RESUMEN
The artificial photosynthesis technology known as the Honda-Fujishima effect, which produces oxygen and hydrogen or organic energy from sunlight, water, and carbon dioxide, is an effective energy and environmental technology. The key component for the higher efficiency of this reaction system is the anode electrode, generally composed of a photocatalyst formed on a glass substrate from electrically conductive fluorine-doped tin oxide (FTO). To obtain a highly efficient electrode, a dense film composed of a nanoparticulate visible light responsive photocatalyst that usually has a complicated multi-element composition needs to be deposited and adhered onto the FTO. In this study, we discovered a method for controlling the electronic structure of a film by controlling the aerosol-type nanoparticle deposition (NPD) condition and thereby forming films of materials with a band gap smaller than that of the prepared raw material powder, and we succeeded in extracting a higher current from the anode electrode. As a result, we confirmed that a current approximately 100 times larger than those produced by conventional processes could be obtained using the same material. This effect can be expected not only from the materials discussed (GaN-ZnO) in this paper but also from any photocatalyst, particularly materials of solid solution compositions.
RESUMEN
A series of quasi-one-dimensional halogen-bridged Ni(III) complexes, [Ni(chxn)(2)X]Y(2) (chxn = 1R,2R-diaminocyclohexane; X = Cl, Br, and mixed halides; Y = Cl, Br, mixed halides, NO(3), BF(4), and ClO(4)) have been synthesized in order to investigate the effect of the bridging halogens and counteranions on their crystal, electronic structures, and moreover the spin density wave strengths. In the crystal structures, the [Ni(chxn)(2)] moieties are symmetrically bridged by halogen ions, forming linear-chain Ni(III)-X-Ni(III) structures. The hydrogen bonds between the aminohydrogens of chxn and the counteranions are constructed not only along the chains but also over the chains, forming the two-dimensional hydrogen-bond networks. While the Ni(III)-X-Ni(III) distances or b axes are almost constant in the compounds with the same bridging halogens, the c axes which correspond to the interchain distances in the directions of the interchain hydrogen bonds are remarkably lengthened with the increase of the ionic radius of the counterions; X < NO(3) < BF(4) < ClO(4). These compounds show the very strong antiferromagnetic interactions among spins on Ni 3d(z)2 orbitals through the superexchange mechanisms via the bridging halogen ions. Judging from the results of X-ray photoelectron spectra (XPS), Auger spectra, and single-crystal reflectance spectra, these Ni compounds are not Mott-insulators but charge-transfer-insulators. Their electronic structures or the spin density wave strengths are found to be tuned by the combinations of the counteranions and the bridging halogens.
RESUMEN
A series of single crystals of quasi-one-dimensional bromo-bridged Ni-Pd mixed-metal MX chain compounds Ni(1)(-)(x)()Pd(x)()(chxn)(2)Br(3) (chxn = 1(R),2(R)-diaminocyclohexane) have been obtained by electrochemical oxidation methods of the mixed methanol solutions of parent Ni(II) complex [Ni(chxn)(2)]Br(2) and Pd(II) complex [Pd(chxn)(2)]Br(2) with various mixing ratios. To investigate the competition between the electron correlation of the Ni(III) states (or spin density wave states) and the electron-phonon interaction of the Pd(II)-Pd(IV) mixed-valence states (or charge density wave states) in the Ni-Pd mixed-metal compounds, IR, Raman, ESR, XP, and Auger spectra have been measured. The IR, resonance Raman, XP, and Auger spectra show that the Pd(II)-Pd(IV) mixed-valence states are influenced and gradually approach the Pd(III) states with the increase of the Ni(III) components. This means that in these compounds the electron-phonon interaction in the Pd(II)-Pd(IV) mixed-valence states is weakened with the strong electron correlation in the Ni(III) states.
RESUMEN
This communication describes the syntheses of the quasi-one-dimensional mixed-halogen-bridged Ni(III) complexes with strong electron correlation [Ni(chxn)(2)Cl(1-x)Br(x)](NO(3))(2) and the tuning of the spin density wave strengths of these compounds. If the Cl 3p and Br 4p make one band in the compounds, we should observe a single peak in the electronic spectra. As a result, we should observe the single peak from 1.45 to 2.00 eV depending on the mixing ratios of Cl and Br ions. Therefore, the Cl 3p and Br 4p make one band. Then, we have succeeded in tuning the spin density wave strengths of the Ni(III) complexes with the strong electron correlation by mixing the bridging halogen ions successively.
RESUMEN
We report on the results of angle-resolved photoemission experiments on a quasi-one-dimensional (1D) MX-chain compound [Ni(chxn)2Br]Br2, which shows a gigantic nonlinear optical effect. A "band" having about 500 meV energy dispersion is found in the first half of the Brillouin zone, but disappears at kb/pi approximately 1/2. These spectral features are well reproduced by the d-p chain model with a small charge-transfer energy Delta compared with that of 1D Cu-O compounds. We propose that this smaller Delta is the origin of the absence of clear spin-charge separation in the photoemission spectra and the strong nonlinear optical effect.