An important step toward molecule-based electronics is to realize a robust and well-ordered molecular network at room temperature. To this end, one key challenge is tuning the molecule–substrate electronic interactions that influence not only the molecular selfassembly but also the stability of the resulting structures. In this study, we investigate the film formation of π-conjugated metal-free phthalocyanine molecules on a 3d-bcc-Fe(001) whisker substrate at 300 K by using ultra-high-vacuum scanning tunneling microscopy. On bare Fe(001), hybridization between the molecular π and the Fe(001) d-states prevents the molecular assembly, resulting in the disordered patchy structures. The second- and third-layer molecules form densely packed films, while the morphologies show clear difference. The second-layer molecules partially form p(5 × 5)-ordered films with the rectangular edges aligned along the [100] and [010] directions, while the edges of the third-layer films are rounded. Remarkably, such film morphologies are stable even at 300 K. These findings suggest that the molecular self-assembly and the resulting morphologies in the second and third layers are affected by the substrate bcc(001), despite that the Fe-d states hybridize only with the first-layer molecules. The possible mechanism is discussed with the kinetic Monte Carlo simulation.

Precise control of organic molecule deposition on a substrate is quite important for fabricating single-molecule-based devices. In this study, we demonstrate whether a quartz-crystal microbalance (QCM) widely used for a film growth calibration has the ability to precisely measure the number of organic molecules adsorbed on a substrate. The well-known Sauerbrey's equation is extended to formulate the relation between QCM resonant frequency shift and the number of adsorbed molecules onto the QCM surface. The formula is examined by QCM measurements of sublimation of π-conjugated organic molecules and direct counting of the deposited molecules one by one onto metal substrates, using ultrahigh vacuum low-temperature scanning tunneling microscopy (STM). It is revealed that the number of adsorbed molecules evaluated by QCM ( N) show good agreement with those counted from the STM images ( N) within the error of ±25%. The results ensure the QCM capability for controlling the deposition number of organic molecules with high accuracy, that is, if one needs to deposit 100 molecules on the substrate, QCM control promises deposition of 100 ± 25 molecules.

The effects of anodization temperature on the photoluminescence (PL) spectrum of porous silicon (Si) have been studied. The luminescence intensity increases exponentially and the peak wavelength decreases monotonically with increasing anodization temperature during formation of pores on Si. The PL intensity increases with decreasing the measurement temperature and reaches the maximum at about 200 K. With a further decrease of the measurement temperature, however, the intensity decreases. The increase rate of the PL intensity with decreasing temperature is found to be much faster for the samples anodized at lower temperatures. Using electron spin resonance the defects of the samples anodized at lower temperatures such as 0 and 10°C are identified to be amorphous centers (a‐centers), while those of the samples anodized at higher temperatures such as 30 and 40°C are attributed to Si dangling bonds.

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