JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2023
·Vol. 34
·期 1
·1-12
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IF 2.8
Liang Xuan,Xue Suting,Wu Wangchen,Feng Qin,Zheng Xudong,Zhang Yakang,Xu Song,Zhou Man,Li Zhongyu
Herein, a series of CuS particles anchored three-dimensional ordered macroporous TiO 2 (CuS/3DOM-TiO 2 ) composites were fabricated by a biocompatible and environmental-friendly biomolecule-assisted route. For the first time in the macroporous 3DOM-TiO 2 , L-cysteine acted as multiple roles including sulfur source and chelating agent for anchoring of CuS particles. During the regulation by Cu/Ti molar ratios from 0.3 to 2, the average size of CuS particle which anchored on inner surface of 3DOM-TiO 2 was well-controlled from about 50 to 20 nm. The photocatalytic activities were investigated by visible-light degradation of methylene blue (MB). The highest activity of CuS/3DOM-TiO 2 was emerged when Cu/Ti equaled to 1. This optimized CuS/3DOM-TiO 2 -1 reached 99% in 180 min, which was 60% higher than that of pure TiO 2 . After four cycles, the photocatalytic activity of CuS/3DOM-TiO 2 retains more than 80% of its original performance. L-cysteine highly promoted the adhesion between CuS and TiO 2 which provided good cycling ability.
研究领域:
材料科学
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环境科学
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生物化学
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高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
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2023
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IF 22.1
Xuewu Deng,Xiaobing Zheng,Feifei Jia,Cuiyao Cao,Haolei Song,Yanjun Jiang,Yunting Liu,Guanhua Liu,Shijie Li,Lihui Wang
The selective oxyfunctionalization of C-H and C C bonds is highly important and catalyzed by unspecific peroxygenases (UPOs) which suffer from inactivation by hydrogen peroxide (H 2 O 2 ). Herein, photo-enzyme integrated catalysts were constructed by immobilizing Aae UPO as cross-linked enzyme aggregates (CLEAs) in Pd-loaded three-dimensional ordered macroporous titania (3DOM TiO 2 ) with in situ photocatalytic H 2 O 2 production. The prepared Aae UPO@3DOM TiO 2 -Pd obtained higher catalytic efficiency compared with CLEAs- Aae UPO. The conversion of ethylbenzene to (R) -1-phenethyl alcohol was significantly improved, reaching 99 % compared with free enzyme (38 %) and CLEAs- Aae UPO (49 %), with ee value of > 99 %. Aae UPO@3DOM TiO 2 -Pd exhibited good stability and reusability attributed to the protection of macropores and in situ H 2 O 2 production. By using the designed 3DOM platform for photocatalysis and enzyme immobilization, the in situ photocatalytic generation of H 2 O 2 was highly efficient, and the monodisperse CLEAs- Aae UPO in the macropores facilitated the contact of substrate and enzyme, thus obtaining excellent photo-enzyme coupled catalysis.
研究领域:
生物化学
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环境科学
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材料科学
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高影响因子
Catalysts
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2021
·Vol. 11
·期 5
·533
·
IF 4.146
Jing Chen,Yingchun Guo,Tengteng Kang,Xingchi Liu,Xiaomei Wang,Xu Zhang
It is wise to mimic a bioinspired system to design a nanoreactor as a catalyst containing multiple components for a cascade reaction. Here, we report the uniform growth of well-dispersed nano-scale ZIF-8 crystals on the pore walls of 3DOM TiO2via the TEA-assisted crystallization process. The UV-vis spectra indicate that the ZIF-8 photosensitizer can extend the visible-light absorption of 3DOM TiO2. The obtained nanoreactor can efficiently catalyze the one-pot aromatic alcohol oxidization and Knoevenagel condensation cascade reaction for larger molecules. This work offers an important strategy for preparing semiconductor–MOF multifunctional composites with a spatially separated compartmentation for the cascade reaction.Keywords:crystal growth;cascade reaction;nanoreactor;semiconductor–MOF composite
研究领域:
材料科学
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催化化学
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高影响因子
MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING
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2019
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IF 2.722
Guo-quan Ma,Fu-sheng Liu,Sheng Wang,Zeng-chao Dang,Jia-wei Zhang,Xiao-jie Fu,Mei-shun Hou
A serial of Bi 2 S 3 /3DOM-TiO 2 (x-BS/3D-Ti, x denotes as the weight percentage of Bi 2 S 3 , x = 5, 10, 15, 20 and 25 wt%) were fabricated and their physico-chemical properties were characterized with the utilization of XRD , SEM, UV–Vis DRS and XPS . The photocatalytic performance was investigated based on photocatalytic degradation of rhodamine B (RhB) solution under simulated solar irradiation . The mechanisms for enhancing the photocatalytic activity and the degradation of RhB occurring on the BS/3D-Ti surface were discussed. The results indicated that 20-BS/3D-Ti exhibited the highest photocatalytic performance among the prepared samples. Although good adsorption property of BS/3D-Ti for RhB could promote the degradation of RhB, effective separation between photoinduced electron and hole was the key influencing factor compared to adsorption. The slightly reducing in the photocatalytic degradation rates after multiple cycles was caused by the adsorption of the oxidation intermediate product of RhB on the surface of BS/3D-Ti, which decreases the absorption of light.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
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2019
·
IF 8.355
Yue Chang,Ying Xuan,Huiying Quan,Hang Zhang,Shuangxi Liu,Zhengcao Li,Kai Yu,Jiangli Cao
As one of the most promising photocatalysts for hydrogen production from water splitting, conventional TiO 2 materials suffer from the low quantum yield and light absorption efficiency. The present study provided a strategy to improve efficiency of TiO 2 -based photocatalysts for hydrogen production from water splitting based on an interesting structure-property relationship. The hydrogen treated Au/TiO 2 photocatalysts with three-dimensionally ordered macroporous (3DOM) structure were successfully synthesized and well characterized through various methods. The 3DOM-structure and Au modification can promote the hydrogenation of TiO 2 . The light absorption can be improved by slow photon effect of the 3DOM structure. And, in the meanwhile, the hydrogenation as well as Au modification can improve the photogenerated carrier separation. In addition, to understand how hydrogenation and Au modification promote electron migration and decrease carrier recombination, the electric band structure for hydrogen treated Au/3DOM-TiO 2 was well studied and we found the local electron field enhancement, surface band bending and the generation of mid-gap state contributed most of enhancement.
研究领域:
材料科学
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能源化学
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高影响因子
CHEMICAL ENGINEERING JOURNAL
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2026
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IF 12.5
Yuxiang Deng,Zhenyu Cai,Libo Yang,Zhiyao Wu,Bihong Chen,Chang Gao,Xinyu Yu,Nannan Wang,Xinpeng Wang
3DOM-TiO 2 /CuO S-scheme heterojunction synthesized via hard templating • Removes 99.06% U(VI) in 120 min; capacity of 1751.33 mg/g • Dynamic Cu valence change & O-vacancy evolution restrain charge recombination. • In situ multi-spectra & DFT reveal charge transfer and U(VI) reduction mechanism. Photocatalysis offers a sustainable approach for uranium-containing wastewater remediation, yet conventional materials still suffer from limited solar-light utilization and rapid charge recombination. Herein, a three-dimensional ordered macroporous TiO 2 /CuO composite (3DOM-TC) was synthesized using resorcinol–formaldehyde resin spheres as a hard template. The ordered macroporous TiO 2 framework enables slow-photon-assisted light harvesting and multiple light scattering, while CuO coupling broadens the light-response range and constructs an S-scheme TiO 2 /CuO heterojunction to promote directional charge separation. Meanwhile, oxygen vacancies mainly serve as electron-trapping and O 2 /intermediate adsorption–activation sites, which are coupled with the dynamic Cu 2+ /Cu + variation during photocatalysis. As a result, 3DOM-TC achieves 99.06% U(VI) removal within 120 min, corresponding to a maximum extraction capacity of 1751.33 mg/g. Photoelectrochemical tests confirm enhanced photocurrent density and efficient interfacial charge transport compared with pristine TiO 2 . In situ EPR, XPS, and DFT calculations reveal the photoinduced charge-transfer pathway and illumination-enhanced oxygen-vacancy signals. Moreover, in situ FTIR spectroscopy confirms that photogenerated ·O 2 − can further convert to H 2 O 2 -related species, thereby promoting U(VI) precipitation as (UO 2 )O 2 ·4H 2 O. This work highlights the synergistic integration of 3DOM-enabled light harvesting, S-scheme charge separation, and vacancy-assisted electron transfer and O 2 activation, providing a promising strategy for efficient photocatalytic U(VI) sequestration. Download: Download high-res image (232KB) Download: Download full-size image
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