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Abstract The engineering of atomically-precise nanopores in two-dimensional materials presents exciting opportunities for both fundamental science studies as well as applications in energy, DNA sequencing, and quantum information technologies. The exceptional chemical and thermal stability of hexagonal boron nitride (h-BN) suggest that exposed h-BN nanopores will retain their atomic structure even when subjected to extended periods of time in gas or liquid environments. Here we employ transmission electron microscopy to examine the time evolution of h-BN nanopores in vacuum and in air and find, even at room temperature, dramatic geometry changes due to atom motion and edge contamination adsorption, for timescales ranging from one hour to one week. The discovery of nanopore evolution contrasts with general expectations and has profound implications for nanopore applications of two-dimensional materials.

In order to improve the performance of the active vibration isolation system (AVIS) with electromagnetic actuator, several problems of vibration control are studied. Position control is a critical component in suspension systems, and the position sensor noise can extremely affect the stability of the system, so a tracking differentiator (TD) is proposed to obtain effective differential signal from relative position sensor. In vibration control, the feedback of acceleration combined with PD position feedback is presented to suppress transmission of periodic vibrations. Then, taking the acceleration transmission as the evaluation index, the acceleration transmission under the presented control method is derived, and the influence of control parameters on vibration isolation performance is discussed in detail. The vibration isolation performance is improved from 24.47 dB to 2.4 dB at resonance frequency, and −34 dB attenuation is achieved at 100 Hz with respect to vibration isolation mount system tested on the ground. The experimental results demonstrate that the performance of active vibration isolation system are improved by the proposed acceleration feedback control.

Hydrogen represents an ideal fuel with environmental‐friendly properties and high energy density. It is attractive to directly produce clean hydrogen from inexhaustible solar energy and the most abundant seawater on the earth. Nevertheless, the search for highly efficient and stable photocatalysts remains a big challenge so far because of the dissolved salts in natural seawater, which may result in the decomposition of photocatalysts and undesirable side reactions. Herein, three polyfluorene‐based conjugated polyelectrolytes (CPEs) with different grafted groups in the polymer backbone for hydrogen production in natural seawater under solar light illumination are reported. The change in the grafted groups on the main chain of CPEs provides them very similar UV light absorption, but PFNH‐Br grafted with H group exhibits significantly improved charge transport and lower emission intensity compared with PFN‐Br (grafted with C8H17) and PFPABr (grafted with CH2CH2N(CH3)3Br). As a result, PFNH‐Br yield the highest hydrogen evolution rate (HER) of 1806 μmol h−1 g−1 without external cocatalysts under simulated solar light, while lower HERs of 356 and 225 μmol h−1 g−1 are found for PFN‐Br and PFPABr, respectively. This study shows that grafted group optimization is a powerful strategy to maximize the activity of polyfluorene‐based CPEs for direct photocatalytic seawater splitting.

In comparison to metal complexes, organic photosensitive dyes employed in photocatalytic hydrogen production exhibit promising developmental prospects. Utilizing the organic dye molecule TA+0 as the foundational structure, a series of innovative organic dyes, denoted as TA1-1 to TA2-6, were systematically designed. Employing first-principles calculations, we methodically explored the modifying effects of diverse electron-donating groups on the R1 and R2 positions to assess their application potential. Our findings reveal that, relative to the experimentally synthesized TATA+03, the TA2-6 molecule boasts a spatial structure conducive to intramolecular electron transfer, showcasing the most negative reduction potential (Ered = -2.11 eV) and the maximum reaction driving force (ΔG02 = -1.26 eV). This configuration enhances its compatibility with the reduction catalyst, thereby facilitating efficient hydrogen evolution. The TA2-6 dye demonstrates outstanding photophysical properties and a robust solar energy capture capacity. Its maximum molar extinction coefficient (ε) stands at 2.616 x 104 M-1·cm-1, representing a remarkable 292.8% improvement over TATA+03. In conclusion, this research underscores the promising potential of the TA2-6 dye as an innovative organic photosensitizer, positioning it as an efficacious component in homogeneous photocatalytic systems. [ABSTRACT FROM AUTHOR]