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排序方式: 共有1308条查询结果,搜索用时 31 毫秒
1.
Weiwen Wang Hui Zhao Peng Pan Kang Xue Zisheng Zhang Jihai Duan 《Ceramics International》2021,47(5):6094-6104
In order to enhance the photocatalytic activity of TiO2 under visible light, Ag nanoparticles were introduced into tridoped B–C–N–TiO2 (TT) catalyst by photoreduction deposition. Ag/B–C–N–TiO2 (ATT) catalysts with the functions of reducing band gap and carrier recombination were prepared. At the same time, the effect of the amount of Ag on the photocatalytic performance of ATT catalyst was investigated. Through XRD, XPS, PL and other characterization methods, the (211)/(101)/Ag interface heterojunction mechanism similar to the traditional Z-scheme heterojunction was proposed. The intervention of Ag nanoparticles changed the P–N interface heterojunction between (211)/(101) to the (211)/(101)/Ag Z-scheme interface heterojunction. The results show that ATT catalyst exhibits the highest photocatalytic activity when the molar amount of Ag is 0.005% with the MB degradation rate of the ATT catalyst (0.01707 min?1), which is 14.59 times of TiO2 (0.00117 min?1) and 2.02 times of TT (0.00847 min?1). In addition, the four cycles efficiencies of ATT for MB degradation were all above 94.00%.This study reveals the possibility of construction of Z-scheme heterojunctions between precious metal nanoparticles and different interfaces of TiO2, and provides a reference for the construction of Z-scheme interface heterojunctions. 相似文献
2.
《International Journal of Hydrogen Energy》2022,47(1):228-241
The construction of semiconductor heterojunction for photocatalytic H2 production from water splitting is an efficient and environment-friendly technology. In this work, ZnO/BiOCl (ZBC) and Sn-doped ZnO/BiOCl (ZBC-S) photocatalysts with Z-scheme heterojunction were successfully prepared by simple hydrothermal method. The photocatalytic H2 evolution from water splitting by the as-prepared photocatalysts was investigated. The formation of ZnO/BiOCl heterojunction reduces the recombination probability of the photogenerated carriers. The impurity levels originated from Sn doping reduce the band gap width of ZnO and BiOCl to some extent, thereby enhancing the light absorption ability. The ZBC-S composite exhibits the best photocatalytic activity. In addition, the photocatalytic efficiency of H2 production was improved by sensitization with Eosin Y (EY) dye. The H2 production rate under simulated sunlight reaches 4146.77 μmol g?1 h?1, which is 27 times higher than that of pure ZnO. Finally, the Z-scheme electron transfer route in ZnO/BiOCl heterojunction was determined, and the photocatalytic H2 production mechanism of EY sensitized ZBC-S was proposed. 相似文献
3.
《International Journal of Hydrogen Energy》2022,47(34):15491-15504
The development of excellent photocatalytic material is highly required for energy and environmental applications. In this study, visible light responsive p-n heterojunction photocatalysts based on CuO/MoO3 with varying ratios of CuO were prepared by the facile hydrothermal method. The crystalline structure, surface morphology, chemical compositions and optical properties of the synthesized photocatalysts were studied using X-ray powder diffraction (XRD), scanning electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared spectroscopy (FTIR), photoluminescence (PL) techniques and UV–Vi's absorption spectroscopy. The results showed that the 5%CuO/MoO3 nanocomposite displayed enhanced photocatalytic performance for the production of hydrogen (98.5 μmol h?1g?1) and degradation of dyes rhodamine B (RhB) and alizarine yellow (AY) than all other samples. Furthermore, 5% CuO/MoO3 composite exhibited excellent stability after five consecutive cycles for both RhB and AY dyes. Overall, the improved photocatalytic performance of 5%CuO/MoO3 composite was due to increased adsorption of visible light, good surface morphology, enhanced charge separation/transfer which inhibited recombination of electrons and holes. This study could encourage the synthesis of novel and effective p-n heterojunction photocatalysts for practical applications. 相似文献
4.
《International Journal of Hydrogen Energy》2022,47(67):28879-28893
A novel Z-type multidimensional FeSe2/CuSe heterojunction photocatalyst was synthesized by a hydrothermal progress. In the reaction, 1D FeSe2 nanorods will load on the surface of 2D CuSe nanosheets to construct heterojunction. This Z-type heterojunction can improve the carriers separated efficiency and reduce internal resistance (as low as 0.31 kΩ). More importantly, the catalysts display both high oxidation and reduction ability confirmed by photocatalytic and photoelectrochemical test. Under the optimum concentration, the catalyst showed 7.4 times of degradation tetracycline hydrochloride rate, and 4 times of photocurrent density than pure CuSe. Active specie O2?? was detected by the electron spin resonance tool during photocatalytic degradation progress which could confirm that a Z-type heterojunction was constructed between CuSe and FeSe2. In this Z-type heterojunction, photoinduced electrons in the conduction band of FeSe2 can directly inject the valence band of CuSe while photoinduced electrons in the conduction band position of CuSe and photoinduced holes in the valence band position of FeSe2 will remain. The remained photoinduced electrons in the conduction band of CuSe can generate O2?? to oxide tetracycline hydrochloride as well as photoinduced electrons to produce hydrogen. This work highlights a simple strategy of Z-tpye selenides heterostructure for oxidation and reduction application. 相似文献
5.
《International Journal of Hydrogen Energy》2022,47(93):39486-39498
Adjusting the band gap of organic-inorganic composites by chemical bonding can effectively construct Step-scheme (S-scheme) heterojunctions, featuring properties of fast photogenerated charge migration and excellent photocatalytic performance. In this work, a novel perylene-3, 4, 9, 10-tetracarboxylicdiimide (PDI)-titanium dioxide (TiO2) heterojunction is elaborately synthesized through simple solvent compounding method. The monodispersed spherical TiO2 nanoparticles was prepared with the capping agents of oleylamine and oleic acid, and suffered by a ligand exchange process with nitrosonium tetrafluoroborate (NOBF4) to remove oleylamine and oleic acid. The NOBF4 ligands were further replaced by PDI super molecular nanosheets to obtain two dimensional (2D)-zero dimensional (0D) PDI-TiO2 composites. TiO2 nanoparticles are evenly anchored on the surface of PDI nanosheets with intimate contact. The PDI-TiO2 composites has emerged considerably superior activity in hydrogen evolution. The highest hydrogen evolution rate for PDI-TiO2composites with the PDI weight percentage of 2.4% was 9766 μmol h?1 g?1 under solar light irradiation, which is 2.56 times of TiO2-NOBF4 catalyst. Moreover, PDI-TiO2 composites possess stoichiometric overall water splitting performance with H2 and O2 release rates of 238.20 and 114.18 μmol h?1 g?1. The superior photocatalytic performance of PDI-TiO2 composites can be attributed to the dramatic increase in visible and NIR light absorption caused by π-π stacking structure of PDI, the prevented charge recombination by the S-scheme heterojunction, and the enhanced oxygen evolution by the stronger oxidation capability of PDI. PDI supramolecular nanosheets may work as a novel functional support for many types of semiconductor nanomaterials as graphene, which will display a wide range of application prospects in the energy and environmental fields. 相似文献
6.
《International Journal of Hydrogen Energy》2022,47(6):3781-3790
A novel heterostructure of g-C3N4/ZnO/Bi4O5Br2 (ZB-3) was designed, and used in the microbial coupled photocatalytic fuel cell (MPFC). It can effectively improve electron utilization efficiency and pollutant degradation using this double Z-scheme heterojunction structure. The current–time (I–t) curves demonstrated that the current density of ZB-3 was higher than that of ZnO, ZnO/Bi4O5Br2 (ZB-1), g-C3N4/ZnO (ZB-2). Electrochemical impedance spectroscopy (EIS) indicated ZB-3 possessed the minimum charge-transfer resistance. This MPFC for degrading rhodamine B (RhB) and tetracycline (TC) under different conditions were developed using these materials. Even in the dark condition, MPFC with g-C3N4/ZnO/Bi4O5Br2 demonstrated 93% and 82% degradation efficiency for RhB and TC, respectively. Furthermore, the electron transport mechanism of the MPFC and ZB-3 were proposed. It paves the approach for more efficient pollutant degradation via MFC photocatalysis. 相似文献
7.
《Advanced Powder Technology》2022,33(11):103777
In this study the constructional modification of Graphitic carbon nitride nanosheet (GCN-ns) has been made with the aid of ZnCr layered double hydroxide (ZC-LDH) in a unique 2D-2D structure to enhance its visible light absorption. Optical and morphological study presents successful incorporation of ZC-LDH on the surface of GCN-ns. Through adjusting of GCN-ns by ZC-LDH lower recombination rate of e?/h+ pairs, longer lifetimes and an increase in contamination reduction was brought out. The binary nanocomposite was employed to effectively degrade Rhodamine B under UV/vis light irradiation. The improvement in photocatalytic abilities was proven to be related to in situ self-production of H2O2 on GCN-ns/ZC-LDH surface by Xe light irradiation which in return accounts for additional hydroxide radical generation. Radical quenching experiments specified the main active species involved while the consequent step-scheme (S-scheme) charge transfer mechanism was proposed. 相似文献
8.
采用直流磁控溅射和后退火氧化工艺在p型GaAs单晶衬底上成功制备了n-VO_2/pGaAs异质结,研究了不同退火温度和退火时间对VO_2/GaAs异质结性能的影响,并分析其结晶取向、化学组分、膜层质量以及光电特性。结果表明,在退火时间2 h和退火温度693 K下能得到相变性能最佳的VO_2薄膜,相变前后电阻变化约2个数量级。VO_2/GaAs异质结在308 K、318 K和328 K温度下具有较好的整流特性,对应温度下的阈值跳变电压分别为6.9 V、6.6 V和6.2 V,该结果为基于VO_2相变特性的异质结光电器件的设计与应用提供了可行性。 相似文献
9.
Jin Wang Mengke Zhang Guanglong Yang Wenwu Song Weiting Zhong Xunyue Wang Minmin Wang Tongming Sun Yanfeng Tang 《Advanced functional materials》2021,31(33):2101532
Highly efficient electrocatalysts composed of earth-abundant elements are desired for water-splitting to produce clean and renewable chemical fuel. Herein, a heteroatomic-doped multi-phase Mo-doped nickel phosphide/nickel sulfide (Mo-NiPx/NiSy) nanowire electrocatalyst is designed by a successive phosphorization and sulfuration method for boosting overall water splitting (both oxygen and hydrogen evolution reactions (HER)) in alkaline solution. As expected, the Mo-NiPx/NiSy electrode possesses low overpotentials both at low and high current densities in HER, while the Mo-NiPx/NiSy heterostructure exhibits high active performance with ultra-low overpotentials of 137, 182, and 250 mV at the current density of 10, 100, and 400 mA cm−2 in 1 m KOH solution, respectively, in oxygen evolution reaction. In particular, the as-prepared Mo-NiPx/NiSy electrodes exhibit remarkable full water splitting performance at both low and high current densities of 10, 100, and 400 mA cm−2 with 1.42, 1.70, and 2.36 V, respectively, which is comparable to commercial electrolysis. 相似文献
10.
《Ceramics International》2021,47(22):31337-31348
In this research work, p-n heterojunction Cu2SnS3/Ti3+-TiO2 photocatalysts were synthesized by using a facile hydrothermal method to degrade tetracycline and produce hydrogen energy. The properties of Cu2SnS3/Ti3+-TiO2 was analyzed by using XRD, SEM, TEM, HRTEM, BET, PL and UV–vis characterization. The HPLC-MS and TOC analyzer systems were used to analyze the intermediate products during the photocatalysis deprivation and total organic carbon. The characterizations showed that the addition of self-doped Ti3+ and Cu2SnS3 into TiO2 enhanced the material's crystallinity, increased the absorption region from 450 nm to 750 nm, increased the surface area of the material from 234 to 583 m2/g and reduced the recombination of charge carriers. Under visible light irradiation, Cu2SnS3/Ti3+-TiO2 exhibited excellent degradation performance and stability. The increase in the efficiency of the material is due to the creation of an internal electric field induced by the p-n heterojunction and reduction in the bandgap of the material, which efficiently reduced the rate of recombination, increased the surface area for light absorption and increased the transfer of charge carriers. The Cu2SnS3/Ti3+-TiO2 photocatalyst degraded 100 % tetracycline and produced 510 μmol/hg hydrogen energy. The Cu2SnS3/Ti3+-TiO2 composite exhibited good stability even after six cycles Cu2SnS3/Ti3+-TiO2 degraded 98–99 % TC under visible light irridiation. The efficiency of Cu2SnS3/Ti3+-TiO2 was also analyzed in the outdoor environment, confirming that this material can be effectively used in practical applications. 相似文献