Search

The crystallization of MAPbI3 perovskite films was purposefully engineered to investigate the governing factors which determine their morphological properties and moisture stability. By modulating nucleation, we obtained a single layer perovskite film with controlled crystal facet orientation and grain size. The lack of perovskite nucleation sites during crystallization allowed us to tailor the resulting crystallization phase. Theoretical calculations indicated that the nucleation sites for perovskite growth are related to the electron density around the oxygen atom (CO and SO) in a Lewis base. A single layer of micrometer-sized and (110)-oriented perovskite crystals was achieved in the optimized MAPbI3 films via suppressing the formation of nucleation sites. We fabricated inverted perovskite solar cells with the structure of glass/ITO/PEDOT:PSS/MAPbI3/PC61BM/Al which exhibited a high power conversion efficiency of 17.5% and a high fill factor over 83%. In addition, a study of the moisture stability indicated that the (110) facet orientation of the perovskite grains plays a more important role in film degradation than grain size.

Uniform, well-ordered sub-20 nm patterns can be generated by the templated self-assembly of block copolymers (BCPs) with a high Flory-Huggins interaction parameter (χ). However, the self-assembled BCP monolayers remain limited in the possible structural geometries. Here, we introduce a multiple self-assembly method which uses di-BCPs to produce diverse morphologies, such as dot, dot-in-honeycomb, line-on-dot, double-dot, pondering, dot-in-pondering, and line-on-pondering patterns. To improve the diversity of BCP morphological structures, we employed sphere-forming and cylinder-forming poly(styrene-block-dimethylsiloxane) (PS-b-PDMS) BCPs with a high χ. The self-assembled mono-layer and double-layer SiOx dot patterns were modified at a high temperature (∼800 °C), showing hexagonally arranged (dot) and double-hexagonally arranged (pondering) SiOx patterns, respectively. We successfully obtained additional new nanostructures (big-dot, dot-in-honeycomb, line-on-dot, pondering, dot-in-pondering, and line-on-pondering types) through a second self-assembly of cylinder-forming BCPs using the dot and pondering patterns as guiding templates. This simple approach can likely be extended to the multiple self-assembly of many other BCPs with good functionality, significantly contributing to the development of various nanodevices.

A cost-effective fabrication method that can produce a remarkable enhancement in the device efficiency along with a reduction in the fabrication cost is one of the crucial requirements for the commercialization of perovskite-based solar cells. Here, we report a low-cost, printable, and highly effective synchronized-pressing annealing (SPA) method for inverted planar perovskite solar cells. In this method, two films are combined face-to-face for annealing, and separated as in a roll-to-roll process. Consequently, the SPA method provides two homogeneous highly crystalline MAPbI3 films with monolithic millimeter-scale crystalline grains by intermediate-induced crystallization engineering. The grains present a tendency of oriented growth along the110direction, parallel to the substrate, which leads to efficient charge transport. The IPSCs fabricated by the SPA method demonstrate a high efficiency of ∼17% with significantly enhanced photocurrents and fill factors. Moreover, the characteristics of both top and bottom devices are very similar, with nearly identical J-V curves and photoresponse spectra. As the SPA method is compatible with the printing technology for mass production, and as it can produce twin devices of high quality via one fabrication process, it can provide a remarkable reduction in the fabrication cost.

The crystallization of MAPbI3 perovskite films was purposefully engineered to investigate the governing factors which determine their morphological properties and moisture stability. By modulating nucleation, we obtained a single layer perovskite film with controlled crystal facet orientation and grain size. The lack of perovskite nucleation sites during crystallization allowed us to tailor the resulting crystallization phase. Theoretical calculations indicated that the nucleation sites for perovskite growth are related to the electron density around the oxygen atom (C[double bond, length as m-dash]O and S[double bond, length as m-dash]O) in a Lewis base. A single layer of micrometer-sized and (110)-oriented perovskite crystals was achieved in the optimized MAPbI3 films via suppressing the formation of nucleation sites. We fabricated inverted perovskite solar cells with the structure of glass/ITO/PEDOT:PSS/MAPbI3/PC61BM/Al which exhibited a high power conversion efficiency of 17.5% and a high fill factor over 83%. In addition, a study of the moisture stability indicated that the (110) facet orientation of the perovskite grains plays a more important role in film degradation than grain size.

Three-dimensional hybrid nanostructures (i.e., Te “nanobranches” on a Si “nanotrunk” or Te “nanoleaves” on a Si “nanotrunk”) were synthesized by combining the gold-assisted chemical etching of Si to form Si “nanotrunks” and the galvanic displacement of Si to form Te “nanobranches” or “nanoleaves.” By adjusting the composition of the electrolyte used for the galvanic displacement reaction, the shape of the Te nanostructures could be changed from nanoleaves to nanobranches. The Si nanotrunks with Te nanobranches showed stronger luminescent emission in the visible region, with their Raman spectrum having a higher wave number, owing to their grain size being larger. This suggested that the optical and photoelectrochemical properties of Te–Si hybrid nanostructures depend on their shape and size. Using this approach, it should be possible to fabricate various hierarchical nanostructures for use in photoelectronic and photoelectrochemical devices.

Correction for ‘Three-dimensional hierarchical Te–Si nanostructures’ by Jae-Hong Lim et al., Nanoscale, 2014, 6, 11697–11702.