The emergence of wearable electronics and optoelectronics requires the development of devices that are not only highly flexible but can also be woven into textiles to offer a truly integrated solution. Here, we report a colour-tunable, weavable fibre-shaped polymer light-emitting electrochemical cell (PLEC). The fibre-shaped PLEC is fabricated using all-solutionbased processes that can be scaled up for practical applications. The design has a coaxial structure comprising a modified metal wire cathode and a conducting aligned carbon nanotube sheet anode, with an electroluminescent polymer layer sandwiched between them. The fibre shape offers unique and promising advantages. For example, the luminance is independent of viewing angle, the fibre-shaped PLEC can provide a variety of different and tunable colours, it is lightweight, flexible and wearable, and it can potentially be woven into light-emitting clothes for the creation of smart fabrics. L ight-emitting electrochemical cells 1-6 , in particular polymer light-emitting electrochemical cells (PLECs), have been widely studied for various applications, including flexible flat panel displays, signage and lighting 4-6 . Like organic light-emitting diodes (OLEDs) and polymer light-emitting diodes (PLEDs), PLECs have a structure that is usually composed of two metal electrodes connected to an organic semiconductor. However, PLECs differ in that mobile ions are incorporated into the organic semiconductor, thereby offering promising advantages such as low operating voltage, high electron/photon conversion efficiency and high power efficiency compared with OLEDs 7-18 . More importantly, PLECs do not require the use of low-workfunction cathodes composed of calcium or magnesium (which are sensitive in air). In contrast, PLEDs require a low-workfunction cathode and high-workfunction anode to realize efficient charge injection 19-21 . In a typical PLEC, the electroluminescent polymer layer forms an in situ light-emitting p-i-n junction for the injection of both electrons and holes from the electrodes 4,5,22 . This means that PLECs can be effectively operated with relatively rougher surfaces than is generally possible with OLEDs and PLEDs, which is advantageous when scaling them up for practical applications with low cost and high efficiency 23-25 .Based on these described advantages, the PLEC is particularly promising for use in portable and wearable electronics, which are being developed for a wide range of applications, from microelectronics to biomedicine, transport and areospace 26-32 . Conventional planar light-emitting devices, including both rigid and flexible films, cannot satisfy the basic requirements for such an application, including softness, light weight and weavability 33,34 . To this end, advances in the textile industry have suggested a useful direction in which to pursue a solution: if a PLEC is made into a continuous fibre using a melting or all-solution-based process, it can be woven into various flexible textiles or integrated into soft substrates for u...

Oxygenic photosynthetic organisms perform solar energy conversion of water and CO2 to O2 and sugar at a broad range of wavelengths and light intensities. These cells also metabolize sugars using a respiratory system that functionally overlaps the photosynthetic apparatus. In this study, we describe the harvesting of photocurrent used for hydrogen production from live cyanobacteria. A non-harmful gentle physical treatment of the cyanobacterial cells enables light-driven electron transfer by an endogenous mediator to a graphite electrode in a bio-photoelectrochemical cell, without the addition of sacrificial electron donors or acceptors. We show that the photocurrent is derived from photosystem I and that the electrons originate from carbohydrates digested by the respiratory system. Finally, the current is utilized for hydrogen evolution on the cathode at a bias of 0.65 V. Taken together, we present a bio-photoelectrochemical system where live cyanobacteria produce stable photocurrent that can generate hydrogen.

Photosystem 1 (PS1) triggers the most energetic light-induced charge-separation step in nature and the in vivo electron-transfer rates approach 50 e(-)  s(-1)  PS1(-1). Photoelectrochemical devices based on this building block have to date underperformed with respect to their semiconductor counterparts or to natural photosynthesis in terms of electron-transfer rates. We present a rational design of a redox hydrogel film to contact PS1 to an electrode for photocurrent generation. We exploit the pH-dependent properties of a poly(vinyl)imidazole Os(bispyridine)2Cl polymer to tune the redox hydrogel film for maximum electron-transfer rates under optimal conditions for PS1 activity. The PS1-containing redox hydrogel film displays electron-transfer rates of up to 335±14 e(-)  s(-1)  PS1(-1), which considerably exceeds the rates observed in natural photosynthesis or in other semiartificial systems. Under O2 supersaturation, photocurrents of 322±19 μA cm(-2) were achieved. The photocurrents are only limited by mass transport of the terminal electron acceptor (O2). This implies that even higher electron-transfer rates may be achieved with PS1-based systems in general.

An oriented photosystem I monolayer with minimised short-circuiting provides anisotropic electron flow, further coupling to a hydrogenase for realising light-induced H2 evolution.

A spun carbon nanotube fiber functions as a torsional actuator in almost all available environmental media such as air, water, organic solvents, and electrolyte solutions. The Ampere's Law among helically aligned carbon nanotubes explains the simultaneous occurrence of lengthwise contraction and rotary torsion upon applying a low current. The produced stress is over 100 times that of the strongest natural skeletal muscle with high reversibility and good stability. The use of torsional fibers for electric motors is demonstrated.