Semiconductors are central to the modern electronics and optics industries. Conventional semiconductive materials bear inherent limitations, especially in emerging fields such as interfacing with biological systems and bottom-up fabrication. A promising candidate for bioinspired and durable nanoscale semiconductors is the family of self-assembled nanostructures comprising short peptides. The highly ordered and directional intermolecular π-π interactions and hydrogen-bonding network allow the formation of quantum confined structures within the peptide self-assemblies, thus decreasing the band gaps of the superstructures into semiconductor regions. As a result of the diverse architectures and ease of modification of peptide self-assemblies, their semiconductivity can be readily tuned, doped, and functionalized. Therefore, this family of electroactive supramolecular materials may bridge the gap between the inorganic semiconductor world and biological systems.

Amino acids and short peptides modified with the 9-fluorenylmethyloxycarbonyl (Fmoc) group possess eminent self-assembly features and show distinct potential for applications due to the inherent hydrophobicity and aromaticity of the Fmoc moiety which can promote the association of building blocks. Given the extensive study and numerous publications in this field, it is necessary to summarize the recent progress concerning these important bio-inspired building blocks. Therefore, in this review, we explore the self-organization of this class of functional molecules from three aspects, i.e., Fmoc-modified individual amino acids, Fmoc-modified di- and tripeptides, and Fmoc-modified tetra- and pentapeptides. The relevant properties and applications related to cell cultivation, bio-templating, optical, drug delivery, catalytic, therapeutic and antibiotic properties are subsequently summarized. Finally, some existing questions impeding the development of Fmoc-modified simple biomolecules are discussed, and corresponding strategies and outlooks are suggested.

To better understand the subsurface behavior of subducting slabs and their relation to the tectonic evolution of the overriding plate, we conduct a full waveform inversion on a large data set to determine a high‐resolution seismic model, FWEA18 (Full Waveform inversion of East Asia in 2018), of the upper mantle beneath eastern Asia. FWEA18 reveals sharper, more intense high‐velocity slabs in the upper mantle under the southern Kuril, Japan, and Ryukyu arcs, than previous studies have found. The subducting Pacific plate is imaged as a roughly 100 km thick high‐velocity slab to near 550 km depth indicating relatively little deformation. Stagnation near 600 km depth is observed over horizontal distances of 600 km or less. The Pacific plate we image accounts for roughly 25 Myr of subduction with older slab likely located in the lower mantle. The Philippine plate, subducting beneath the Ryukyu Islands, has a clear termination at about 450 km depth. This may indicate a tearing event in the past or that less Philippine Sea plate has subducted than previously thought. We found a double‐layer high‐velocity anomaly above and below 660 km under the Yellow Sea and eastern coast of North China. This may correspond to parts of the Philippine Sea plate that detached in the past and Pacific plate that have intersected at depth or a complicated behavior of the Pacific plate at that depth. Slow cylindrical anomalies cross the entire upper mantle are imaged beneath major Holocene volcanoes, which are likely upwellings associated with the edges of deep slabs that are entering the lower mantle.

Despite the impressive merits of low-cost and high-safety electrochemical energy storage for aqueous zinc ion batteries, researchers have long struggled against the unresolved issues of dendrite growth and the side reactions of zinc metal anodes. Herein, a new strategy of zinc-electrolyte interface charge engineering induced by amino acid additives is demonstrated for highly reversible zinc plating/stripping. Through electrostatic preferential absorption of positively charged arginine molecules on the surface of the zinc metal anode, a self-adaptive zinc-electrolyte interface is established for the inhibition of water adsorption/hydrogen evolution and the guidance of uniform zinc deposition. Consequently, an ultra-long stable cycling up to 2200 h at a high current density of 5 mA cm −2 is achieved under an areal capacity of 4 mAh cm −2 . Even cycled at an ultra-high current density of 10 mA cm −2 , 900 h-long stable cycling is still demonstrated, demonstrating the reliable self-adaptive feature of the zinc-electrolyte interface. This work provides a new perspective of interface charge engineering in realizing highly reversible bulk zinc anode that can prompt its practical application in aqueous rechargeable zinc batteries.