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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2022 · IF 5.141

Enhancement of power conversion efficiency by chlorophyll and carotenoid co-sensitization in the biosolar cells

Jiaxin Ye,Na Li,Xiao-Feng Wang,Ritsuko Fujii,Yumiko Yamano,Shin-ichi Sasaki

Photosynthetic pigment-based biosolar cells (BSCs) have attracted much attention over the past few years in the field of artificial photosynthesis . To further improve the power conversion efficiency (PCE) of chlorophyll (Chl)-based bilayer BSCs, co-sensitization effects of three carboxylated chromophores , methyl trans -3 2 -carboxy-pyropheophorbide- a ( H 2 Chl-1 ), methyl 7-deformyl-7-( trans -carboxyethenyl)-pyropheophorbide- b ( H 2 Chl-2 ), and β -apo-8′-carotenoic acid ( Car ) were investigated as H 2 Chl-1 : H 2 Chl-2 , H 2 Chl-1 : Car , and H 2 Chl-2 : Car combinations. The homogeneously co-sensitized mesoporous TiO 2 ( m -TiO 2 ) layer (TiO 2 – H 2 Chl : Car ) serves as the photoactive and electron extraction layer, while a Chl- a derivative, zinc methyl 3-devinyl-3-hydroxymethyl-pyropheophorbide- a ( ZnChl ) forms J -type self-aggregation film and acts as electron donor layer. The light absorption and electron injection efficiency of the TiO 2 sensitized H 2 Chl-1 : Car blends are better than those of other types of co-sensitization after optimizing the blend ratio of each type. The electron absorption spectrum of TiO 2 –( H 2 Chl-1 : Car ) at the best mass ratio of 10:3 (molar ratio of 12:5) showed wider absorption band in 350–450 nm region compared to the spectrum of sole TiO 2 –( H 2 Chl-1 ). The charge transfer resistance was significantly reduced when TiO 2 –( H 2 Chl-1 : Car ) was applied for BSCs. The best PCE of 2.13% was achieved using TiO 2 –( H 2 Chl-1 : Car  = 10:3), which corresponds to 40% increase of PCE compared to the device using TiO 2 –( H 2 Chl-1 ) without Car .

研究领域: 植物学 · 生物物理学 · 可再生能源
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ELECTROCHIMICA ACTA · 2012 · IF 3.832

Strategies to prepare an efficient photoanode for ZnO nanowires-based CdS–CdSe co-sensitized solar cells

Xingtian Yin,Wenxiu Que,Duan Fei,Haixia Xie,Zuoli He,Gangfeng Wang

Strategies employed to fabricate an efficient photoanode with ZnO nanowires (NWs) arrays and CdS–CdSe co-sensitizers were investigated. A detailed procedure for growing long ZnO NWs which are suitable for the application in quantum dot sensitized solar cells was discussed, and several optimized parameters were obtained for fabrication of the ZnO NWs with large aspect ratio. CdS and CdSe layers were deposited on the surface of the ZnO NWs by a successive ionic-layer adsorption and reaction method and the deposition process was optimized according to the performance of the solar cells fabricated with the ZnO/CdS NWs and the ZnO/CdS/CdSe NWs arrays, respectively. The relationship between the thickness of the sensitizer layer and the performance of the devices was also discussed in detail. Transmission electron microscopy observation shows that ∼7   nm thick CdS layer and ∼5   nm thick CdSe layer can be easily achieved on the ZnO NWs at an optimal deposition condition. UV–vis absorption spectra demonstrate that the light absorption range of the ZnO/CdS/CdSe NWs can be almost extended to the whole visible range. Through an optimization of the photoanode fabrication, which mainly includes the synthesis of the ZnO NWs arrays and the deposition of the CdS and CdSe layers, a short circuit current density as high as 18.63   mA/cm 2 with an overall efficiency of 3.06% can be obtained for the resulting device.

CAS / MDL: 9002-98-6
研究领域: 材料科学 · 能源科学
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CHEMICAL ENGINEERING JOURNAL · 2013 · IF 3.473

Synthesis of CdS quantum dots (QDs) via a hot-bubbling route and co-sensitized solar cells assembly

Ting Yang,Mengmeng Lu,Xiaoli Mao,Wenhong Liu,Lei Wan,Shiding Miao,Jinzhang Xu

More than 5.0   g luminescent CdS quantum dots (QDs) were synthesized via a hot-bubbling route. The synthetic parameters including temperature, growth time, feeding ratio Cd/S and capping ligands were studied to show great influence on the optical properties . Two types of CdS “magic-sized” clusters (MSCs) emitting at 313   nm and 323   nm were obtained at temperature lower than 80   °C. The PL quantum yields of the CdS QDs reaches 11.6% when trioctyphosphine oxide was used as ligand. The prepared CdS QDs have been transferred into aqueous solution via ligand exchange (LE). To expand the spectral response in photovoltaic devices, two different sizes of CdS QDs were deposited on mesoporous TiO 2 /SiO 2 electrode, and the co-sensitized solar cells (SCs) were prepared. It was found that the co-sensitized SCs show a higher conversion efficiency ( η   =   1.55%) than the single sized QDs sensitized SCs ( η   =   0.53%). The incident photon-to-current conversion efficiency (IPCE) of co-sensitized SCs showed two peaks at 370   nm and 460   nm which resembles the absorption peaks of the two different sized QDs.

研究领域: 材料科学 · 纳米技术 · 光电子学
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MATERIALS RESEARCH BULLETIN · 2021 · IF 4.641

Cosensitization-based halide perovskite in aqueous solution: A photoelectrochemical and first-principles investigation

Lei Zhang,Shuai Lin

The halide perovskite films suffer from poor photoelectrochemical performance in aqueous solution, inhibiting their further industrial deployment. Here, we propose a new concept of “cosensitized perovskites” that employ the cosensitization strategy to improve the photoelectrochemical properties of the prototypical CH 3 NH 3 PbI 3 film in the aqueous solution via two commercial coumarin dyes. The resulting photocurrent of the cosensitization-modified perovskite film in the aqueous solution increases by 40 % than those of the single dye-based films, and is several orders of magnitude higher than that offered by the bare perovskite film under the same conditions. The first-principles calculations reveal the detailed atomic and electronic structures of the cosensitized systems, and suggest that the improved photoelectrochemical performance is attributed to the multiple types of surface coordination when the cosensitization is available and the conjugation in the dye molecules; these effectively reduce the surface charge traps. This study serves as the first example to highlight the cosensitization strategy for the perovskite materials, and expects the cosensitization method for a wide range of perovskite-based applications, including solar cells, photodetectors, light-emitting diodes, photocatalysts, and water-splitting systems.

研究领域: 材料科学 · 物理化学
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RSC Advances · 2017 ·Vol. 7 ·期 17 ·10494-10502 · IF 3.108

Stepwise co-sensitization of two metal-based sensitizers: probing their competitive adsorption for improving the photovoltaic performance of dye-sensitized solar cells

Yanming Zhao,Futai Lu,Jie Zhang,Yuze Dong,Bao Zhang,Yaqing Feng

How to graft co-sensitizers with different binding strengths onto TiO2 surfaces for enhancing the performance of dye-sensitized solar cells (DSSCs) has not been discussed very much. Herein a ruthenium-based sensitizer (N719) and a porphyrin molecule (LP-2) with complementary absorption spectra (300–750 nm) have been chosen to investigate how the dye loading procedure would influence the photovoltaic performance of co-sensitized solar cells. Interestingly, it is found that 54.7% of the loading amounts of pre-adsorbed LP-2 are replaced by the post-adsorption of N719. The replacement adsorption is not observed when the two molecules are loaded in reverse order, which is attributed to their different adsorption configurations and binding energies. The competitive adsorption between co-sensitizers is thus systematically investigated by UV-visible absorption spectroscopy, energy dispersive spectrometry (EDS) and electron probe microanalysis (EPMA). Upon optimization, the device sequentially sensitized with LP-2 and N719 exhibits efficiency (7.72%) enhancement of 38.6% and 18.0% compared with those fabricated with single LP-2 and N719, respectively. The results provide a new vision on the stepwise sensitization of TiO2 films using co-sensitizers with a difference in adsorption properties, suggesting that complementary spectral absorption of co-sensitizers can lead to excellent cell performance by choosing an appropriate dye loading procedure.

研究领域: 材料科学 · 化学
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RSC Advances · 2020 ·Vol. 10 ·期 71 ·43290-43298 · IF 3.119

The influence of three diphenylpyran isomer co-sensitizers with different sterical structures on N719-based dye sensitized solar cells

Xinxin Wang,Xiuhua Hang,Altan Bolag,Wu Yun,Tana Bao,Jun Ning,Hexig Alata,Tegus Ojiyed

Aiming to explore the relationship between the molecular structure and photovoltaic performance, three pyran isomer dyes DO, DM and DP were synthesized and applied as a co-sensitizer with N719 dye in dye-sensitized solar cells (DSCs). These sensitizers were investigated by theoretical calculation, UV-vis absorption spectroscopy and cyclic voltammetry measurement to understand their structure, optical and electrochemical properties. The DSC devices based on N719 and the co-sensitizers were characterized using I–V tests, incident photon-to-current conversion efficiency and electrochemical impedance spectroscopy measurements. As compared to the standard N719-based DSCs, the co-sensitization system of N719 and DM with the most sterical structure exhibited an enhancement of the power conversion efficiency (PCE) by 18% from 7.60% to 8.96%. Both the short-circuit photocurrent density (Jsc) and open-circuit voltage (Voc) of the co-sensitized systems were increased resulting from the better maintained N719 dye loading amount on TiO2 as well as the prevention of dye aggregation. Co-sensitization of the DO molecule with less steric hindrance reduced the desorbed N719 dye amount by half leading to a decline of the photo-harvesting ability and photocurrent generation in DSCs.

研究领域: 材料科学 · 物理化学
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OPTICS COMMUNICATIONS · 2015 · IF 1.449

CdS/CdSe co-sensitized SnO2 photoelectrodes for quantum dots sensitized solar cells

Yibing Lin,Yu Lin,Yongming Meng,Yongguang Tu,Xiaolong Zhang

SnO 2 nanoparticles were synthesized by hydrothermal method and applied to photo-electrodes of quantum dots-sensitized solar cells (QDSSCs). After sensitizing SnO 2 films via CdS quantum dots , CdSe quantum dots was decorated on the surface of CdS/SnO 2 photo-electrodes to further improve the power conversion efficiency. CdS and CdSe quantum dots were deposited by successive ionic layer absorption and reaction method (SILAR) and chemical bath deposition method (CBD) respectively. Scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD) were used to identify the surface profile and crystal structure of SnO 2 photo-electrodes before and after deposited quantum dots. After CdSe co-sensitized process, an overall power conversion efficiency of 1.78% was obtained in CdSe/CdS/SnO 2 QDSSC, which showed 66.4% improvement than that of CdS/SnO 2 QDSSC.

研究领域: 材料科学 · 能源技术
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JOURNAL OF ALLOYS AND COMPOUNDS · 2015 · IF 2.999

CdS/Cu2S co-sensitized TiO2 branched nanorod arrays of enhanced photoelectrochemical properties by forming nanoscale heterostructure

Lin Tang,Yaocheng Deng,Guangming Zeng,Wei Hu,Jiajia Wang,Yaoyu Zhou,Jingjing Wang,Jing Tang,Wei Fang

This paper described a facile method for the design and utilization of three-dimensional TiO 2 branched nanorod arrays with CdS and Cu 2 S quantum dots co-sensitized photoelectrode for photoelectrochemical water splitting . CdS and Cu 2 S quantum dots were attached on the surface of TiO 2 BNRs by successive ionic layer adsorption and reaction (SILAR). The morphology and element composition of the fabricated samples were characterized by field emission scanning electron microscopy (FE-SEM), high resolution transmission electron microscopy (HR-TEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and the optical features were measured by UV–vis diffuse reflection spectroscopy (UV–vis DRS) and photocurrent density–voltage (I–V) curves. The photocurrent value can be significantly enhanced due to the introduction of CdS and Cu 2 S quantum dots on the TiO 2 BNRs surface. The 9 cycles of CdS and 6 cycles of Cu 2 S presented the best performance and reached a high photocurrent density to 13.65 mA at 0 V versus Ag/AgCl and hydrogen generation efficiency of 7.74% at −0.467 V versus Ag/AgCl. This enhancement can be attributed to the improved light absorption and the heterojunction formed between CdS and Cu 2 S, which can greatly promote the introduction and transportation of the photo electrons. This work provided a facile way for the synthesis of high performance photoelectrode for photoelectrochemical water splitting.

CAS / MDL: 5593-70-4 7550-45-0
研究领域: 材料科学 · 纳米技术 · 能源科学
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CERAMICS INTERNATIONAL · 2017 · IF 2.986

Enhanced charge separation of CuS and CdS quantum-dot-cosensitized porous TiO2-based photoanodes for photoelectrochemical water splitting

Jimin Du,Mengke Yang,Fangfang Zhang,Xuechun Cheng,Haoran Wu,Huichuang Qin,Qingsong Jian,Xialing Lin,Kaidi Li,Dae Joon Kang

Photoelectrochemical (PEC) water splitting using high-performance catalysts shows considerable promise in generating environment-friendly hydrogen energy. Its practical applications, however, suffer from several shortcomings, such as low photocurrent density, large onset-voltage value, and poor durability. In this study, CuS and CdS quantum-dot-cosensitized porous TiO 2 -based PEC catalysts (CuS-CT) have been successfully synthesized via in situ sulfuration of CuO and CdO coexisting inside a porous TiO 2 monolith by a hydrothermal method . Compared to porous TiO 2 , CuS-sensitized porous TiO 2 (CuS-TiO 2 ), and CdS-sensitized porous TiO 2 (CdS-TiO 2 ) in terms of PEC performance, the CuS-CT photoanode exhibited a significantly high anodic photocurrent for water splitting under simulated sunlight radiation. The photocurrent produced by the optimized sample of 7% CuS-5% CdS-TiO 2 (7% CuS-CT) was nearly 2.7 times higher than that of pure porous TiO 2 at 1.0   V versus a reversible hydrogen electrode (RHE). Porous TiO 2 possesses large surface areas that can drive fast electrolyte transport and afford more surface reaction active sites. On the other hand, CuS and CdS quantum dots not only broaden the visible light absorption range, but also improve photoinduced electron-hole separation efficiency. The co-sensitized multi-nanostructures photoanodes lead to a remarkable and promising application in PEC water splitting reactions.

研究领域: 材料科学 · 光化学 · 能源材料 · 纳米技术
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Nanoscale Research Letters · 2016 ·Vol. 11 ·期 1 ·1-7 · IF 2.584

CdS/CdSe Co-sensitized Solar Cells Based on Hierarchically Structured SnO2/TiO2 Hybrid Films

Chen Zeng,Wei Chaochao,Li Shengjun,Diao Chunli,Li Wei,Kong Wenping,Zhang Zhenlong,Zhang Weifeng

SnO 2 nanosheet-structured films were prepared on a fluorine-doped tin oxide (FTO) substrate using ZnO nanosheet as template. The as-prepared SnO 2 nanosheets contained plenty of nano-voids and were generally vertical to the substrate. TiO 2 nanoparticles were homogeneously deposited into the intervals between the SnO 2 nanosheets to prepare a hierarchically structured SnO 2 /TiO 2 hybrid film. The hybrid films were co-sensitized with CdS and CdSe quantum dots. The sensitized solar cells assembled with the SnO 2 /TiO 2 hybrid film showed much higher photoelectricity conversion efficiency than the cells assembled with pure TiO 2 films. The lifetime of photoinduced electron was also investigated through electrochemical impedance spectroscopy, which showed that the SnO 2 /TiO 2 hybrid film electrode is as long as the TiO 2 film electrode.

CAS / MDL: 64-17-5 67-56-1
研究领域: 材料科学 · 能源科学
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DALTON TRANSACTIONS · 2018 ·Vol. 47 ·期 7 ·2214-2221 · IF 4.099

Charge recombination control for high efficiency CdS/CdSe quantum dot co-sensitized solar cells with multi-ZnS layers

Qiang Wu,Juan Hou,Haifeng Zhao,Zhiyong Liu,Xuanyu Yue,Shanglong Peng,Haibin Cao

ZnS as an inorganic passivation agent has been proven to be effective in suppressing charge recombination and enhancing power conversion efficiency (PCE) in quantum dot-sensitized solar cells (QDSCs). In the present study, we constructed a novel TiO2/ZnS/CdS/ZnCdS/CdSe/ZnS photoelectrode via successive ionic layer adsorption and reaction (SILAR) and chemical bath deposition (CBD). The complementary effects of multi-ZnS layers on the optical and electrochemical performance of the QDSCs were systematically investigated. The multi-ZnS can not only facilitate the growth and distribution of QDs, but also suppress the different interface charge recombination effectively. We suggest that the formation of the ZnCdS intermediate layers via ion-exchange route during CBD process contributes to the higher photoelectrochemical cell performance of the QDSCs with the middle ZnS layer. When the three-layer ZnS was employed in CdS/CdSe co-sensitized system, the PCE reached 6.05%, which is much higher than that observed for solar cells with the conventional single ZnS treatments and the two layers inserted at the interface between CdS QDs and CdSe QDs and electrolyte (4.80% and 5.42%, respectively).

研究领域: 材料科学 · 纳米科技 · 光电子学 · 能源化学 · 半导体器件
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TALANTA · 2022 · IF 6.556

Ultrasensitive photoelectrochemical biosensor for DNA 5-methylcytosine analysis based on co-sensitization strategy combined with bridged DNA nanoprobe

Chuiyu Zhu,Xiao Tian,Qiuyan Li,Zichang Dai,Lina Wang,Huamin Liu,Chenghong Li,Kashif Rafiq Zahid,Chunmei Wu,Hui Huang,Lichao Fang,Qiyuan Huang,Feixue Liu,Jun Deng,Yan Li,Tao Zeng,Junsong Zheng

Altered DNA methylation in the form of 5-methylcytosine (5-mC) patterns is correlated with disease diagnosis, prognosis, and treatment response. Therefore, accurate analysis of 5-mC is of great significance for the diagnosis of diseases. Here, an efficient enhanced photoelectrochemical (PEC) biosensor was designed for the quantitative analysis of DNA 5-mC based on a cascaded energy level aligned co-sensitization strategy coupling with the bridged DNA nanoprobe (BDN). Firstly, Au nanoparticle/graphite phase carbon nitride/titanium dioxide (AuNPs/g-C 3 N 4 @TiO 2 ) nanocomposite was synthesized through in situ growth of AuNPs on g-C 3 N 4 @TiO 2 surface as a matrix to provide a stable background signal. Next, BDN with a high mass transfer rate synthesized from a pair of DNA tetrahedral as nanomechanical handles was used as a capture probe to bind to the target sequence. The polydopamine nanosphere was applied to load with CdTe QDs (PDANS-CdTe QDs) as a photocurrent label of 5-mC antibodies. When the 5-mC existed, a large number of PDANS-Ab-CdTe QDs were introduced to the electrode surface, the formed CdTe QDs/AuNPs/g-C 3 N 4 @TiO 2 co-sensitive structure could effectively enhance the electron transfer capability and photocurrent response rate due to the effective cascade energy level arrangement, leading to a significantly enhanced photocurrent signal. The proposed PEC biosensor manifested a wide range from 10 −17  M to 10 −7  M and a detection limit of 2.2 aM. Meanwhile, the excellent performance indicated the practicability of the designed strategy, thus being capable of the clinical diagnosis of 5-mC.

研究领域: 生物医学工程 · 分析化学 · 分子生物学
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