Fuel cells are clean, sustainable energy conversion devices for power generation, and they most commonly use platinum as the electrocatalyst.[1] However, Pt-based catalysts suffer from very limited reserves, high cost, and inactivation by CO poisoning; these are major obstacles that fuel cells have to overcome for commercialization. [1][2][3][4][5][6] Thus, exploring nonprecious metal or even metal-free catalysts to rival platinum in activity and durability is absolutely crucial, with a potentially revolutionary impact on fuel-cell technologies. Very recently, metal-free PEDOT [6] and nitrogen-doped carbon nanotubes (NCNTs) [7,8] have shown a striking electrocatalytic performance for the oxygen reduction reaction (ORR). These breakthroughs have activated an exciting field for exploring the advanced metal-free electrocatalysts and understanding the related mechanism.As one of the most important carbon nanostructures, carbon-based nanotubes have been widely studied as the support of electrocatalysts for fuel cells in recent years. [9][10][11][12] Recent progress involving doping carbon nanotubes (CNTs) with electron-rich nitrogen to transform CNTs into superb metal-free electrocatalysts for the ORR [7,8] has motivated our curiosity to examine the corresponding performance of its counterpart by doping CNTs with electron-deficient boron. Intuitively, the adsorption of O 2 on boron dopant should be quite easy owing to the large difference of electronegativity between boron and oxygen, which is the precondition for the subsequent O 2 dissociation. In this study, BCNTs with tunable boron content of 0-2.24 atom % were synthesized. The ORR onset and peak potentials shift positively and the current density increases noticeably with increasing boron content, indicating a strong dependence of the ORR performance on boron content. Moreover, the origin of the electrocatalytic activity of BCNTs including the role of the boron dopant has been revealed by density functional theory (DFT) calculations. The experimental and theoretical results provide a new strategy to explore carbon-based metal-free electrocatalysts that are significant to the development of fuel cells.Using chemical vapor deposition (CVD) with benzene, triphenylborane (TPB), and ferrocene as precursors and catalyst, BCNTs were synthesized with tunable boron content of 0-2.24 at % by using different TPB concentrations. BCNTs with boron content of 0.86, 1.33, and 2.24 at %, as determined by X-ray photoelectron spectroscopy (XPS), were denoted as B 1 CNTs, B 2 CNTs, and B 3 CNTs, respectively (Supporting Information, S1
Fuel cells are clean, sustainable energy conversion devices for power generation, and they most commonly use platinum as the electrocatalyst. [1] However, Pt-based catalysts suffer from very limited reserves, high cost, and inactivation by CO poisoning; these are major obstacles that fuel cells have to overcome for commercialization. [1][2][3][4][5][6] Thus, exploring nonprecious metal or even metal-free catalysts to rival platinum in activity and durability is absolutely crucial, with a potentially revolutionary impact on fuel-cell technologies. Very recently, metal-free PEDOT [6] and nitrogen-doped carbon nanotubes (NCNTs) [7,8] have shown a striking electrocatalytic performance for the oxygen reduction reaction (ORR). These breakthroughs have activated an exciting field for exploring the advanced metal-free electrocatalysts and understanding the related mechanism.As one of the most important carbon nanostructures, carbon-based nanotubes have been widely studied as the support of electrocatalysts for fuel cells in recent years. [9][10][11][12] Recent progress involving doping carbon nanotubes (CNTs) with electron-rich nitrogen to transform CNTs into superb metal-free electrocatalysts for the ORR [7,8] has motivated our curiosity to examine the corresponding performance of its counterpart by doping CNTs with electron-deficient boron. Intuitively, the adsorption of O 2 on boron dopant should be quite easy owing to the large difference of electronegativity between boron and oxygen, which is the precondition for the subsequent O 2 dissociation. In this study, BCNTs with tunable boron content of 0-2.24 atom % were synthesized. The ORR onset and peak potentials shift positively and the current density increases noticeably with increasing boron content, indicating a strong dependence of the ORR performance on boron content. Moreover, the origin of the electrocatalytic activity of BCNTs including the role of the boron dopant has been revealed by density functional theory (DFT) calculations. The experimental and theoretical results provide a new strategy to explore carbon-based metal-free electrocatalysts that are significant to the development of fuel cells.Using chemical vapor deposition (CVD) with benzene, triphenylborane (TPB), and ferrocene as precursors and catalyst, BCNTs were synthesized with tunable boron content of 0-2.24 at % by using different TPB concentrations. BCNTs with boron content of 0.86, 1.33, and 2.24 at %, as determined by X-ray photoelectron spectroscopy (XPS), were denoted as B 1 CNTs, B 2 CNTs, and B 3 CNTs, respectively (Supporting Information, S1.
This study compares the electrocatalytic activity of nitrogen-doped carbon nanotubes (NCNTs) with multiwalled carbon nanotubes (MWCNTs). Results indicate that NCNTs possess a marked electrocatalytic activity toward oxygen reduction reaction (ORR) by an efficient four-electron process in the alkaline condition, while the process of MWCNTs is through a two-electron pathway. Meanwhile, NCNTs show a very attractive electrochemical performance for the redox reaction of hydrogen peroxide (H2O2) and could be employed as a H2O2 sensor at a low potential of +0.3 V. The sensitivity of the NCNT-based biosensor reaches 24.5 microA/mM, more than 87 times that of the MWCNT-based one. Moreover, NCNTs exhibit striking analytical stability and reproducibility, which enables a reliable and sensitive determination of glucose by monitoring H2O2 produced by an enzymatic reaction between glucose oxidase/glucose or choline oxidase/choline at +0.3 V without the help of the electron mediator. The NCNT-based glucose biosensor has a linear range from 2 to 140 microM with an extremely high sensitivity of 14.9 microA/mM, and the detection limit is estimated to be 1.2 microM at a signal-to-noise ratio of 3. The results indicate that the NCNTs are good nanostructured materials for potential application in biosensors.
Recently, step‐scheme (S‐scheme) photocatalysts have received widespread attention in the field of solar fuel development and transformation because of efficient charge spatial separation along with strong redox capabilities. Herein, the development history of S‐scheme photocatalysts is summarized and reviewed, from Z‐scheme photocatalysts to S‐scheme photocatalysts. Advantages of S‐scheme photocatalysts are also discussed in depth and detail, including design principles and construction strategies as well as charge transfer mechanisms. In addition, identification characterizations for S‐scheme photocatalysts and their solar energy conversion applications are also reviewed. Finally, conclusions and outlooks for solar energy conversion challenges are demonstrated. It provides insights and up‐to‐date information to enable the scientific community to fully tap into the potential of S‐scheme photocatalysts in renewable energy generation and environmental remediation.
Low efficient transfer of photogenerated charge carriers to redox sites along with high surface reaction barrier is a bottleneck problem of photocatalytic H2O overall splitting. Here, in the absence of cocatalysts, H2O overall splitting has been achieved by single-atomic S vacancy hexagonal CdS with a spin polarization electric field (PEF). Theoretical and experimental results confirm that single-atomic S vacancy-induced spin PEF with opposite direction to the Coulomb field accelerates charge carrier transport dynamics from the bulk phase to surface-redox sites. By systematically tuning the spin PEF intensity with single-atomic S vacancy content, common pristine CdS is converted to a photocatalyst that can efficiently complete H2O overall splitting by releasing a great number of H2 bubbles under natural solar light. This work solves the bottleneck of solar energy conversion in essence by single atom vacancy engineering, which will promote significant photocatalytic performance enhancement for commercialization.
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