Bibliometric and visualization analysis of the application of inorganic nanomaterials to autoimmune diseases.

Objective: To conduct bibliometric analysis of the application of inorganic nanomaterials to autoimmune diseases to characterize current research trends and to visualize past and emerging trends in this field in the past 15 years. Methods: The evolution and thematic trends of the application of inorganic nanomaterials to autoimmune diseases from January 1, 1985, to March 15, 2024, were analyzed by bibliometric analysis of data retrieved and extracted from the Web of Science Core Collection (WoSCC) database. A total of 734 relevant reports in the literature were evaluated according to specific characteristics such as year of publication, journal, institution, country/region, references, and keywords. VOSviewer was used to build co-authorship analysis, co-occurrence analysis, co-citation analysis, and network visualization. Some important subtopics identified by bibliometric characterization are further discussed and reviewed. Result: From 2009 to 2024, annual publications worldwide increased from 11 to 95, an increase of 764%. ACS Nano published the most papers (14) with the most citations (1372). China (230 papers, 4922 citations) and the Chinese Academy of Sciences (36 papers, 718 citations) are the most productive and influential country and institution, respectively. The first 100 keywords were co-clustered to form four clusters: (1) the application of inorganic nanomaterials in drug delivery, (2) the application of inorganic nano-biosensing to autoimmune diseases, (3) the use of inorganic nanomaterials for imaging applied to autoimmune diseases, and (4) the application of inorganic nanomaterials in the treatment of autoimmune diseases. Combination therapy, microvesicles, photothermal therapy (PTT), targeting, diagnostics, transdermal, microneedling, silver nanoparticles, psoriasis, and inflammatory cytokines are the latest high-frequency keywords, marking the emerging frontier of inorganic nanomaterials in the field of autoimmune diseases. Sub-topics were further discussed to help researchers determine the scope of research topics and plan research directions. Conclusion: Over the past 39 years, the application of inorganic nanotechnology to the field of autoimmune diseases shows extensive cooperation between countries and institutions, showing a continuous increase in the number of reports in the literature, and has clinical translation prospects. Future research should further improve the safety of inorganic nanomaterials, clarify the mechanism of action of nanomaterials, establish a standardized nanomaterial preparation and performance evaluation system, and ultimately achieve the goal of early detection and precise treatment of autoimmune diseases.

g-C3N4/Ag@AgCl with Z-scheme heterojunction and Ag electron bridge for enhanced photocatalytic degradation of tetracycline wastewater.

Building Z-scheme heterojunctions with an electron bridge is a favored function for increasing photocatalytic activity. A facile approach for preparing g-C3N4/Ag@AgCl ternary heterojunctions by co-precipitation and photoreduction was established in this work. First, via co-precipitation, AgCl was modified on the surface of g-C3N4 to create a broad contact area between AgCl and g-C3N4. The AgCl is then reduced to Ag via an in-situ photoreduction technique, resulting in the formation of a ternary composite. The experimental results showed that when g-C3N4 modified 25% of the Ag@AgCl, that is, g-C3N4/Ag@AgCl-25 had the best photocatalytic performance, 94.9% of TC was degraded within 240 min, and the reaction rate to TC was 0.1214 min-1, which was 4.49 times and 8.12 times higher than that of g-C3N4 and Ag/AgCl, respectively. The excellent photocatalytic performance of g-C3N4/Ag@AgCl is attributed to the LSPR effect of Ag NPs and O-doping g-C3N4, which broadens the absorbance performance of g-C3N4, the establishment of Z-type heterojunctions between AgCl NPs and g-C3N4 NSs and Ag NPs as an electron transport bridge accelerate the photogenerated electrons transfer between AgCl and g-C3N4.

Rational construction of porous N-doped Fe2O3 films on porous graphene foams by molecular layer deposition for tunable microwave absorption.

Graphene-based materials with porous microstructure have attracted immense attentions due to their wide application in microwave absorption. However, constructing magnetic film with both porous microstructure and uniform pore size by using traditional methods still remains a challenge. To overcome this problem, we reported a facile strategy of molecular layer deposition (MLD) for successfully fabrication of the hybrid-architecture of porous graphene foams and nitrogen-doped porous Fe2O3 films. The surfaces of porous graphene foams are uniformly covered by porous Fe2O3 films without aggregation and the pore structures are widely distributed. The porous graphene-based composites exhibit remarkably enhanced microwave absorption performance compared to the pristine graphene foams. The minimum reflection loss value is increased by approximately 8 times, reaching -64.36 dB with a thickness of only 2.18 mm. More importantly, the absorption property can be precisely modulated by tuning the MLD cycle numbers and effective absorption bandwidth covers 3.04-18.0 GHz by adjusting the thickness from 1.0 to 5.0 mm. This work provides new insights for exploring novel and high-performance graphene-based microwave absorbents and offers a new idea to rationally design three-dimensional composites with porous magnetic films.

Origin of synergistic effects in bicomponent cobalt oxide-platinum catalysts for selective hydrogenation reaction.

The synergistic nature of bicomponent catalysts remains a challenging issue, due to the difficulty in constructing well-defined catalytic systems. Here we study the origin of synergistic effects in CoOx-Pt catalysts for selective hydrogenation by designing a series of closely contacted CoOxPt/TiO2 and spatially separated CoOx/TiO2/Pt catalysts by atomic layer deposition (ALD). For CoOx/TiO2/Pt, CoOx and platinum are separated by the walls of titania nanotubes, and the CoOx-Pt intimacy can be precisely tuned. Like CoOxPt/TiO2, the CoOx/TiO2/Pt shows higher selectivity to cinnamyl alcohol than monometallic TiO2/Pt, indicating that the CoOx-Pt nanoscale intimacy almost has no influence on the selectivity. The enhanced selectivity is ascribed to the increased oxygen vacancy resulting from the promoted hydrogen spillover. Moreover, platinum-oxygen vacancy interfacial sites are identified as the active sites by selectively covering CoOx or platinum by ALD. Our study provides a guide for the understanding of synergistic nature in bicomponent and bifunctional catalysts.

Controllable n-Fe2O3@graphene nanomaterials by ALD applied in an aptasensor with enhanced electrochemical performance for thrombin detection.

An elegant atomic layer deposition (ALD) method has been employed for the controllable preparation of a uniform Fe2O3-coated graphene nanostructure (Fe2O3@graphene). The Fe2O3 coating thickness of the Fe2O3@graphene nanostructure can be tuned by varying the cycle number of Fe2O3 ALD. The produced Fe2O3@graphene composites are characterized by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy and cyclic voltammetry (CV). It is revealed that Fe2O3 is effectively deposited on the surface of graphene. Combined with the high affinity and specificity of an aptamer, a simple, rapid and sensitive electrochemical aptasensor was successfully fabricated for thrombin detection. The resulting electrochemical aptasensor displays a linear response to thrombin in the 1.0 × 10-11 to 4.0 × 10-9 M concentration range with the detection limit of 1.0 × 10-12 M (at an S/N of 3). The described controllable multifunctional graphene nanomaterials from ALD are expected to be applied in a biosensing platform which will exhibit wide applications in biological, medical, and environmental fields.