Publications by authors named "Ruiping Qin"

Although Metal oxide ZnO is widely used as electron transport layers in all-inorganic PSCs due to high electron mobility, high transmittance, and simple preparation processing, the surface defects of ZnO suppress the quality of perovskite film and inhibit the solar cells' performance. In this work, [6,6]-Phenyl C butyric acid (PCBA) modified zinc oxide nanorods (ZnO NRs) is employed as electron transport layer in perovskite solar cells. The resulting perovskite film coated on the zinc oxide nanorods has better crystallinity and uniformity, facilitating charge carrier transportation, reducing recombination losses, and ultimately improving the cells' performance.

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A J-type dimer PMI-2, two perylene monoimides linked by butadiynylene bridger was prepared, and its excited-state dynamics was studied using ultrafast femtosecond transient absorption spectroscopy, along with steady-state spectroscopy and quantum chemical calculations. It is evidently demonstrated that the symmetry-breaking charge separation (SB-CS) process in PMI-2 is positively mediated by an excimer, which is mixed by localized Frenkel excitation (LE) and an interunit charge transfer (CT) state. Kinetic studies show that, with the polarity increasing of the solvent, the transformation of excimer from a mixture to the CT state (SB-CS) is accelerated, and the recombination time of the CT state is reduced obviously.

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Reducing the interfacial defects of perovskite films is key to improving the performance of perovskite solar cells (PSCs). In this study, two kinds of perylene monoimide (PMI) derivative phosphonium bromide salts were designed and used as a multifunctional interface-modified layer in PSCs. These two molecules are inserted between SnO and perovskite to produce a bidirectional passivation effect.

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Germanium selenide (GeSe), as a typical member of 2D wide bandgap semiconductors (WBSs), shows great potential in ultraviolet (UV) optoelectronics due to its excellent flexibility, superior environmental stability, competitive UV absorption coefficient, and significant spectral selectivity. However, the GeSe-based UV photodetector suffers from high operation voltages and low photocurrent, which prevents its practical imaging applications. In this work, we report an elevated photocurrent generation in a vertical stacking graphene/GeSe/graphene heterostructure with low operation voltage and low power consumption.

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Phenyl-C61-butyric acid methyl ester (PCBM) has been widely researched as a passivate electron transport layer in planar n-i-p-type perovskite solar cells (PSCs). However, due to the terrible wettability of PCBM, the growth of perfect large-area perovskite films on the electron transport layer treated by PCBM is a huge challenge, which limits the commercial application of PSCs. Herein, we incorporate a hydrophilic polymer polyethylene glycol (PEG) into PCBM to ameliorate its wettability.

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Despite the successful enhancement in the high-power conversion efficiency (PCE) of perovskite solar cells (PSCs), the poor stability of PSCs is one of the major issues preventing their commercialization. The attenuation of PSCs may be due to the lower heat resistance of the organic charge transport layer and the tendency to aggregate at high temperatures. Here we report cerium oxide (CeO ) as an electron transport layer (ETL) prepared through a simple solution processed at a low temperature (∼100 °C) to replace the organic charge transport layer on top of the inverted planar PSCs.

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Despite the successful improvement in the power conversion efficiency (PCE) of perovskite solar cells (PSCs), the issue of instability is still a serious challenge for their commercial application. The issue of the PSCs mainly originates from the decomposition of the organic-inorganic hybrid perovskite materials, which will degrade upon humidity and suffer from the thermal environment. In addition, the charge transport layers also influence the stability of the whole devices.

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This work investigates the photovoltaic properties of polymers that include different carbazole blocks as electron donors (D) but the same benzothiadiazole derivative as the electron acceptor (A). Five D-A copolymers are studied with ultrafast intramolecular exciton splitting and recombination dynamics to acquire the single-molecule structure and their photovoltaic performance relationship. The photovoltaic parameters such as energy level, optical band gap, and light-harvesting ability are highly dependent on the molecular structure of the donor monomer (including their appended flexible alkyl chain).

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The efficiency enhancement mechanism of the alkali-treated Si nanowire (SiNW) solar cells is discussed and analyzed in detail, which is important to control the useful photovoltaic process. All the results demonstrate that the photovoltaic performance enhancement of alkali-treated SiNW device steps from the formation of the good core-shell heterojunction, which consequently enhances the junction area, promotes fast separating and transporting of electron and hole pairs, and reduces the carrier surface combination. It also indicates that alkali treatment for SiNWs is a promising processing as an economical method for the formation of good core-shell SiNW/polymer heterojunction.

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A set of monodisperse 2,7-linked carbazole oligomers (3-mer, 5-mer, 7-mer, and 9-mer) was synthesized, and their photophysical, electrochemical, and thermal properties were investigated. In solutions, these oligomers exhibited bright blue emission with almost quantitative fluorescence quantum yield. The emission spectra of these oligomers in films are quite different.

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An alternating copolymer, poly(2-(5-(5,6-bis(octyloxy)-4-(thiophen-2-yl)benzo[c][1,2,5]thiadiazol-7-yl)thiophen-2-yl)-9-octyl-9H-carbazole) (HXS-1), was designed, synthesized, and used as the donor material for high efficiency polymer solar cells. The close packing of the polymer chains in the solid state was confirmed by XRD. A J(sc) of 9.

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