The power conversion efficiency of perovskite solar cells (PSCs) has ascended from 3.8% to 22.1% in recent years. ZnO has been well-documented as an excellent electron-transport material. However, the poor chemical compatibility between ZnO and organo-metal halide perovskite makes it highly challenging to obtain highly efficient and stable PSCs using ZnO as the electron-transport layer. It is demonstrated in this work that the surface passivation of ZnO by a thin layer of MgO and protonated ethanolamine (EA) readily makes ZnO as a very promising electron-transporting material for creating hysteresis-free, efficient, and stable PSCs. Systematic studies in this work reveal several important roles of the modification: (i) MgO inhibits the interfacial charge recombination, and thus enhances cell performance and stability; (ii) the protonated EA promotes the effective electron transport from perovskite to ZnO, further fully eliminating PSCs hysteresis; (iii) the modification makes ZnO compatible with perovskite, nicely resolving the instability of ZnO/perovskite interface. With all these findings, PSCs with the best efficiency up to 21.1% and no hysteresis are successfully fabricated. PSCs stable in air for more than 300 h are achieved when graphene is used to further encapsulate the cells.

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Surface and interfacial engineering of heterogeneous metal catalysts is effective and critical for optimizing selective hydrogenation for fine chemicals. By using thiol-treated ultrathin Pd nanosheets as a model catalyst, we demonstrate the development of stable, efficient, and selective Pd catalysts for semihydrogenation of internal alkynes. In the hydrogenation of 1-phenyl-1-propyne, the thiol-treated Pd nanosheets exhibited excellent catalytic selectivity (>97%) toward the semihydrogenation product (1-phenyl-1-propene). The catalyst was highly stable and showed no obvious decay in either activity or selectivity for over ten cycles. Systematic studies demonstrated that a unique Pd-sulfide/ thiolate interface created by the thiol treatment was crucial to the semihydrogenation. The high catalytic selectivity and activity benefited from the combined steric and electronic effects that inhibited the deeper hydrogenation of C=C bonds. More importantly, this thiol treatment strategy is applicable to creating highly active and selective practical catalysts from commercial Pd/C catalysts for semihydrogenation of internal alkynes.

Air-stable atomically thick copper nanosheets are prepared and used for selective electrochemical reduction of CO2 into CO.

Electrochemical conversion of CO into fuels using electricity generated from renewable sources helps to create an artificial carbon cycle. However, the low efficiency and poor stability hinder the practical use of most conventional electrocatalysts. In this work, a 2D hierarchical Pd/SnO structure, ultrathin Pd nanosheets partially capped by SnO nanoparticles, is designed to enable multi-electron transfer for selective electroreduction of CO into CH OH. Such a structure design not only enhances the adsorption of CO on SnO , but also weakens the binding strength of CO on Pd due to the as-built Pd-O-Sn interfaces, which is demonstrated to be critical to improve the electrocatalytic selectivity and stability of Pd catalysts. This work provides a new strategy to improve electrochemical performance of metal-based catalysts by creating metal oxide interfaces for selective electroreduction of CO .

Janus nanoparticles (JNPs) offer unique features, including the precisely controlled distribution of compositions, surface charges, dipole moments, modular and combined functionalities, which enable excellent applications that are unavailable to their symmetrical counterparts. Assemblies of NPs exhibit coupled optical, electronic and magnetic properties that are different from single NPs. Herein, we report a new class of double-layered plasmonic-magnetic vesicle assembled from Janus amphiphilic Au-Fe O NPs grafted with polymer brushes of different hydrophilicity on Au and Fe O surfaces separately. Like liposomes, the vesicle shell is composed of two layers of Au-Fe O NPs in opposite direction, and the orientation of Au or Fe O in the shell can be well controlled by exploiting the amphiphilic property of the two types of polymers.

The poor UV, thermal, and interfacial stability of perovskite solar cells (PSCs) makes it highly challenging for their technological application, and has drawn increasing attention to resolving the above issues. In nature, plants generally sustain long exposure to UV illumination without damage, which is attributed to the presence of the organic materials acting as sunscreens. Inspired by the natural phenomenon, a natural plant sunscreen, sinapoyl malate, an ester derivative of sinapic acid, is employed to modify the surface of electron transport materials (ETMs). The interfacial modification successfully resolved the UV stability and reduced the poor interfacial contact between ETM and perovskite. The best efficiency of fabricated PSCs is up to 19.6%. Furthermore, we employed a mixture of Co(II) and Co(III)-based porphyrin compounds containing the excellent Co(II)/Co(III) redox couple to substitute the commonly used hole transport material, 2,2',7,7'-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spiro-bifluorene (spiro-OMeTAD), to resolve the thermal degradation of PSCs noted at and above 80 °C that originates from ion diffusion of I and CH NH (MA ) ions from perovskite into spiro-OMeTAD. Finally, the stable PSCs with the best efficiency up to 20.5% are successfully fabricated.

Crown ether effectively stabilizes the cubic phase of CsPbI3 to inhibit the moisture invasion and phase transformation of CsPbI3 films, producing large-area devices and improving device performance.