Cesium-Doped Vanadium Oxide as the Hole Extraction Layer for Efficient Perovskite Solar Cells

In this study, we report the utilization of low-temperature solution-processed Cs-doped VO_X thin films as the hole extraction layers (HELs) in perovskite solar cells (PSCs). It is found that the VO_X:<i>y</i>Cs (where <i>y</i> is the mole ratio of Cs versus V and <i>y</i> = 0.1, 0.3, and 0.5) thin films possess better electrical conductivities than that of the pristine VO_X thin film. As a result, the PSCs incorporated with the VO_X:<i>y</i>Cs HEL exhibit large fill factors and high short-circuit currents, with consequently high power conversion efficiencies, which is more than 30% enhancement as compared with pristine VO_X HEL. Our studies provide a facial way to enhance the electrical conductivity of the hole extraction layer for boosting device performance of perovskite solar cells

Polyaniline-Modified Oriented Graphene Hydrogel Film as the Free-Standing Electrode for Flexible Solid-State Supercapacitors

In this study, we report polyaniline (PANI)-modified oriented graphene hydrogel (OGH) films as the free-standing electrode for flexible solid-state supercapacitors (SCs). The OGH films are prepared by a facile filtration method using chemically converted graphene sheets and then introduced to PANI on the surface of OGH films by in situ chemical polymerization. The PANI-modified OGH films possess high flexibility, high electrical conductivity, and mechanical robustness. The flexible solid-state SCs based on the PANI-modified OGH films exhibit a specific capacitance of 530 F/g, keeping 80% of its original value up to 10 000 charge–discharge cycles at the current density of 10 A/g. Remarkably, the flexible solid-state SCs maintain ∼100% capacitance retention bent at 180° for 250 cycles. Moreover, the flexible solid-state SCs are further demonstrated to be able to light up a red-light-emitting diode. These results indicate that the flexible solid-state SCs based on PANI-modified OGH films as the free-standing electrode have potential applications as energy-storage devices

Comparative Study of Graphene Hydrogels and Aerogels Reveals the Important Role of Buried Water in Pollutant Adsorption

Water as the universal solvent has well-demonstrated its ability to dissolve many substances, but buried water inside different nanoporous materials always exhibits some unusual behaviors. Herein, 3D porous graphene hydrogel (GH) is developed as a super-adsorbent to remove different pollutants (antibiotics, dyes, and heavy ions) for water purification. Due to its highly porous structure and high content of water, GH also demonstrated its super adsorption capacity for adsorbing and removing different pollutants (antibiotics, dyes, and heavy ions) as compared to conventional graphene aerogel (GA). More fundamentally, the buried-water enhanced adsorption mechanism was proposed and demonstrated, such that buried water in GH plays the combinatorial roles as (1) supporting media, (2) transport nanochannels, and (3) hydrogen bondings in promoting pollutant adsorption. In parallel, molecular dynamics simulations further confirm that buried water in GH has the stronger interaction with pollutants via hydrogen bonds than other buried alcohols. GH integrates the merit of both graphene (e.g., fine chemical resistance and excellent mechanical property) and hydrogel (e.g., high water content, porous structure, and simple solution-based processability and scalability), giving it promising potential for environmental applications

Synthesis of Anthracene-Based Donor–Acceptor Copolymers with a Thermally Removable Group for Polymer Solar Cells

A highly soluble anthracene cyclic adduct with a thermally cleavable substituent was synthesized, and it was used as a donor unit in a series of donor–acceptor type conjugated copolymers with improved processability. The removable group was eliminated under elevated temperature through retro Diels–Alder reaction, which offered the corresponding copolymers with better planarity and rigidity. Thermogravimetric analysis (TGA), FT-IR, and UV–vis spectroscopy were carried out to study the thermal cleavage process. Uniform films were easily formed from these precursor copolymers due to their good solution processabilty. Polymer solar cells were successfully fabricated through applying thermal annealing treatment on the blend films that were spin-coated from solutions of the precursor copolymers blended with fullerene derivatives. The best polymer solar cell device with a power conversion efficiency (PCE) of 2.15% was achieved based on copolymer PCOAEHDPP

Enhanced Thermoelectric Properties of Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) by Binary Secondary Dopants

To simultaneously increase the electrical conductivity and Seebeck coefficient of poly­(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS) was a challenge for realizing efficient organic thermoelectrics. In this study, for the first time, we report both increased electrical conductivities and Seebeck coefficients, hence, enhanced thermoelectric properties of PEDOT:PSS thin films by doped with binary secondary dopants, dimethyl sulfoxide (DMSO) and poly­(ethylene oxide) (PEO). Without modifying film morphology, the molar ratios of PEDOT to PSS are tuned by PEO, resulting in increased proportions of PEDOT in the bipolaron states. Our study provides a facile route to optimizing thermoelectric properties of PEDOT:PSS thin films

Efficient Polymer Solar Cells by Lithium Sulfonated Polystyrene as a Charge Transport Interfacial Layer

In this paper, we report the highly efficient bulk heterojunction (BHJ) polymer solar cells (PSCs) with an inverted device structure via utilizing an ultrathin layer of lithium sulfonated polystyrene (LiSPS) ionomer to reengineer the surface of the solution-processed zinc oxide (ZnO) electron extraction layer (EEL). The unique lithium-ionic conductive LiSPS contributes to enhanced electrical conductivity of the ZnO/LiSPS EEL, which not only facilitates charge extraction from the BHJ active layer but also minimizes the energy loss within the charge transport processes. In addition, the organic–inorganic LiSPS ionomer well circumvents the coherence issue of the organic BHJ photoactive layer on the ZnO EEL. Consequently, the enhanced charge transport and the lowered internal resistance between the BHJ photoactive layer and the ZnO/LiSPS EEL give rise to a dramatically reduced dark saturation current density and significantly minimized charge carrier recombination. As a result, the inverted BHJ PSCs with the ZnO/LiSPS EEL exhibit an approximatively 25% increase in power conversion efficiency. These results indicate our strategy provides an easy, but effective, approach to reach high performance inverted PSCs

Two-Dimensional Metal Halide Perovskites Created by Binary Conjugated Organic Cations for High-Performance Perovskite Photovoltaics

Studies indicated that two-dimensional (2D) metal halide perovskites (MHPs) embodied with three-dimensional (3D) MHPs were a facile way to realize efficient and stable perovskite solar cells (PSCs) and perovskite photodetectors (PPDs). Here, high-performance PSCs and PPDs, which are based on 2D/3D MHPs bilayer thin films, where the 2D MHPs are created by binary conjugated organic cations, are reported. Systemically studies reveal that the above novel 2D/3D MHPs bilayer thin films possess an enlarged crystal size, balanced charge transport, reduced charge carrier recombination, smaller charge-transfer resistance, and accelerated charge-extraction process compared to the 2D/3D MHPs bilayer thin films, where the 2D MHPs are created by a single conjugated organic cation. As a result, the PSCs based on the above novel 2D/3D MHPs bilayer thin film exhibit a power conversion efficiency of 22.76%. Moreover, unencapsulated PSCs possess dramatically enhanced stability compared with those based on the 2D/3D MHPs bilayer thin films, where the 2D MHPs are created by a single conjugated organic cation. In addition, the PPDs based on the above novel 2D/3D MHPs bilayer thin film exhibit a projected detectivity of 1016 cm Hz1/2/W and a linear dynamic range of 108 dB at room temperature. Our studies indicate that the development of binary conjugated organic cation-based 2D MHPs incorporated with 3D MHPs is a simple method to realize high-performance PSCs and PPDs

Understanding the Halogenation Effects in Diketopyrrolopyrrole-Based Small Molecule Photovoltaics

Two molecules containing a central diketopyrrolopyrrole and two oligothiophene units have been designed and synthesized. Comparisons between the molecules containing terminal F (FDPP) and Cl (CDPP) atoms allowed us to evaluate the effects of halogenation on the photovoltaic properties of the small molecule organic solar cells (OSCs). The OSCs devices employing FDPP:PC₇₁BM films showed power conversion efficiencies up to 4.32%, suggesting that fluorination is an efficient method for constructing small molecules for OSCs