Laiquan Li

Bio: Laiquan Li is an academic researcher from University of Adelaide. The author has contributed to research in topics: Electrocatalyst & Carbon. The author has an hindex of 17, co-authored 21 publications receiving 1877 citations. Previous affiliations of Laiquan Li include Center for Advanced Materials & Nanyang Technological University.

Binary metal oxide: advanced energy storage materials in supercapacitors

Abstract: Binary transition metal oxides (BTMOs) possess higher reversible capacity, better structural stability and electronic conductivity, and have been widely studied to be novel electrode materials for supercapacitors. In this review, we present an extensive description of BTMO materials and the most commonly used synthetic methods. Furthermore, we review several notable BTMOs and their composites in application of supercapacitors. With the increasing attention for energy storage, more and more exciting results about BTMO materials will be reported in the future.

Two-dimensional mosaic bismuth nanosheets for highly selective ambient electrocatalytic nitrogen reduction

Abstract: Electrochemical fixation of N2 to ammonia is a promising strategy to store renewable energy and mitigate greenhouse gas emissions. However, it usually suffers from extremely low ammonia yield and Faradaic efficiency because of the lack of efficient electrocatalysts and the competing hydrogen evolution reaction. Herein, we report that the semiconducting bismuth can be a promising catalyst for ambient electrocatalytic N2 reduction reaction (NRR). A two-dimensional mosaic bismuth nanosheet (Bi NS) was fabricated via an in situ electrochemical reduction process and exhibited favorable average ammonia yield and Faradaic efficiency as high as 2.54 ± 0.16 μgNH3 cm–2 h–1 (∼13.23 μg mgcat.–1 h–1) and 10.46 ± 1.45% at −0.8 V versus reversible hydrogen electrode in 0.1 M Na2SO4. The high NRR electrocatalytic activity of the Bi NS could be attributed to the sufficient exposure of edge sites coupled with effective p-orbital electron delocalization in the mosaic bismuth nanosheets. In addition, the semiconducting featu...

Nitrogen Vacancies on 2D Layered W2N3: A Stable and Efficient Active Site for Nitrogen Reduction Reaction

Abstract: Electrochemical nitrogen reduction reaction (NRR) under ambient conditions provides an avenue to produce carbon-free hydrogen carriers. However, the selectivity and activity of NRR are still hindered by the sluggish reaction kinetics. Nitrogen Vacancies on transition metal nitrides are considered as one of the most ideal active sites for NRR by virtue of their unique vacancy properties such as appropriate adsorption energy to dinitrogen molecule. However, their catalytic performance is usually limited by the unstable feature. Herein, a new 2D layered W2 N3 nanosheet is prepared and the nitrogen vacancies are demonstrated to be active for electrochemical NRR with a steady ammonia production rate of 11.66 ± 0.98 µg h-1 mgcata-1 (3.80 ± 0.32 × 10-11 mol cm-2 s-1 ) and Faradaic efficiency of 11.67 ± 0.93% at -0.2 V versus reversible hydrogen electrode for 12 cycles (24 h). A series of ex situ synchrotron-based characterizations prove that the nitrogen vacancies on 2D W2 N3 are stable by virtue of the high valence state of tungsten atoms and 2D confinement effect. Density function theory calculations suggest that nitrogen vacancies on W2 N3 can provide an electron-deficient environment which not only facilitates nitrogen adsorption, but also lowers the thermodynamic limiting potential of NRR.

Tailoring Acidic Oxygen Reduction Selectivity on Single-Atom Catalysts via Modification of First and Second Coordination Spheres.

Abstract: Product selectivity in multielectron electrocatalytic reactions is crucial to energy conversion efficiency and chemical production. However, a present practical drawback is the limited understanding of actual catalytic active sites. Here, using as a prototype single-atom catalysts (SACs) in acidic oxygen reduction reaction (ORR), we report the structure-property relationship of catalysts and show for the first time that molecular-level local structure, including first and second coordination spheres (CSs), rather than individual active atoms, synergistically determines the electrocatalytic response. ORR selectivity on Co-SACs can be tailored from a four-electron to a two-electron pathway by modifying first (N or/and O coordination) and second (C-O-C groups) CSs. Using combined theoretical predictions and experiments, including X-ray absorption fine structure analyses and in situ infrared spectroscopy, we confirm that the unique selectivity change originates from the structure-dependent shift of active sites from the center Co atom to the O-adjacent C atom. We show this optimizes the electronic structure and *OOH adsorption behavior on active sites to give the present "best" activity and selectivity of >95% for acidic H2O2 electrosynthesis.

Heteroatom-Doped Transition Metal Electrocatalysts for Hydrogen Evolution Reaction

Abstract: Developing efficient and low-cost electrocatalysts for the hydrogen evolution reaction (HER) is important for clean energy systems. Non-noble transition metals are the most promising candidates for...

Graphitic Carbon Nitride (g-C3N4)-Based Photocatalysts for Artificial Photosynthesis and Environmental Remediation: Are We a Step Closer To Achieving Sustainability?

Abstract: As a fascinating conjugated polymer, graphitic carbon nitride (g-C3N4) has become a new research hotspot and drawn broad interdisciplinary attention as a metal-free and visible-light-responsive photocatalyst in the arena of solar energy conversion and environmental remediation. This is due to its appealing electronic band structure, high physicochemical stability, and “earth-abundant” nature. This critical review summarizes a panorama of the latest progress related to the design and construction of pristine g-C3N4 and g-C3N4-based nanocomposites, including (1) nanoarchitecture design of bare g-C3N4, such as hard and soft templating approaches, supramolecular preorganization assembly, exfoliation, and template-free synthesis routes, (2) functionalization of g-C3N4 at an atomic level (elemental doping) and molecular level (copolymerization), and (3) modification of g-C3N4 with well-matched energy levels of another semiconductor or a metal as a cocatalyst to form heterojunction nanostructures. The constructi...

g-C3N4-Based Heterostructured Photocatalysts

Abstract: Photocatalysis is considered as one of the promising routes to solve the energy and environmental crises by utilizing solar energy. Graphitic carbon nitride (g-C3N4) has attracted worldwide attention due to its visible-light activity, facile synthesis from low-cost materials, chemical stability, and unique layered structure. However, the pure g-C3N4 photocatalyst still suffers from its low separation efficiency of photogenerated charge carriers, which results in unsatisfactory photocatalytic activity. Recently, g-C3N4-based heterostructures have become research hotspots for their greatly enhanced charge carrier separation efficiency and photocatalytic performance. According to the different transfer mechanisms of photogenerated charge carriers between g-C3N4 and the coupled components, the g-C3N4-based heterostructured photocatalysts can be divided into the following categories: g-C3N4-based conventional type II heterojunction, g-C3N4-based Z-scheme heterojunction, g-C3N4-based p–n heterojunction, g-C3N4/metal heterostructure, and g-C3N4/carbon heterostructure. This review summarizes the recent significant progress on the design of g-C3N4-based heterostructured photocatalysts and their special separation/transfer mechanisms of photogenerated charge carriers. Moreover, their applications in environmental and energy fields, e.g., water splitting, carbon dioxide reduction, and degradation of pollutants, are also reviewed. Finally, some concluding remarks and perspectives on the challenges and opportunities for exploring advanced g-C3N4-based heterostructured photocatalysts are presented.

Towards flexible solid-state supercapacitors for smart and wearable electronics

Abstract: Flexible solid-state supercapacitors (FSSCs) are frontrunners in energy storage device technology and have attracted extensive attention owing to recent significant breakthroughs in modern wearable electronics In this study, we review the state-of-the-art advancements in FSSCs to provide new insights on mechanisms, emerging electrode materials, flexible gel electrolytes and novel cell designs The review begins with a brief introduction on the fundamental understanding of charge storage mechanisms based on the structural properties of electrode materials The next sections briefly summarise the latest progress in flexible electrodes (ie, freestanding and substrate-supported, including textile, paper, metal foil/wire and polymer-based substrates) and flexible gel electrolytes (ie, aqueous, organic, ionic liquids and redox-active gels) Subsequently, a comprehensive summary of FSSC cell designs introduces some emerging electrode materials, including MXenes, metal nitrides, metal–organic frameworks (MOFs), polyoxometalates (POMs) and black phosphorus Some potential practical applications, such as the development of piezoelectric, photo-, shape-memory, self-healing, electrochromic and integrated sensor-supercapacitors are also discussed The final section highlights current challenges and future perspectives on research in this thriving field

Spinels: Controlled Preparation, Oxygen Reduction/Evolution Reaction Application, and Beyond

Abstract: Spinels with the formula of AB2O4 (where A and B are metal ions) and the properties of magnetism, optics, electricity, and catalysis have taken significant roles in applications of data storage, biotechnology, electronics, laser, sensor, conversion reaction, and energy storage/conversion, which largely depend on their precise structures and compositions. In this review, various spinels with controlled preparations and their applications in oxygen reduction/evolution reaction (ORR/OER) and beyond are summarized. First, the composition and structure of spinels are introduced. Then, recent advances in the preparation of spinels with solid-, solution-, and vapor-phase methods are summarized, and new methods are particularly highlighted. The physicochemical characteristics of spinels such as their compositions, structures, morphologies, defects, and substrates have been rationally regulated through various approaches. This regulation can yield spinels with improved ORR/OER catalytic activities, which can furth...