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Progress in Natural Science-Materials International · 2019 ·Vol. 29 ·期 4 ·379-383 · IF 3.31

Photo-improved hydrogen evolution reaction activity of the Pt/CdS electrocatalyst

Yongsheng Fu,Jun Li,Jianguo Li

The effect of CdS content on the photo-induced improvement of hydrogen evolution reaction activity of the Pt/CdS electrocatalyst was investigated. Although the electrons transferred from CdS to Pt in the Pt/CdS electrocatalyst increased with the CdS content under illumination, the electrochemical active surface area of the Pt/CdS electrocatalyst decreased with the CdS content, resulting that the photo-induced improvement of hydrogen evolution reaction activity of the Pt/CdS electrocatalyst decreased with the CdS content.

研究领域: 材料科学 · 催化化学 · 物理化学 · 纳米材料 · 能源化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF SOLID STATE CHEMISTRY · 2021 · IF 3.498

Crystallization behavior of boron in low-temperature immobilization of iodine waste

Yaxin Feng,Guilin Wei,Yi Liu,Wenhong Han,Yan Chen,Runjie Sun,Lin Peng,Meihua Ma,Yu Zhang,Zhentao Zhang,Xirui Lu

The immobilization of iodine waste is a challenge in the field of nuclear waste . In this work, iodine waste (silver-coated silica gel with different iodine loadings) was immobilized at low-sintering temperatures (500, 550, and 600 ​°C). XRD represented that the crystallized phases of the sintered matrix consist of AgI and B 2 O 3 . The crystallization behavior of boron can be found as the sintering temperature increased from 500 ​°C to 600 ​°C. FT-IR results proved that in the process of crystallization, part of the microstructure related to B–O stretching transformed from [BO 4 ] to [BO 3 ] units, which benefits low-temperature iodine waste immobilization due to the bonding energy of [BO 3 ] is higher than that of [BO 4 ]. Our work reveals the B-related microstructure transition in low-temperature immobilization iodine waste.

研究领域: 核废物处理 · 材料科学 · 无机化学 · 放射化学 · 环境工程
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2015 ·Vol. 41 ·期 3 ·1550-1558 · IF 3.313

Cation ordering/disordering effects upon photocatalytic activity of CrNbO4, CrTaO4, Sr2CrNbO6 and Sr2CrTaO6

Meilin Lv,Shuang Ni,Zhuo Wang,Tongcheng Cao,Xiaoxiang Xu

Doping has generally been served as one of the most efficient strategies for the improvement of wide band gap semiconductor photocatalysts . However, atomic arrangements of doped elements in the host crystal structure have often been overlooked, particularly during the investigation and evaluation of dopant functionality. It is known that electronic structures of a semiconductor are profoundly controlled by atomic occupancies in different crystallographic positions. Knowledge about dopant accommodations in the crystal structure and their influence towards photocatalytic performance is highly desired. Here, we investigated four compositional and structural relevant compounds CrNbO 4 , CrTaO 4 , Sr 2 CrNbO 6 and Sr 2 CrTaO 6 with the aim to study the effects of cation ordering/disordering upon their photocatalytic activity . Our results showed that ordered cations, namely Cr and Nb/Ta, are detrimental to the photocatalytic performance. Theoretical calculations indicate that cation ordering would enlarge the band gap and inhibit charge transfer between Cr and Nb/Ta. Our findings imply that ordered dopants in photocatalytic materials would severely offset the benefits of doping and might be a reason for the decreased activity at high doping levels often encountered.

研究领域: 材料科学 · 半导体物理 · 光催化 · 固体化学 · 能源材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Novel MoS2/montmorillonite hybrid aerogel encapsulated PEG as composite phase change materials with superior solar-thermal energy harvesting and storage

Qijing Guo,Hao Yi,Feifei Jia,Shaoxian Song

Phase change materials (PCMs) offer significant advantages in energy conversion and storage by facilitating the storage and release of thermal energy during phase transition processes. However, challenges such as leakage during PCM phase transitions and poor light absorption properties have constrained their application in the field of photothermal energy storage. In this study, Montmorillonite (Mt) and molybdenum disulfide (MoS 2 ) has been used to design and synthesize hybrid aerogels (MoS 2 /Mt) boasting high mechanical strength and excellent photothermal conversion performance. These aerogels are then used to encapsulate polyethylene glycol (PEG) to prepare composite PCMs with outstanding solar-thermal conversion and storage performances. The results show that the synthesized MoS 2 /Mt-PEG composite PCMs exhibit high enthalpies of melting and solidification of 169.16 J/g and 170.78 J/g, respectively, while the aerogel supporting material has a high compressive modulus of 1.96 MPa. Moreover, the composite material displayed excellent thermal stability and leakage resistance after undergoing 30 melting-cooling cycles. Furthermore, the incorporation of MoS 2 imparted outstanding light absorption properties to the MoS 2 /Mt-PEG composite, resulting in a high light absorption and photothermal conversion-storage efficiency of 93.4 % and 96.47 %, respectively. Synthesized composite PCMs also demonstrate outstanding performance in solar-thermal-electricity conversion, achieving a voltage output of 458 mV under illumination conditions and maintaining a sustainable voltage output even after removing the light source. Thus, the composite PCMs prepared in this work can meet the requirements of high enthalpy, effective leakage prevention, efficient solar-thermal conversion and solar-thermal-electricity conversion performance, thereby presenting potential applications in practical solar energy collection, conversion, and storage.

研究领域: 材料科学 · 能源化学 · 纳米复合材料 · 热能存储 · 光热转换
✓ 已验证 DOI 高影响因子
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RSC Advances · 2015 ·Vol. 6 ·期 3 ·2241-2251 · IF 3.84

Synthesis of porous Al doped ZnO nanosheets with high adsorption and photodecolorizative activity and the key role of Al doping for methyl orange removal

Xiaohua Sun,Weilong Luo,Linlin Chen,Linjie Zheng,Chao Bao,Panpan Sun,Niu Huang,Yihua Sun,Liang Fang,Lei Wang

Porous Al doped ZnO (AZO) nanosheets have been prepared as an efficient multifunctional water treatment material. Their fundamental properties were characterized by various spectroscopic testing methods. The AZO nanosheets displayed very rapid adsorption rate and high adsorption capacity for methyl orange (MO) dye. The kinetics and equilibrium of adsorption process were found to follow the pseudo-second-order kinetic and Langmuir isotherm models, respectively. Furthermore, the AZO nanosheets exhibited superior photodecolorizative activity compared with the commercial P25 TiO2 nanoparticles. It was found that Al doping increased the zeta potential of AZO nanosheets and then significantly enhanced the adsorption capacity for MO dye and, at the same time, retarded the recombination of photoexcited electron–hole pairs, and prolonged the lifetime of the photo-generated carriers, and then improved the semiconductor photocatalytic activity. In addition, the visible-light-driven dye photosensitized degradation was also an important reason for enhanced photodecolorizative activity. Therefore, AZO nanosheets are a potential multifunctional water treatment material combining highly efficient adsorption and photocatalytic degradation.

研究领域: 材料科学 · 环境化学 · 纳米技术 · 光催化 · 水处理
✓ 已验证 DOI 高影响因子
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JOURNAL OF LUMINESCENCE · 2013 · IF 2.144

Comparative study of the binding of trypsin to caffeine and theophylline by spectrofluorimetry

Ruiyong Wang,Xiaohui Kang,Ruiqiang Wang,Rui Wang,Huanjing Dou,Jing Wu,Chuanjun Song,Junbiao Chang

The interactions between trypsin and caffeine/theophylline were investigated by fluorescence spectroscopy , UV–visible absorption spectroscopy , resonance light scattering and synchronous fluorescence spectroscopy under mimic physiological conditions . The results revealed that the fluorescence quenching of trypsin by caffeine and theophylline was the result of the formed complex of caffeine–trypsin and theophylline–trypsin. The binding constants and thermodynamic parameters at three different temperatures were obtained. The hydrophobic interaction was the predominant intermolecular forces to stabilize the complex. Results showed that caffeine was the stronger quencher and bound to trypsin with higher affinity than theophylline .

研究领域: 生物化学 · 分子药理学 · 药物代谢 · 蛋白质-配体相互作用 · 光谱学
✓ 已验证 DOI 高影响因子
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APPLIED SURFACE SCIENCE · 2017 · IF 3.387

Highly efficient dye-sensitized solar cell with a novel nanohybrid film of Cu2ZnSnS4-MWCNTs as counter electrode

Hui Chen,Jinfeng Wang,Chenchen Jia,Junpeng Mou,Lei Zhu

For the purpose of increasing the power conversion efficiency (PCE) meanwhile decreasing the cost of dye-sensitized solar cell (DSSC), Cu 2 ZnSnS 4 - multiwall carbon nanotubes (CZTS-MWCNTs) nanohybrid Pt-free counter electrode (CE) was prepared via a facile fabricating route. In brief, CZTS nanoparticles were synthesized by a solvothermal method and the composite film was fabricated by spin coating the aqueous solution of the composite. The short-circuit current density and PCE of the DSSC with CZTS-MWCNTs CE were found to be 16.62   mA   cm −2 and 9.04%, respectively. But the corresponding values were 15.42   mA   cm −2 and 8.74% for a DSSC with a pure Pt-CE. This is owing to the synergistic effect of the intrinsic superior electrocatalytic activity of the CZTS nanoparticles and highly specific surface area and high electrical conductivity of the MWCNTs . The presence and distribution of CZTS-MWCNTs on the CE were characterized by X-Ray Diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscope (SEM), respectively. Cyclic voltammetry (CV) and electrochemical impedance spectra (EIS) were examined for confirming the high electrocatalytic efficiency of this nanohybrid system.

研究领域: 材料科学 · 能源化学 · 纳米技术 · 电化学 · 光伏器件
✓ 已验证 DOI 高影响因子
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2015 · IF 7.435

Comparing the degradation of acetochlor to RhB using BiOBr under visible light: A significantly different rate-catalyst dose relationship

Peng Yi-Zhu,Ma Wan-Hong,Jia Man-Ke,Zhao Xiao-Rong,David M. Johnson,Huang Ying-Ping

In this study, a weakly polar pesticide acetochlor in water was tried to degrade by BiOBr catalysts under visible light irradiation. Its degradation reaction rate increased exponentially with increasing catalyst dosage, which was significantly different from conventional photocatalytic patterns established for polar or water-soluble pollutants. Thus, the rate-dosage relationship of BiOBr/acetochlor was compared to that of BiOBr/Rhodamine B (RhB) (a typical strong polar dye pollutant in water) at different BiOBr dosages. The degradation rate of RhB increased with the BiOBr dosage and then plateaued due to more catalyst particles blocking the light into the inner solution, which is a typical behavior for heterogeneous photocatalysis of polar organic compounds in aqueous solution. While acetochlor behaved differently, its degradation rate increased exponentially with the BiOBr dosage, and no plateau was observed even up to 9.0   g/L BiOBr dosage. This special rate-dose relationship for weakly polar acetochlor was correlated with a unique adsorption property of BiOBr to acetochlor in water solution. There was a re-distribution effect that always exclude excessive acetochlor adsorbed on BiOBr surface regardless either substrates or BiOBr overdose. This finally resulted in every BiOBr particle having enough adsorption sites available for dissolved dioxygen to function thereby accelerate the degradation of weakly polar organic compounds in water.

研究领域: 环境化学 · 光催化 · 水污染控制 · 环境功能材料 · 污染物降解机制
✓ 已验证 DOI 高影响因子
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APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Hydrophilic, self-cleaning, and recyclable La-TiO2/PAN nanofibrous membranes rapidly fabricated via electro-centrifugal spinning for photocatalytic organic pollutants

Jingying Xu,Teng Hou,Jing Zhou,Hao Ye,Yaru Wang,Lvzhu Cheng,Xianglong Li,Bin Yang

Photocatalytic fibrous membranes are regarded as one of the most proficient materials for environmental remediation because of their excellent photocatalytic activity, porous structure, and outstanding recyclability. However, the poor dispersion performance of photocatalysts in the polymer matrix and the low migration ability to the surface constrain the development of this technology. In this study, a versatile strategy was developed to facilitate the design of hydrophilic nanofibrous membranes with promising photocatalytic activity and robust recyclability by combining the loaded rare earth element La 3+ modified TiO 2 photocatalyst, introducing hyperbranched polymers as dispersants within electro-centrifugal spinning, and applying post-treatment to construct hydrophilic sites. Significantly, the removal efficiency of the fibrous membrane materials on the dye wastewater was as high as 89.34 %, and the treatment efficiency can still reach 81.68 % after five cycles. In addition, the photocatalytic mechanism for the degradation of organic pollutants was also analyzed. This work provides a new method for building advanced photocatalytic nanofibrous membranes, which is expected to be used in the treatment and remediation of environmental wastewater.

研究领域: 环境科学 · 材料科学 · 纳米技术 · 化学工程 · 光催化 · 高分子材料 · 水处理技术
✓ 已验证 DOI 高影响因子
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2019 · IF 14.229

In situ exsolution of silver nanoparticles on AgTaO3-SrTiO3 solid solutions as efficient plasmonic photocatalysts for water splitting

Jinxing Yu,Lei Zhang,Jun Qian,Zhirong Zhu,Shuang Ni,Gang Liu,Xiaoxiang Xu

Starting from two wide band gap semiconductors AgTaO 3 and SrTiO 3 , we managed to reduce the band gap by forming their solid solutions, i.e. (AgTaO 3 ) 1-x (SrTiO 3 ) x (0.0 ≤ x ≤ 1.0). These solid solutions all adopt cubic perovskite structure similar to SrTiO 3 and high temperature phase of AgTaO 3 , suggesting that SrTiO 3 is helpful to stabilize AgTaO 3 in its high temperature cubic phase. Substantial improvements over photocatalytic hydrogen production were realized in these solid solutions which clearly outperform their parent compounds AgTaO 3 and SrTiO 3 . In-situ exolution of silver nanoparticles at the surface of solid solutions (x = 0.2) substantially strengthen the visible light absorption due to localized surface plasmons of these silver nanoparticles . This contributes to further improvements on both photocatalytic hydrogen and oxygen production under visible light illumination (λ ≥ 400 nm). Apparent quantum efficiency as high as ˜ 2.02% and ˜ 0.11% was achieved at solid solutions (x = 0.2) decorated with silver nanoparticles for full range (λ ≥ 250 nm) and visible light (λ ≥ 400 nm) illumination respectively. Photoelectrochemical analysis suggests that solid solutions own a better charge separation conditions than their parent compounds. Furthermore, the band edge positions of solid solutions (x = 0.2) lie approximately in the middle between AgTaO 3 and SrTiO 3 , being ideal for solar water splitting reactions.

研究领域: 材料科学 · 光催化 · 能源化学 · 半导体物理 · 纳米材料
✓ 已验证 DOI 高影响因子
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Advances in Experimental Medicine and Biology · 2016 · IF 1.953

The Role of Free Radicals in the Photodynamic Treatment of Fibrotic Skin Diseases

Yan Heping,Chen Yashun,Zhang Jucheng,Liu Wei,Chen Rui

The first derivatives of gelatin and type I collagen fluorescence spectra were characterized in order to describe the effect of free radicals on pyridinoline (PYD) cross-links. The different gas saturation conditions were used to investigate the effect of different free radicals. An analysis of first derivative fluorescence spectra suggests that PYD cross-link fluorescence emission is composed of three peaks in gelatin, but only two in type I collagen. The PYD cross-link was photo-degraded more than other gases in the presence of O 2 . This suggests that the singlet oxygen ( 1 O 2 ) plays a key role when using photodynamic therapy to treat skin fibrosis disease with Hypocrellin B (HB).

研究领域: 光生物学 · 皮肤科学 · 分子生物学 · 结缔组织病 · 自由基化学 · 光动力学 · 纤维化疾病
✓ 已验证 DOI 高影响因子
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RSC Advances · 2013 ·Vol. 3 ·期 45 ·23133-23138 · IF 2.562

Ultra-high payload of doxorubicin and pH-responsive drug release in CuS nanocages for a combination of chemotherapy and photothermal therapy

Yang Wang,Yun Xiao,Hangyu Zhou,Wei Chen,Ruikang Tang

A novel versatile system combining chemotherapy and photothermal therapy for cancer cells using CuS NCs is reported. CuS NCs were synthesized by a solid–liquid reaction between Cu2O nanocubes and thiourea. While the hollow nanocage can be used to load anticancer drugs for chemotherapy, the CuS can convert NIR light into heat for photothermal therapy. More importantly, CuS NCs display exceptionally high drug loading capacity of DOX with 500 wt% and release of DOX is pH-controllable, which is a spontaneous process under intracellular conditions. Compared with chemotherapy or photothermal therapy alone, the combination of chemotherapy and phototherapy can significantly improve the therapeutic efficacy. This improvement strategy using multifunctional nanomaterials may be particularly useful in biomedical applications.

研究领域: 肿瘤学 · 纳米医学 · 药物递送 · 转化医学 · 生物材料
✓ 已验证 DOI 高影响因子
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