RENEWABLE ENERGY
·
2017
·
IF 4.357
Rongshu Zhu,Fei Tian,Sainan Che,Gang Cao,Feng Ouyang
A series of RGO/La-ZnIn 2 S 4 photocatalysts were successfully synthesized using the hydrothermal method with different amount of RGO (0 wt%, 0.1 wt%, 0.5 wt%, 1.0 wt%, 2.0 wt%, 5.0 wt%) and La (0 wt%, 0.1 wt%, 0.5 wt%, 1.0 wt%, 2.0 wt%, 5.0 wt%) and characterized by various analysis techniques, such as XRD , Raman, SEM, UV–Vis, TEM, BET and PL. The photocatalytic H 2 evolution activities have also been evaluated under visible-light irradiation. The H 2 production activity of RGO/La-ZnIn 2 S 4 was influenced by both La and RGO significantly. The activity reached the best when the amounts of La and RGO were both 1.0 wt%. The hydrogen production rate of 1.0Pt/1.0RGO/1.0La-ZnIn 2 S 4 was 2255 μmol g −1 h −1 and the apparent quantum yield and the energy conversion efficiency were 29.45% and 18.79% at 420 nm respectively. The activity was related to the BET surface area, the pore microstructure and the synergistic effect of RGO and La. On the basis of the characterization of the catalysts, the synergistic effect of RGO and La on the photocatalytic activity of RGO/La-ZnIn 2 S 4 was discussed in detail.
研究领域:
材料科学
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催化化学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF MATERIALS CHEMISTRY
·
2012
·Vol. 22
·期 42
·22619-22623
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IF 5.968
Yuhan Lin,Fang Zhang,Daocheng Pan
A series of (ZnS)x(CuInS2)1−x hierarchical micro/nano-structured solid solutions with precisely controlled chemical composition were synthesized via a facile one-pot solvothermal method. ZnO, Cu2O, and In(OH)3 are used as the starting materials and dissolved in ethanol dithiocarbamic acid which is formed from CS2 and ethanolamine in situ. The ethanol dithiocarbamic acid not only serves as a thermally-degradable ligand, but also acts as sulfur source during synthesis, and can be completely removed by a simple calcination process. As-prepared (ZnS)x(CuInS2)1−x microspheres have a hierarchical micro/nano structure composed of around 7 nm nanoparticles. These samples show excellent photocatalytic H2 evolution activity under visible-light irradiation without any noble metal loading owing to their high surface area (as high as 101.6 m2 g−1) and unique hierarchical structure.
研究领域:
材料科学
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能源化学
✓ 已验证
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2018
·
IF 4.439
Li Liu,Mengting Yue,Jinrong Lu,Jinshan Hu,Yinghua Liang,Wenquan Cui
This paper reports that hybrid titanium dioxide (TiO 2 ) packaged self-assembly perylenetetracarboxylic acid diimide (PTCDI) by self-assembly. These were synthesized through simple mechanical milling that has great photocatalytic performance under visible light . The PTCDI@TiO 2 composite had high activity for the degradation of phenol and 2,4-dichlorophenol, which were 2.3 and 3.2 times of the monomer PTCDI, respectively. After three cycles, the activity of the composite catalyst remained at 70%. Further analysis showed that the photocatalytic activity and stability are mainly due to the enhancement of the charge mobility by the π-π conjugated structure in PTCDI. Moreover, the good energy level matching between PTCDI and TiO 2 helps to separate the electron-hole, thus improving the photocatalytic performance of the composite. The origin of photocatalytic activity was greatly improved due to holes and O 2 − , which was mainly attributed to the strong interaction between PTCDI and TiO 2 .
研究领域:
材料科学
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环境科学
✓ 已验证
DOI
高影响因子
MOLECULES
·
2024
·Vol. 29
·期 2
·493
·
IF 4.2
Ligang Ma,Chao Lin,Wenjun Jiang,Shun Yan,Huilin Jiang,Xiang Song,Xiaoqian Ai,Xiaoxiao Cao,Yihuan Ding
Selective supported catalysts have emerged as a promising approach to enhance carrier separation, particularly in the realm of photocatalytic hydrogen production. Herein, a pioneering exploration involves the loading of PdS and Pt catalyst onto g-C3N4nanosheets to construct g-C3N4@PdS@Pt nanocomposites. The photocatalytic activity of nanocomposites was evaluated under visible light and full spectrum irradiation. The results show that g-C3N4@PdS@Pt nanocomposites exhibit excellent properties. Under visible light irradiation, these nanocomposites exhibit a remarkable production rate of 1289 μmol·g−1·h−1, marking a staggering 60-fold increase compared to g-C3N4@Pt (20.9 μmol·g−1·h−1). Furthermore, when subjected to full spectrum irradiation, the hydrogen production efficiency of g-C3N4@PdS@Pt-3 nanocomposites reaches an impressive 11,438 μmol·g−1·h−1, representing an eightfold enhancement compared to g-C3N4@Pt (1452 μmol·g−1·h−1) under identical conditions. Detailed investigations into the microstructure and optical properties of g-C3N4@PdS catalysts were conducted, shedding light on the mechanisms governing photocatalytic hydrogen production. This study offers valuable insights into the potential of these nanocomposites and their pivotal role in advancing photocatalysis.
研究领域:
材料科学
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能源科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
NANOTECHNOLOGY
·
2020
·Vol. 31
·期 30
·305704
·
IF 3.551
Hong Li,Weizhe Song,Xingqiang Cui,Yanhui Li,Baorong Hou,Xiaoping Zhang,Yuqi Wang,Lianjun Cheng,Pengfei Zhang,Junru Li
AgInS2 nanoparticle and graphene nanosheet co-sensitized anatase TiO2 nanotube array films were fabricated by a combination of hydrothermal reaction and electrochemical anodization on titanium sheets. The results showed that the co-sensitization of AgInS2 nanoparticles and graphene nanosheets extended the photoresponse of TiO2 nanotubes into the visible-light region, and improved the photogenerated charge separation and transfer capability. The photocurrent density of the AgInS2/graphene/TiO2 composites (about 4.0 mA cm−2) was 20 times that of bare TiO2 (only 0.2 mA cm−2) under visible-light illumination. The potential negative shift value of AgInS2/graphene/TiO2 composites was up to 0.68 V versus saturated calomel electrode. The AgInS2/graphene/TiO2 composites can provide Q235 carbon steel with highly efficient photocathodic protection under visible-light illumination.
研究领域:
材料科学
·
电化学
·
腐蚀防护
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2020
·
IF 16.683
Yanbiao Shi,Xiaobing Wang,Xiufan Liu,Cancan Ling,Wenjuan Shen,Lizhi Zhang
We demonstrate that visible light irradiation can promote Fe 3 S 4 Fenton oxidation of atrazine. The visible light irradiation could increase the atrazine Fenton degradation rate by 4.9 times. The enhanced atrazine degradation activity under visible light was attributed to the higher surficial Fe(II)/Fe(III) ratio of Fe 3 S 4 and the efficient surface iron redox cycle triggered by visible light. Experimental results revealed that the operando formation of FeOOH on the Fe 3 S 4 surface blocked the iron redox cycle and inhibited the H 2 O 2 decomposition, accounting for the largely decreased Fenton activity of Fe 3 S 4 in dark, while these problems were successfully solved by the introduction of visible light irradiation, which excite Fe 3 S 4 to produce abundant photo-generated electrons and O 2 − for efficient regeneration of active Fe(II) species of Fe 3 S 4 and in-situ formed FeOOH.
研究领域:
环境科学
·
化学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2017
·
IF 3.387
Yuan Bian,Yongjin Ma,Yanyang Shang,Pengfei Tan,Jun Pan
Bi 2 O 2 CO 3 with a narrow band gap ( Eg ∼ 2.93 eV) was self-assembled by Bi 2 O 2 CO 3 nanosheets via a hydrothermal method, and the β-Bi 2 O 3 /Bi 2 O 2.33 @Bi 2 O 2 CO 3 composites were further fabricated using Bi 2 O 2 CO 3 as template by slow thermal decomposition for 4 h, described as: Bi 2 O 2 CO 3 → β-Bi 2 O 3 /Bi 2 O 2.33 @Bi 2 O 2 CO 3 (300 °C) → β-Bi 2 O 3 /Bi 2 O 2.33 (320 °C) → β-Bi 2 O 3 (350 °C). Deep investigation towards the generation and existence of β-Bi 2 O 3 and Bi 2 O 2.33 on the surfaces and interfaces of Bi 2 O 2 CO 3 were also carefully conducted by XRD, HRTEM and XPS analysis. In comparison with pure Bi 2 O 2 CO 3 , β-Bi 2 O 3 /Bi 2 O 2.33 @Bi 2 O 2 CO 3 displayed superior photocatalytic degradation efficiency and stability to cationic dyes under visible-light irradiation. Especially, the as-prepared BOC–300 °C with relatively high specific surface area (12.11 m 2 g −1 ) could entirely remove Rh-B and MB in 45 min and 60 min, which were approximately 4.7 and 6.6 times as high as that of pure Bi 2 O 2 CO 3 , respectively. Further study demonstrated that the enhanced photocatalytic degradation efficiency of β-Bi 2 O 3 /Bi 2 O 2.33 @Bi 2 O 2 CO 3 is surely owing to the well matched band gap and p - n heterojunction, which made it possible for much faster charge transfer rather than electron-hole pairs recombination process.
研究领域:
材料科学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY
·
2016
·Vol. 80
·期 3
·719-727
·
IF 1.473
Sun Shanfu,Sun Mingxuan,Kong Yuanyuan,Fang Yalin,Yao Yuan
Abstract There has been considerable progress in the field of semiconductor photocatalysis; nevertheless, developing low-cost and high-activity photocatalysts are still a challenge at the present. Here, a series of graphene/MoS 2 /Fe 2 O 3 ternary composites (MG/Fe 2 O 3 ) were prepared via a two-step simple hydrothermal process using H 2 MoO 4 , CH 4 N 2 S, graphene oxide, and Fe(NO 3 ) 3 ·9H 2 O as the starting materials, respectively. Various techniques such as X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, photoluminescence spectra, and UV–Vis diffuse reflectance spectroscopy were adopted to characterize the as-prepared samples. The results suggested that MoS 2 /graphene hybrids were successfully composited with Fe 2 O 3 . A redshift of absorption edge in the light region and more absorption in the visible light region were confirmed for the prepared ternary composites. The highest photocatalytic activity of MG/Fe 2 O 3 composites (3.01 × 10 −3 min −1 ) was observed, which was 1.5 times higher than that of pure Fe 2 O 3 (1.97 × 10 −3 min −1 ). The effect of ultrasound on photocatalytic reactions was investigated, and its photodegradation rate was improved 2.2 times than the photoreactor system without sonication. The results indicated that the positive synergetic effect of the MoS 2 and graphene components in this hybrid cocatalyst, which extended the light response and acted as a charges transfer medium, respectively, is the key to improve photocatalytic performance of Fe 2 O 3 . This research may provide new concepts for the design of high-efficiency photocatalysts and broaden the potential of application of Fe 2 O 3 in photocatalytic fields. Graphical Abstract MoS 2 /graphene/Fe 2 O 3 nanocomposites were successfully fabricated via a simple two-step hydrothermal process and a considerably enhanced activity of visible light-induced photodecomposition of MB was demonstrated.
研究领域:
材料科学
·
环境科学
·
化学
✓ 已验证
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2021
·
IF 19.503
Yingtong Zou,Yezi Hu,Andrej Uhrich,Zewen Shen,Baoxiang Peng,Zhuoyu Ji,Martin Muhler,Guixia Zhao,Xiangke Wang,Xiaoxiang Xu
We provide a distinct understanding on the role of oxygen vacancies (OVs) for visible light-triggered aerobic oxidation of alcohols via comparative studies on three kinds of Nb 2 O 5 , i.e., undoped, Ti-doped and Ce-doped Nb 2 O 5 . With benzyl alcohol and 5-hydroxymethylfurfural as representative alcohol substrates, we show that fast alcohol oxidation with high selectivity can be achieved on these doped Nb 2 O 5 containing abundant OVs. However, the functionality of OVs is dependent on the properties of dopants as Ce-doped Nb 2 O 5 exhibits a better performance than Ti-doped one. Investigations indicate that the Ce dopants incur little distortion to the structure of Nb 2 O 5 and induce more accessible OVs than Ti dopants for the dissociative chemisorption of alcohol molecules which supports favorable interfacial electron migration process. The present work not only reveals the difference of oxygen vacancies caused by varied metal doping but provides a unique insight in the relation between OVs structure and photocatalytic alcohol oxidation.
研究领域:
催化化学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Xiaobin Dong,Han Wang,Xiaolong Li,Pedram Fatehi,Shoujuan Wang,Qin Wu,Keyin Liu,Fangong Kong
Graphitic carbon nitride is a very potential photocatalytic catalyst for H 2 production, but its practical application is seriously limited by the fast recombination of photogenerated carriers and insufficient utilization of surface charge. In order to solve these problems, herein, a series of g-C 3 N 4 -NiO-NiS x photocatalysts were synthesized by first calcining the precursor to load NiO on g-C 3 N 4 and subsequently partial sulfidation of NiO into NiS x in situ via a hydrothermal process. Under the irradiation of visible light, the photocatalytic H 2 production rate of g-C 3 N 4 -NiO-0.4T can be up to 1248.1 μmol·g −1 ·h −1 using triethanolamine as sacrificial agent. In addition, recycling test also confirmed g-C 3 N 4 -NiO-0.4T has excellent photostability. It is believed that the formation of p-n junction between NiO and g-C 3 N 4 and the presence of NiS x promote the spatially fast separation of photogenerated carriers, while the abundant interface of NiS 2 and NiS also leads to the good proton trapping ability. These two factors jointly determine the efficient H 2 production of the composite photocatalysts. Furthermore, the detailed energy band structure and plausible photocatalytic mechanism of g-C 3 N 4 -NiO-NiS x are also proposed. This work can offer a new route and useful reference for the design and research of high efficiency composite photocatalysts for H 2 production.
研究领域:
材料科学
·
能源化学
✓ 已验证
产品关联
DOI
高影响因子
Frontiers of Chemical Science and Engineering
·
2021
·Vol. 15
·期 6
·1561-1571
·
IF 4.204
Quan Huiying,Qian Kejiang,Xuan Ying,Lou Lan-Lan,Yu Kai,Liu Shuangxi
It is of broad interest to develop emerging photocatalysts with excellent light-harvesting capacity and high charge carrier separation efficiency for visible light photocatalytic hydrogen evolution reaction. However, achieving satisfying hydrogen evolution efficiency under noble metal-free conditions remains challenging. In this study, we demonstrate the fabrication of three-dimensionally ordered macroporous SrTiO3 decorated with Zn x Cd 1 − x S nanoparticles for hydrogen production under visible light irradiation (λ > 420 nm). Synergetic enhancement of photocatalytic activity is achieved by the slow photon effect and improved separation efficiency of photogenerated charge carriers. The obtained composites could afford very high hydrogen production efficiencies up to 19.67 mmol·g −1 ·h −1 , with an apparent quantum efficiency of 35.9% at 420 nm, which is 4.2 and 23.9 times higher than those of pure Zn0.5Cd0.5S (4.67 mmol·g −1 ·h −1 ) and CdS (0.82 mmol·g −1 ·h −1 ), respectively. In particular, under Pt-free conditions, an attractive hydrogen production rate (3.23 mmol·g −1 ·h −1 ) was achieved, providing a low-cost and high-efficiency strategy to produce hydrogen from water splitting. Moreover, the composites showed excellent stability, and no obvious loss in activity was observed after five cycling tests.
研究领域:
材料科学
·
能源化学
✓ 已验证
DOI
高影响因子
DALTON TRANSACTIONS
·
2018
·Vol. 47
·期 30
·10046-10056
·
IF 4.099
Xiang Li,Mengyuan Su,Guifen Zhu,Kaige Zhang,Xia Zhang,Jing Fan
In this study, a novel few-layer WS2/Bi2MoO6 heterojunction with greatly enhanced visible light photocatalytic performance was synthesized via a facile hydrothermal method. The results indicated that Bi2MoO6 nanosheets were directly grown on the surface of few-layer WS2 and form plate-on-plate heterojunctions. The synthesized nanocomposites exhibited excellent photocatalytic activity under visible-light irradiation. The optimal composite with 5 wt% WS2 showed the highest photocatalytic activity, whose degradation efficiencies and TOC removal were 99.5% and 91.7% for rhodamine B (RhB), 98.9% and 89.8% for ciprofloxacin (CIP), 76.0% and 67.8% for methylene blue (MB), and 69.3% and 58.6% for methimazole (MMI), respectively. Their excellent photocatalytic performance was predominantly ascribed to the construction of a plate-on-plate heterojunction structure between WS2 and Bi2MoO6, which could promote charge separation efficiency and enhance light harvesting efficiency. The present work provides a new understanding for extending the application of transition-metal dichalcogenides in the field of photocatalysis.
研究领域:
材料科学
·
环境科学
·
化学
✓ 已验证
DOI
高影响因子