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Abstract Colloidal Ag(In,Ga)S2 nanocrystals (AIGS NCs) with the band gap tunability by their size and composition within visible range have garnered surging interest. High absorption cross-section and narrow emission linewidth of AIGS NCs make them ideally suited to address the challenges of Cd-free NCs in wide-ranging photonic applications. However, AIGS NCs have shown relatively underwhelming photoluminescence quantum yield (PL QY) to date, primarily because coherent heteroepitaxy has not been realized. Here, we report the heteroepitaxy for AIGS-AgGaS2 (AIGS-AGS) core-shell NCs bearing near-unity PL QYs in almost full visible range (460 to 620 nm) and enhanced photochemical stability. Key to the successful growth of AIGS-AGS NCs is the use of the Ag-S-Ga(OA)2 complex, which complements the reactivities among cations for both homogeneous AIGS cores in various compositions and uniform AGS shell growth. The heteroepitaxy between AIGS and AGS results in the Type I heterojunction that effectively confines charge carriers within the emissive core without optically active interfacial defects. AIGS-AGS NCs show higher extinction coefficient and narrower spectral linewidth compared to state-of-the-art heavy metal-free NCs, prompting their immediate use in practicable applications including displays and luminescent solar concentrators (LSCs).

Dissimilar surface and interfacial energies of the two blocks in BCP thin films favour parallel orientations, whereas a perpendicular orientation is essential for directed self-assembly. Here, the authors demonstrate perpendicular microdomain orientations by filtered plasma treatment of the surface of the BCP film.

Colloidal semiconductor nanocrystals, referred to as quantum dots (QDs), have unique and superb photophysical properties, promising a variety of applications ranging from optoelectronics and energy harvesting to agriculture. The last decade witnessed a tremendous advance in QDs and their successful debut in displays, and now, QDs are equipped with environmental benignity to expand their territory to everyday life. From this perspective, the current research status and future perspective of environmentally benign QDs as building blocks for light-generating and light-harvesting applications are provided. Also provided is an overview of the progress made in the chemistry (colloidal synthesis, surface chemistry, and heterostructuring) and in their photophysical and electrical properties from the viewpoint of their use in light-emitting or light-harvesting applications. Grounded on the current status of heavy-metal-free QDs compared with cutting-edge technologies, the perspective of environmentally benign QDs for practical use and future research directions is discussed.

Abstract Recent research has built a consensus that the binder plays a key role in the performance of high‐capacity silicon anodes in lithium‐ion batteries. These anodes necessitate the use of a binder to maintain the electrode integrity during the immense volume change of silicon during cycling. Here, Zn2+–imidazole coordination crosslinks that are formed to carboxymethyl cellulose backbones in situ during electrode fabrication are reported. The recoverable nature of Zn2+–imidazole coordination bonds and the flexibility of the poly(ethylene glycol) chains are jointly responsible for the high elasticity of the binder network. The high elasticity tightens interparticle contacts and sustains the electrode integrity, both of which are beneficial for long‐term cyclability. These electrodes, with their commercial levels of areal capacities, exhibit superior cycle life in full‐cells paired with LiNi0.8Co0.15Al0.05O2 cathodes. The present study underlines the importance of highly reversible metal ion‐ligand coordination chemistries for binders intended for high capacity alloying‐based electrodes.

Quasi-type II heterostructured nanocrystals (NCs) have been of particular interest due to their great potential for controlling the interplay of charge carriers. However, the lack of material choices for quasi-type II NCs restricts the accessible emission wavelength from red to near-infrared (NIR), which hinders their use in light-emitting applications that demand a wide range of visible colors. Herein, we demonstrate a new class of quasi-type II nanoemitters formulated in ZnSe/ZnSe1-XTeX/ZnSe seed/spherical quantum well/shell heterostructures (SQWs) whose emission wavelength ranges from blue to orange. In a given geometry, ZnSe1-XTeX emissive layers grown between the ZnSe seed and the shell layer are strained to fit into the surrounding media, and thus, the lattice mismatch between ZnSe1-XTeX and ZnSe is effectively alleviated. In addition, composition of the ZnSe1-XTeX emissive layer and the dimension of the ZnSe shell layer are engineered to tailor the distribution and energy of electron and hole wave functions. Benefitting from the capabilities to tune the charge carriers on demand and to form defect-free heterojunctions, ZnSe/ZnSe1-XTeX/ZnSe/ZnS NCs show near-unity photoluminescence quantum yield (PL QY>90%) in a broad range of emission wavelengths (peak PL from 450 nm to 600 nm). Finally, we exemplify dichromatic white NC-based light-emitting diodes (NC-LEDs) employing the mixed layer of blue- and yellow-emitting ZnSe/ZnSe1-XTeX/ZnSe/ZnS SQW NCs.