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Superhydrophobic surfaces possess enormous potential in various applications on account of their versatile functionalities. However, artificial superhydrophobic surfaces with ultralow solid/liquid adhesion often require complicated structure fabrication and surface fluorination processes. Here, we designed a superhydrophobic surface possessed of micro/nanoscale structures by employing facile and low-cost demolding and initiated chemical vapor deposition (iCVD) processes. The achieved micro/nanostructured superhydrophobic surface has a maximum static contact angle of ∼170°, a roll-off angle and contact angle hysteresis below 1°, ultralow solid/liquid adhesion for water droplets, and maintains excellent superhydrophobicity after exposure to strongly corrosive species, like strong acid/base and salt solutions, for 60 h. This reasonability-designed method of creating the superhydrophobic surface could provide valuable guidelines for the manufacture of transferable superhydrophobic surfaces and facilitate potential applications extending from optoelectronic devices to self-cleaning materials, such as solar cells, windows, and electronic displays.

CsPbIxBry-based all-inorganic perovskite materials are a potential candidate for stable semitransparent and tandem structured photovoltaic devices. However, poor film (morphological and crystalline...

Nanofabrication schemes usually suffer challenges in direct growth on complex nanostructured substrates. We provide a new technology that allows for the convenient, selective growth of complex nanostructures directly on three-dimensional (3D) homogeneous semiconductor substrates. The nature of the selectivity is derived from surface states modulated electrochemical deposition. Metals, metal oxides, and compound semiconductor structures can be prepared with high fidelity over a wide scale range from tens of nanometers to hundreds of microns. The utility of the process for photoelectrochemical applications is demonstrated by selectively decorating the sidewalls and tips of silicon microwires with cuprous oxide and cobalt oxides catalysts, respectively. Our findings indicate a new selective fabrication concept applied for homogeneous 3D semiconductor substrates, which is of high promise in community of photoelectronics, photoelectrochemistry, photonics, microelectronics, etc.

Layered metal thiophosphates with a general formula MPX3 (M is a group VIIB or VIII element and X is a chalcogen) have emerged as a novel member in a two-dimensional (2D) family with fascinating physical and chemical properties. Herein, the photoelectric performance of the few-layer MnPSe3 was studied for the first time. The multilayer MnPSe3 shows p-type conductivity and its field-effect transistor delivers an ultralow dark current of about 0.1 pA. The photoswitching ratio reaches ∼103 at a wavelength of 375 nm, superior to that of other thiophosphates. A responsivity and detectivity of 392.78 mA/W and 2.19 × 109 Jones, respectively, have been demonstrated under irradiation of 375 nm laser with a power intensity of 0.1 mW/cm2. In particular, the photocurrent can be remarkably increased up to 30 times by integrating a layer of Au nanoparticle array at the bottom of the MnPSe3 layer. The metal-semiconductor interfacial electric field and the strain-induced flexoelectric polarization field caused by the underlying nanorugged Au nanoparticles are proposed to contribute together to the significant current improvement.

Modulating and optimizing the diverse parameters of photocatalysts synergistically as well as exerting these advantages fully in photocatalytic reactions are crucial for the sufficient utilization of solar energy but still face various challenges. Herein, a novel and facile urea- and KOH-assisted thermal polymerization (UKATP) strategy is first developed for the preparation of defect-modified thin-layered and porous g-C3N4 (DTLP-CN), wherein the thickness of g-C3N4 was dramatically decreased, and cyano groups, nitrogen vacancies, and mesopores were simultaneously introduced into g-C3N4. Importantly, the roles of thickness, pores, and defects can be targetedly modulated and optimized by changing the mass ratio of urea, KOH, and melamine. This can remarkably increase the specific area, improve the light-harvesting capability, and enhance separation efficiency of photoexcited charge carriers, strengthening the mass transfer in g-C3N4. Consequently, the photocatalytic hydrogen evolution efficiency of the DTLP-CN (1.557 mmol h-1 g-1, λ > 420 nm) was significantly improved more than 48.5 times with the highest average apparent quantum yield (AQY) of 18.5% and reached as high as 0.82% at 500 nm. This work provides an effective strategy for synergistically regulating the properties of g-C3N4, and opens a new horizon to design g-C3N4-based catalysts for highly efficient solar-energy conversion.

The development of highly crystalline perovskite films with large crystal grains and few surface defects is attractive to obtain high-performance perovskite solar cells (PSCs) with good device stability. Herein, we simultaneously improve the power conversion efficiency (PCE) and humid stability of the CH

Although ternary polymer solar cells have more potential in realizing a high power conversion efficiency than the binary counterparts, the mechanism of exciton separation and charge transport in such complicated ternary systems is far from being understood. Herein, we focus on this issue and give a clear view on the detailed roles of the ternary components contributing to the device performance, through utilizing the technique of pump-probe photoconductivity spectroscopy combined with transient photoluminescence spectroscopy, for the first time for ternary polymer solar cells. The ternary photovoltaic devices are based on PBDB-T:ITIC:PC71BM and present a dramatic improvement in efficiency in comparison to that of the binary counterparts. Systematic investigation reveals that the excitons generated in ITIC could be separated at the interface of PBDB-T:ITIC rather than ITIC:PC71BM with holes injecting to PBDB-T. These holes together with those generated in PBDB-T contribute to the photocurrent of the devices. The aggregation of holes in PBDB-T would also weaken the exciton generation herein, and the electron injection to PC71BM and ITIC would also be influenced. The key role of PC71BM in the ternary devices is accepting the electrons from PBDB-T and transporting them to the cathode with a higher rate than that of ITIC. Thus, this article is of importance in constructing high-efficiency ternary polymer solar cells.

Extensive efforts have been undertaken on the photoelectric physics of hybrid organolead halide perovskites to unveil the reason for the attractive photovoltaic performance. Yet, the resulting evidence is far from being fully conclusive. Herein, we provide another direct support for this issue. In addition to the observation on the conventional band edge at 1.58 eV that presents a blueshift toward temperature increase, interestingly, we also observe an unusual optical band edge at 1.48 eV in CH3NH3PbI3 perovskite single crystals for the first time. Contrary to the conventional band edge, this one shows an obvious redshift toward the enhancement in temperature, in agreement with the Varshni relation. More interestingly, the unusual band edge exhibits a series of obvious absorption and photocurrent signals, but the according photoluminescence signals are not observable. This indicates that this band edge is particularly beneficial for the photovoltaic effect due to the inhibited radiative recombination. The...

A complete mechanistic study on the nucleation of polymeric nanoparticles covering the generation of the clusters and the forthcoming aggregation to the nuclei is performed by in situ 1H nuclear ma...