g-C3N4: Properties, Pore Modifications, and Photocatalytic Applications

Graphitic carbon nitride (g-C3N4), as a polymeric semiconductor, is promising for ecological and economical photocatalytic applications because of its suitable electronic structures, together with the low cost, facile preparation, and metal-free feature. By modifying porous g-C3N4, its photoelectric behaviors could be facilitated with transport channels for photogenerated carriers, reactive substances, and abundant active sites for redox reactions, thus further improving photocatalytic performance. There are three types of methods to modify the pore structure of g-C3N4: hard-template method, soft-template method, and template-free method. Among them, the hard-template method may produce uniform and tunable pores, but requires toxic and environmentally hazardous chemicals to remove the template. In comparison, the soft templates could be removed at high temperatures during the preparation process without any additional steps. However, the soft-template method cannot strictly control the size and morphology of the pores, so prepared samples are not as orderly as the hard-template method. The template-free method does not involve any template, and the pore structure can be formed by designing precursors and exfoliation from bulk g-C3N4 (BCN). Without template support, there was no significant improvement in specific surface area (SSA). In this review, we first demonstrate the impact of pore structure on photoelectric performance. We then discuss pore modification methods, emphasizing comparison of their advantages and disadvantages. Each method’s changing trend and development direction is also summarized in combination with the commonly used functional modification methods. Furthermore, we introduce the application prospects of porous g-C3N4 in the subsequent studies. Overall, porous g-C3N4 as an excellent photocatalyst has a huge development space in photocatalysis in the future.

Green and Highly-Efficient Microwave Synthesis Route for Sulfur/Carbon Composite for Li-S Battery

Multiporous carbons (MPCs) are prepared using ZnO as a hard template and biomass pyrolysis oil as the carbon source. It is shown that the surface area, pore volume, and mesopore/micropore ratio of the as-prepared MPCs can be easily controlled by adjusting the ZnO/oil ratio. Sulfur/MPC (S/MPC) composite is prepared by blending sulfur powder with the as-prepared MPCs followed by microwave heating at three different powers (100 W/200 W/300 W) for 60 s. The unique micro/mesostructure characteristics of the resulting porous carbons not only endow the S/MPC composite with sufficient available space for sulfur storage, but also provide favorable and efficient channels for Li-ions/electrons transportation. When applied as the electrode material in a lithium-ion battery (LIB), the S/MPC composite shows a reversible capacity (about 500 mAhg−1) and a high columbic efficiency (>95%) after 70 cycles. Overall, the method proposed in this study provides a simple and green approach for the rapid production of MPCs and S/MPC composite for high-performance LIBs.

Enhanced the Synergistic Effect of Tetracycline Adsorption and Photocatalytic Degradation on a Novel Mesoporous Carbon Nitride

A novel mesoporous g-C3N4 with guanidine hydrochloride as precursor was prepared by molten salt assisted hard template of silica (SiO2) aerogel for photocatalytic degradation of tetracycline (TC). The textural structure, chemical composition, morphology and optical properties of mesoporous g-C3N4 were characterized by a series of means, and the synergistic effect of adsorption and photocatalytic degradation of TC was elucidated. The results show that the successfully synthesized mesoporous g-C3N4 presented a coral-like rod shaped and heptazine ring structure. When the amount of SiO2 aerogel template was 1.4 g, the richer nitrogen defects of the sample (GM-1.4) with the lower band gap (2.42 eV) was displayed.The photocatalytic degradation rate of GM-1.4 for TC was reached to 83.4% under visible illumination for 120 min. Furthermore, the •O2- and h+ were proved to be the main active species, and the reasons of TC photodegradation were associated with the destruction of TC molecular structure.

Medium-Low-Temperature NO2 Sensor Based on YSZ Solid Electrolyte and Mesoporous WO3 Sensing Electrode for Detection of Vehicle Emissions

A mixed potential-type NO2 sensor was fabricated using yttria-stabilized zirconia (YSZ) as the electrolyte and mesoporous WO3 as the sensing electrode for the detection of NO2 in vehicle exhausts. The mesoporous WO3 with a diameter of 7 nm was synthesized using the hard template method. The sensor showed excellent performance in the detection of 30–500[Formula: see text]ppm of NO2 at 300∘C and 500∘C. However, commercial WO3 only operate well at 500∘C. The response of the mesoporous WO3 was higher and the test temperature was lower compared to that of commercial WO3. XPS combined with NO2-TPD was used to explain the high activity of mesoporous WO3 at medium-low temperature, and the mechanism of mixed electromotive force was verified by electrochemical impedance spectroscopy. Furthermore, the sensor exhibited high NO2 selectivity in the presence of interfering gases, such as NO, CO, CO2 and NH3. Most importantly, the sensor had excellent repeatability and stability.

Mesoporous LaFeO3: Synergistic Effect of Adsorption and Visible Light Photo-Fenton Processes for Phenol Removal from Refinery Wastewater

Mesoporous LaFeO3 as a visible light-driven photocatalyst was prepared by a nanocasting method using mesoporous silica (SBA-15) as a hard template. The as-prepared LaFeO3 photocatalyst was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N2 adsorption-desorption, X-ray photoelectron spectroscopy (XPS), and optical absorption spectra. The characterization studies and experimental results showed that LaFeO3 with porous structure caused by the removal of SBA-15 hard template could enhance the specific surface area of the resulting photocatalyst, which improves the phenol adsorption ability of the photocatalyst and in turn enhances its photo-Fenton catalytic activity. The photo-Fenton catalytic activity of the photocatalyst was investigated by photo-Fenton degradation of aqueous phenol under visible light irradiation. The effects of catalyst dosage, H2O2 concentration, and solution pH on the photo-Fenton catalytic degradation of phenol using mesoporous LaFeO3 were studied and optimized. Under the optimal conditions of 20 mg L−1 phenol, 1.0 g L−1 catalyst, and 10 mM H2O2 at pH = 5, the photo-Fenton degradation of phenol (93.47%) was achieved in 180 min under visible light irradiation. Furthermore, our results proved the stability and reusability of mesoporous LaFeO3 and revealed its catalytic mechanism for the photo-Fenton degradation of phenol.