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Single-wall carbon nanotubes (SWCNTs) have a high aspect ratio, large surface area, good stability and unique metallic or semiconducting electrical conductivity, they are therefore considered a promising candidate for the fabrication of flexible gas sensors that are expected to be used in the Internet of Things and various portable and wearable electronics. In this review, we first introduce the sensing mechanism of SWCNTs and the typical structure and key parameters of SWCNT-based gas sensors. We then summarize research progress on the design, fabrication, and performance of SWCNT-based gas sensors. Finally, the principles and possible approaches to further improving the performance of SWCNT-based gas sensors are discussed.

Inorganic chalcogenides are traditional high-performance thermoelectric materials. However, they suffer from intrinsic brittleness and it is very difficult to obtain materials with both high thermoelectric ability and good flexibility. Here, we report a flexible thermoelectric material comprising highly ordered Bi2Te3 nanocrystals anchored on a single-walled carbon nanotube (SWCNT) network, where a crystallographic relationship exists between the Bi2Te3 <\\[\\bar{1}2\\bar{1}0\\]> orientation and SWCNT bundle axis. This material has a power factor of ~1,600 μW m−1 K−2 at room temperature, decreasing to 1,100 μW m−1 K−2 at 473 K. With a low in-plane lattice thermal conductivity of 0.26 ± 0.03 W m−1 K−1, a maximum thermoelectric figure of merit (ZT) of 0.89 at room temperature is achieved, originating from a strong phonon scattering effect. The origin of the excellent flexibility and thermoelectric performance of the Bi2Te3–SWCNT material is attributed, by experimental and computational evidence, to its crystal orientation, interface and nanopore structure. Our results provide insight into the design and fabrication of high-performance flexible thermoelectric materials.

Bifacial perovskite solar cells have shown great promise for increasing power output by capturing light from both sides. However, the suboptimal optical transmittance of back metal electrodes together with the complex fabrication process associated with front transparent conducting oxides have hindered the development of efficient bifacial PSCs. Here, we present a novel approach for bifacial perovskite devices using single-walled carbon nanotubes as both front and back electrodes. single-walled carbon nanotubes offer high transparency, conductivity, and stability, enabling bifacial PSCs with a bifaciality factor of over 98% and a power generation density of over 36%. We also fabricate flexible, all-carbon-electrode-based devices with a high power-per-weight value of 73.75 W g −1 and excellent mechanical durability. Furthermore, we show that our bifacial devices have a much lower material cost than conventional monofacial PSCs. Our work demonstrates the potential of SWCNT electrodes for efficient, stable, and low-cost bifacial perovskite photovoltaics. The suboptimal optical transmittance of back electrodes and complex fabrication process hindered development of bifacial perovskite solar cells. Here, authors apply single-walled carbon nanotubes as front and back electrodes, achieving power generation density of 36% and bifaciality factor of 98%.

The keen interest in fuel cells and metal‐air batteries stimulates a great deal of research on the development of a cost‐efficient and high‐performance catalyst as an alternative to traditional Pt to boost the sluggish oxygen reduction reaction (ORR) at the cathode. Herein, we report a facile and scalable strategy for the large‐scale preparation of a free‐standing and flexible porous atomically dispersed Fe–N‐doped carbon microtube (FeSAC/PCMT) sponge. Benefiting from its unique structure that greatly facilitates the catalytic kinetics, mass transport, and electron transfer, our FeSAC/PCMT electrode exhibits excellent performance with an ORR potential of 0.942 V at −3 mA cm−2. When the FeSAC/PCMT sponge was directly used as an oxygen electrode for liquid‐state and flexible solid‐state zinc‐air batteries, high peak power densities of 183.1 and 58.0 mW cm−2 were respectively achieved, better than its powdery counterpart and commercial Pt/C catalyst. Experimental and theoretical investigation results demonstrate that such ultrahigh ORR performance can be attributed to atomically dispersed Fe–N5 species in FeSAC/PCMT. This study presents a cost‐effective and scalable strategy for the fabrication of highly efficient and flexible oxygen electrodes, provides a significant new insight into the catalytic mechanisms, and helps to realize significant advances in energy devices. A metal–organic framework‐graft‐derived approach is proposed for bulk preparation of free‐standing and flexible porous atomically dispersed Fe–N‐doped carbon microtube films. Theoretical calculation and experimental results demonstrate that this ultrahigh‐performance film catalyst benefits from the cross‐wrapped carbon microtube network structure that ensures fast electron transfer capability, shortens mass transport pathways, and enhances the utilization of high‐activity Fe–N5 sites for oxygen reduction.

Carbon nanotubes (CNTs) are considered a promising candidate for the detection of toxic gases because of their high specific surface area and excellent electrical and mechanical properties. However, the detecting performance of CNT-based detectors needs to be improved because covalently bonded CNTs are usually chemically inert. We prepared a nitrogen-doped single-wall CNT (SWCNT) film by means of gas-phase fluorination followed by thermal annealing in NH3. The doped nitrogen content could be changed in the range of 2.9–9.9 at%. The N-doped SWCNT films were directly used to construct flexible and transparent gas sensors, which can work at a low voltage of 0.01 V. It was found that their NO2 detection performance was closely related to their nitrogen content. With an optimum nitrogen content of 9.8 at%, a flexible sensor had a detection limit of 500 ppb at room temperature with good cycling ability and stability during bending.

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. A multifunctional Lewis acid (p‐toluenesulfonic acid, TsOH) is used to significantly reduce the energy loss in single‐wall carbon nanotube/silicon (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, which effectively suppresses the recombination of photogenerated carriers. As a result, a champion power conversion efficiency of 17.7% is achieved.

The growth of high-quality semiconducting single-wall carbon nanotubes with a narrow band-gap distribution is crucial for the fabrication of high-performance electronic devices. However, the single-wall carbon nanotubes grown from traditional metal catalysts usually have diversified structures and properties. Here we design and prepare an acorn-like, partially carbon-coated cobalt nanoparticle catalyst with a uniform size and structure by the thermal reduction of a [Co(CN) 6 ] 3− precursor adsorbed on a self-assembled block copolymer nanodomain. The inner cobalt nanoparticle functions as active catalytic phase for carbon nanotube growth, whereas the outer carbon layer prevents the aggregation of cobalt nanoparticles and ensures a perpendicular growth mode. The grown single-wall carbon nanotubes have a very narrow diameter distribution centred at 1.7 nm and a high semiconducting content of >95%. These semiconducting single-wall carbon nanotubes have a very small band-gap difference of ∼0.08 eV and show excellent thin-film transistor performance. Growth of high-quality semiconducting single-wall carbon nanotubes is crucial for high-performance devices. Here, the authors report a partially carbon-coated cobalt nanoparticle catalyst which catalyzes growth of predominantly semiconducting single-wall carbon nanotubes with a narrow band-gap distribution.

Noble‐metal free, cost‐effective, and highly stable catalysts with efficient activity for both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) have attracted tremendous research interest in recent years. Here, a flexible, self‐standing hybrid film comprising a N‐doped single‐wall carbon nanotube (SWCNT) network on which are anchored Ni nanoparticles encapsulated by a monolayer of N‐doped carbon (NCNi) is reported. The films are prepared by floating catalyst chemical vapor deposition followed by NH3 treatment. The material obtained at optimum conditions shows excellent bifunctional electrocatalytic activity in alkaline media with low overpotentials of 190 and 270 mV for HER and OER, respectively, to reach a current density of 10 mA cm−2. A current density of 10 mA cm−2 at 1.57 V is achieved when this freestanding and binder‐free rod‐shaped NCNi/SWCNT assembly is used as cathode and anode in 1 m KOH solution for overall water splitting, presenting one of the best values reported to date. A support‐free film of single‐wall carbon nanotubes decorated with small‐sized Ni nanoparticles covered by N‐doped monolayer carbon shows excellent electrocatalytic activity at low overpotentials for overall water splitting. The optimized electrocatalyst gives a current density of 10 mA cm−2 at an overpotential of 270 and 190 mV for the oxygen evolution reaction and hydrogen evolution reaction, and 1.57 V for total water splitting.

Fe-N-C has emerged as a promising noble-metal-free catalyst for the oxygen reduction reaction (ORR). However, achieving a catalytic activity comparable to that of Pt in acidic medium remains a great challenge. Here we report a N-doped carbon nanotube (CNT) catalyst in which a high concentration of single Fe atoms has been dispersed (CNT@Fe-N-PC). The catalyst was prepared by a simple and scalable atomic isolation method, in which a metal isolation agent was introduced to isolate Fe atoms and was then evaporated to produce abundant micropores that host single Fe atom active sites. The CNT@Fe-N-PC catalyst contained a high concentration of single Fe atom active sites and exhibited ultrahigh ORR activity with a half-wave potential of 0.82 V, comparable to that of Pt/C in an acidic medium. A high concentration of Fe-Nx active sites was created on a flexible single-wall CNT film and carbon cloth using this technique, and these materials showed even better ORR performance, that is, 40-60 mV more positive onset potentials than those of a commercial Pt/C catalyst. These catalysts exhibit excellent catalytic activity, good durability and low cost, and show great potential for commercial use as substitutes for current Pt-based catalysts.

The development of low-cost, high-activity, and durable integrated bifunctional flexible air electrodes for use in Zn-air batteries is both challenging and important. We report a simple and scalable electropolymerization method used to prepare an electrode material comprising heavily N-doped carbon covering single-walled carbon nanotube (N/C-SWCNT) networks. The resulting core/shell structure of the hybrid electrode enabled the flexibility, mechanics, and three-dimensional interconnected porous structure of SWCNT films while containing abundant pyridinic N, which provided excellent catalytic activity for both the oxygen reduction and evolution reactions (overpotential gap = 0.76 V). A binder-free Zn-air battery using the N/C-SWCNT film as an oxygen electrode was assembled and showed a high peak power density of 181 mW/cm 2 , a high specific capacity of 810 mAh/g and stable discharge‒charge cycling performance. We also constructed a flexible solid-state Zn-air battery featuring not only a high power density of 22 mW/cm 2 but also good flexibility and stability. A core/shell structured hybrid film comprised of N-doped carbon covering on single-wall carbon nanotubes (SWCNTs) were synthesized by a rapid electropolymerization method, which not only contains abundant exposed pyridinic N that leads to excellent catalytic activity for both ORR and OER, but also perfectly inherits the high conductivity, excellent flexibility, and porous structure of original SWCNT film, making it a desirable integrated oxygen electrode for Zn-air batteries.