Hongzheng Chen

Enhanced Photovoltaic Performance of CH3NH3PbI3 Perovskite Solar Cells through Interfacial Engineering Using Self-Assembling Monolayer

Morphology control is critical to achieve high efficiency CH3NH3PbI3 perovskite solar cells (PSC). The surface properties of the substrates on which crystalline perovskite thin films form are expected to affect greatly the crystallization and, thus, the resulting morphology. However, this topic is seldom examined in PSC. Here we developed a facile but efficient method of modifying the ZnO-coated substrates with 3-aminopropanioc acid (C3-SAM) to direct the crystalline evolution and achieve the optimal morphology of CH3NH3PbI3 perovskite film. With incorporation of the C3-SAM, highly crystalline CH3NH3PbI3 films were formed with reduced pin-holes and trap states density. In addition, the work function of the cathode was better aligned with the conduction band minimum of perovskite for efficient charge extraction and electronic coupling. As a result, the PSC performance remarkably increased from 9.81(±0.99)% (best 11.96%) to 14.25(±0.61)% (best 15.67%). We stress the importance of morphology control through substrate surface modification to obtain the optimal morphology and device performance of PSC, which should generate an impact on developing highly efficient PSC and future commercialization.

Surface Doping of Conjugated Polymers by Graphene Oxide and Its Application for Organic Electronic Devices

Conjugated polymers are a novel class of solution-processable semiconducting materials with intriguing optoelectronic properties. [ 1 ] They have received great attention as active components in organic electronic devices such as organic photovoltaic cells (OPVs), organic light-emitting diodes (OLEDs), and organic fi eld-effect transistors (OFETs) due to their light weight, facile tuning of electronic properties through molecular engineering, and ease of processing. The performance and lifetime of conjugated polymer-based electronic devices are critically dependent on the bulk properties of the active materials and the interfacial properties of electrode/polymer contacts. [ 2–4 ] In these devices, the electrode(s) either inject charge into or extract charges from the organic semiconductor layer(s). Mismatch of the work functions between metal or metal oxide electrodes and molecular orbital energy levels of organic semiconductors can lead to high contact resistance, which decreases the charge injection and extraction effi ciency. Therefore, it is essential to minimize contact resistance at the electrode/organic semiconductor interface. To improve charge injection/extraction across the electrode/ organic semiconductor interface, several strategies have been developed. One is to tune the interfacial dipole across the electrode/semiconductor interface to reduce the injection/collection energy barrier. This can be achieved by modifying the electrode surface with self-assembled dipolar molecules to tune the energy level alignment at the semiconductor/electrode interface. [ 5–7 ] Alternatively, the introduction of a thin layer of polymer surfactant that contains polar side chains between the conjugate polymer/electrode interface can also be used to improve the interfacial properties. The polar side chains can provide not

A spirobifluorene and diketopyrrolopyrrole moieties based non-fullerene acceptor for efficient and thermally stable polymer solar cells with high open-circuit voltage

In this study, we design and synthesize a new non-fullerene electron acceptor, SF(DPPB)4, in which a spirobifluorene (SF) core is installed with four benzene endcapped diketopyrrolopyrrole (DPP) arms. SF(DPPB)4 exhibits energy levels matching perfectly with those of the commonly used poly(3-hexyl thiophene) (P3HT) donor in polymer solar cells (PSCs). Furthermore, a designed cross-shaped molecular geometry helps in suppressing strong intermolecular aggregation in the P3HT : SF(DPPB)4 blend, leading to efficient non-fullerene PSCs. The resultant devices give a maximum power conversion efficiency (PCE) of 5.16% with an extremely high open-circuit voltage (Voc) of 1.14 V. In contrast, the devices based on P3HT : PC61BM blends provide a PCE of 3.18% with a Voc of 0.62 V. Finally, we observe that the P3HT : SF(DPPB)4 devices exhibit significantly improved thermal stability from that of the P3HT : PC61BM devices; upon thermal treatment at 150 °C for 3 h, the PCEs of P3HT : SF(DPPB)4 devices remain unchanged, whereas those of the P3HT : PC61BM devices drop drastically to below 1%. The abovementioned results demonstrate that the new design strategy of employing a high-performance non-fullerene acceptor, SF(DPPB)4, is promising for the future practical application of PSCs.

Dopant-Free Hole-Transporting Material with a C3h Symmetrical Truxene Core for Highly Efficient Perovskite Solar Cells.

Herein we present a new structural design of hole-transporting material, Trux-OMeTAD, which consists of a C3h Truxene-core with arylamine terminals and hexyl side-chains. This planar, rigid, and fully conjugated molecule exhibits excellent hole mobility and desired surface energy to the perovskite uplayer. Perovskite solar cells fabricated using the p-i-n architecture with Trux-OMeTAD as the p-layer, show a high PCE of 18.6% with minimal hysteresis.

Superhydrophobic cotton fabrics prepared by sol-gel coating of TiO2 and surface hydrophobization.

Abstract By coating fibers with titania sol to generate a dual-size surface roughness, followed by hydrophobization with stearic acid, 1H,1H,2H,2H-perfluorodecyltrichlorosilane or their combination, hydrophilic cotton fabrics were made superhydrophobic. The surface wettability and topology of cotton fabrics were studied by contact angle measurement and scanning electron microscopy. The UV-shielding property of the treated fabrics was also characterized by UV-vis spectrophotometry.

Atomically monodispersed and fluorescent sub-nanometer gold clusters created by biomolecule-assisted etching of nanometer-sized gold particles and rods.

Atomically monodispersed gold clusters were synthesized by etching gold nanocrystals (particles and rods) with the assistance of biomolecules (amino acids, peptides, proteins, and DNA) under sonication in water. The resulting gold clusters were exclusively composed of eight atoms, as demonstrated by photoluminescence, optical absorption, electrospray ionization mass spectrometry, and transmission electron microscopy measurements. The gold clusters exhibited solvent-dependent photoluminescence properties when exposed to organic solvents, such as chloroform, tetrahydrofuran, or N,N-dimethylformamide, which was attributed to the rich surface properties of the clusters. This strategy, based on top-down etching, offers an approach to create metal clusters from nanomaterials, which show great potential applications in biological labeling/imaging and sensors that utilize photoluminescence properties as the response.

Anode modification of inverted polymer solar cells using graphene oxide

A simple method has been developed to modify the anode interface of inverted bulk-heterojunction (BHJ) polymer solar cells by spin-coating a thin layer of graphene oxide (GO) on top of the organic active layer. The device with GO exhibited a remarkable improvement in power conversion efficiency compared to devices without any interfacial layer, indicating that GO can effectively modify the BHJ/metal anode interface to facilitate efficient hole collection. The dependence of the device performance on the GO layer thickness was also investigated showing an optimum performance from a GO thickness of ∼2–3 nm.

Fluorescence near gold nanoparticles for DNA sensing.

We investigated fluorescence quenching and enhancement near gold nanoparticles (GNP) of various sizes using fluorescently labeled hairpin DNA probes of different lengths. A closed hairpin caused intimate contact between the fluorophore and the gold, resulting in an efficient energy transfer (quenching). Upon hybridization with complementary DNA, the DNA probes were stretched yielding a strong increase in fluorescence signal. By carefully quantifying the amount of bound fluorescent probes and the GNP concentrations, we were able to determine the quenching and enhancement efficiencies. We also studied the size and distance dependence theoretically, using both FDTD simulations and the Gersten-Nitzan model and obtained a good agreement between experiments and theory. On the basis of experimental and theoretical studies, we report over 96.8% quenching efficiency for all particle sizes tested and a maximal signal increase of 1.23 after DNA hybridization. The described results also demonstrate the potential of gold nanoparticles for label free DNA sensing.

Recent advances in perovskite solar cells: efficiency, stability and lead-free perovskite

With the rapid growth of efficiency from 3.8% to 22.1% in recent years, perovskite solar cells (PVSCs) have drawn significant attention of researchers from both academia and industry. However, significant barriers remain standing in the pathway of PVSC advancement. To develop high-efficiency and stable devices as well as environmentally benign perovskites is critical, yet challenging aspects remain in PVSC research. In this review article, we focused on the recent advances in related subjects. The approaches for high-efficiency PVSCs have been introduced and then the instability issues and lead-free perovskite have been discussed. Finally, the conclusion along with brief perspectives has been provided on further advancing PVSCs towards use in efficient and stable solar-to-electricity technologies.

Design of a versatile interconnecting layer for highly efficient series-connected polymer tandem solar cells

A versatile interconnecting layer (ICL) based on reflective ultra-thin Ag (8–14 nm) was developed to enable the fabrication of a series-connected micro-cavity tandem polymer solar cell. This novel ICL can manipulate the optical field distribution between the constituent sub-cells to address the challenge of current matching. As a result, a very high power conversion efficiency (∼11%) and high summed external quantum efficiency of >90% were demonstrated.