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Direct methane conversion (DMC) to oxygenates at low temperature is of great value but remains challenging due to the high energy barrier for C−H bond activation. Here, we report that in situ decoration of Pd1‐ZSM‐5 single atom catalyst (SAC) by CO molecules significantly promoted the DMC reaction, giving the highest turnover frequency of 207 h−1 ever reported at room temperature and ~100 % oxygenates selectivity with H2O2 as oxidant. Combined characterizations and DFT calculations illustrate that the C‐atom of CO prefers to coordinate with Pd1, which donates electrons to the Pd1−O active center (L−Pd1−O, L=CO) generated by H2O2 oxidation. The correspondingly improved electron density over Pd−O pair renders a favorable heterolytic dissociation of C−H bond with low energy barrier of 0.48 eV. Applying CO decoration strategy to M1‐ZSM‐5 (M=Pd, Rh, Ru, Fe) enables improvement of oxygenates productivity by 3.2–11.3 times, highlighting the generalizability of this method in tuning metal‐oxo electronic structure of SACs for efficient DMC process. [ABSTRACT FROM AUTHOR]

The responses of magnetic moments to external stimuli such as magnetic-field, heat, light and electric-field have been utilized to manipulate the magnetism in magnetic semiconductors, with many of the novel ideas applied even to ferromagnetic metals. Here, we review a new experimental development on the control of magnetism in (Ga,Mn)As thin films by surface decoration of organic molecules: Molecules deposited on the surface of (Ga,Mn)As thin films are shown to be capable of significantly modulating their saturation magnetization and Curie temperature. These phenomena are shown to originate from the carrier-mediated ferromagnetism in (Ga,Mn)As and the surface molecules acting as acceptors or donors depending on their highest occupied molecular orbitals, resembling the charge transfer mechanism in a pn junction in which the equilibrium state is reached on the alignment of Fermi levels.

Highly effective, hybrid separation materials for water purification were generated following a bioinspired system available in nature. The desert beetle was the inspiration for the generation of separation materials. Using the hydrophobic poly(vinylidene fluoride) (PVDF) membrane as the basis, the membrane was first activated and then furnished with silane-based linkers, and the covalent anchoring of chitosan was successfully accomplished. The obtained surface architecture was a copy of the desert beetle's armor possessing a hydrophobic matrix with hydrophilic domains. The modification was done in the presence or the lack of catalyst ( N , N -diisopropylethylamine) that made it possible to tune easily wettability, roughness, and material as well as adhesive features. The membrane morphology and surface chemistry were studied by applying a series of analytical techniques. As a result of chitosan attachment, substantial improvement in transport and separation was reported. Pristine PVDF was characterized by a water flux of 5.28 kg m -2 h -1 and an activation energy of 48.16 kJ mol -1 . The water flux and activation energy for a hybrid membrane with chitosan were equal to 15.55 kg m -2 h -1 and 33.98 kJ mol -1 , respectively. The hybrid materials possessed enhanced stability and water resistance that were maintained after 10 cycles of membrane distillation tests.