Search

The surface morphologies, crystallinities, and excitonic characteristics of MAxCs1−xPb(IxBr1−x)3 thin films deposited on top of the P3CT‐Na/ITO/glass substrates are investigated by using the atomic‐force microscopic images, absorbance spectra, grazing incidence X‐ray diffraction patterns, photoluminescence (PL) spectra, and Raman scattering spectra. The P3CT‐Na‐based perovskite solar cell shows a stable and efficient maximum power density curve due to the formation of a graded MA0.83Cs0.17Pb(I0.83Br0.17)3 alloy thin film which is confirmed by using the surface‐sensitive PL and Raman scattering spectra. The highest power conversion efficiency (PCE) of the P3CT‐Na‐based MA0.83Cs0.17Pb(I0.83Br0.17)3 solar cells is 15.93% mainly due to the high fill factor of 79.4%. Besides, the PCE of the nonencapsulated solar cell slowly decreases to a moderate value (10.48%) within 157 days under an uncontrolled environment (55–60 relative humidity%) at room temperatures (22–25 °C). [ABSTRACT FROM AUTHOR]

Atomic-force microscopic images, x-ray diffraction patterns, Urbach energies and photoluminescence quenching experiments show that the interfacial contact quality between the hydrophobic [6,6]-phenyl-C61-buttric acid methyl ester (PCBM) thin film and hydrophilic CH3NH3PbI3 (MAPbI3) thin film can be effectively improved by using a binary antisolvent mixture (toluene:dichloromethane or chlorobenzene:dichloromethane) in the anti-solvent mixture-mediated nucleation process, which increases the averaged power conversion efficiency of the resultant PEDOT:PSS (P3CT-Na) thin film based MAPbI3 solar cells from 13.18% (18.52%) to 13.80% (19.55%). Beside, the use of 10% dichloromethane (DCM) in the binary antisolvent mixture results in a nano-textured MAPbI3 thin film with multicrystalline micrometer-sized grains and thereby increasing the short-circuit current density and fill factor (FF) of the resultant solar cells. It is noted that a remarkable FF of 80.33% is achieved, which can be used to explain the stable photovoltaic performance without additional encapsulations. [ABSTRACT FROM AUTHOR]

The averaged power conversion efficiency of polyelectrolytes (P3CT-Na) based MAPbI3 solar cells can be increased from 14.94% to 17.46% with a wetting method before the spin-coating process of MAPbI3 precursor solutions. The effects of the wetting process on the surface, structural, optical and excitonic properties of MAPbI3 thin films are investigated by using the atomic-force microscopic images, x-ray diffraction patterns, transmittance spectra, photoluminescence spectra and Raman scattering spectra. The experimental results show that the wetting process of MAPbI3 precursor solution on top of the P3CT-Na/ITO/glass substrate can be used to manipulate the molecular packing structure of the P3CT-Na thin film, which determines the formation of MAPbI3 thin films. [ABSTRACT FROM AUTHOR]

This paper describes a method for fabricating silicon heterojunction thin film solar cells with an ITO/p-type a-Si : H/n-type cSi structure by radiofrequency magnetron sputtering. A short-circuit current density and efficiency of 28.80 mA/cm² and 8.67% were achieved. Novel nanopatterned silicon wafers for use in cells are presented. Improved heterojunction cells are formed on a nanopatterned silicon substrate that is prepared with a self-assembled monolayer of SiO2 nanospheres with a diameter of 550 nm used as an etching mask. The efficiency of the nanopattern silicon substrate heterojunction cells was 31.49% greater than that of heterojunction cells on a flat silicon wafer. [ABSTRACT FROM AUTHOR]

In this study, the CuIn(Ga)Se2 (CIGS) crystalline quality and MoSe2 thickness of films produced by the rapid thermal selenization process under various selenization pressures were investigated. When the selenization pressure increased from 48 Pa to 1.45 x 104 Pa, the CIGS films were smooth and uniform with large crystals of varying sizes. However, the MoSe2 thicknesses increased from 50 nm to 2,109 nm, which created increased contact resistivity for the CIGS/MoSe2/Mo structures. The efficiency of CIGS solar cells could be increased from 1.43% to 4.62% due to improvement in the CIGS crystalline quality with increasing selenization pressure from 48 Pa to 1.02 x 10³ Pa. In addition, the CIGS crystalline quality and MoSe2 thickness were modified by the pressure released valve (PRV) selenization process method. The crystalline qualities of the CIGS films were similarly affected by the selenization pressure at 1.02 x 10³ Pa in the PRV selenization method and the MoSe2 thicknesses were reduced from 1,219 nm to 703 nm. A higher efficiency of 5.2% was achieved with the thinner MoSe2 obtained by using the PRV selenization method. [ABSTRACT FROM AUTHOR]

The absorption coefficient at 1.4 eV is divided by the value at 0.9 eV to obtain the factor used to judge the quality of µc-Si:H. PV device performance can be predicted by multiplying Voc with Isc when using this layer as an intrinsic layer. The results show a good relationship between the quality factor and the product of open-circuit voltage and short-circuit current. However, the final efficiency is influenced by the identities of the interface in the multilayer structure. [ABSTRACT FROM AUTHOR]

A graded fullerene derivative thin film was used as a dual-functional electron transport layer (ETL) in CH3NH3PbI3 (MAPbI3) solar cells, to improve the fill factor (FF) and device stability. The graded ETL was made by mixing phenyl-C61-butyric acid methyl ester (PCBM) molecules and C60-diphenylmethanofullerene-oligoether (C60-DPM-OE) molecules using the spin-coating method. The formation of the graded ETLs can be due to the phase separation between hydrophobic PCBM and hydrophilic C60-DPM-OE, which was confirmed by XPS depth-profile analysis and an electron energy-loss spectroscope. Comprehensive studies were carried out to explore the characteristics of the graded ETLs in MAPbI3 solar cells, including the surface properties, electronic energy levels, molecular packing properties and energy transfer dynamics. The elimination of the s-shape in the current density–voltage curves results in an increase in the FF, which originates from the smooth contact between the C60-DPM-OE and hydrophilic MAPbI3 and the formation of the more ordered ETL. There was an improvement in device stability mainly due to the decrease in the photothermal induced morphology change of the graded ETLs fabricated from two fullerene derivatives with distinct hydrophilicity. Consequently, such a graded ETL provides dual-functional capabilities for the realization of stable high-performance MAPbI3 solar cells. [ABSTRACT FROM AUTHOR]

A series of alcohols (methanol, ethanol and isopropyl alcohol) were added to poly(3,4-ethylenedioxythiophene): (polystyrene sulfonate) (PEDOT: PSS) aqueous solutions in order to manipulate the molecular structure of the PEDOT chains in PEDOT: PSS hole transporting materials (HTMs) and thus to improve the power conversion efficiency of CH 3 NH 3 PbI 3 based solar cells. The structural and electronic characteristics of the resultant PEDOT: PSS HTMs were analyzed using atomic-force microscopy, contact angle measurement, Raman scattering spectrometry and photoelectron spectrometry. The properties of the PEDOT: PSS thin films could be controlled by tuning the viscosity of the PEDOT: PSS solutions. High viscosity PEDOT: PSS solutions resulted in linear structured PEDOT chains, which increased the work function of the PEDOT: PSS HTMs thereby improving the open-circuit voltage of the CH 3 NH 3 PbI 3 solar cells. The surface roughness and surface free energy of the PEDOT: PSS HTMs influence the structural properties of CH 3 NH 3 PbI 3 thin films, which determines the exciton dissociation at the CH 3 NH 3 PbI 3 /PEDOT: PSS interface (short-circuit current density) and the carrier recombination at the CH 3 NH 3 PbI 3 /[6,6]-phenyl-C61-butyric acid methyl ester (PC 61 BM) interface (fill factor). In addition, it is predicted that the power conversion efficiency can be further improved by increasing the crystallinity of the CH 3 NH 3 PbI 3 thin film. [ABSTRACT FROM AUTHOR]

A series of nonpolar antisolvents (chlorobenzene, bromobenzene, iodobenzene and toluene) were used to assist in the formation of smooth and crystalline CH 3 NH 3 PbI 3 thin films by a one-step spin-coating method. The structural, optical and excitonic characteristics of the resultant CH 3 NH 3 PI 3 thin films were analyzed using an atomic-force microscope, X-ray diffractometer, absorbance spectrum, photoluminescence (PL) spectrum, time-resolved PL and temperature-dependent PL. The properties of the CH 3 NH 3 PbI 3 thin films are dependent on the relative polarity and boiling point of the nonpolar antisolvents used in the washing treatment process. The interplay between nucleation (relative polarity) and crystal growth (boiling point) during the formation of CH 3 NH 3 PbI 3 thin films influences the short-circuit current density (J SC ) and power conversion efficiency (PCE) of the corresponding solar cells. The experimental results demonstrate that iodobenzene can be substituted for toluene as a more efficient antisolvent in the washing treatment process during the fabrication of CH 3 NH 3 PbI 3 thin films. In addition, it is predicted that the J SC and PCE can be further improved by increasing the crystallinity of the CH 3 NH 3 PbI 3 thin film. [ABSTRACT FROM AUTHOR]

Transmittance spectra, atomic-force microscopic images, energy-dispersive X-ray spectra and droplet contact angle images show that a facile wet etching process can be used to manipulate the thickness, surface roughness, surface chemical composition and surface wettability of the indium-tin oxide (ITO) thin films, which influences the molecular packing structure of the P3CT-Na thin films and thereby dominating the crystal quality of the CH 3 NH 3 PbI 3 (MAPbI 3) thin films. The power conversion efficiency (PCE) of the P3CT-Na based MAPbI 3 solar cells can be improved from 17.02% to 19.35% by increasing the Sn/In concentration ratio of the ITO thin films from 0.36 to 0.47 with a facile wet etching process at a constant temperature of 40 °C. It is noted that the PCE of the optimal solar cell decreases slowly toward a stable PCE of 16% for more than 60 days under moderate environment conditions (55 ± 10 RH%). • Surface properties of the ITO/glass substrates can be varied by the wet etching process. • The contact quality at the P3CT-Na/ITO interface can be improved. • The contact quality at the MAPbI3/P3CT-Na interface can be improved. • After 60 days, the PCE slowly decreased from 19.35% to 16.03%. [ABSTRACT FROM AUTHOR]

An Ag modified bathocuproine:ZnO nanoparticles (BCP:ZnO NPs) thin film was used as the buffer layer of inverted-type perovskite solar cells, which increased the bifacial power conversion efficiency from 6.82% to 15.50%. The surface-enhanced Raman scattering and absorbance spectra show that the Ag modified BCP small molecules can effectively passivate the surface oxygen defects of ZnO NPs and thereby increasing the crystallinity, which simultaneously increases the short-circuit current density (J SC) and fill factor. It is noted that a high incident photon-to-electron conversion efficiency (IPCE) of 92% is achieved at the wavelength of 587 nm due to the constructive interference effect in the multilayer structure, which can be used to explain the high photocurrent generation in a semi-transparent solar cell. In addition, the light intensity-dependent experimental results of the bifacial perovskite solar demonstrates that the hole transportation is better than the electron transportation in the perovskite thin film. This concept can be readily used in the optimization of high-efficiency bifacial perovskite solar cells. [Display omitted] • A bifacial PCE of 15.50% is achieved in the bifacial inverted-type MAPbI 3 solar cells. • Ag modified BCP:ZnO NPs thin film is used as the electron buffer layer of MAPbI3 solar cells. • The higher deposition rate of Ag results in the higher FF and PCE. • The asymmetric FF implies that the hole mobility is higher than electron mobility in MAPbI 3 thin films. [ABSTRACT FROM AUTHOR]

—The structural, optical and excitonic characteristics of urea doped CH 3 NH 3 PbI 3 (MAPbI 3) multi-crystalline thin films were investigated by using the X-ray diffraction patterns, atomic-force microscopic images, absorbance spectra, photoluminescence (PL) spectra and Raman scattering spectra. The surface-sensitive Raman scattering spectra show that the urea small molecules are mainly distributed in the top region of the MAPbI 3 thin films and thereby effectively passivating the electron-poor defects (interfacial MA cations) of MAPbI 3 thin films. Besides, the thermal annealing temperature and the concentration of urea additive both strongly influence the formation of MAPbI 3 thin films, which dominates the photovoltaic performance. The use of 5-wt% urea can increase the open-circuit voltage (V OC) and short-circuit current density (J SC) of the MAPbI 3 solar cells from 0.88 V to 19.75 mA/cm2 to 0.94 V and 22.97 mA/cm2, respectively. In addition, the reduced current hysteresis in the J-V curves of the MAPbI 3 solar cells can be explained as due to the effective defect passivation in the top region of the MAPbI 3 thin film by the oxygen-donors of the urea small molecules. Image 1 • The optoelectronic properties of urea-doped MAPbI 3 thin films are investigated. • The 5-wt% urea-doped MAPbI 3 thin film has the disk-like shaped grains. • The urea small molecules are mainly distributed in the top region of MAPbI3 thin films. • The V OC and J SC of MAPbI3 solar cells are simultaneously increased by using the urea additive. [ABSTRACT FROM AUTHOR]

CH 3 NH 3 PbI 3 (MAPbI 3) perovskite thin films were fabricated by using the one-step spin-coating method with a washing-enhanced nucleation (WEN) process under various dropping times, and the resultant thin films were characterized through the reflected-type optical microscope, atomic force microscope, transmittance spectrometer, X-ray diffractometer, photoluminescence spectrometer and water droplet contact-angle imaging system. The experimental results show that the dropping time for the WEN process strongly influences the surface morphology, surface wettability, crystallinity and refractive index of the resultant MAPbI 3 thin films, which dominates the contact at the hydrophilic MAPbI 3 /hydrophobic 6,6-phenyl C 61 butyric acid methyl ester (PCBM) interface and thereby determines the photovoltaic performance. In addition, this investigation helps further understand the effects of the WEN process on the formation of a closely-packed MAPbI 3 thin film. Image 1 • The dropping time for the WEN process highly influences the formation of perovskite films. • The dropping time largely changes the optical and structural properties of perovskite films. • The dropping time can change the surface wettability of perovskite films. • The dropping time dominates the photovoltaic performance of perovskite solar cells. [ABSTRACT FROM AUTHOR]