Collagen films with proton conduction are a candidate of next generation of fuel-cell electrolyte. To clarify a relation between proton conductivity and formation of water networks in the collagen film originating from a tilapia’s scale, we systematically measured the ac conductivity, infrared absorption spectrum, and weight change as a function of relative humidity (RH) at room temperature. The integrated absorbance concerning an O–H stretching mode of water molecules increases above 60% RH in accordance with the weight change. The dc conductivity varies in the vicinity of 60 and 83% RH. From those results, we have determined the dc conductivity vs. hydration number (N) per unit (Gly-X-Y). The proton conduction is negligible in the collagen molecule itself, but dominated by the hydration shell, the development of which is characterized with three regions. For 0 < N < 2, the conductivity is extremely small, because the water molecule in the primary hydration shell has a little hydrogen bonded with each other. For 2 < N < 4, a quasi-one-dimensional proton conduction occurs through intra-water bridges in the helix. For 4 < N, the water molecule fills the helix, and inter-water bridges are formed in between the adjacent helices, so that a proton-conducting network is extended three dimensional.

Electrical conductivity, DTA (differential thermal analysis) and NMR measurements have been performed on the KHSO₄ crystal. The results of DTA indicates that the KHSO₄ crystal shows thermal anomalies at T c ₂ = 393 K and T c ₁ = 451 K. It is observed that electrical conductivity increases steeply above T c ₂ . Especially, the motion of proton in each phase was investigated by the NMR measurements. It is also found that the NMR absorption lines above T c ₁ become narrow, although the NMR absorption line at 77 K is broad. it is expected that all protons in the crystal move rapidly above T c ₁ . Moreover electrical conductivity is 10⁻¹ S/cm above T c ₁ . These results indicate that the KHSO₄ crystal becomes super-ionic conductor above T c ₁ .

In pure pentacene film and iodine doped pentacene film, X-ray and electric conductivity measurements were performed. It was found from X-ray diffraction data that the iodine doped pentacene possess the stage-2 structure in addition to the stage-1 structure. The c axis lattice constant of the stage-2 structure, which is the length of the interval between the layers, was determined to be 33.2 Å. Moreover, electric conductivity was measured in pentacene doped with iodine at the various doping temperatures T _d. This result was compared with the results obtained from X-ray diffraction data.

Biomaterials attract a lot of attention as next-generation materials. Especially in the energy field, fuel cells based on biomaterials can further develop clean next-generation energy and are focused on with great interest. In this study, solid-state hydrogen fuel (PSII–chitin composite) composed of the photosystem II (PSII) and hydrated chitin composite was successfully created. Moreover, a biofuel cell consisting of the electrolyte of chitin and the hydrogen fuel using the PSII–chitin composite was fabricated, and its characteristic feature was investigated. We found that proton conductivity in the PSII–chitin composite increases by light irradiation. This result indicates that protons generate in the PSII–chitin composite by light irradiation. It was also found that the biofuel cell using the PSII–chitin composite hydrogen fuel and the chitin electrolyte exhibits the maximum power density of 0.19 mW/cm². In addition, this biofuel cell can drive an LED lamp. These results indicate that the solid-state biofuel cell based on the bioelectrolyte “chitin” and biofuel “the PSII–chitin composite” can be realized. This novel solid-state fuel cell will be helpful to the fabrication of next-generation energy.

Recently, it was reported that chitin and chitosan exhibited high-proton conductivity and function as an electrolyte in fuel cells. In particular, it is noteworthy that proton conductivity in the hydrated chitin becomes 30 times higher than that in the hydrated chitosan. Since higher proton conductivity is necessary for the fuel cell electrolyte, it is significantly important to clarify the key factor for the realization of higher proton conduction from a microscopic viewpoint for the future development of fuel cells. Therefore, we have measured proton dynamics in the hydrated chitin using quasi-elastic neutron scattering (QENS) from the microscopic viewpoint and compared the proton conduction mechanism between hydrated chitin and chitosan. QENS results exhibited that a part of hydrogen atoms and hydration water in chitin are mobile even at 238 K, and the mobile hydrogen atoms and their diffusion increase with increasing temperature. It was found that the diffusion constant of mobile protons is two times larger and that the residence time is two times faster in chitin than that in chitosan. In addition, it is revealed from the experimental results that the transition process of dissociable hydrogen atoms between chitin and chitosan is different. To realize proton conduction in the hydrated chitosan, the hydrogen atoms of the hydronium ions (H₃O⁺) should be transferred to another hydration water. By contrast, in hydrated chitin, the hydrogen atoms can transfer directly to the proton acceptors of neighboring chitin. It is deduced that higher proton conductivity in the hydrated chitin compared with that in the hydrated chitosan is yielded by the difference of diffusion constant and the residence time by hydrogen-atom dynamics and the location and number of proton acceptors.

Energies based on biomaterials attract a lot of interest as next-generation energy because biomaterials are environmentally friendly materials and abundant in nature. Fuel cells are also known as the clean and important next-generation source of energy. In the present study, to develop the fuel cell based on biomaterials, a novel biofuel cell, which consists of collagen electrolyte and the hydrogen fuel generated from photochemical system II (PSII) in photosynthesis, has been fabricated, and its property has been investigated. It was found that the PSII solution, in which PSII was extracted from the thylakoid membrane using a surfactant, generates hydrogen by the irradiation of light. The typical hydrogen-generating rate is approximately 7.41 × 10¹⁴ molecules/s for the light intensity of 0.5 mW/cm² for the PSII solution of 5 mL. The biofuel cell using the PSII solution as the fuel exhibited approximately 0.12 mW/cm². This result indicates that the fuel cell using the collagen electrolyte and the hydrogen fuel generated from PSII solution becomes the new type of biofuel cell and will lead to the development of the next-generation energy.