Two-dimensional (2D) layered transition metal dichalcogenides (TMDs) have recently emerged as a new class of atomically thin semiconductors for diverse electronic, optoelectronic, and valleytronic applications. To explore the full potential of these 2D semiconductors requires a precise control of their band gap and electronic properties, which represents a significant challenge in 2D material systems. Here we demonstrate a systematic control of the electronic properties of 2D-TMDs by creating mixed alloys of the intrinsically p-type WSe2 and intrinsically n-type WS2 with variable alloy compositions. We show that a series of WS2xSe2-2x alloy nanosheets can be synthesized with fully tunable chemical compositions and optical properties. Electrical transport studies using back-gated field effect transistors demonstrate that charge carrier types and threshold voltages of the alloy nanosheet transistors can be systematically tuned by adjusting the alloy composition. A highly p-type behavior is observed in selenium-rich alloy, which gradually shifts to lightly p-type, and then switches to lightly n-type characteristics with the increasing sulfur atomic ratio, and eventually evolves into highly n-doped semiconductors in sulfur-rich alloys. The synthesis of WS2xSe2-2x nanosheets with tunable optical and electronic properties represents a critical step toward rational design of 2D electronics with tailored spectral responses and device characteristics.

Energy devices such as rechargeable batteries, fuel cells, and solar cells are central to powering a renewable, mobile, and electrified future. To advance these devices requires a fundamental understanding of the complex chemical reactions, material transformations, and charge flow that are associated with energy-conversion processes. Analytical in situ transmission electron microscopy (TEM) offers a powerful tool for directly visualizing these complex processes at the atomic scale in real time and in operando. Recent advancements in energy materials and devices that have been enabled by in situ TEM are reviewed. Firstly, the evolutionary development of TEM nanocells from the open-cell configuration to the close-cell, and finally the full-cell, design is reviewed. Next, in situ TEM studies of rechargeable ion batteries in a practical operation environment are explored, followed by applications of TEM for in situ observation of electrocatalyst formation, evolution, and degradation in proton-exchange-membrane fuel cells, and investigations of new energy materials such as perovskites for solar cells through in situ TEM. Finally, recent advances in the use of environmental TEM and cryogenic electron microscopy in probing clean-energy materials are presented and emerging opportunities and challenges in in situ TEM research of energy materials and devices are discussed.

Recent studies have identified unique properties of organic battery electrode materials such as moderate redox potentials and mechanical softness which are uniquely beneficial for all-solid-state batteries based on ceramic electrolytes. Here, we further explore the promise of organic materials and demonstrate a sulfide electrolytebased organic-lithium battery with a specific energy of 828 Wh kg −1 , rivaling the state-ofthe-art of all-solid-state batteries. Two innovation steps are responsible for the accomplishment. First, the combination of lithium anode and the high-capacity cathode material pyrene-4,5,9,10-tetraone ensures a high theoretical specific energy. Second, the microstructure of the organic cathode is optimized with the introduction of cryomilling, a technique common to processing soft materials but not familiar to electrode fabrication. The cathode material utilization increases to 99.5% as a result, up from the 55−89% previously reported for ceramic electrolyte-based solid-state organic batteries. The improvement highlights the special requirements of solid-state organic electrodes for microstructural engineering while preserving the chemical integrity of components.