Chi Li

Single‐Junction Polymer Solar Cells Exceeding 10% Power Conversion Efficiency

A single-junction polymer solar cell with an efficiency of 10.1% is demonstrated by using deterministic aperiodic nanostructures for broadband light harvesting with optimum charge extraction. The performance enhancement is ascribed to the self-enhanced absorption due to collective effects, including pattern-induced anti-reflection and light scattering, as well as surface plasmonic resonance, together with a minimized recombination probability.

Halide-Substituted Electronic Properties of Organometal Halide Perovskite Films: Direct and Inverse Photoemission Studies

Solution-processed perovskite solar cells are attracting increasing interest due to their potential in next-generation hybrid photovoltaic devices. Despite the morphological control over the perovskite films, quantitative information on electronic structures and interface energetics is of paramount importance to the optimal photovoltaic performance. Here, direct and inverse photoemission spectroscopies are used to determine the electronic structures and chemical compositions of various methylammonium lead halide perovskite films (MAPbX3, X = Cl, Br, and I), revealing the strong influence of halide substitution on the electronic properties of perovskite films. Precise control over halide compositions in MAPbX3 films causes the manipulation of the electronic properties, with a qualitatively blue shift along the I → Br → Cl series and showing the increase in ionization potentials from 5.96 to 7.04 eV and the change of transport band gaps in the range from 1.70 to 3.09 eV. The resulting light absorption of MAPbX3 films can cover the entire visible region from 420 to 800 nm. The results presented here provide a quantitative guide for the analysis of perovskite-based solar cell performance and the selection of optimal carrier-extraction materials for photogenerated electrons and holes.

Outcoupling-Enhanced Flexible Organic Light-Emitting Diodes on Ameliorated Plastic Substrate with Built-in Indium–Tin-Oxide-Free Transparent Electrode

Enhancing light outcoupling in flexible organic light-emitting diodes (FOLEDs) is an important task for increasing their efficiencies for display and lighting applications. Here, a strategy for an angularly and spectrally independent boost in light outcoupling of FOLEDs is demonstrated by using plastic substrates with a low refractive index, consisting of a bioinspired optical coupling layer and a transparent conductive electrode composed of a silver network. The good transmittance to full-color emission (>94% over the whole visible wavelength range), ultralow sheet resistance to carrier injection (<5 Ω sq(-1)), and high tolerance to mechanical bending of the ameliorated plastic substrates synergistically optimize the device performance of FOLEDs. The maximum power efficiencies reach 47, 93, 56, and 52 lm W(-1) for red, green, blue, and white emissions, which are competitive with similarly structured OLEDs fabricated on traditional indium-tin-oxide (ITO) glass. This paradigm for light outcoupling enhancement in ITO-free FOLEDs offers additional features and design freedoms for highly efficient flexible optoelectronics in large-scale and low-cost manufacturing without the need for a high-refractive-index plastic substrate.

Polymer Solar Cells with 90% External Quantum Efficiency Featuring an Ideal Light‐ and Charge‐Manipulation Layer

Rapid progress in the power conversion efficiency (PCE) of polymer solar cells (PSEs) is beneficial from the factors that match the irradiated solar spectrum, maximize incident light absorption, and reduce photogenerated charge recombination. To optimize the device efficiency, a nanopatterned ZnO:Al2 O3 composite film is presented as an efficient light- and charge-manipulation layer (LCML). The Al2 O3 shells on the ZnO nanoparticles offer the passivation effect that allows optimal electron collection by suppressing charge-recombination loss. Both the increased refractive index and the patterned deterministic aperiodic nanostructure in the ZnO:Al2 O3 LCML cause broadband light harvesting. Highly efficient single-junction PSCs for different binary blends are obtained with a peak external quantum efficiency of up to 90%, showing certified PCEs of 9.69% and 13.03% for a fullerene blend of PTB7:PC71 BM and a nonfullerene blend, FTAZ:IDIC, respectively. Because of the substantial increase in efficiency, this method unlocks the full potential of the ZnO:Al2 O3 LCML toward future photovoltaic applications.

Biomaterial functionalized graphene oxides with tunable work function for high sensitive organic photodetectors

Graphene acts as an ideal material for transparent conductive electrodes in optoelectronic devices attributed to its excellent electrical conductivity, optical transparency, and mechanical properties. Graphene oxide (GO) in the form of a colloidal suspension is considered to be more commonly useful because of its low cost and high volume production. However, controlling the work function of graphene and GO as transparent electrodes in optoelectronic devices is still a challenging task, since it is important to match the energy level of the active materials. In this study, GO sheets functionalized with amino acids were fabricated via a mild and environmentally friendly approach. The work functions of the novel amino acid functionalized graphenes and their compounds with poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) were tuned over a wide range, which matched well with the energy of various semiconductors. Organic photodetectors with the functionalized GO exhibited the highest normalized detectivity of 5.7 × 1012 jones at −0.1 V. The results indicated that the synthesized solution-processable GO exhibits promising potential as transparent electrodes for various photoelectric devices.

Switching Hole and Electron Transports of Molecules on Metal Oxides by Energy Level Alignment Tuning

Charge transport at organic/inorganic hybrid contacts significantly affects the performance of organic optoelectronic devices because the unfavorable energy level offsets at these interfaces can hinder charge injection or extraction due to large barrier heights. Herein, we report a technologically relevant method to functionalize a traditional hole-transport layer of solution-processed nickel oxide (NiOx) with various interlayers. The photoemission spectroscopy measurements reveal the continuous tuning of the NiOx substrate work function ranging from 2.5 to 6.6 eV, enabling the alignment transition of energy levels between the Schottky-Mott limit and Fermi level pinning at the organic/composite NiOx interface. As a result, switching hole and electron transport for the active organic material on the composite NiOx layer is achieved due to the controlled carrier injection/extraction barriers. The experimental findings indicate that tuning the work function of metal oxides with optimum energy level offsets can facilitate the charge transport at organic/electrode contacts.