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Resolution and field-of-view often represent a fundamental tradeoff in microscopy. Atomic force microscopy (AFM), in which a cantilevered probe deflects under the influence of local forces as it scans across a substrate, is a key example of this tradeoff with high resolution imaging being largely limited to small areas. Despite the tremendous impact of AFM in fields including materials science, biology, and surface science, the limitation in imaging area has remained a key barrier to studying samples with intricate hierarchical structure. Here, we show that massively parallel AFM with >1000 probes is possible through the combination of a cantilever-free probe architecture and a scalable optical method for detecting probe–sample contact. Specifically, optically reflective conical probes on a comparatively compliant film are found to comprise a distributed optical lever that translates probe motion into an optical signal that provides sub-10 nm vertical precision. The scalability of this approach makes it well suited for imaging applications that require high resolution over large areas.

For thousands of years, carbon ink has been used as a black color pigment for writing and painting purposes. However, recent discoveries of nanocarbon materials, including fullerenes, carbon nanotubes, graphene, and their various derivative forms, together with the advances in large‐scale synthesis, are enabling a whole new generation of carbon inks that can serve as an intrinsically programmable materials platform for developing advanced functionalities far beyond color. The marriage between these multifunctional nanocarbon inks with modern printing technologies is facilitating and even transforming many applications, including flexible electronics, wearable and implantable sensors, actuators, and autonomous robotics. This review examines recent progress in the reborn field of carbon inks, highlighting their programmability and multifunctionality for applications in flexible electronics and stimuli‐responsive devices. Current challenges and opportunities will also be discussed from a materials science perspective towards the advancement of carbon ink for new applications beyond color.

Organic color‐centers (OCCs) have emerged as promising single‐photon emitters for solid‐state quantum technologies, chemically specific sensing, and near‐infrared bioimaging. However, these quantum light sources are currently synthesized in bulk solution, lacking the spatial control required for on‐chip integration. The ability to pattern OCCs on solid substrates with high spatial precision and molecularly defined structure is essential to interface electronics and advance their quantum applications. Herein, a lithographic generation of OCCs on solid‐state semiconducting single‐walled carbon nanotube films at spatially defined locations is presented. By using light‐driven diazoether chemistry, it is possible to directly patternp‐nitroaryl OCCs, which demonstrate chemically specific spectral signatures at programmed positions as confirmed by Raman mapping and hyperspectral photoluminescence imaging. This light‐driven technique enables the fabrication of OCC arrays on solid films that fluoresce in the shortwave infrared and presents an important step toward the direct writing of quantum emitters and other functionalities at the molecular level.

Incorporating photonic crystals with nanoplasmonic building blocks gives rise to novel optoelectronic properties that promise designing advanced multifunctional materials and electronics. Herein, the free‐standing chiral plasmonic composite films are designed by coassembling anisotropic plasmonic gold nanorods (GNRs) and rod‐like cellulose nanocrystals (CNCs). The effects of surface charge and concentration of the GNRs on the structure and optical properties of the CNC/GNR films are examined within this study. The CNC/GNR hybrid films retain the photonic characteristic of the CNCs host while concomitantly possessing the plasmonic resonance of GNRs. The negatively charged GNRs distribute uniformly in the layered CNCs host, inducing strong electrostatic repulsion among the CNCs and thus promoting the formation of a larger helical pitch than the case without GNRs. The positively charged GNRs decrease the chiroptical activity in the composite films with increasing the concentration of GNR, which is confirmed by the circular dichroism spectra. Notably, the surface plasmon resonances of GNRs enhance the fluorescence emission, which has been demonstrated by surface‐enhanced fluorescence signals in this work. This study sheds light on fabricating functional chiral plasmonic composite films with enhanced chiral plasmonics by utilizing CNCs as a dynamic chiral nematic template and adjusting surface charges.