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Mechanically resilient optoelectronic devices are relevant for a wide range of applications, including portable and wearable devices. Perovskite thin film‐based devices are a suitable choice for designing such resilient systems as it demonstrates high performance while preserving moderate mechanical compliance. Yet its mechanical property can be improved further by integrating the energy dissipation system and self‐healing ability into the thin film. Copolymers containing Lewis‐base functional groups, elastomer chains, and cyclic linkages are synthesized and introduced into the perovskite precursor. The polymers impart multifunctional effect of controlled crystal growth, defect passivation, protection against moisture, mechanical energy dissipation, and self‐recoverability. The polymer‐added perovskite solar cells are shown to provide a power conversion efficiency of 23.25% (a steady‐state efficiency of 22.61%), due to the strong coordinative covalent interaction between the polymer and the perovskite. An operational lifetime of solar cells under harsh conditions is also substantially extended by the polymer incorporation. Furthermore, the interchain hydrogen‐bond strength controlled by the cyclic linkage, and hybrid cross‐linked network formed within the thin film significantly improves the mechanical stability and self‐recoverability of the thin film. As a result, the devices demonstrate robustness under 2000 cyclic flex tests at a bending radius of 1 mm. [ABSTRACT FROM AUTHOR]

Narrowband photodetector (NB‐PD) with selective light detection is critical for artificial vision and imaging. Intrinsic (optical‐filter‐free) NB‐PDs using conjugated organics or halide perovskite materials have been developed for eliminating the current complex filtering systems in NB‐PDs. However, the poor performance and external driving circuit of organic NB‐PDs as well as complex doping and uncontrollable recombination reactions in typical perovskite NB‐PDs have limited their applicational diversification. A p‐type self‐doped perovskite for intrinsic NB detection is reported which exhibits unique unbalanced electron–hole transfer kinetics. In conjunction with the optical field distribution, an unbalanced charge transport within the self‐doped perovskite triggers a wavelength‐dependent photo‐carrier collection, resulting in a novel spontaneous internal quantum efficiency narrowing mechanism. As a result, by reverting the device architectural polarity, an NB detection at a monochromic light of either red or UV is observed. Using such a revertible asymmetric device design, self‐powered NB‐PDs are successfully achieved. Briefly, the corresponding NB‐PDs exhibit excellent narrow response with a response window of ≈100 nm, high detectivity ≈1011 Jones, and fast response speed (f−3dB ≈ 60 kHz) at zero bias. These results demonstrate a new strategy of manipulating internal charge transport to realize power‐free and filter‐free intrinsic NB‐PDs. [ABSTRACT FROM AUTHOR]

With the power conversion efficiencies of perovskite solar cells (PSCs) exceeding 25%, the PSCs are a step closer to initial industrialization. Prior to transferring from laboratory fabrication to industrial manufacturing, issues such as scalability, material cost, and production line compatibility that significantly impact the manufacturing remain to be addressed. Here, breakthroughs on all these fronts are reported. Carbon‐based PSCs with architecture fluorine doped tin oxide (FTO)/electron transport layer/perovskite/carbon, that eliminate the need for the hole transport layer and noble metal electrode, provide ultralow‐cost configuration. This PSC architecture is manufactured using a scalable and industrially compatible electrospray (ES) technique, which enables continuous printing of all the cell layers. The ES deposited electron transport layer and perovskite layer exhibit properties comparable to that of the laboratory‐scale spin coating method. The ES deposited carbon electrode layer exhibits superior conductivity and interfacial microstructure in comparison to films synthesized using the conventional doctor blading technique. As a result, the fully ES printed carbon‐based PSCs show a record 14.41% power conversion efficiency, rivaling the state‐of‐the‐art hole transporter‐free PSCs. These results will immediately have an impact on the scalable production of PSCs. [ABSTRACT FROM AUTHOR]

1D ferroelectric nanostructures are promising for enhanced ferroelectric and piezoelectric performance on the nanoscale, however, their synthesis at the wafer scale using industrially compatible processes is challenging. In order to advance the nanostructure-based electronics, it is imperative to develop a silicon-compatible growth technique yielding high volumetric density and an ordered arrangement. Here, a major breakthrough is provided in addressing this need and ordered and close-packed single crystalline ferroelectric nanorod arrays, of composition PbZr0.52Ti0.48O3 (PZT), grown on commercial grade 3 in. silicon wafer are demonstrated. PZT nanorods exhibit enhanced piezoelectric and ferroelectric performance compared to thin films of similar dimensions. Sandwich structured architecture utilizing 1D PZT nanorod arrays and 2D reduced graphene oxide thin film electrodes is fabricated to provide electrical connection. Combined, these results offer a clear pathway toward integration of ferroelectric nanodevices with commercial silicon electronics. [ABSTRACT FROM AUTHOR]

In article number 1804419, Congcong Wu, Shashank Priya, and co‐workers develope a dual‐functional PMMA‐fullerene complex, where the fullerene C60 dwells in the caves of the PMMA polymer chain. The PMMA‐fullerene complex is incorporated into the perovskite layer, which resides along the grain boundary of the perovskites. The fullerene reduces the charge carrier recombination and the PMMA polymer improves the stability of the perovskite solar cell. [ABSTRACT FROM AUTHOR]

Lead halide perovskite solar cells (PSCs) have demonstrated great potential for realizing low‐cost and easily fabricated photovoltaics. At this juncture, power conversion efficiency and long‐term stability are two important factors limiting their transition. PSCs exhibit rapid environmental degradation since the perovskite layer is very sensitive to factors such as humidity, temperature, and ultraviolet light. Here, a novel successful approach is demonstrated that simultaneously improves the efficiency and stability of PSCs. This approach relies on incorporation of a dual‐functional polymethyl methacrylate (PMMA)–fullerene complex into the perovskite layer. The fullerene within perovskite layer forms a localized dipole‐like electric field that favors electron–hole separation, resulting in significant improvement in current density and fill factor with conversion efficiency reaching 18.4%. The molecular‐scale coating of hydrophobic PMMA on the perovskite grain boundary effectively blocks moisture penetration into the perovskite, thereby, significantly improving the stability against moisture, heat, and light. The PSCs with PMMA–fullerene complex showed no photovoltaic performance degradation for 250 d and exhibited 60 times higher stability compared to the state‐of‐the‐art devices under continuous 1 sun illumination in ambient air. Polymethyl methacrylate is coated on a perovskite grain boundary, blocking moisture penetration. The distributed C60 clusters create a dipole‐like electric field inside the perovskite layer, which favors exciton dissociation, and improves the conversion efficiency of perovskite solar cells. [ABSTRACT FROM AUTHOR]