Peng Huang

Bio: Peng Huang is an academic researcher from Hunan University. The author has contributed to research in topics: Materials science & Electrode. The author has an hindex of 3, co-authored 5 publications receiving 48 citations.

Sub-Thick Electrodes with Enhanced Transport Kinetics via In Situ Epitaxial Heterogeneous Interfaces for High Areal-Capacity Lithium Ion Batteries.

Abstract: The ever-growing portable electronics and electric vehicle draws the attention of scaling up of energy storage systems with high areal-capacity The concept of thick electrode designs has been used to improve the active mass loading toward achieving high overall energy density However, the poor rate capabilities of electrode material owing to increasing electrode thickness significantly affect the rapid transportation of ionic and electron diffusion kinetics Herein, a new concept named "sub-thick electrodes" is successfully introduced to mitigate the Li-ion storage performance of electrodes This is achieved by using commercial nickel foam (NF) to develop a monolithic 3D with rich in situ heterogeneous interfaces anode (Cu3 P-Ni2 P-NiO, denoted NF-CNNOP) to reinforce the adhesive force of the active materials on NF as well as contribute additional capacity to the electrode The as-prepared NF-CNNOP electrode displays high reversible and rate areal capacities of 681 and 150 mAh cm-2 at 040 and 60 mA cm-2 , respectively The enhanced Li-ion storage capability is attributed to the in situ interfacial engineering within the NiO, Ni2 P, and Cu3 P and the 3D consecutive electron conductive network In addition, cyclic voltammetry, charge-discharge curves, and symmetric cell electrochemical impedance spectroscopy consistently reveal improved pseudocapacitance with enhanced transports kinetics in this sub-thick electrodes

Tailoring the cationic and anionic sites of LaFeO3-based perovskite generates multiple vacancies for efficient water oxidation

Abstract: Perovskite transition metal oxides with ABO3 structure are considered as potential alternative non-precious metal electrocatalysts for designing highly active and durable electrocatalysis for the oxygen evolution reaction (OER). Herein, we successfully enable LaFeO3 coated on nickel foam (denoted LFO@NF) perovskite with impressive OER activity by systematically tailoring the Fe cation sites and the introduction of oxygen vacancies. The cationic site involves dual cation modulation with Cr and Mo, which creates lattice distortions inducing strong electronic interaction, while the anionic site entails reduction via a hydrogen-treatment process, creating oxygen vacancy sites to improve the electronic conductivity of the perovskite oxide. As a result, the optimized LFO-based catalyst, specifically hydrogenated LaFe0.75Cr0.15Mo0.10O3-coated on the nickel foam (denoted H-LFCMO@NF), requires the lowest overpotential of 263 mV at 10 mA cm−2, and has superior kinetics and excellent stability, which are superior to its counterparts. Theoretical analysis also confirmed that the tailoring of the LFO@NF perovskite leads to an increase in the exposure of active sites, optimization of the adsorption energy of reaction intermediates and enhanced electronic conductivity. This work may provide a promising concept to enhance the performance of LFO-based perovskite electrocatalysts for alkaline OER and beyond.

Advanced trifunctional electrodes for 1.5 V-based self-powered aqueous electrochemical energy devices

Abstract: A novel 1.5 V aqueous self-powered electrochemical energy device involving the integration of asymmetric supercapacitors and overall water splitting is designed, where the phosphorus-doped NiMoO4/MoO2 electrode plays a trifunctional role in the device.

Advanced Tri-Layer Carbon Matrices with π-π Stacking Interaction for Binder-Free Lithium-Ion Storage.

Abstract: Enabling materials with distinct features toward achieving high-performance energy storage devices is of huge importance but highly challenging. Commercial carbon cloth (CC), because of its appealing chemical and mechanical properties, has been proven to be an excellent conductive substrate for active electrode materials. However, its performance is notably poor when directly used as an electrode in energy storage, due to its low theoretical capacity and surface area. Herein, we successfully endow the CC with enhanced storage capacity via formation of a π-π stacking interaction by integrating electrochemically activated CC (denoted CC/ACC) with biomass-derived carbon (BMDC) (denoted π-CC/ECC@BMDC). The π-CC/ECC@BMDC electrode displays excellent storage performance with a high capacity of 2.53 mAh cm-2 under 0.2 mA cm-2 when used as anode material for lithium ion batteries (LIBs). Due to the induction energy, the negatively charged molecules of the CC/ACC functional groups interact with the BMDC during carbonization, creating the π-π stacking interaction. Based on first-principles calculations, the structural design of the tri-layer carbon enables the movement of electrons around the π-π stacking interaction, which significantly facilitates rapid transportation of electrons, creates three-dimensional (3D) ion tunnels for fast transportation of ions, and improves the electrode's mechanical and electronic properties.

Water electrolysis: from textbook knowledge to the latest scientific strategies and industrial developments

Abstract: Replacing fossil fuels with energy sources and carriers that are sustainable, environmentally benign, and affordable is amongst the most pressing challenges for future socio-economic development. To that goal, hydrogen is presumed to be the most promising energy carrier. Electrocatalytic water splitting, if driven by green electricity, would provide hydrogen with minimal CO2 footprint. The viability of water electrolysis still hinges on the availability of durable earth-abundant electrocatalyst materials and the overall process efficiency. This review spans from the fundamentals of electrocatalytically initiated water splitting to the very latest scientific findings from university and institutional research, also covering specifications and special features of the current industrial processes and those processes currently being tested in large-scale applications. Recently developed strategies are described for the optimisation and discovery of active and durable materials for electrodes that ever-increasingly harness first-principles calculations and machine learning. In addition, a technoeconomic analysis of water electrolysis is included that allows an assessment of the extent to which a large-scale implementation of water splitting can help to combat climate change. This review article is intended to cross-pollinate and strengthen efforts from fundamental understanding to technical implementation and to improve the ‘junctions’ between the field's physical chemists, materials scientists and engineers, as well as stimulate much-needed exchange among these groups on challenges encountered in the different domains.

Oxygen Vacancy-Based Metal Oxides Photoanodes in Photoelectrochemical Water Splitting

Abstract: Photoelectrochemical (PEC) water splitting is considered as a promising technology for producing clean energy such as hydrogen. The urgent challenge in this field is how to prepare highly efficient electrode materials. The introduction of oxygen vacancies (OVs) into catalytic materials has been confirmed to be an effective strategy toward enhancing the performance of PEC water splitting by both theoretical calculations and experiment results. Herein, the existing strategies for introducing OVs into nanomaterials are discussed in this minireview. In addition, the effect of OVs on PEC water splitting to improve the light absorption efficiency, charges transfer efficiency, and charge injection efficiency was summarized. Finally, we propose several challenges that need to be addressed in the field of PEC water splitting in the future. This minireview could offer some important contributions to the future synthesis of nanomaterials with rich OVs for PEC application.