Glycol Oxidation Reaction Research Articles

Segmentation and Re-encapsulation of Porous PtCu Nanoparticles by Generated Carbon Shell for Enhanced Ethylene Glycol Oxidation and Oxygen-Reduction Reaction.

Hierarchical porous carbon-encapsulated ultrasmall PtCu (UsPtCu@C) nanoparticles (NPs) were constructed based on segmentation and re-encapsulation of porous PtCu NPs by using glucose as a green biomass carbon source. The synergistic electronic effect from the bimetallic elements can enhance the catalytic activity by adjusting the surface electronic structure of Pt. Most importantly, the generated porous carbon shell provided a large contact surface area, excellent electrical conductivity, and structural stability, and the ultrasmall PtCu NPs exhibited an increased electrochemical performance compared with their PtCu matrix because of the exposure of more catalytically active centers. This synergistic relationship between the components resulted in enhanced catalytic activity and better stability of the obtained UsPtCu@C for ethylene glycol oxidation reaction and the oxygen-reduction reaction in alkaline electrolyte, which was higher than the PtCu NPs and commercial Pt/C (20 wt % Pt on Vulcan XC-72). The electrochemically active surface areas of the UsPtCu@C, PtCu NPs, and commercial Pt/C were calculated to be approximately 230.2, 32.8, and 64.0 m2/gPt, respectively; the mass activity of the UsPtCu@C for the ethylene glycol oxidation reaction was 8.5 A/mgPt, which was 14.2 and 8.5 times that of PtCu NPs and commercial Pt/C, respectively. The specific activity of UsPtCu@C was 3.7 mA/cmpt2, which was 2.1 and 2.3 times that of PtCu NPs and commercial Pt/C, respectively. The onset potential (Eon-set) of UsPtCu@C for the oxygen-reduction reaction was 0.96 V (vs reversible hydrogen electrode, RHE), which was 110 and 60 mV higher than PtCu and commercial Pt/C, respectively. The half-wave potentials (E1/2) of UsPtCu@C, PtCu, and Pt/C were 0.88, 0.56, and 0.82 V (vs RHE), respectively, which indicated that the UsPtCu@C catalyst had an excellent bifunctional electrocatalytic activity.

Highly Adjustable Three-Dimensional Hollow Pt(Au)Cu Nanonetwork Structures as Enhancing Electrocatalysts for Alcohol Oxidation Reaction

Pt-based nanomaterials are proven as one of the most efficient catalysts for direct alcohol fuel cells. However, it is a challenge to construct Pt-based catalysts with high catalytic activity and less Pt. In this work, we develop a new strategy to prepare three-dimensional (3D) nanonetwork structures (NNWs) like hollow Pt(Au)Cu (3D h-Pt(Au)Cu NNWs). 3D Cu nanonetworks (3D Cu NNWs) were firstly synthesized as template, and then by replacing Cu with Pt precursors or Pt and Au precursors, 3D h-Pt42Cu58 NNWs and 3D h-Pt38Au17Cu45 NNWs were obtained. Among the NNWs and commercial Pt/C, the 3D h-Pt38Au17Cu45 NNWs owned the best catalytic activity for methanol, ethanol and ethylene glycol oxidation reaction with the mass activity of 6.12 A mgPt−1, 8.53 A mgPt−1 and 12 A mgPt−1, which are 3.84-fold, 7.35-fold and 4.23-fold higher than that of commercial Pt/C. The study provides a simple strategy for preparing novel 3D hollow Pt-based polymetallic nanostructures, showing great potential in synthesizing and designing high-efficiency Pt-based electrocatalysts.

Efficient polyalcohol oxidation electrocatalysts enabled by PtM (M = Fe, Co, and Ni) nanocubes surrounded by (200) crystal facets.

Due to the high-density (200) crystal planes and abundant active sites, cubic platinum nanomaterials have become outstanding electrocatalysts in promoting fuel cell reactions. However, because of the fact that the facet-controlled synthesis is difficult, it is still a grand challenge to synthesize a sequence of Pt-based nanocubes via a universal method. Herein, we report a general and simple eco-friendly solvothermal method to prepare (200)-enclosed PtM nanocubes. Different from the other nanomaterials, nanocubes are conducive to mass transfer. Moreover, the synergistic and electronic effects between M and Pt are profitable to improve the utilization of precious metals. We used (200)-encapsulated nanocrystals to evaluate their electrocatalytic performance towards glycerol and ethylene glycol oxidation reactions in an alkaline medium. In particular, Pt4Co nanocubes showed superior mass activities in glycerol and ethylene glycol oxidation reactions, which are 6.2- and 5.0-fold higher than those obtained for commercial Pt/C catalysts, respectively. Meanwhile, Pt4M catalysts manifested excellent stability in the endurance test, which is attributed to the alloying effect promoting the electrooxidation of intermediates. Our study provides an ideal method for the construction of Pt-based bimetallic nanocubes, which can be used for anode reactions of polyol fuel cells and beyond.

One-step aqueous synthesis of hierarchically multi-branched PdRuCu nanoassemblies with highly boosted catalytic activity for ethanol and ethylene glycol oxidation reactions

Shaped-controlled synthesis of high-efficiency electrocatalysts towards ethanol oxidation reaction (EOR) and ethylene glycol oxidation reaction (EGOR) is important for development of alcohol alkaline fuel cells. Herein, one-step aqueous method was developed for constructing hierarchically multi-branched PdRuCu nanoassemblies (NAs) under the guidance of octylphenoxypolyethoxyethanol (NP-40) and NaBr. The as-obtained PdRuCu NAs exhibited dramatically enhanced electrocatalytic activity and improved stability for EOR and EGOR in alkaline solution. The mass/specific activity of the as-prepared catalysts for EOR (1.16 A mg−1Pd/3.78 mA cm−2) and EGOR (1.29 A mg−1Pd/4.19 mA cm−2) were steeply higher than those of commercial Pd black (0.17 A mg−1Pd/1.81 mA cm−2; 0.21 A mg−1Pd/2.27 mA cm−2), respectively. This work would provide some valuable insights for synthesis of advanced polymetallic electrocatalysts in fuel cells.

Snowflake-like Cu2S as visible-light-carrier for boosting Pd electrocatalytic ethylene glycol oxidation under visible light irradiation

Photo-assisted electrocatalytic oxidation alcohol molecule holds promise for both sustainable energy generation and energy conversion in direct alcohol fuel cells (DAFCs). Herein, we demonstrate that snowflake-like Cu2S on which Pd nanoparticles are grown, which acts as an excellent catalyst for ethylene glycol oxidation reaction (EGOR) under visible light irradiation. The peak current density of Pd–Cu2S electrode reaches to 3254 mA mg−1Pd under visible light irradiation, which is 1.7 and 5.5 times than that of Pd–Cu2S electrode and commercial Pd/C electrode under dark condition. In the chronopotentiometry experiments, the sustained time of Pd–Cu2S electrode under visible light illumination is 2.9 and 5.0 times longer than that of Pd–Cu2S electrode and commercial Pd/C electrode in dark. These results indicate that Pd–Cu2S catalyst exhibits excellent catalytic activity and stability for EGOR under photoelectric cooperation. Meanwhile, the present work indicates that Cu2S snowflake as the traditional noble metal electrocatalyst carrier demonstrates promising prospects in efficient and stable solar fuel conversion and fuel cell reaction.

Porous dendritic PtRuPd nanospheres with enhanced catalytic activity and durability for ethylene glycol oxidation and oxygen reduction reactions

Developing highly active and durable catalyst is of pivotal importance in fuel cells, owing to excessive consumption of fossil fuels. Herein, porous dendritic PtRuPd nanospheres (PtRuPd NSs) were synthesized by a facile hexadecylpyridinium chloride (HDPC)-mediated one-pot aqueous method with ascorbic acid (AA) as the reducing agent. The as-obtained PtRuPd NSs displayed high-efficient catalytic activity and durability for ethylene glycol oxidation reaction (EGOR) and oxygen reduction reaction (ORR). It exhibited enlarged mass activity (MA, 1.368 A mg−1) compared to commercial Pt/C (1.100 A mg−1) for EGOR. Besides, the onset potential (Eonset, 0.930 V) and half-wave potential (E1/2, 0.852 V) of PtRuPd NSs were more positive relative to homemade PtPd NSs (0.905 and 0.840 V), PdRu NSs (0.895 and 0.839 V), and commercial Pt/C (0.910 and 0.822 V) toward ORR. This work provides some valuable guidelines for producing novel trimetallic nanocatalysts in fuel cells.

Trimetallic PtRhCo petal-assembled alloyed nanoflowers as efficient and stable bifunctional electrocatalyst for ethylene glycol oxidation and hydrogen evolution reactions

Controllable synthesis of multimetal nanocrystals with hierarchical structures and tunable compositions are feasible to steeply improve the catalytic properties in fuel cells. Herein, trimetallic PtRhCo petal-assembled alloyed nanoflowers (PtRhCo PAANFs) were fabricated via a one-pot solvothermal method, which showed remarkable enlargement in specific activity and mass activity over PtRh0.25Co nanodentrites (NDs), PtRh1.5Co NDs, PtCo NDs and commercial Pt/C catalysts for ethylene glycol oxidation in 0.5 M KOH solution. The as-developed catalyst exhibited dramatically better CO tolerance and recoverability, coupling with the superior activity and durability for hydrogen evolution reaction (HER) in the alkaline electrolyte. This work demonstrates the significance of Rh in the alloy for improving the stability. This work offers a promising strategy for preparation of advanced trimetallic electrocatalysts for energy conversion applications.

Ultrathin PdFePb nanowires: One-pot aqueous synthesis and efficient electrocatalysis for polyhydric alcohol oxidation reaction

Synthesis of high-efficiency catalysts for alcohol oxidation reaction caused great interest in direct alcohol fuel cells (DAFCs). Ultrathin PdFePb nanowires (NWs) with an average diameter of 2.3 nm were synthesized by a simple and fast one-pot aqueous synthesis, using octylphenoxypolyethoxyethanol (NP-40) as the structure-directing agent. The as-prepared PdFePb NWs displayed an increscent electrochemically active surface area (ECSA, 121.18 m2 g−1 Pd). For ethylene glycol oxidation reaction (EGOR) and glycerol oxidation reaction (GOR), PdFePb NWs exhibited much higher activity and superior stability, outperforming those of homemade PdFe NWs, PdPb NWs, commercial Pd black and Pd/C (20 wt%). These results reveal dramatically high catalytic activity and durability of ultrathin PdFePb NWs in enhancing polyols electrooxidation.

Pd-Ru-Bi nanoalloys modified three-dimensional reduced graphene oxide/MOF-199 composites as a highly efficient electrocatalyst for ethylene glycol electrooxidation

Abstract Well-dispersed trimetallic Pd-Ru-Bi alloy nanoparticles (NPs) were successfully embedded in the three-dimensional (3D) rGO/MOF-199 by a facile hydrothermal and in situ impregnation-reduction method. Among the mono-, bi- and tri-metal@rGO/MOF-199 electrocatalysts, the trimetallic PdRuBi@rGO/MOF-199 exhibited the highest catalytic activity and durability towards ethylene glycol oxidation reaction (EGOR) under the alkaline condition, as high as 213.93 mA cm−2, is about 7.23 times higher than that of commercial Pd/C. The outstanding electrocatalysis oxidation performance of the PdRuBi@rGO/MOF-199 is attributed to the unique 3D structures with trimetallic composition and strong synergistic effects of Pd, Ru and Bi nanoalloys that providing plenty of interfaces and achievable reaction active sites. Furthermore, the introduction of GO in MOF-199 matrix conduces to the superior electron transfer and large surface area, which are beneficial to improve the catalytic ability of the catalyst. The study on the new composites offers a conception and applicable way to develop the advanced Pd-based electrocatalysts for high performance direct ethylene glycol fuel cells.

Graphene supported palladium-phosphorus nanoparticles as a promising catalyst for ethylene glycol oxidation

Abstract In this work, a novel composite catalyst, consisting of palladium (Pd), non-metallic phosphorus (P) and graphene (GE) has been successfully prepared by a facile sodium borohydride (NaBH4) reduction method and investigated as a catalyst for ethylene glycol oxidation reaction (EGOR) in alkaline media. Transmission electron microscopy (TEM) images exhibit that PdP nanoparticles (NPs) are evenly dispersed on the GE surface. X-ray photoelectron spectroscopy (XPS) measurement reveals that P could modify the electronic structure of Pd and a stronger electronic interaction exists between them. Electrochemical tests demonstrate that the as-prepared Pd-P/GE catalyst displays higher electrocatalytic performance and better electrochemical stability toward EGOR in comparison with the monometallic Pd catalyst (Pd/GE), with the best performance observed for the PdP(1:1)/GE catalyst. All results suggest that the introduction of non-metallic P is indeed a useful way to enhance the electrocatalytic performance of Pd, which is expected to shed some light on the design of catalysts containing non-metal P or even other nonmetals to accelerate the commercialization of fuel cells.

Polydopamine functionalized multi-walled carbon nanotubes supported PdAu nanoparticles as advanced catalysts for ethylene glycol oxidation

Design of high performance and low cost electrocatalysts for the oxidation of small organic molecules remains a great challenge for the practical application of direct fuel cells. Herein, a novel composite catalyst composed of PdAu nanoparticles (NPs) uniformly dispersed on the polydopamine functionalized MWCNTs (PDA-MWCNTs) has been synthesized. TEM images indicate that MWCNTs are successfully coated by PDA, and the as-prepared PdAu NPs are homogeneously dispersed on the PDA functional MWCNTs with smaller sizes than those on pristine MWCNTs. Electrochemical tests reveal that PDA-MWCNTs is a promising catalyst carrier for direct ethylene glycol fuel cell (DEGFC), and the PdAu(1:1)/PDA-MWCNTs catalyst displays the highest peak current density among all catalysts towards ethylene glycol oxidation reaction (EGOR) in alkaline medium, with mass activity of 1540.3 mA mgPd−1, which is 1.5, 2.6, 9.8, 13.4 and 2.0 times greater than those of PdAu(1:3)/PDA-MWCNTs, PdAu(3:1)/PDA-MWCNTs, Pd/PDA-MWCNTs, Pd/MWCNTs and commercial Pd/C catalysts, respectively. In addition, PdAu(1:1)/PDA-MWCNTs catalyst also exhibits the best stability. These findings are valuable for the development of advanced Pd-based catalysts, which will help promote the industrialization of direct fuel cell.

Palladium/Copper Nanoalloy Supported on Carbon Nanotubes for the Electrooxidation of Methanol and Ethylene Glycol

AbstractHerein, we demonstrate the ultrasonic‐assisted synthesis of Palladium/Copper nanoalloy supported on carbon nanotubes (PdCu/CNT) towards the electro‐oxidation of methanol and ethylene glycol using Triton X‐100 as a stabilizer. Structural and morphological analysis manifests the formation of PdCu nanoalloy on the surface of CNTs. For the electrochemical comparison, PdCu on Vulcan carbon (PdCu/VC) also synthesized in the same procedure and characterized thoroughly. The electrochemical evaluations of the PdCu/CNT reveal the better mass activity of 1021.6 mA mg[pd]−1 which is 1.6‐fold higher than PdCu/VC and 5.9 times advanced than commercial Pd/C catalysts towards methanol electrooxidation. Also, for electrooxidation of ethylene glycol, the mass activity of the PdCu/CNT is more of about 1219.8 mA mg[pd]−1 which is around 1.7 times enhanced than PdCu/VC and 4.1 times improved than commercial Pd/C catalysts. Furthermore, sonochemically prepared PdCu/CNT provides improved stability up to 3600s in both methanol and ethylene glycol oxidation reactions. The accredited activity enhancement due to its unique construction of zero‐dimensional structured PdCu nanoalloy with one‐dimensional CNTs and modified electronic effect of Pd on it.

Shape-controlled PdSn alloy as superior electrocatalysts for alcohol oxidation reactions

Abstract At present, it is still a great challenge to control the morphology and size of nanoparticles for obtaining more efficient and stable catalysts for direct fuel cell reactions. Herein, we have synthesized a series of Pd3Sn bimetallic catalysts with different morphologies that transitioned from nanonetwork to nanostrips and then to nanodots by altering the varieties of reducing agents and the amount of surfactant. And the formation mechanisms of nanocatalysts were also investigated. It is worth noting that Pd3Sn-dots, due to the unique structure, uniform dispersion and ultra-small size, exhibit excellent electrocatalytic activity for ethanol oxidation reaction and ethylene glycol oxidation reaction, which distinctly higher than the other Pd3Sn catalysts and commercial Pd/C catalysts. Moreover, the as-prepared Pd3Sn catalysts also performed greater long-term durability due to the electronic and synergistic effects. This work provides guidance on the morphology-dependent nanocrystals, which will show a great potential as anodic catalysts in direct fuel cell applications.

2D Semiconductor Bi2WO6 Nanosheets as the Pt Carriers for Ethylene Glycol Oxidation Reaction with Photoelectric Interaction

Ethylene glycol oxidation reaction (EGOR) is a key anode reaction in direct ethylene glycol fuel cells (DEGFCs). Herein, 2D semiconductor bismuth tungstate (Bi2WO6) nanosheets are facilely prepared and used as carriers for the deposition of platinum nanoparticles (Pt NPs). The resultant material is used as the working electrode in the application of DEGFCs. Due to the excellent absorption property of Bi2WO6 in visible light, the optimized Pt‐Bi2WO6 electrode (Pt at 20 wt%) shows improved catalytic activity and stability with visible‐light illumination. The current density using the Pt‐Bi2WO6 electrode reaches 492.5 mA mg−1Pt with visible‐light irradiation, which is about 4.2 fold higher in comparison with the same electrode in dark conditions. This 2D sheet‐like support, together with the visible‐light response of Bi2WO6, induces the deposition of ultra‐small sizes of Pt (5.4 nm) and the synergistic effect of electrocatalytic and photocatalytic ethylene glycol oxidation, thus greatly improving the photoelectric catalytic property of EGOR.

Monodispersed bimetallic platinum-copper alloy nanospheres as efficient catalysts for ethylene glycol electrooxidation

Designing and fabricating highly active and efficient catalysts are of vital importance for the practical applications of direct ethylene glycol fuel cells (DEGFCs). In this study, we employ a feasible one-pot synthetic method to construct highly monodispersed PtCu nanospheres (NSs) as high-efficiency anode electrocatalysts for DEGFCs. Interestingly, the optimized carbon supported Pt1Cu1 NSs can display the highest mass activity of 2146.9 mA mg−1 in 1 M KOH + 1 M EG solution under the scan rate of 50 mV s−1, which is 1.9 times higher than that of commercial Pt/C catalysts. This is ascribed to the favorable electronic effect between Pt and Cu, which is beneficial for ethylene glycol oxidation reaction (EGOR) in fuel cells. Meanwhile, such monodispersed Pt1Cu1 NSs can also exhibit excellent durability, where the Pt1Cu1 catalyst retains 62.6% of the initial value after the cyclic voltammetry of 500 cycles. This work not only provides a significant approach for designing catalysts for fuel cells, but also constructs a novel class of active and stable electrocatalysts for EGOR.

Catalytic Ru containing Pt3Mn nanocrystals enclosed with high-indexed facets: Surface alloyed Ru makes Pt more active than Ru particles for ethylene glycol oxidation

Tuning the surface property of Pt based nanocrystals at the atomic level is of vital significance to meet superior electrocatalytic performance criteria. In this work, a new strategy to advance fundamental surface study on Pt based nanocrystals is addressed by implanting foreign metals as “active auxiliaries” onto the surface of Pt based nanocrystals to engineer a stable structured catalyst. Under the guidance of this concept, the Ru component was selected as “active auxiliary” to construct Ru containing Pt3Mn catalysts by doping the isolated Ru atoms (Pt3Mn–Ru) and Ru nanoparticles (Pt3Mn@Ru) onto surface layer of Pt3Mn concave nanocubes (CNCs). Strikingly, the Pt3Mn–Ru CNCs showed the most optimal catalytic activity, durability and CO anti-poisoning ability toward ethylene glycol oxidation reaction (EGOR). The specific activity of Pt3Mn–Ru CNCs is 1.32 mA cm−2, which is 1.47 and 3.07 times higher than Pt3Mn@Ru CNCs (0.90 mA cm−2) and pure Pt3Mn CNCs (0.43 mA cm−2). The results of in situ Fourier transform infrared spectroscopy experiments revealed that Pt3Mn–Ru CNCs were more in favor of CC bond cleavage of EG and rapid oxidation/removal of intermediate poisonous COads. Furthermore, the theoretical calculations revealed that the Pt3Mn–Ru CNCs possessed a lower reaction barrier (1.69 eV) for oxidation of COads assisted by adsorbed OHads species, and an energy-favorable position (2.88 Å) for reaction between COads and OHads. This work disclosed a new tactics to develop a novel structured catalyst in possession of excellent electrocatalytic performance, which provided a promising methodology for designing Pt-based nanoparticles as efficient fuel cell catalysts.

Superior liquid fuel oxidation electrocatalysis enabled by novel bimetallic PtNi nanorods

Great research attention is raised in the field of direct alcohol fuel cells due to their advantages such as potential for clean, renewability, and high energy density. However, the preparation and optimization of high-efficiency anode electrocatalysts are highly desirable yet challenging, which is an essential part in fuel cells. We thereby design a simple but efficient method and then synthesize a series of novel one dimension PtNi nanorods electrocatalysts. The as-prepared PtNi nanorods exhibit excellent electrocatalytic performance towards alcohol oxidations in alkaline medium. The Pt3Ni nanorods with optimized composition show the best mass and activity of 4601.5 mA mg−1 (11.4 mA cm−2) and 7260 mA mg−1 (18.1 mA cm−2) towards glycerol oxidation reaction and ethylene glycol oxidation reaction respectively, 4.6 (5.4) and 6.1 (7.2) times higher than commercial Pt/C catalysts. The present work in situ offers a practical synthetic approach of electrocatalysts and their better catalytic properties in alcohol oxidation reactions, which has a promoting effect for development of liquid fuel cells.

Highly efficient ethylene glycol electrocatalytic oxidation based on bimetallic PtNi on 2D molybdenum disulfide/reduced graphene oxide nanosheets

In this paper, a two-dimensional (2D) hybrid material of molybdenum disulfide (MoS2)/reduced graphene oxide (RGO) is facilely synthesized and used as an ideal support for the deposition of Pt nanoparticles. The as-prepared Pt/MoS2/RGO composites are further worked as electrocatalysts towards ethylene glycol oxidation reaction (EGOR). In addition, when alloying with Ni, the composite shows obvious enhancement in electrocatalytic performance for EGOR. Specifically, the optimized molar ratio of Pt to Ni is 3:1, namely Pt3Ni/MoS2/RGO performs the strongest current density of 2062 mA mg−1Pt, which is 11.1, 5.80 and 2.40 times higher than those of Pt, Pt3Ni and Pt/MoS2/RGO electrodes, respectively. The systematically electrochemical measurements indicate that the largely promoted electrocatalytic performances of Pt3Ni/MoS2/RGO are mainly attributed to the synergistic effect of Ni and Pt, and 2D sheets of MoS2/RGO. This excellent performance indicates that the reported electrocatalytic material could be an efficient catalyst for the application in direct ethylene glycol fuel cell and beyond.

Ultrafine two-dimensional alloyed PdCu nanosheets-constructed three-dimensional nanoflowers enable efficient ethylene glycol electrooxidation

Constructing efficient catalysts for the electrooxidation of fuels is of vital importance for realizing the commercialization of fuel cells. Unfortunately, most of catalysts (e.g. Pt) suffer from limited activity and poor durability for the electrooxidation of liquid fuel. Also, the drawbacks of extremely high cost and nature scarcity have also severely hindered their large-scale applications. Here, we demonstrated the synthesis of a new class of well-defined and three-dimensional (3D) flower-like nanocatalysts which assembled by ultrafine two-dimensional (2D) alloyed PdCu nanosheets. Structurally, the as-obtained PdCu alloy nanoflowers (NFs) possessed high surface area with abundant surface active sites. Benefiting from the unique structural properties and the strong alloy effect, the as-obtained PdCu NFs can display greatly enhanced performances toward ethylene glycol oxidation reaction (EGOR) with the mass/specific activity of 4714.1 mA mg−1/13.7 mA cm−2, which are 4.4 and 6.85 times of Pd/C catalysts, respectively. Most strikingly, such 2D nanosheets-constructed 3D nanoflower-like structure also enables the PdCu catalysts with high long-term stability for EGOR. As a proof of concept, this work not only presents the rational design and construction of catalysts with well-defined structure for the fuel cells reactions but also provides a promising method to largely promote the electrochemical performances of catalysts.

The chain-typed nanoflowers structure endows PtBi with highly electrocatalytic activity of ethylene glycol oxidation

Pursuing high-effective electrocatalysts is of paramount importance yet a great challenge, drawbacks such as irregular morphology, weak corrosion resistance, and poor anti-poisoning that limited their catalytic performance. Kinds of strategies have been developed to synthesize nanocatalysts with properties of low-cost, high-performance, and long lifetime. Pt-based catalyst is one of the most effective anodic materials for direct fuel cells (DFCs), especially towards ethylene glycol oxidation reaction (EGOR). Herein, we integrate the advantages of both composition and morphology to finally synthesize a series of PtBi chain-typed nanoflowers (NFs) serving as high-efficiency anode catalysts. The Pt1Bi1 chain-typed NFs show much higher catalytic performances than Pt1Bi2, Pt2Bi1, and commercial Pt/C catalysts with the mass activity (1.17, 1.64, and 5.71 times higher, respectively) and retained mass activities (1.68, 3.26, and 13.1 times higher, respectively). Our present work opens a new way to promote the electrocatalytic activity and stability via synthesizing well-defined PtBi NFs with chain-typed structure. We also believe that the as-obtained PtBi NFs can be one of the candidates as promising anodic catalysts in DFCs.