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International Journal of Bioprinting                             Bacteriorhodopsin-embedded hydrogel device
























            Figure 3. Photoelectric response of bacteriorhodopsin (br)-embedded hydrogel construct. (A) The composite square-differential photoelectrical response
            of hydrogel construct containing br. A constant photocurrent and a differential response were observed when the construct was illuminated by white LED
            with a wavelength span of 420–700 nm. (B) The square-wave photoelectric response of a hydrogel construct containing no br. The square-wave response
            originated from the indium tin oxide (ITO) glass substrate under the illumination of white LED. (C) The pure differential photoelectrical response of the
            br-embedded hydrogel construct under pulsing light with 1 Hz frequency from a 543 nm laser. No square-wave photoelectrical response was observed.


            wave response of ITO glass due to the heating effect of   nearly all br molecules contribute to the photoelectric
            its blue light component. To validate this hypothesis, a   response as they are all attached to the working electrode.
            543 nm green laser, containing no blue light component   Additionally,  in  the  br-embedded  hydrogel,  protonation
            and  having significantly  less  heat  effect,  was  utilized  for   and deprotonation occur within the hydrogel environment,
            the photoelectrical characterization, and pure differential   while in a br film-based photovoltaic cell, these processes
            photoelectrical response was observed (Figure 3C). These   take place in the liquid aqueous environment. Since proton
            results  explained  the  composite  photoelectrical  response   mobility is restricted in the hydrogel matrix, this could also
            of the br-embedded hydrogel construct immobilized on   lead to a reduction in the photocurrent of br-embedded
            the ITO glass substrate under the illumination of a white   hydrogel. Consequently, the photocurrent generated by the
            LED light source. Therefore, the 543 nm green laser light   br-embedded hydrogel in a three-electrode photovoltaic
            source was used in the pattern recognition experiment as it   setup is notably lower than the photocurrent produced by
            introduces no observable artifacts.
                                                               the br film under the same light intensity.
               The differential response, which refers to the response
            of the material to changes in light intensity rather than the   In addition to the amperometric i-t mode, linear sweep
            light itself, is a critical characteristic of the photoelectrical   voltammetry and open circuit potential-time mode were
            response of br. This phenomenon is commonly observed   employed to further characterize the photoelectrochemical
            in devices incorporating br films as photosensitive   properties of the br-embedded hydrogel. In the linear
            elements. 21,26,55,67  When br is immobilized as thin films   sweep voltammetry test, a 5 Hz pulsing laser served as the
            on an electrode, exposure to light leads to the transfer of   light source, and data was recorded both with and without
            protons to the electrode, resulting in the generation of a   illumination. The difference between the two linear sweep
            potential difference between the electrodes. This potential   voltammetry curves is illustrated in Figure 4A, displaying
            difference gradually diminishes as it drives the electron   an alternating photocurrent under illumination. The open
            movement, thereby causing the differential response.  The   circuit potential-time analysis (Figure  4B) displayed a
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            photovoltaic mechanism of the br molecule in the hydrogel   differential response pattern similar to the photocurrent
            is thus very similar, if not identical, to that of the br molecule   curve in Figure 3A, where an initial upward peak was noted
            in a solid film, where the br molecule facilitates proton   at the onset of illumination, followed by a subsequent
            transfer between the working electrode and the electrolyte.   downward peak after the illumination period.
            Nevertheless, there  are several  distinctions  between  br-
            embedded hydrogel and br films. For instance, in a three-  The relationship between light intensity and the
            electrode photovoltaic cell configuration in this study, the   amplitude of photocurrent is illustrated in Figure 4C. The
            br molecules embedded in the hydrogel can only produce   photocurrent increased as the light intensity increased,
            detectable photocurrent when they are closely attached to   and a linear correlation was observed as presented in the
            the working electrode, whereas in a br film-based device,   following equation:


            Volume 10 Issue 6 (2024)                       522                                doi: 10.36922/ijb.4454
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