Flexible and portable devices are a mainstream direction in modern electronics and related multidisciplinary fields. To this end, they are generally required to be stretchable to satisfy various substrates. [1,2] As a result, stretchable devices, such as electrochemical supercapacitors, [3][4][5][6] lithium-ion batteries, [7] organic solar cells, [8] organic light-emitting diodes, [9,10] field-effect transistors, [11] and artificial skin sensors [12] have been widely studied. However, these stretchable devices are made in a conventional planar format that has largely hindered their development. For the portable applications, the devices need to be lightweight and small, though it is difficult for them to be made into efficient microdevices. In particular, it is challenging or even impossible for them to be used in electronic circuits and textiles that are urgently required also in a wide variety of other fields, such as microelectronic applications.Recently, some attempts have been made to fabricate wire-shaped microdevices, such as electrochemical supercapacitors. They have been generally produced by twisting two fiber electrodes with electrolytes coated on the surface. [13][14][15][16][17][18][19] Several examples have been also successfully shown to make fiber-shaped supercapacitors with a coaxial structure. [20,21] Compared with their planar counterparts, the wire or fiber shape enables promising advantages such as being lightweight and woven into textiles. Although the wire and fiber-shaped supercapacitors are also flexible with high electrochemical performance, they are not stretchable, which is critically important for many applications. For instance, the resulting electronic textiles could easily break during the use if they were not stretchable.To the best of our knowledge, herein we have, for the first time, developed a novel family of highly stretchable, fibershaped high-performance supercapacitors. Aligned carbon nanotube (CNT) sheets that are sequentially wrapped on an elastic fiber serve as two electrodes. The use of aligned CNT sheets offers combined remarkable properties including high flexibility, tensile strength, electrical conductivity, and

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Aligned carbon-nanotube (CNT) sheets are used as building blocks to prepare light-weight, frequency-tunable and high-performance microwave absorbers, and the absorption frequency can be accurately controlled by stacking them with different intersectional angles. A remarkable reflection loss of -47.66 dB is achieved by stacking four aligned CNT sheets with an intersectional angle of 90° between two neighboring ones. The incorporation of a second phase such as a metal and a conducting polymer greatly enhances the microwave-absorption capability.

Organic-inorganic hybrid perovskite multijunction solar cells have immense potential to realize power conversion efficiencies (PCEs) beyond the Shockley-Queisser limit of single-junction solar cells; however, they are limited by large nonideal photovoltage loss (V ) in small- and large-bandgap subcells. Here, an integrated approach is utilized to improve the V of subcells with optimized bandgaps and fabricate perovskite-perovskite tandem solar cells with small V . A fullerene variant, Indene-C bis-adduct, is used to achieve optimized interfacial contact in a small-bandgap (≈1.2 eV) subcell, which facilitates higher quasi-Fermi level splitting, reduces nonradiative recombination, alleviates hysteresis instabilities, and improves V to 0.84 V. Compositional engineering of large-bandgap (≈1.8 eV) perovskite is employed to realize a subcell with a transparent top electrode and photostabilized V of 1.22 V. The resultant monolithic perovskite-perovskite tandem solar cell shows a high V of 1.98 V (approaching 80% of the theoretical limit) and a stabilized PCE of 18.5%. The significantly minimized nonideal V is better than state-of-the-art silicon-perovskite tandem solar cells, which highlights the prospects of using perovskite-perovskite tandems for solar-energy generation. It also unlocks opportunities for solar water splitting using hybrid perovskites with solar-to-hydrogen efficiencies beyond 15%.

A low-bandgap (1.33 eV) Sn-based MA FA Pb Sn I perovskite is developed via combined compositional, process, and interfacial engineering. It can deliver a high power conversion efficiency (PCE) of 14.19%. Finally, a four-terminal all-perovskite tandem solar cell is demonstrated by combining this low-bandgap cell with a semitransparent MAPbI cell to achieve a high efficiency of 19.08%.

Two-dimensional perovskites have emerged as more intrinsically stable materials for solar cells. Chemical tuning of spacer organic cations has attracted great interest due to their additional functionalities. However, how the chemical nature of the organic cations affects the properties of two-dimensional perovskites and devices is rarely reported. Here we demonstrate that the selection of spacer cations (i.e., selective fluorination of phenethylammonium) affects the film properties of two-dimensional perovskites, leading to different device performance of two-dimensional perovskite solar cells (average n = 4). Structural analysis reveals that different packing arrangements and orientational disorder of the spacer cations result in orientational degeneracy and different formation energies, largely explaining the difference in film properties. This work provides key missing information on how spacer cations exert influence on desirable electronic properties and device performance of two-dimensional perovskites via the weak and cooperative interactions of these cations in the crystal lattice.

The efficiencies of perovskite solar cells (PSCs) are now reaching such consistently high levels that scalable manufacturing at low cost is becoming critical. However, this remains challenging due to the expensive hole-transporting materials usually employed, and difficulties associated with the scalable deposition of other functional layers. By simplifying the device architecture, hole-transport-layer-free PSCs with improved photovoltaic performance are fabricated via a scalable doctor-blading process. Molecular doping of halide perovskite films improved the conductivity of the films and their electronic contact with the conductive substrate, resulting in a reduced series resistance. It facilitates the extraction of photoexcited holes from perovskite directly to the conductive substrate. The bladed hole-transport-layer-free PSCs showed a stabilized power conversion efficiency above 20.0%. This work represents a significant step towards the scalable, cost-effective manufacturing of PSCs with both high performance and simple fabrication processes.

Light my wire: Aligned carbon nanotube (CNT) fibers are wrapped around a TiO2 nanowire that is several centimeters long. Treating the ends of the nanotube wire with a light‐sensitive dye and an electrolyte, creates photoelectric‐conversion and energy‐storage regions in the same device (see scheme). The “wire” shows a high overall photoelectric conversion and storage efficiency of 1.5 %.