Redesigning heterogeneous
catalysts so that they can simultaneously
integrate the efficiency and durability under reaction environments
with respect to gas fuel production, such as hydrogen (H2), oxygen (O2), or carbon monoxide (CO), has proven challenging.
In this work, we report the successful template-assisted printing-based
assembly of platinum (Pt) nanoparticles (NPs) into striped-pattern
(SP) superlattices to produce H2. In comparison to drop-casting
flat Pt NPs films, SP superlattices lead to higher mass transference
and smaller bubble stretch force, representing a general strategy
to improve the efficiency and durability of pre-existed Pt catalysts
for the hydrogen evolution reaction (HER), as well as higher current
densities than commercial Pt/C, Pt NP films, and many of the other
Pt-based or non-Pt-based HER catalysts reported in the literature.
The generic nature of template-assisted printing leads to flexibility
in the composition, size, and shape of the constituent NPs or molecules,
and thus extends such an accelerated technique for producing the oxygen
evolution reaction and electrochemical reduction of CO2 to CO.
B and T lymphocyte attenuator (BTLA) is one of the most important cosignaling molecules. It belongs to the CD28 superfamily and is similar to programmed cell death-1 (PD-1) and cytotoxic T lymphocyte associated antigen-4 (CTLA-4) in terms of its structure and function. BTLA can be detected in most lymphocytes and induces immunosuppression by inhibiting B and T cell activation and proliferation. The BTLA ligand, herpesvirus entry mediator (HVEM), does not belong to the classic B7 family. Instead, it is a member of the tumor necrosis factor receptor (TNFR) superfamily. The association of BTLA with HVEM directly bridges the CD28 and TNFR families and mediates broad and powerful immune effects. Recently, a large number of studies have found that BTLA participates in numerous physiopathological processes, such as tumor, inflammatory diseases, autoimmune diseases, infectious diseases, and transplantation rejection. Therefore, the present work aimed to review the existing knowledge about BTLA in immunity and summarize the diverse functions of BTLA in various immune disorders.
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