摘要：Sub-1 nm nanowires(SNWs) can not only be processed like polymers due to their polymer-analogue properties but also show multifunctions owing to their well-manipulated compositions and structures. Rationally designed and engineered multicomponent heterostructure SNWs can further enhance their multifunction performance while it is very challenging to achieve such SNWs at ***, we synthesized Bi_(2)O_(3)-polyoxometalate heterostructure SNWs(PMB SNWs), and fabricated super-aligned PMB SNWs films(S-PMB SNWs films), which can serve as interlayers to efficiently suppress lithium polysulfide(LPS)shuttling, intrinsically promote the redox kinetics of the LPS conversion and substantially protect the Li anode. The lithium-sulfur(Li-S) battery with the S-PMB SNWs film as the interlayer showcases an ultralow capacity decay rate with 0.013% per cycle over 850 cycles. This study demonstrates the potential of heterostructure SNWs to improve the performance of Li-S batteries.

摘要：In this work we used CdS NWs(nanowires)with vanadium carbide(VC)attached via facile electrostatic self‐assembly and calcination *** results showed that compared to pristine CdS NWs,the photocatalytic activity of CdS NWs loaded with the particular amount of VC was dramatically *** them,the VC/CS‐15 indicated the highest enhancement for simultaneous production of H2 with selective oxidation of benzyl alcohol(BO)into benzaldehyde(BD).The highest hydrogen evolution rate of 20.5 mmol g^(-1)h^(-1)was obtained with more than 99%selectivity for BD production under visible light(λ˃420 nm)irradiation for 2 h,which was almost 661 times higher than the pristine CdS *** enhancement of photocatalytic activity is due to the VC,which provides a favorable attraction for BO by lowering the zeta potential,along with the active site for hydrogen production,and retard the recombination of electron‐hole pairs by increasing the conductivity of the ***,the apparent quantum efficiency(AQE)of VC/CS‐15 for BD and H_(2)production at monochromatic 420 nm is about 7.5%.At the end of the hydrogen evolution test,the selective oxidation with more than 99%selectivity was *** hopes this work will prove its future significance and move scientific community toward a more economical way for achieving the commercialization of H_(2) by photocatalysis.

摘要：To optimize the electronic structure of photocatalyst,a facile one‐step approach is developed for the simultaneous realization of Zn‐doping and surface oxygen vacancies(SOVs)formation on SnO_(2).The Zn‐doped SnO_(2)with abundant SOVs exhibits efficient and stable performance for photocatalytic degradation of toluene under both low and high relative *** and theoretical calculations results show that the synergistic effects of Zn‐doping and SOVs on SnO_(2)can considerably boost the charge transfer and separation *** the in situ DRIFTS and theoretical calculations methods,it is revealed that the benzene ring of toluene is opened at benzoic acid on the SnO_(2)surface and selectively at benzaldehyde on the Zn‐doped SnO_(2)*** implies that Zn‐doped SnO_(2)photocatalysts shorten the pathway of toluene degradation,and toxic intermediates can be significantly *** work could provide a promising and sustainable route for safe and efficient removal of aromatic VOCs with photocatalytic technology.