fe2O3/Cu2O Heterostructures under Visible Light Irradiation

Hematite-cuprous oxide (α-Fe2O3/Cu2O) nanocomposites are synthesized based on the design of Z-scheme photocatalyst for CO2 reduction. The band structure for the typical Fe2O3/Cu2O (with 1:1 mole ratio) is characterized by UV-vis reflectance spectroscopy and X-ray/ultraviolet photoelectron spectroscopy, and its heterojunction is determined to be Type II band alignment. The photoreduction CO2 activities of the heterostructures are investigated in the presence of water vapor. The CO yields are changed with Fe/Cu mole ratio, and the maximal CO yield attains 5.0 μmol·g cat(-1) after 3 h of visible-light irradiation. Besides the effect of light wavelength, H2O/CO2 molar ratio and temperature on the products is studied. The selectivity of the prepared catalysts is tunable by modulating the light wavelength. The reaction mechanism is proposed and further confirmed experimentally. The results gained herein may provide some insights into the design of Z-scheme photocatalysts for CO2 reduction.

Synergistic photocatalysis of Cr(VI) reduction and 4-Chlorophenol degradation over hydroxylated α-Fe2O3 under visible light irradiation.

A series of Fe2O3 materials with hydroxyl are synthesized in different monohydric alcohol (C2-C5) solvents by solvothermal method and characterized by XRD, BET, XPS, TG and EA. The amount of hydroxyl is demonstrated to be emerged on the surface of the as-synthesized Fe2O3 particles and their contents are determined to be from 7.99 to 3.74 wt%. The Cr(VI) reduction experiments show that the hydroxyl content of Fe2O3 samples exacts great influence on the photocatalytic activity under visible light irradiation (λ>400 nm) and that the Fe2O3 sample synthesized in n-butyl alcohol exhibits the optimal photocatalytic activity. The synergistic photocatalysis for 4-Chlorophenol (4-CP) degradation and Cr(VI) reduction over above Fe2O3 sample is further investigated. The photocatalytic ratio of Cr(VI) reduction are enhanced from 24.8% to 70.2% while that of 4-CP oxidation are increased from 13.5% to 47.8% after 1 h visible light irradiation. The Fe2O3 sample keeps good degradation rates of mixed pollutants after 9 runs. The active oxygen intermediates O2(-)˙, ˙OH and H2O2 formed in the photoreaction process are discovered by ESR measurement and UV-vis test. The photocatalytic degradation mechanism is proposed accordingly.