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Journal of Materials Chemistry C · 2019 ·Vol. 7 ·期 33 ·10379-10388 · IF 6.641

Effect of structural engineering of π-spacers on anti-aggregation of D–A–π–A dyes

Tao Hua,Keyi Zhang,Zu-Sheng Huang,Lingyun Wang,Hao Tang,Herbert Meier,Derong Cao

In this paper, the encapsulated insulated molecular wire (EIMW) and 2′,7′-bis(hexyloxy)spiro[cyclopenta[2,1-b:3,4-b′]dithiophene-4,9′-fluorene] (SPDF) were specifically designed as efficient anti-aggregation π-bridges for two novel D–A–π–A metal-free sensitizers (IBT1 and IBT2). Compared with the reference dye IBT3 with 3,3′-dihexyl-2,2′-bithiophene (DHBT) as an anti-aggregation π-bridge, both the dyes IBT1 with EIMW and IBT2 with SPDF as π-bridges can suppress intermolecular aggregation more efficiently. The π-bridge of SPDF shows the strongest anti-aggregation ability due to the rigid ‘T’ configuration among these dyes. Meanwhile, the π-bridge of EIMW shows better anti-aggregation ability than DHBT because of the larger steric hindrance of the former. Finally, when the dyes IBT1 and IBT2 are co-sensitized with IBT3, respectively, the new devices exhibit high efficiencies of 7.85% and 7.64%, respectively, which are comparable to that of N719 (7.85%). The results demonstrate that the dyes with EIMW and SPDF as anti-aggregation π-bridges are promising candidates for efficient DSSCs and dye aggregation can be effectively inhibited by structural engineering of the π-spacer.

研究领域: 材料科学 · 化学工程
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Applied Nanoscience · 2022 ·Vol. 12 ·期 12 ·3995-4004 · IF 3.869

Preparation and photocatalytic properties of dye-sensitization titanium dioxide/graphene composites for removal of MB

Bao Li-hong,Wen Yu-xin,Ling Jia-wen,Guan Fang-lan,Nie Jin-mei,Zhang Mei

In this study, titanium dioxide (TiO 2 ) and graphene oxide (GO) were used to make a titanium dioxide/reduced graphene oxide (TG) composite under hydrothermal condition, and the TG composite was subsequently dye-sensitization (DTG). TEM, XRD, Raman, XPS, and UV–vis DRS spectroscopy were used to examine the structure and morphology of DTG, and the results revealed that the grafting rate of dye molecules on TG was approximately 20.4% and the band-gap value for TiO 2 , TG and DTG were 3.21, 3.03, 2.57 eV, respectively. The photocatalytic performances of DTG, TG, and TiO 2 were investigated under the illumination of a xenon lamp, and it was discovered that the final removal rates of MB by TiO 2 and TG were only 21.53% and 50.37%, but DTG can remove 97.67% of MB, the COD value of the effluent decreased by 88.24%. Furthermore, the elimination rate of MB maintained over 90% after 5 cycles of photocatalytic tests, indicating that DTG had good endurance.

CAS / MDL: 7782-42-5
研究领域: 材料科学 · 环境科学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2018 · IF 11.698

High efficient photocatalytic hydrogen evolution from formaldehyde over sensitized Ag@Ag-Pd alloy catalyst under visible light irradiation

Hongxia Liu,Meng Wang,Xuqiang Zhang,Jiantai Ma,Gongxuan Lu

The development of an active but cheaper catalyst is critical for efficient photocatalytic hydrogen from renewable source. In this study, we develop a high active catalyst for hydrogen evolution from formaldehyde via alloying of Pd with Ag and sensitization with a dye eosin Y (EY). The XRD, XPS, TEM and HRTEM characterizations indicate that the catalyst exhibits a core-shell structure (Ag core and Ag-Pd shell). Alloying Pd with Ag not only provides more efficient catalytic sites than single component Pd catalyst, but greatly promotes the efficient electron transfer and prolongs the lifetime of photogenerated electrons, enhances the charge separation efficiency and the photocatalytic hydrogen evolution activity significantly. The catalyst activity for hydrogen is highly dependent on the adsorption energies of HCHO and H 2 O molecules on metal surface of the alloy catalyst. Our results disclose a new route to high efficient catalyst development for solar hydrogen generation from formaldehyde.

研究领域: 材料科学 · 能源化学
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NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 19 ·8886-8895 · IF 2.7

Visible light active dye-sensitizing titanium dioxide/graphene composites with excellent photocatalytic activity

Keyu Li,Miaoqing Liang,Fanglan Guan,Mei Zhang,Jinmei Nie,Lihong Bao

TiO2/rGO (TG) composites were synthesized using a hydrothermal reduction method, with titanium dioxide and graphene as the starting materials. Subsequently, dye-sensitizing titanium dioxide/graphene photocatalytic composites, named DTG and APTG, were prepared by covalently attaching C.I. Direct Black 17 or C.I. Acid Violet 3 dye onto TG. The composites were characterized using FTIR, TEM, UV-vis DRS, EDS, and Raman spectroscopy. The EDS surface scanning results of APTG and D2.70TG composites have shown that Ti and S atoms are uniformly distributed on the graphene sheets. The presence of characteristic peaks for S2p and N1s near 166 eV and 399 eV in D2.70TG and APTG was intensified compared to those of TG composites. The grafting rate reached its peak when the amount of C.I. Direct Black 17 was 2.70 and the fixed amount of TG was 0.1 g. The UV-vis diffuse reflectance spectroscopy study results demonstrated a shift in the response range to visible light after dye modification for DTGs and APTG. Photocatalytic experiments showed that D2.70TG was capable of removing over 99% of MB within 1 hour. Furthermore, after 5 cycles of photocatalytic experiments, the removal rate of MB remained at above 95%.

CAS / MDL: 7782-42-5
研究领域: 材料科学 · 环境科学
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Surfaces and Interfaces · 2022 · IF 6.137

Layer assembled polyaniline and CuWO4 film as Pt-free efficient counter electrodes of dye-sensitized solar cells

Kezhong Wu,Zejin Wang,Hui Zhao,Bei Ruan,FeiFei Nie,Rufen Chen,Mingxing Wu

The development of transition metal compounds (TMCs) and conductive polymers composite catalysts substitute for the traditional scarce Pt-based catalysts of counter electrodes (CEs) has been recognized as one of the distinguishing paths to enhance power conversion efficiency (PCE) and decrease manufacturing costs of dye-sensitized solar cells (DSSCs). At present, various thin film preparations have been developed and applied to prepare assortment CEs. Herein, both polyaniline (PANI) and CuWO 4 film were prepared, and further to fabricate layer-by-layer composite CEs of CuWO 4 /PANI, PANI/CuWO 4 , CuWO 4 /PANI/CuWO 4 , PANI/CuWO 4 /PANI, aiming to promote the charge transfer capability and thus improve catalytic activity. And then, PANI, CuWO 4 and four composite layered CEs obtained PCE values of 5.14, 5.64, 5.96, 6.21, 4.96 and 4.24% toward the regeneration of I 3 − /I − redox couples in the assembled DSSCs, respectively. Particularly, the fascinating performance of the bilayer PANI/CuWO 4 CEs inherits the excellent electrical conductivity and the abundant porous structure of PANI skeletons for effective electrolyte diffusion. Meanwhile, the CuWO 4 layer was coupled to the layers of PANI by thermal activation annealing treatment to furnish rich inner active sites for the regeneration of I 3 − /I − couples. Benefit from the synergistic effects of PANI and CuWO 4 , the as-prepared PANI/CuWO 4 CEs manifests the highest PCE of 6.21%, indicating an inspiring strategy by the layered assembly Pt-free CEs with the cost effective and high-performance as an alternative Pt-based catalyst for DSSC.

研究领域: 材料科学 · 能源科学
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SOLAR ENERGY · 2021 · IF 5.742

Screen-printed carbon black/SiO2 composite counter electrodes for dye-sensitized solar cells

Abdelaal S.A. Ahmed,Wanchun Xiang,Fatma S.M. Hashem,Xiujian Zhao

Platinum (Pt)-based counter electrodes (CEs) are promising electrocatalysts for dye-sensitized solar cells (DSSCs). However, replacing the expensive Pt with low-cost materials and comparable catalytic activity still a big challenge. Here, we prepared CB-SiO 2 composites by blending various weights of SiO 2 (1, 3, and 5 wt%) with carbon black (CB), followed by screen printed onto the FTO substrate to utilized as CEs for DSSCs. In comparison with pure CB, CB-SiO 2 composite CEs showed higher transferability and higher electrocatalytic activity toward I 3 - / I - I3-/I- redox couple. Among all, CB-SiO 2 -1% composite CE with 4 µm showed the best catalytic performance, and the related DSSC showed a power conversion efficiency of 6.38%. Increasing the CE thickness significantly enhances the catalytic ability and the total performance of the assembled devices, whereas the power conversion efficiency of the DSSC with CB-SiO 2 -1% composite CE in 8 µm thick was 7.99%, which is close to that achieved by Pt-based device under the same conditions.

研究领域: 材料科学 · 能源研究
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ELECTROCHIMICA ACTA · 2014 · IF 4.086

Phosphotungstic acid and WO3 incorporated TiO2 thin films as novel photoanodes in dye-sensitized solar cells

Wenzhang Li,Guanhua Jin,Haishi Hu,Jie Li,Yanghui Yang,Qiyuan Chen

Dye-sensitized solar cells (DSSCs) based on phosphotungstic acid–TiO 2 composites (PT) and WO 3 nanoparticle incorporated TiO 2 photoanodes were successfully constructed by doctor blading TiO 2 paste containing PT and various amounts of WO 3 . Film features were investigated by scanning electron microscopy, X-ray photoelectron spectroscopy, X-ray diffraction, transmission electron microscopy, and ultraviolet–visible spectroscopy. Photoelectrochemical properties were examined by the photocurrent–voltage ( J – V ) curves as well as monochromatic incident photon-to-photocurrent conversion efficiency and electrochemical impedance spectroscopy (EIS) measurements. Compared with the DSSC based on pure P25 films, that based on PT/P25 films yielded a 16.9% higher J sc and a 21.3% higher η , while that based on PT/P25   +   1/70WO 3 films resulted in a 49.2% higher J sc and a 40.3% higher η . EIS data demonstrated that charge transfer resistance was clearly reduced by introducing PT and WO 3 into TiO 2 films. The introduction of PT and WO 3 was observed to promote electron transfer and retard recombination synergistically, leading to a significant improvement in cell performance.

研究领域: 材料科学 · 能源科学
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Journal of Renewable Materials · 2020 ·Vol. 8 ·期 4 ·431-446 · IF 1.341

Sunflower-Like SrCo2S4@f-MWCNTs Hybrid Wrapped by Engineering N-Reduced Graphene Oxide for High Performance Dye-Sensitized Solar Cells

Zhang Weiming,Wasim Muhammad,Zuo Xueqin,Yang Qun,Tang Huaibao,Jin Shaowei,Li Guang

A novel sunflower-like nanocomposite of SrCo2S4 nanoflakes and functionalized multiwall carbon nanotubes (f-MWCNTs) entanglement enveloped in nitrogen-reduced graphene oxide (N-RGO) is prepared by a cheap process. The unique entanglement structure of the material exhibits higher specific surface area, better electrical conductivity and other properties. This helps to reduce the transfer resistance in the photoelectric process of the battery and improve the electrochemical activity, thus increasing the photoelectric conversion efficiency of the battery. The new ternary cobalt-based sulfide material can replace platinum as the counter electrode (CE) material loaded on dye-sensitized solar cells (DSSCs). DSSCs with SrCo2S4@f-MWCNTs@N-RGO (SCS@f-M@N-R) as CE material show excellent photoelectric conversion efficiency (PCE, 8.06%), even surpassing than that of Pt CE material (7.51%). The low cost, excellent electrocatalytic performance and simple preparation method of SCS@f-M@N-R nanomaterial provide feasibility for replacing platinum material as the CE material of DSSCs, which is of great significance and persuasion.

CAS / MDL: 10377-51-2
研究领域: 材料科学 · 能源科学
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Catalysts · 2022 ·Vol. 12 ·期 12 ·1583 · IF 4.501

Design and Architecture of P-O Co-Doped Porous g-C3N4 by Supramolecular Self-Assembly for Enhanced Hydrogen Evolution

Ximiao Zhu,Fan Yang,Jinhua Liu,Guangying Zhou,Dongdong Chen,Zhang Liu,Jianzhang Fang

A novel phosphorus and oxygen co-doped graphitic carbon nitride (sheetP-O-CNSSA) photocatalyst was successfully synthesized and applied for H2evolution under visible light. In the synthesis process ofsheetP-O-CNSSA, the supramolecular complex was developed by the self-assembly and copolymerization reaction among melamine, cyanuric acid (CA) and trithiocyanuric acid (TCA) to act as g-C3N4precursors, while (NH4)2HPO4was applied as P and O precursors for element doping. The chemical structures, morphologies, and optical properties of thesheetP-O-CNSSAwere characterized by a series of measurements, i.e., XRD, FT-IR, SEM, TEM, UV-vis DRS, and PL. The results suggested that the introduction of P and O elements could enhance the separation and migration efficiency of photogenerated electrons and holes in the energy band of g-C3N4. The photocatalytic tests over Erythrosin B (EB) sensitizedsheetP-O-CNSSAindicated that the hydrogen evolution was greatly enhanced compared with other catalysts and non-sensitizedsheetP-O-CNSSAunder visible light irradiation. Finally, a possible dye-sensitized photocatalysis mechanism was also proposed on the basis of the as-obtained results.Keywords:P-O-co-doped g-C3N4;self-assembly;dye sensitization;hydrogen evolution

研究领域: 材料科学 · 光催化
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Materials · 2023 ·Vol. 16 ·期 13 ·4743 · IF 3.4

Synthesis of Single Crystal 2D Cu2FeSnS4 Nanosheets with High-Energy Facets (111) as a Pt-Free Counter Electrode for Dye-Sensitized Solar Cells

Jianming Wen,Suqin Chen,You Xu,Tuxiang Guan,Xiaoyan Zhang,Ningzhong Bao

Two-dimensional Cu2FeSnS4(CFTS) nanosheets with exposed high-energy facets (111) have been synthesized by a facile, scalable, and cost-effective one-pot heating process. The CFTS phase formation is confirmed by both X-ray diffraction and Raman spectroscopy. The formation mechanism of exposed high-energy facet CFTS growth is proposed and its electrochemical and photoelectrochemical properties are investigated in detail to reveal the origin of the anisotropic effect of the high-energy facets. Dye-sensitized solar cells (DSSC) achieve a favorable power conversion efficiency of 5.92% when employing CFTS thin film as a counter electrode, suggesting its potential as a cost-effective substitute for Pt in DSSCs.Keywords:Cu2FeSnS4nanosheets;high-energy facets;counter electrode;dye-sensitized solar cells

研究领域: 材料科学 · 能源科学
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RSC Advances · 2017 ·Vol. 7 ·期 7 ·4102-4107 · IF 3.108

Immobilising a cobalt cubane catalyst on a dye-sensitised TiO2 photoanode via electrochemical polymerisation for light-driven water oxidation

Jialing Li,Yi Jiang,Qian Zhang,Xiaochen Zhao,Na Li,Haili Tong,Xiaoxuan Yang,Lixin Xia

A simple and effective method to prepare photocatalytically active electrodes for water oxidation is described in this paper. The precious-metal-free catalyst, Co4O4(O2CMe)4(4-vinylpy)4 (py = pyridine) was electrochemically polymerised on a RuP-sensitised TiO2 (RuP = [Ru(bpy)2(4,4′-(PO3H2)2bpy2)]Cl2) and on a TiO2 surface codecorated with vinyl phosphate (Vpa) and RuP for applications in molecular photoelectrochemical (PEC) devices. With a Vpa chain as the anchoring group, the photoanode poly-Co4O4+Vpa/RuP/TiO2 demonstrated a significantly higher PEC performance compared to poly-Co4O4/RuP/TiO2. The introduction of a Vpa chain allows better immobilisation of catalyst and enhances the electron transport between the photosensitiser and the catalyst. A photocurrent density of ∼100 μA cm−2 was achieved in a Na2SO4 solution at pH 7.0 under a 0.4 V external bias, with a faradaic efficiency of 76% for oxygen production.

研究领域: 材料科学 · 电化学 · 催化化学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2018 · IF 11.698

Visible light-induced selective oxidation of alcohols with air by dye-sensitized TiO2 photocatalysis

Xia Li,Ji-Long Shi,Huimin Hao,Xianjun Lang

Visible light-induced selective oxidation of alcohols to aldehydes or ketones with atmosphere oxygen was triumphantly achieved devoid of any redox mediator. A paradigm of dye-sensitized TiO 2 photocatalysis was capable of animating selective oxidation of a myriad of alcohols by 0.67 mol% of alizarin red S anchored onto TiO 2 surface under the irradiation of green light-emitting diodes. In essence, both a robust dye like ARS and anatase TiO 2 with a high specific surface area hold the key to unlock the high photocatalytic activity; and superoxide is pivotal in affording the selective oxidation product. This discovery could shed light on the design of visible light photocatalysis for selective organic transformations under ambient conditions by harvesting the cooperation between an organic dye and a metal oxide.

研究领域: 化学 · 材料科学
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