Single-wall carbon nanotube/silicon (SWCNT/Si) heterojunction shows appealing potential for use in photovoltaic devices. However, the relatively low conductivity of SWCNT network and interfacial recombination of carriers have limited their photovoltaic performance. Herein, a multifunctional Lewis acid (p-toluenesulfonic acid, TsOH) is used to significantly reduce the energy loss in SWCNT/Si solar cells. Owing to the charge transfer doping effect of TsOH, the conductivity and work function of SWCNT films are optimized and tuned. More importantly, a chemical bridge is constructed at the interface of SWCNT/Si heterojunction. Experimental studies indicate that the phenyl group of TsOH can interact with SWCNTs through π-π interaction, meanwhile, the oxygen in the sulfonic functional group of the TsOH molecule can graft on the dangling bonds of the Si surface. The chemical bridge structure effectively suppresses the recombination of photogenerated carriers. The TsOH coating also works as an antireflection layer, leading to a 19% increment of the photocurrent. As a result, a champion power conversion efficiency of 17.7% is achieved for the TsOH-SWCNT/Si device, and it also exhibits an excellent stability, retaining more than 96% of the initial efficiency in the ambient air after 1 month.
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http://dx.doi.org/10.1002/advs.202206989 | DOI Listing |
J Am Chem Soc
January 2025
Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, 123 Bevier Road, Piscataway, New Jersey 08854, United States.
Electrostatic interactions, hydrogen bonding, and solvation effects can alter the free energies of ionizable functional groups in proteins and other nanoporous architectures, allowing such structures to tune acid-base chemistry to support specific functions. Herein, we expand on this theme to examine how metal sites ( = H, Zn, Co, Co) affect the p of benzoic acid guests bound in discrete porphyrin nanoprisms () in CDCN. These host-guest systems were chosen to model how porous metalloporphyrin electrocatalysts might influence H transfer processes that are needed to support important electrochemical reactions (e.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
College of Materials Science and Engineering, Hunan University, Changsha 410082, PR China.
High-voltage LiCoO is a promising cathode material for ultrahigh-energy lithium-ion batteries, particularly in the commercialization of 5G technology. However, achieving long-term operational stability remains a significant challenge. Herein, a quaterpolymer additive with multiple functional groups is introduced to enhance the electrochemical performance of LiCoO cathode at 4.
View Article and Find Full Text PDFInorg Chem
December 2024
School of Materials Science and Chemical Engineering, Resource Recycling of Ningbo University - Ningbo Shuangneng Environmental Technology Co., Ltd., Ningbo University, Ningbo 315211, China.
The utilization of metal-organic frameworks (MOFs) as fluorescent sensors for the detection of environmental and chemical reagent pollutants as well as heterogeneous catalysis for CO conversion represents a crucial avenue of research with significant implications for the protection of human health. In this work, a Tb(III)-based three-dimensional metal-organic framework, [Tb(L)·4DMF] (Tb-MOF) (HL = 5'-(4-carboxy-3-hydroxyphenyl)-3,3″-dihydroxy-[1,1':3',1″-terphenyl]-4,4″-dicarboxylic acid), has been structurally conformed by single-crystal X-ray crystallography. It possesses a 1D rhombus channel along the [010] direction, featuring a pore size of 6.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, 14117-13116 Tehran, Islamic Republic of Iran.
A multifunctional magnetic chiral metal-organic framework (MOF) was developed for asymmetric applications by utilizing strategies of chiralization and multifunctionalization. Cu(l-proline)-Triazine/FeO@SiO-NH was employed as a chiral secondary agent to synthesize a chiral hybrid nanocomposite within a MOF. The use of a chiral secondary agent efficiently induces chirality in an achiral MOF structure that cannot be directly chiralized.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
Department of Medicinal Chemistry, Uppsala University, 751 23 Uppsala, Sweden.
A new functional group transformation allowing the synthesis of methyl-dithioesters from readily available trifluoromethyl arenes defluorinative functionalization has been developed. This microwave-assisted method is operationally simple, rapid, and eliminates the need for pre-functionalization while accommodating a broad range of functional groups. In addition, it does not rely on highly odorous thiol sources, and utilizes the commercially available reagent BFSMe complex as a multifunctional Lewis acid/sulfur source/defluorination and demethylation agent.
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