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As Geordie Rose was to QC; Jim Al-Khalili is to Quantum Biology. QC and QB will together make a new advance quantum tech world complete as both are needed to advance both the foundation(infrastructure) and the products and services we love and rely on.


What is quantum biology? Philip Ball explains how strange quantum effects take place in the messy world of biology, and how these are behind familiar biological phenomena such as smell, enzymes and bird’s migration.
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In this guest curated event on quantum biology, Jim Al-Khalili invited Philip Ball to introduce how the mysteries of quantum theory might manifest themselves at the biological level. Here he explains how the baffling yet powerful theory of the baffling yet powerful theory of the subatomic world might play an important role in biological processes.

Bohr’s atomic model was utterly revolutionary when it was presented in 1913 but, although it is still taught in schools, it became obsolete decades ago. However, its creator also developed a much wider-ranging and less known quantum theory, the principles of which changed over time. Researchers at the University of Barcelona have now analysed the development in the Danish physicist’s thought — a real example of how scientific theories are shaped.

Most schools still teach the atomic model, in which electrons orbit around the nucleus like the planets do around the sun. The model was proposed more than a century ago by Danish physicist Niels Bohr based on Rutherford’s first model, the principles of classical mechanics and emerging ideas about ‘quantisation’ (equations to apply initial quantum hypotheses to classical physical systems) advanced by Max Planck and Albert Einstein.

As Blai Pié i Valls, a physicist at the University of Barcelona, explains: “Bohr published his model in 1913 and, although it was revolutionary, it was a proposal that did little to explain highly varied experimental results, so between 1918 and 1923 he established a much more wide-ranging, well-informed theory which incorporated his previous model.”

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A purely organic p–n junction is used as the luminescent center in a novel planar device that exhibits a high external quantum efficiency and an extremely low driving voltage.

In recent years, organic LEDs (OLEDs) have become a popular option for creating digital displays. These devices generally consist of three types of semiconductors (i.e., a p-type hole-transport layer, an n-type electron-transport layer, and an emission layer).1–3 The emission layer (normally capable of bipolar transport) provides a platform for carrier capture, exciton generation, and transition, and the luminescent property of an OLED mainly depends on the fluorescence behavior of single-molecule emitters. However, the incorporation of the emission layer within the structure of an OLED causes two energy barriers to be induced at the interfaces with the emission and transport layers. This means that the driving voltages for OLEDs are generally much larger than for traditional inorganic LEDs (with similarly chromatic emission). Moreover, the excitons that are generated at most purely organic emitters have a strong binding energy.

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Nice report published in Jan on.


The mechanism of selectivity in ion channels is still an open question in biology for more than half a century. Here, we suggest that quantum interference can be a solution to explain the selectivity mechanism in ion channels since interference happens between similar ions through the same size of ion channels. In this paper, we simulate two neighboring ion channels on a cell membrane with the famous double-slit experiment in physics to investigate whether there is any possibility of matter-wave interference of ions via movement through ion channels. Our obtained decoherence timescales indicate that the quantum states of ions can only survive for short times, i.e. ≈100 picoseconds in each channel and ≈17–53 picoseconds outside the channels, giving the result that the quantum interference of ions seems unlikely due to environmental decoherence. However, we discuss our results and raise few points, which increase the possibility of interference.

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Photoswitchable molecules are able to isomerize between two metastable forms through light stimuli. Originally being studied by photochemists, this type of molecule has now found a wide range of applications within physics, chemistry and biology. The extensive usage of photochromic molecules is due to the two isomers having fundamentally different physical and chemical properties. The most important attribute of a photoswitch is the photoisomerization quantum yield, which defines the efficiency of the photoisomerization event. Here we show how to determine the photoisomerization quantum yield in the solid state and in solution when taking thermal processes into account. The described method together with provided software allows for rapid and accurate determination of the isomerization process for this important class of molecules.

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