This paper describes a bifacial passivation strategy for the metal/Si interface of metal–insulator–semiconductor (MIS) photoelectrodes, achieving record high activities for water oxidation and reduction for Si-based MIS electrodes.
Water splitting for hydrogen production by harvesting sunlight is widely accepted as one of the most promising routes to relieve the energy crisis and environmental issues caused by excessive use of fossil fuels. Earth-abundant silicon (Si) is emerging as a suitable candidate for a photoelectrode material for efficient solar water splitting. This review describes the current status and prospects of single-crystal Si-based photoelectrodes in photoelectrochemical (PEC) water splitting for hydrogen production. We start with highlighting the recent achievements in single-crystal Si-based photocathodes and photoanodes for PEC water reduction and oxidation. We then discuss the recent progress in the design and fabrication of unbiased solar water splitting cells with single-crystal Si-based photoelectrodes. Finally, we provide an overview from the optimization of a single-crystal Si-based electrode (both a photocathode and a photoanode) to the integration of a full cell for unassisted overall solar water splitting.
Aiming at the problem that it is difficult to control the mechanical assembly error in the process of transmission, this paper presents a dynamic model simulation method of error transmission system. By analyzing the component structure of worm meta-action assembly unit, combining the error source and assembly dimension chain, the corresponding error transfer model of mechanical meta-action assembly process is established, and the assembly error transfer digraph is constructed; Based on the directed graph and using Vensim_ Ple software, the assembly error transfer accumulation model under system dynamics is established and simulated. The simulation results show that the assembly error transfer accumulation of worm rotating meta-action unit is a step-up trend. The comparison between the test results and the simulation results shows that the dynamic model of the error transfer accumulation system established has a high accuracy. The simulation results have a certain practical significance for guiding the assembly error control in the transfer process.
PJA2 is documented to degrade various substrates. Nevertheless, the role of PJA2 as an E3 ubiquitin-protein ligase in colorectal cancer (CRC) progression remains unexplored. The correlation between PJA2 mRNA levels and clinical characteristics is investigated using data from The Cancer Genome Atlas (TCGA) database. Quantitative real-time polymerase chain reaction (qRT-PCR) and immunohistochemistry (IHC) are utilized to evaluate PJA2 expression levels in CRC tissues. The biological functions of PJA2 are confirmed through colony formation assays and azoxymethane/dextran sulfate sodium (AOM/DSS) mouse model of CRC, among other experimental approaches. The underlying molecular mechanisms of PJA2 action are elucidated using RNA sequencing (RNA-seq), co-immunoprecipitation (co-IP), proximity ligation assay (PLA), and chromatin immunoprecipitation (ChIP). Our research discovered that PJA2 is downregulated in CRC tissues and decreased PJA2 expression correlates with poor prognosis. Functionally, in vivo and in vitro experiments uncovered that PJA2 inhibits tumor cell proliferation and promotes apoptosis. Mechanistically, PJA2 recognized histone deacetylase 2 (HDAC2) via its RING-B-box domain (RBD) and bind to the N-terminal of HDAC2, facilitating ubiquitination at the lysine 90 (K90) residue. PJA2-mediated degradation of HDAC2 counteracts the transcriptional repression of the interferon-induced protein with the tetratricopeptide repeats (IFIT) family, thereby suppressing CRC progression. The data demonstrates that PJA2 suppresses CRC progression through the PJA2/HDAC2/IFIT axis, and its expression is regulated by HDAC2, thus constituting a positive feedback loop. Consequently, PJA2 may serve as a potential therapeutic target for CRC, and interrupting this feedback loop can represent a viable treatment strategy to restrain CRC progression.
Most Bi-based photoelectrodes have suitable band gaps and can effectively promote the water oxidation reaction. However, simple preparation methods for Bi-based binary metal oxides as photoanodes are scarce. This paper describes a simple hydrothermal anion exchange method to synthesize Bi-based binary metal oxides with controlled morphologies. This synthesis process uses BiOI as the template and Bi source, which is eventually converted to Bi-based porous nanoflake photoanodes upon reaction with MO x (M = W, V, and Mo)-containing precursors. The photoanodes show well-shaped porous nanoflake morphologies and exhibit impressive photoelectrochemical properties compared to Bi-based photoanodes synthesized by conventional methods. These three samples possess long-term stability under solar irradiation and show considerable photocurrent for sulfite oxidation.
'/%3e%3cuse xlink:href='%23a' transform='rotate(23.036 .093 25.536)'/%3e%3cuse xlink:href='%23a' transform='rotate(45.87 1.273 16.18)'/%3e%3cuse xlink:href='%23a' transform='rotate(69.945 .996 12.078)'/%3e%3cuse xlink:href='%23a' transform='rotate(20.66 -19.689 31.932)'/%3e%3c/svg%3e)