Chang-Wen Chen

Efficient and Uniform Planar‐Type Perovskite Solar Cells by Simple Sequential Vacuum Deposition

A novel sequential layer-by-layer sub-100 °C vacuum-sublimation method to fabricate planar-type organometal halide perovskite solar cells is developed. Very uniform and highly crystalline perovskite thin films with 100% surface coverage are produced. The cells attain maximum and average efficiencies up to 15.4% and 14%, respectively. This low- temperature, all-vacuum process is suitable for a wide variety of rigid and flexible applications.

A Low-Energy-Gap Organic Dye for High-Performance Small-Molecule Organic Solar Cells

A novel donor-acceptor-acceptor (D-A-A) donor molecule, DTDCTB, in which an electron-donating ditolylaminothienyl moiety and an electron-withdrawing dicyanovinylene moiety are bridged by another electron-accepting 2,1,3-benzothiadiazole block, has been synthesized and characterized. A vacuum-deposited organic solar cell employing DTDCTB combined with the electron acceptor C(70) achieved a record-high power conversion efficiency (PCE) of 5.81%. The respectable PCE is attributed to the solar spectral response extending to the near-IR region and the ultracompact absorption dipole stacking of the DTDCTB thin film.

Optical properties of organometal halide perovskite thin films and general device structure design rules for perovskite single and tandem solar cells

The optical constants of a CH3NH3PbI3−xClx perovskite thin film were acquired for the first time. With this optical constant information, detailed optical modelling and optimization were performed and the calculations suggest that power conversion efficiencies of up to 20% and 29% are feasible in planar-type single and tandem cells.

Microcavity‐Embedded, Colour‐Tuneable, Transparent Organic Solar Cells

In this work microcavity-capped colour-tuneable SMOSCs are evaluated. By adopting a microcavity-structured cathode with optical spacer layers of different thicknesses fabricated in a Ag/NPB/Ag structure, the transmission spectra of complete devices can be tuned over the entire visible-light region (400-750 nm). The fabricated semitransparent colour-tuneable solar cells show an average efficiency of 4.78% under 1-sun illumination.

Insight into Evolution, Processing and Performance of Multi-length-scale Structures in Planar Heterojunction Perovskite Solar Cells.

The structural characterization correlated to the processing control of hierarchical structure of planar heterojunction perovskite layer is still incomplete due to the limitations of conventional microscopy and X-ray diffraction. This present study performed the simultaneously grazing-incidence small-angle scattering and wide-angle scattering (GISAXS/GIWAXS) techniques to quantitatively probe the hierarchical structure of the planar heterojunction perovskite solar cells. The result is complementary to the currently microscopic study. Correlation between the crystallization behavior, crystal orientation, nano- and meso-scale internal structure and surface morphology of perovskite film as functions of various processing control parameters is reported for the first time. The structural transition from the fractal pore network to the surface fractal can be tuned by the chloride percentage. The GISAXS/GIWAXS measurement provides the comprehensive understanding of concurrent evolution of the film morphology and crystallization correlated to the high performance. The result can provide the insight into formation mechanism and rational synthesis design.

Spontaneous formation of light-trapping nano-structures for top-illumination organic solar cells

By introduction of nano-structured crystallite capping layers, the power conversion efficiency of top-illumination organic solar cells is improved from 4.2 ± 0.1% to 6.0 ± 0.2%, representing a 44% enhancement. This is caused by the increase in JSC and led by the enhancement in the local E distribution inside the active layers. Comprehensive finite-difference time domain simulation reveals two main reasons for this enhancement: (1) the nano-structured capping layers can be treated as gradient-index films that effectively increase the light entering the devices. (2) The nano-structured capping layers can also diffract the light from original normal-incident paths, hence increasing the absorption length inside the active layers.