Power conversion efficiencies (PCEs) of polymer solar cells (PSCs) have exceeded 18% in the last few years. Stability has therefore become the next most important issue before commercialization. Herein, the degradation behaviors of the inverted PM6:IT‐4F (PBDB‐T‐2F:3,9‐bis(2‐methylene‐((3‐(1,1‐dicyanomethylene)‐6,7‐difluoro)‐indanone))‐5,5,11,11‐tetrakis(4‐hexylphenyl)‐dithieno[2,3‐d:2′,3′‐d′]‐s‐indaceno[1,2‐b:5,6‐b′]dithiophene) solar cells with different ZnO layers are systematically investigated. The PCE decay rates of the cells and the photobleaching process of the IT‐4F containing organic films on ZnO surface are directly correlated with the light‐absorption ability of the ZnO layer in the visible light range, indicating that photochemical decomposition of IT‐4F is initiated by the light absorption of ZnO layer. By analyzing the products of the aged ZnO/IT‐4F films with matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry (MALDI‐TOF‐MS), it is confirmed that photochemical reactions at the IT‐4F/ZnO interface include de‐electron‐withdrawing units and dealkylation on the side‐phenyl ring. Hydroxyl radicals generated by the photo‐oxidation of dangling hydroxide by ZnO are confirmed by electron spin resonance (ESR) spectroscopy measurements, which is attributed as the main reason causing the decomposition of IT‐4F. Surface treatment of ZnO with hydroxide and/or hydroxyl radical scavenger is found to be able to improve the stability of the PSCs, which further supports the proposed degradation mechanism.

With the rapid progress of organic solar cells (OSCs), improvement in the efficiency of large‐area flexible OSCs (>1 cm2) is crucial for real applications. However, the development of the large‐area flexible OSCs severely lags behind the growth of the small‐area OSCs, with the electrical loss due to the large sheet resistance of the electrode being a main reason. Herein, a high conductive and high transparent Ag/Cu composite grid with sheet resistance <1 Ω sq−1 and an average visible light transparency of 84% is produced as the transparent conducting electrode of flexible OSCs. Based on this Ag/Cu composite grid electrode, a high efficiency of 12.26% for 1 cm2 flexible OSCs is achieved. The performances of large‐area flexible OSCs also reach 7.79% (4 cm2) and 7.35% (9 cm2), respectively, which are much higher than those of the control devices with conventional flexible indium tin oxide electrodes. Surface planarization using highly conductive PEDOT:PSS and modification of the ZnO buffer layer by zirconium acetylacetonate (ZrAcac) are two necessary steps to achieve high performance. The flexible OSCs employing Ag/Cu grid have excellent mechanical bending resistance, maintaining high performance after bending at a radius of 2 mm.

Intermolecular electron transfer between piperazine and PC61BM leading to a simultaneous performance and stability improvement.

Dedicated to Professor Baowen Zhang on the occasion of her 80th birthday. Despite the tremendous efforts in developing non-fullerene acceptor (NFA) for polymer solar cells (PSCs), only few researches are done on studying the NFA molecular structure dependent stability of PSCs, and long-term stable PSCs are only reported for the cells with low efficiency. Herein, the authors compare the stability of inverted PM6:NFA solar cells using ITIC, IT-4F, Y6, and N3 as the NFA, and a decay rate order of IT-4F > Y6 ≈ N3 > ITIC is measured. Quantum chemical calculations reveal that fluorine substitution weakens the C═C bond and enhances the interaction between NFA and ZnO, whereas the 𝜷-alkyl chains on the thiophene unit next to the C═C linker blocks the attacking of hydroxyl radicals onto the C═C bonds. Knowing this, the authors choose a bulky alkyl side chain containing molecule (named L8-BO) as the acceptor, which shows slower photo bleaching and performance decay rates. A combination of ZnO surface passivation with phenylethanethiol (PET) yields a high efficiency of 17% and an estimated long T 80 and Ts 80 of 5140 and 6170 h, respectively. The results indicate functionalization of the 𝜷-position of the thiophene unit is an effective way to improve device stability of the NFA.

Electromagnetic (EM) absorbers serving in the megahertz (MHz) band and a wide temperature range (from −50 to 150 °C) require high and temperature-stable permeability for outstanding EM absorption performance. Herein, FeCoNiCr0.4Cu X high-entropy alloy (HEA) powders with a unique nanocrystalline structure separated by a thin amorphous layer (NTA) are designed to improve permeability and enhance intergranular coupling. Simultaneously, the long-range anisotropy is introduced via devising the preparation process and tuning the chemical composition, such that the intergranular exchange interaction is further strengthened for stable permeability and EM wave absorption in a wide temperature range. FeCoNiCr0.4Cu0.2 HEAs exhibit a near-zero permeability temperature coefficient (5.7 × 10–7 °C–1) a in wide temperature range. The maximum reflection loss (RL) of FeCoNiCr0.4Cu0.2 HEAs is higher than −7 dB with 5 mm thickness at −50–150 °C, and the absorption bandwidth (RL < −7 dB) can almost cover 400–1000 MHz. Furthermore, FeCoNiCr0.4Cu0.2 HEAs also have a high Curie temperature (770 °C) and distinguished oxidation resistance. The permeability temperature dependence of FeCoNiCr0.4Cu X HEAs is investigated in-depth in light of the microstructural change induced by tuning the chemical composition, and a new inspiration is provided for the design of magnetic applications serving in wide temperature, such as transformers, sensors, and EM absorbers.

Piperazine has been recently reported as a stabilizer for polymer:fullerene solar cells that can minimize the “burn-in” degradation of the cell. In this paper, the influence of N-substituents on the stabilization effect of piperazine in P3HT:PC61BM cells was investigated. Results confirmed that only piperazine derivatives (PZs) with N–H bonds showed the stabilization effect, whereas the bis-alkyl-substituted piperazine compounds cannot improve the stability. An efficient photon-induced electron transfer (PET) process between PZ and PC61BM was only detected for the N–H-containing PZ:PC61BM blends, corresponding very well to the stabilization effect of the PZs, which indicates that the PET process between PZ and PC61BM stabilizes the cell performance, and the N–H bond plays a critical role ensuring the PET process and the consequent stabilization effect. Both 1H-NMR spectroscopy and theoretical calculations confirmed the formation of N–H···O–C and N–H···π bonds for the PC61BM:piperazine adduct, which was considered as the driving force that promotes the PET process between these two components. In addition, comparison of the calculated electron affinity energy (E A) and excitation energy (E Ex) of PC61BM with/without piperazine confirmed that piperazine doping is able to promote the electron transfer (which leads to the formation of PC61BM anions) than the energy transfer (leads to the formation of PC61BM excitons) between P3HT and PC61BM, which is beneficial for the performance and stability improvement.

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Methylglyoxal (MG) is a cytotoxic by-product of glycolysis. MG inhibits the growth of glucose-fermenting yeast cells by inhibiting glycolysis. MG does so by inducing endocytosis and degradation of the cell-surface glucose sensors Rgt2 and Snf3, which are required for glucose induction of HXT (glucose transporter) gene expression.