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In this work, we present new oligonucleotide derivatives containing inter-nucleotide N -benzimidazole, N -benzoxazole, N -benzothiazole, and 1,3-dimethyl- N -benzimidazole (benzoazoles) phosphoramide groups. These modifications were introduced via the Staudinger reaction with appropriate azides during standard automated solid-phase oligonucleotide synthesis. The principal structural difference between the new azido modifiers and those already known is that they are bulk heterocyclic structures, similar to purine nucleoside bases. Modified oligonucleotides with one and two modifications at different positions and multiple modified heteronucleotide sequences were obtained with high yields. The possibility of multiple modifications in the process of automatic DNA synthesis is fundamental and critical for further application of our oligonucleotide derivatives. Initial studies on the properties of new oligonucleotides were carried out. The stability of the oligodeoxyribonucleotide duplex containing phosphoramide groups of N -benzoazoles with complementary DNA or RNA is slightly lower than that of native complexes., Competing Interests: The authors declare no competing financial interest., (© 2022 The Authors. Published by American Chemical Society.)

Recent years have seen a resurgence of interest in crystalline silicon Schottky junction solar cells distinguished by the use of low density of electronic states (DOS) nanocarbons (nanotubes, graphene) as the metal contacting the Si. Recently, unprecedented modulation of the power conversion efficiency in a single material system has been demonstrated in such cells by the use of electronic gating. The gate field induced Fermi level shift in the low-DOS carbon serves to enhance the junction built-in potential, while a gate field induced inversion layer at the Si surface, in regions remote from the junction, keeps the photocarriers well separated there, avoiding recombination at surface traps and defects (a key loss mechanism). Here, we extend these results into the third dimension of a vertical Si nanowire array solar cell. A single wall carbon nanotube layer engineered to contact virtually each n-Si nanowire tip extracts the minority carriers, while an ionic liquid electrolytic gate drives the nanowire body into inversion. The enhanced light absorption of the vertical forest cell, at 100 mW/cm(2) AM1.5G illumination, results in a short-circuit current density of 35 mA/cm(2) and associated power conversion efficiency of 15%. These results highlight the use of local fields as opposed to surface passivation as a means of avoiding front surface recombination. A deleterious electrochemical reaction of the silicon due to the electrolyte gating is shown to be caused by oxygen/water entrained in the ionic liquid electrolyte. While encapsulation can avoid the issue, a nonencapsulation-based approach is also implemented.

The hydrogen evolution reaction, 2H(+) + 2e(–) → H2, and its converse, the hydrogen oxidation reaction, H2 → 2H(+) + 2e(–), are central to any realization of a hydrogen economy. Various forms of carbon have been used for decades as the precious metal catalyst support in these reactions. Here we report the unexpected result that single-wall carbon nanotubes and some graphitic carbons, activated by brief exposure to electrochemical potentials that induce hydrogen evolution in intercalating acids combined with extended soak times in such acids, acquire an activity for these reactions that exceeds that of known nonprecious metal catalysts.

Black-to-transmissive switching polymer electrochromic devices (ECDs) were designed using a set of spray-processable cathodically coloring polymers, a non-color-changing electroactive polymer poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methacrylate) (PTMA) as the charge-compensating counter electrode, and a highly conducting gel electrolyte (6.5 mS cm(-1)). The color "black" was obtained by utilizing (1) individual copolymers absorbing across the visible spectrum, and (2) blends and bilayers of several polymer electrochromes with complementary spectral absorption. Neutral-state black and ink-like dark purple-blue (or "ink-black") donor-acceptor (DA) copolymers composed of the electron-donor 3,4-propylenedioxythiophene (ProDOT) and the electron-acceptor 2,1,3-benzothiadiazole (BTD) building units, which possess relatively homogeneous absorption profiles across the visible spectrum, were chosen for their propensity to switch to transmissive states upon electrochemical oxidation. A blend of magenta and cyan polymers (PProDOT-(CH(2)OEtHx)(2) and P(ProDOT-BTD-ProDOT), respectively) was produced with the goal of generating the same dark purple-blue color as that obtained with the "ink-black" DA copolymer. While the multi-polymer ECDs demonstrate high contrasts (up to 50%T), and switch from a saturated purple-blue color (L*=32, a*=13, b*=-46) to a light green-blue transmissive state (L*=83, a*=-3, b*=-6), devices made with the DA electrochromic copolymers switch more than two times faster (0.7 s to attain 95% of the full optical change) than those involving the polymer blends (1.6 s), and exhibit more neutral achromatic colors (L*=38, a*=5, b*=-25 for the colored state and L*=87, a*=-3, b*=-2 for the bleached state, correspondingly). The results obtained suggest that these materials should prove to be applicable in both transmissive- (window-type) and reflective-type ECDs., (© 2011 American Chemical Society)

Dual polymer absorptive/transmissive electrochromic (EC) window devices have been assembled using the solution-processable and high-EC-contrast polymer PProDOT-(CH(2)OEtHx)(2) as the EC material, along with a non-color-changing electroactive polymer, poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methacrylate) (PTMA), as the counter electrode material. Indium-tin oxide (ITO) and highly transmissive single-walled carbon nanotube (SWNT) film coated glass electrodes are used as electrode substrates. The use of the EC/non-color-changing polymer combination allowed us to construct window devices that rapidly switch between magenta and highly transmissive (>95% T for ITO and approximately 79% T for SWNT) states with large optical modulation (>71% DeltaT for ITO and 66% DeltaT for SWNT). The devices showed effective coloration and bleaching: the lightness parameter (L*) changing from 67 to 95 for ITO (approximately 50-92 for SWNT), essentially reaching a diffuse white upon oxidation. The color modulates from highly pure magenta with a* = 28 (red hue) and b* = -28 (blue chroma) for ITO (a* = 40 and b* = -36 for SWNT) to nearly colorless with a* = 1 and b* = -1 for ITO (a* = -2 and b* = -3 for SWNT) devices. Increasing the switching voltage from 2.55 V up to 3.5 V resulted in faster SWNT-based window device performance.