Small-Molecule Copper Chloride Modulating the Buried Interfaces of Perovskite Solar Cells.

In perovskite solar cells (PSCs), tin dioxide (SnO2) is a highly effective electron transport material. On the other hand, the low intrinsic conductivity of SnO2, the high trap-state density on the surface and bulk of SnO2, and inadequate interface contacts between SnO2 and perovskite significantly impact device performance. Herein, small-molecule copper(II) chloride (CuCl2) is introduced into the SnO2 dispersion, which inhibits the agglomeration of SnO2 colloids and improves the quality of the electron transport layer. Furthermore, the introduction of CuCl2 optimizes the energy-level array between the ETL and perovskite layer (PVK) and passivates the anion/cation defects in SnO2, perovskite, and their interface, realizing the systematic modulation of the photoelectronic properties of the ETLs and PVKs as well as the PVK/ETL. As a result, the CuCl2-opmized PSC exhibits an impressive power conversion efficiency of 23.71%, along with improved stability.

Poly(3-hexylthiophene)/perovskite Heterointerface by Spinodal Decomposition Enabling Efficient and Stable Perovskite Solar Cells.

The best research-cell efficiency of perovskite solar cells (PSCs) is comparable with that of mature silicon solar cells (SSCs); However, the industrial development of PSCs lags far behind SSCs. PSC is a multiphase and multicomponent system, whose consequent interfacial energy loss and carrier loss seriously affect the performance and stability of devices. Here, by using spinodal decomposition, a spontaneous solid phase segregation process, in situ introduces a poly(3-hexylthiophene)/perovskite (P3HT/PVK) heterointerface with interpenetrating structure in PSCs. The P3HT/PVK heterointerface tunes the energy alignment, thereby reducing the energy loss at the interface; The P3HT/PVK interpenetrating structure bridges a transport channel, thus decreasing the carrier loss at the interface. The simultaneous mitigation of energy and carrier losses by P3HT/PVK heterointerface enables n-i-p geometry device a power conversion efficiency of 24.53% (certified 23.94%) and excellent stability. These findings demonstrate an ingenious strategy to optimize the performance of PSCs by heterointerface via Spinodal decomposition.

Synergistic Effect of 2-(Trifluoromethyl) Benzimidazole on the Stability and Performance of Perovskite Solar Cells.

The quality of the perovskite active layer directly impacts the photovoltaic performance of perovskite solar cells (PSCs). Unfortunately, perovskite films produced through solution methods often have a significant number of defects on their surface, which lead to a substantial degradation in the performance of devices. For this reason, a multifunctional additive 2-(trifluoromethyl) benzimidazole (TFMBI) is introduced into perovskite films. Based on the Lewis acid/base coordination principle, the TFMBI double site cooperatively passivates surface defects, inhibiting carrier non-radiative recombination. Simultaneously, the hydrophobic solid group (-CF3) of TFMBI covers the surface, establishing a moisture-oxygen barrier and improving the environmental stability of the devices. In consequence, the power conversion efficiency (PCE) of TFMBI-modified PSCs reached 23.16%, significantly higher than the pristine one with a PCE of 20.62%. Additionally, the unencapsulated target device retained 90.32% of its initial PCE even after being reserved in the air with a relative humidity of 20-30% for 60 days.

Synergistic Ionic Liquid in Hole Transport Layers for Highly Stable and Efficient Perovskite Solar Cells.

Perovskite solar cells (PSCs) with n-i-p structures often utilize an organic 2,2',7,7'-tetrakis (N, N-di-p-methoxyphenyl-amine) 9,9'-spirobifluorene (spiro-OMeTAD) along with additives of lithium bis(trifluoromethanesulfonyl)imide salt (LiTFSI) and tert-butylpyridine as the hole transporting layer (HTL). However, the HTL lacks stability in ambient air, and numerous defects are often present on the perovskite surface, which is not conducive to a stable and efficient PSC. Therefore, constructive strategies that simultaneously stabilize spiro-OMeTAD and passivate the perovskite surface are required. In this work, it is demonstrated that a novel ionic liquid of dimethylammonium bis(trifluoromethanesulfonyl)imide (DMATFSI) could act as a bifunctional HTL modulator in n-i-p PSCs. The addition of DMATFSI into spiro-OMeTAD can effectively stabilize the oxidized spiro-OMeTAD+ cation radicals through the formation of spiro-OMeTAD+ TFSI- because of the excellent charge delocalization of the conjugated CF3 SO2 - moiety within TFSI- . In addition, DMA+ cations could move toward the perovskite from the HTL, resulting in the passivation of defects at the perovskite surface. Accordingly, a power conversion efficiency of 23.22% is achieved for PSCs with DMATFSI and LiTFSI co-doped spiro-OMeTAD. Moreover, benefiting from the improved ion migration barrier and hydrophobicity of the HTL, still retained nearly 80% of their initial power conversion efficiency after 36 days of exposure to ambient air.

Single-atom sites on perovskite chips for record-high sensitivity and quantification in SERS.

Surface enhanced Raman scattering (SERS) is a rapid and nondestructive technique that is capable of detecting and identifying chemical or biological compounds. Sensitive SERS quantification is vital for practical applications, particularly for portable detection of biomolecules such as amino acids and nucleotides. However, few approaches can achieve sensitive and quantitative Raman detection of these most fundamental components in biology. Herein, a noble-metal-free single-atom site on a chip strategy was applied to modify single tungsten atom oxide on a lead halide perovskite, which provides sensitive SERS quantification for various analytes, including rhodamine, tyrosine and cytosine. The single-atom site on a chip can enable quantitative linear SERS responses of rhodamine (10-6-1 mmol L-1), tyrosine (0.06-1 mmol L-1) and cytosine (0.2-45 mmol L-1), respectively, which all achieve record-high enhancement factors among plasmonic-free semiconductors. The experimental test and theoretical simulation both reveal that the enhanced mechanism can be ascribed to the controllable single-atom site, which can not only trap photoinduced electrons from the perovskite substrate but also enhance the highly efficient and quantitative charge transfer to analytes. Furthermore, the label-free strategy of single-atom sites on a chip can be applied in a portable Raman platform to obtain a sensitivity similar to that on a benchtop instrument, which can be readily extended to various biomolecules for low-cost, widely demanded and more precise point-of-care testing or in-vitro detection. Electronic Supplementary Material: Supplementary material is available for this article at 10.1007/s40843-022-1968-5 and is accessible for authorized users.

High-efficiency and ultraviolet stable carbon-based CsPbIBr2 solar cells from single crystal three-dimensional anatase titanium dioxide nanoarrays with ultraviolet light shielding function.

TiO2 is commonly used to prepare electron transport layers (ETLs) in perovskite solar cells (PSCs). However, conventional TiO2 ETLs suffer from low electron mobility and charge recombination. Here, we report the direct growth of TiO2 ETLs on fluorine doped conductive (FTO) glasses with titanium tetrafluoride (TiF4) as the reactant by hydrothermal method. The TiO2 ETLs have pure anatase phase, single crystal structure and three-dimensional (3D) nanoarrays morphology. This 3D-TiO2 ETLs mainly consist of thermodynamically stable surfaces {101} and more reactive surfaces {001}. Compared with the conventional TiO2 ETLs, the 3D-TiO2 ETLs can effectively optimize energy level matching and charge transfer dynamics. The special morphology of 3D-TiO2 ETLs can well assist to form high quality CsPbIBr2 with larger crystal grains. The champion CsPbIBr2 PSC with 3D-TiO2 ETL achieves an efficiency as high as 10.65%, which is equal to the one with hole-transport and Au electrode structure (10.79%) and much higher than the pristine one (7.16%) with the conventional TiO2 ETL. Furthermore, the 3D-TiO2 ETLs show ultraviolet (UV) shielding function, which can effectively overcome the UV instability defect of conventional TiO2 ETLs and obviously enhance UV stability of CsPbIBr2 and the corresponding PSCs. Therefore, the 3D-TiO2 ETLs can be good candidates for preparing high-efficiency and UV stable carbon-based CsPbIBr2 PSCs.

Bulky ammonium iodide and in-situ formed 2D Ruddlesden-Popper layer enhances the stability and efficiency of perovskite solar cells.

The practical applications of perovskite solar cells (PSCs) are limited by the further improvement of their stability and performance. Interface engineering is a promising strategy to solve these pain points. Herein, we design (R)-(-)-1-cyclohexylethylamine iodide (R-CEAI), composed of positively charged hydrophobic R-CEA+ and negatively charged I-, to post-treat the interface of 3D mixed-cation/halide perovskite with assist one of isopropyl alcohol (IPA). R-CEAI treatment not only passivates the defects at surface and grain boundaries of perovskite, but also in-situ grows quasi 2D Ruddlesden-Popper perovskite at the interface between 3D perovskite and hole transport layer, which reduces trap density of states, tunes energy level and alleviates lattice distortion. As a result, R-CEAI treated 2D/3D PSCs yield a champion PCE of 22.52%, with an improved open-circuit voltage of 1.195 V and retain 84.34% of their initial efficiency in long-term stability test, while the pristine device provides a PCE of 19.43% with only 54.30% retention.

Surface Reconstruction and In Situ Formation of 2D Layer for Efficient and Stable 2D/3D Perovskite Solar Cells.

The 2D/3D composite structure possesses both the excellent stability of 2D perovskite and the excellent performance of 3D perovskite, which recently have attracted special attention. Different from the popular isopropanol, a novel additive solvent-polypropylene glycol bis (2-aminopropyl ether) (A-PPG) is introduced here to dissolve excess PbI2 and perovskite, and then reconstruct and in situ form the quasi-2D perovskite layer on 3D perovskite bulk. The lone electron pairs of the ether-oxygen and amino in A-PPG can form coordination bonds with Pb2+ . The introduction of A-PPG tunes the energy array of functional layers, passivates defects, and mitigates carrier nonradiative recombination. Consequently, the 2D/3D perovskite device exhibits a championship efficiency of 22.24% with a distinguished open-circuit voltage of 1.21 V (the thermodynamic limit of 1.30 V). Moreover, the 2D/3D device still maintains 90% of the original efficiency in the ambient atmosphere with a relative humidity of 30 ± 10% after 50 days.

Alkali Metal Fluoride-Modified Tin Oxide for n-i-p Planar Perovskite Solar Cells.

The practical applications of perovskite solar cells (PSCs) are limited by further improvement of their stability and performance. Additive engineering and interface engineering are promising medicine to cure this stubborn disease. Herein, an alkali metal fluoride as an additive is introduced into the tin oxide (SnO2) electron transport layer (ETL). The formation of coordination bonds of F- ions with the oxygen vacancy of Sn4+ ions decreases the trap-state density and improves the electron mobility; the hydrogen bond interaction between the F ion and amine group (FA+) of perovskite inhibits the diffusion of organic cations and promotes perovskite (PVK) stability. Meanwhile, the alkali metal ions (K+, Rb+, and Cs+) permeated into PVK fill the organic cation vacancies and ameliorate the crystal quality of PVK films. Consequently, a SnO2-based planar PSC exhibits a power conversion efficiency (PCE) of 20.24%, while the PSC modified by CsF achieves a PCE of 22.51%, accompanied by effective enhancement of stability and negligible hysteresis. The research results provide a typical example for low-cost and multifunctional additives in high-performance PSCs.

Enhanced photovoltage and stability of perovskite photovoltaics enabled by a cyclohexylmethylammonium iodide-based 2D perovskite passivation layer.

Regardless of the impressive progress that perovskite solar cells (PSCs) have achieved, especially considering their power conversion efficiency (PCE) over 25%, traditional PSCs still contend with an inherent instability with exposure to humidity, which remains as a critical issue for the realization of commercial production. Herein, we proposed an effective pathway to relieve the instability of PSCs without sacrificing efficiency by introducing a 2D phase at the surface of the 3D perovskite film, based on a novel organic cyclohexylmethylammonium iodide (CMAI). The self-assembled thin 2D capping layer atop the 3D perovskite layer can not only reduce the ionic defects, but also serve as a protective barrier against moisture. Consequently, the champion device incorporating 2D perovskite capping layers delivered an open-circuit voltage (Voc) of 1.19 V, which contributes to an impressive PCE of 22.06% on account of the improved charge extraction and decreased non-radiative recombination. More importantly, an excellent long-term stability along with mitigated hysteresis was observed for the modified devices as a result of the suppressed ion migration and high humidity resistance of the 2D perovskite film. Our finding provides a comprehensive approach for simultaneously enhancing the efficiency and stability of PSCs through dimension engineering utilizing CMA-based 2D perovskite materials.

High-Efficiency, Low-Hysteresis Planar Perovskite Solar Cells by Inserting the NaBr Interlayer.

With great research potential, the perovskite solar cells (PSCs) have been well developed in recent years, but there are still some urgent issues like efficiency and hysteresis defects that severely limit their commercialization. Interface modification is a significant measure to reduce defects and promote performance. In the article, an easy and effective strategy of modifying the electron transport layer (ETL) with NaBr is proposed to improve efficiency and reduce hysteresis. The charge carrier dynamics can be greatly optimized by diffusing NaBr on the ETL. The efficiency of the NaBr coated device can achieve 21.16%, which is extremely higher than the control one and shows low hysteresis behavior with a hysteresis index reduced from 0.135 to 0.025. The results indicate that the NaBr modification provides a novel strategy for preparing PSCs with high efficiency and low hysteresis.

[Implementation of a WeChat small program assisted process assessment system in "Experiment of Inorganic Chemistry" for Biological Engineering undergraduates].

The convenience of "no installation, available at your fingertips" of the WeChat small program makes it unique in the application of mobile terminal auxiliary experimental teaching. In order to optimize the assessment system and improve the quality and outcomes of experimental teaching, a self-designed WeChat small program was used to assist the development of the process assessment system. This system was applied to the teaching practice of "Experiment of Inorganic Chemistry" course for the first-year undergraduates majored in Biological Engineering, with the aim to promote teaching and learning by assessment. The results showed that course scores of the students who used this small program were superior to the control group and the correlation between the process assessment and final examination results was significant. These results indicated the WeChat small program assisted process assessment could effectively improve the learning outcomes of students, enable them to grasp the knowledge of Experiment of Inorganic Chemistry efficiently. The results of the questionnaire for the teachers and students also showed a high recognition of the WeChat small program assisted teaching.

Additive Engineering by Bifunctional Guanidine Sulfamate for Highly Efficient and Stable Perovskites Solar Cells.

High efficiency and good stability are the challenges for perovskite solar cells (PSCs) toward commercialization. However, the intrinsic high defect density and internal nonradiative recombination of perovskite (PVK) limit its development. In this work, a facile additive strategy is devised by introducing bifunctional guanidine sulfamate (GuaSM; CH6 N3 + , Gua+ ; H2 N-SO3 - , SM- ) into PVK. The size of Gua+ ion is suitable with Pb(BrI)2 cavity relatively, so it can participate in the formation of low-dimensional PVK when mixed with Pb(BrI)2 . The O and N atoms of SM- can coordinate with Pb2+ . The synergistic effect of the anions and cations effectively reduces the trap density and the recombination in PVK, so that it can improve the efficiency and stability of PSCs. At an optimal concentration of GuaSM (2 mol%), the PSC presents a champion power conversion efficiency of 21.66% and a remarkably improved stability and hysteresis. The results provide a novel strategy for highly efficient and stable PSCs by bifunctional additive.

Highly Efficient CsPbBr3 Planar Perovskite Solar Cells via Additive Engineering with NH4SCN.

Improving stability is a major aspect for commercial application of perovskite solar cells (PSCs). The all-inorganic CsPbBr3 perovskite material has been proven to have excellent stability. However, the CsPbBr3 film has a small range of light absorption and serious charge recombination at the interface or inside the device, so the power conversion efficiency is still lower than that of the organic-inorganic hybrid one. Here, we successfully fabricate high-quality CsPbBr3 films via additive engineering with NH4SCN. By incorporating NH4+ and pseudo-halide ion SCN- into the precursor solution, a smooth and dense CsPbBr3 film with good crystallinity and low trap state density can be obtained. At the same time, the results of a series of photoluminescence and electrochemical analyses including electrical impedance spectroscopy, space-charge limited current method, Mott-Schottky data, and so on reveal that the NH4SCN additive can greatly reduce the trap state density of the CsPbBr3 film and also effectively inhibit interface recombination and promote charge transport in the CsPbBr3 planar PSC. Finally, the CsPbBr3 planar PSC prepared with a molar ratio of 1.5% NH4SCN achieves a champion efficiency of 8.47%, higher than that of the pure one (7.12%).

Strong electron acceptor additive based spiro-OMeTAD for high-performance and hysteresis-less planar perovskite solar cells.

As the most popular hole-transporting material (HTM), spiro-OMeTAD has been extensively applied in perovskite solar cells (PSCs). Unluckily, the pristine spiro-OMeTAD film has inferior conductivity and hole mobility, thus limiting its potential for application in high-performance PSCs. To ameliorate the electrical characteristics of spiro-OMeTAD, we employ 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) as a strong electron acceptor into spiro-OMeTAD in PSCs. The incorporation of DDQ with spiro-OMeTAD not only improves the conductivity and the Fermi energy level, but also reduces the trap states and nonradiative recombination, which accounts for the remarkable enhancement in both the fill factor (FF) and open-circuit voltage (V OC) of PSCs. Consequently, the champion PSC with DDQ doped hole transport layer (HTL) generates a boosted power conversion efficiency (PCE) of 21.16% with an FF of 0.796 and a V OC of 1.16 V. Remarkably, DDQ modified devices exhibit superb device stability, as well as mitigated hysteresis. This study provides a facile and viable strategy for dopant engineering of HTL to realize highly efficient PSCs.

Suppressing Vacancy Defects and Grain Boundaries via Ostwald Ripening for High-Performance and Stable Perovskite Solar Cells.

As one kind of promising next-generation photovoltaic devices, perovskite solar cells (PVSCs) have experienced unprecedented rapid growth in device performance over the past few years. However, the practical applications of PVSCs require much improved device long-term stability and performance, and internal defects and external humidity sensitivity are two key limitation need to be overcome. Here, gadolinium fluoride (GdF3 ) is added into perovskite precursor as a redox shuttle and growth-assist; meanwhile, aminobutanol vapor is used for Ostwald ripening in the formation of the perovskite layer. Consequently, a high-quality perovskite film with large grain size and few grain boundaries is obtained, resulting in the reduction of trap state density and carrier recombination. As a result, a power conversion efficiency of 21.21% is achieved with superior stability and negligible hysteresis.

Toward Highly Reproducible, Efficient, and Stable Perovskite Solar Cells via Interface Engineering with CoO Nanoplates.

It is well-known that solution-processed polycrystalline perovskite films show a high density of parasitic traps and the defects mainly exist at grain boundaries and surfaces of polycrystal perovskite films, which would limit potential device performance by triggering the undesired recombination and impair device long-term stability by accelerating the degradation of perovskite films. In this regard, defect passivation is highly desirable for achieving efficient and stable perovskite solar cells (PSCs). Here, we report the fabrication of highly reproducible, efficient, and stable PSCs via interface engineering with CoO nanoplates. When a suitable concentration of CoO nanoplates solution is spin-coated on perovskite film, a discontinuous CoO nanoplates modified layer is obtained, which is advantageous to achieving highly photovoltaic performance of the device because the uncovered perovskite crystalline grains can guarantee the unobstructed transport of holes from perovskite layers to hole transport layers. Furthermore, the hydrophobic oleylamine ligands capped CoO nanoplates are well filled in the boundaries of perovskite crystalline grains to effectively passivate the trap states, suppress dark recombination, and enhance moisture-resistance. These benefits are propitious to achieving a 20.72% champion efficiency and a 20.20% steady-state efficiency of the devices with good reproducibility and stability.

The Dawn of Lead-Free Perovskite Solar Cell: Highly Stable Double Perovskite Cs2AgBiBr6 Film.

Recently, lead-free double perovskites have emerged as a promising environmentally friendly photovoltaic material for their intrinsic thermodynamic stability, appropriate bandgaps, small carrier effective masses, and low exciton binding energies. However, currently no solar cell based on these double perovskites has been reported, due to the challenge in film processing. Herein, a first lead-free double perovskite planar heterojunction solar cell with a high quality Cs2AgBiBr6 film, fabricated by low-pressure assisted solution processing under ambient conditions, is reported. The device presents a best power conversion efficiency of 1.44%. The preliminary efficiency and the high stability under ambient condition without encapsulation, together with the high film quality with simple processing, demonstrate promise for lead-free perovskite solar cells.

Mixed-Organic-Cation Tin Iodide for Lead-Free Perovskite Solar Cells with an Efficiency of 8.12.

In this work, a fully tin-based, mixed-organic-cation perovskite absorber (FA) x (MA)1-x SnI3 (FA = NH2CH = NH2+, MA = CH3NH3+) for lead-free perovskite solar cells (PSCs) with inverted structure is presented. By optimizing the ratio of FA and MA cations, a maximum power conversion efficiency of 8.12% is achieved for the (FA)0.75(MA)0.25SnI3-based device along with a high open-circuit voltage of 0.61 V, which originates from improved perovskite film morphology and inhibits recombination process in the device. The cation-mixing approach proves to be a facile method for the efficiency enhancement of tin-based PSCs.

High Crystallization of Perovskite Film by a Fast Electric Current Annealing Process.

High-efficiency organic-inorganic hybrid perovskite solar cells have experienced rapid development and attracted significant attention in recent years. Crystal growth as an important factor would significantly influence the quality of perovskite films and ultimately the device performance, which usually requires thermal annealing for 10 min or more. Herein, we demonstrate a new method to get high crystallization of perovskite film by electric current annealing for just 5 s. In contrast to conventional thermal annealing, a homogeneous perovskite film was formed with larger grains and fewer pinholes, leading to a better performance of the device with higher open-circuit voltage and fill factor. An average power conversion efficiency of 17.02% with electric current annealing was obtained, which is higher than that of devices with a conventional thermal annealing process (16.05%). This facile electric current annealing process with less energy loss and time consumption shows great potential in the industrial mass production of photovoltaic devices.